Abstract
Silicon (Si) serves as bioactive beneficial element. Si is highly abundant in soil, and occurs ubiquitously in all organisms including plants and humans. During the last three decades, nutritional significance of Si for plant and human health has received increasing attention. Plant Si plays a pivotal role in growth and development, and this beneficial effect depends usually on accumulation in plant tissues, which are then protected from various forms of biotic and abiotic stresses. Likewise, human exposure to Si imparts health benefits and essentially occurs through plant-derived food products. Si bioavailability in human diet, e.g., strengthens bones and improves immune response, as well as neuronal and connective tissue health. Despite this empiric knowledge, the essentiality of Si still remains enigmatic. Thus the link between Si availability for plant development and its profound implication for human welfare should receive attention. This review aims to provide a broad perspective on Si as important element for plant and human nutrition and to define research fields for interdisciplinary research.
Introduction
Silicon (Si) is omnipresent and takes part in global biogeochemical Si cycles, both in oceans and on terrestrial areas (). Until 1960s, the essentiality of Si was best known for lower forms of life, in particular diatoms, sponges and corals. Si is required for normal cell growth and imparts structural benefits to diatoms, radiolarians, and some sponges (). However, Si also cycles between plants and the environment thereby realizing multiple functional benefits. Ferns and many monocots accumulate Si to high amounts (). Thus functional significance of Si in modulating growth performance and ameliorating stress in higher plants is widely accepted. This view is based upon a range of field and laboratory experiments indicating that Si serves manifold roles in plants (, ; Rafi and Epstein, 1999; Rains et al., 2006; Ma et al., 2011).
The ample Si supply from soil to plants exceeds uptake of essential nutrients in several species including cereals (). Plants grown under natural conditions are exposed to diverse biotic (diseases caused by viral and bacterial pathogens or fungi and herbivores) (Miyake and Takahashi, 1983; ; Savant et al., 1997) and abiotic (salinity, heat, cold, wind, water, and mineral deficiency or excess) stresses, often in combinations (Ma et al., 2001; Ma, 2004; ). Thus plants face an enormous combinatorial complexity with basically infinite environmental conditions. Si enhances physical and chemical defense power of plants (). However, beneficial effects of Si are most obvious in high Si-accumulating plant species (Ma et al., 2011). Investigation of crop species of the Si-accumulating type including cereals revealed an active mode of Si uptake and transport system, which enable them to realize the high Si requirements of their plant body (Ma et al., 2006, 2011). On the other hand, Si deficiency does not interrupt the life cycle in plants, therefore its absolute requirement and essentiality continues to be debated (Marschner, 1995). During recent years along with the growing interest of plant biologists to understand Si dependencies and anomalies in plants, the nutritional function of Si has also received attention in human biology, where equally important features have been established by now. Silica is prevalent in the typical human diet with concentrations tending to be much higher in plant based foods and has a multitude of uses, e.g., strengthen bones and connective tissues, reduces risks of alopecia, Alzheimer’s and cardiovascular diseases (Jugdaohsingh et al., 2000; Jugdaohsingh, 2007; Nielsen, 2014). Thus Si plays a significant role in modulating physiological and metabolic responses both in plant and human biology. Most of the previously published reviews focused on either aspect of nutritional significance of Si (; Wu et al., 2013; Nielsen, 2014; Zhu and Gong, 2014; Pontigo et al., 2015). There is a need for comprehensive information covering the breadth and versatility of silica. Therefore, the intent of this review is to critically evaluate both types of evidences available to support the nutritional significance of silica for plant stress tolerance and health benefits of dietary silica primarily derived from plant-based foods. The article compiles the present state of knowledge on the availability, uptake, distribution and positive potential of Si, but also shows that the molecular understanding of involved mechanisms of beneficial action still awaits clarification which is critical to fostering the much needed research at interdisciplinary level. Further, the information from this review shall be used to develop strategies to manipulate plant silica contents for enhanced plant tolerance against various kinds of environmental stresses and improved nutritional quality for human health.
Good Nutritional Diet Begins with the Soil
Silicon is the second most abundant element in the earth crust with a mean share of 28.8% (dry weight basis) () mostly ranging between 50 and 400 g Si kg-1 of soil (Kovda, 1973). Generally, Si compounds exist in different soil fractions such as solid, adsorbed or liquid phases (Sauer et al., 2006) (Figure 1a). The pre-dominant Si forms in mineral soils include silica (SiO2), and primary (e.g., quartz, feldspar, mica) or secondary (e.g., clay minerals) silicate minerals which contain Si, oxygen, and metals like Al (aluminosilicates) and Mg (talc) (; Rezanka and Sigler, 2008). SiO2 comprises up to 45% of soil mass and represents >95% of the secondary Si-enriched horizons (Summerfield, 1983). Additionally, Si compounds exist in various amorphous forms of biogenic origin such as phytoliths and silica rich plants (). The biogenic silica contributes 1–3% of total Si pool in soil ().
FIGURE 1
Weathering of silicate-containing minerals is the major source of chemical elements for terrestrial plants, and, thus for the whole nutritional chain. The mineral breakdown releases soluble silica mainly as silicic acid (H4SiO4) into the soil solution (liquid phase), surface water and other natural water bodies with variable contents of 0.1–0.6 mM. This is about twofold the average soil phosphorous contents and similar to macro-nutrients such as calcium, potassium, and sulfur (). However, the dissolved Si concentration varies considerably depending on the type of minerals and the biotic and abiotic environment (; ). Silicic acid is weakly acidic (pKa1 = 9.70 and pKa2 = 12) and below pH 9 it commonly occurs as uncharged monomeric form [(H4SiO4)o] which is the most readily absorbable form of Si in humans and plants (Weast and Astle, 1983; Knight and Kinrade, 2001; Jugdaohsingh et al., 2002; Ma et al., 2008).
Some of the released silica is adsorbed to soil minerals such as Fe and Al oxides/hydroxides () and competes with other anions for sorption sites (Figure 1a). Despite the fact that most soil reservoirs are rich in Si, plant-available Si may be limited depending on soil type and seasonal changes. Young mineral soils which are less weathered usually supply more Si than completely weathered acidic soils to the biosphere (Skjemstad et al., 1992).
Ex Planta Benefits of Silicon Relate to Abundance in Soil
Silicon release from weathering of silicate-containing minerals activates plant acclimation responses against multiple abiotic stresses. Improved stress tolerance has partly been related to silica presence in the soil inducing ex planta benefits in the rhizosphere and to the silica pool that has entered the plant body causing positive in planta effects (Figures 1b,c). Indigenous Si pools or artificial amendment of soils with silicate-containing fertilizers affect soil properties and improve availability of essential elements such as phosphorous (; ). In addition, reported that the beneficial effect of Si under phosphorous deficiency is attributed to increased levels of organic phosphoesters, thereby improved utilization of phosphorous inside plant body. Later on confirmed the correlation between phosphorous availability and Si presence outside the plant tissue and concluded that Si fertilization improves phosphate availability to plants in low phosphorous soils. Interestingly the opposite response was seen under conditions where excess phosphorous was applied. Then Si application reduced toxic effects of phosphorous by limiting its availability, and ultimately reduced chlorosis (Ma et al., 2001). Thus Si establishes a phosphorous buffer system.
Similarly, soil Si immobilizes toxic metal ions such as alumi num (Al), arsenic (As), cadmium (Cd), iron (Fe), manganese (Mn), and zinc (Zn) via complexation, ultimately removing them from the rhizosphere as insoluble precipitates (Liang et al., 2005; ; Naeem et al., 2014). For instance, Si forms complexes with Al creating inert hydroxyl-aluminosilicates (HAS) in soil solution and reduces bioavailability of toxic Al ions (; Li et al., 1996; Liang et al., 2007). In maize, Si stimulates root exudation of phenolic compounds which form complexes with Al ions and reduces their uptake by plant roots (Kidd et al., 2001). Additionally, Si in the growth media ameliorates As toxicity in rice. Both Si and As share common root uptake and transport pathway. Therefore elevated Si abundance in the soil solution reduces As uptake and subsequent accumulation in rice shoots (Ma et al., 2008). Further, exogenous application of Si increases soil pH and decreases solubility and thus availability of toxic metals. For example, addition of furnace slag as Si source in paddy field reduced Cd uptake possibly by increasing soil pH and subsequently also root to shoot translocation (Shi et al., 2005; Liang et al., 2007; Lu et al., 2014). However, an alternative explanation was proposed by who found that applied calcium silicate reduced Cd and Zn concentrations in maize shoots by changing metal ion speciation in the soil solution without affecting soil pH. Similarly, the beneficial effect of Si application to reduce Mn toxicity is attributed to enhanced Mn deposition in the cell wall and hence reduced uptake in the cytoplasm (Rogalla and Romheld, 2002; Wiese et al., 2007). Likewise, Ma and Takahashi (2002) found that Si application reduced Fe toxicity in rice. Under such conditions, oxidative activity of rice roots increased by Si fertilization, thereby stimulating conversion of Fe2+ (ferrous; soluble form) to Fe3+ (ferric; insoluble form). This process resulted in the precipitation of Fe in the growth media or at the root surface (iron plaque; ) and ultimately reduced Fe uptake and toxicity in plants. All these reports highlight the importance of bioactive silica in soil reservoirs which interact with toxic metals and reduce their availability by increasing soil pH, metal immobilization in the growth media and also by changing metal distribution inside the plant.
Contrarily, the beneficial role of Si under metal deficiency conditions has also been recently assessed in several plant species (; Pavlovic et al., 2013; ). Generally, immobilized metal pools formed under both metal toxic and non-toxic conditions are known to serve as source for plant nutrition through remobilization during micronutrient deficiency periods (; ; Waters et al., 2009). As discussed above, the formation of Fe, Mn, and Zn deposits in the cell wall of roots by the application of Si under metal toxic conditions provide general evidence in this regard (Rogalla and Romheld, 2002; Wiese et al., 2007; ; ). However, the effect of Si addition was further investigated under Fe deficiency in cucumber and soybean (; Pavlovic et al., 2013; ). The results demonstrated that total plant Fe contents did not improve significantly by pre-application of Si during sufficiency period, while more Fe accumulated in roots of Si-treated cucumber and soybean plants, owing to its precipitation at the root surface and high Fe accumulation in the root apoplast (Pavlovic et al., 2013). Subsequently, root Fe apoplastic pool decreased dramatically after the first day of Fe deficiency until complete depletion of Fe in the root apoplastic pool within next 5 days. In contrast, Fe concentration in the xylem sap and its subsequent distribution in plant body improved significantly by the supplementation of Si to Fe-deficient plants. Under such conditions, citrate production in xylem sap, root, and leaf tissues of Si-treated cucumber plants increased significantly, thereby facilitating long distance transport of Fe through the xylem and improving utilization in leaves (Rellán-Alvarez et al., 2010; Pavlovic et al., 2013; ). Apparently Si application promotes Fe storage in the root apoplast during sufficiency/excess toxicity periods. Fe remobilization during deficiency periods seems to be the main factor contributing to the beneficial effect of Si under Fe deficiency conditions. Similarly under Mn and Zn toxicity, enhanced metal immobilization in root cell wall due to presence of Si are reported in several studies (; ), while little is known about their occurrence under normal growth conditions and the beneficial role of Si in their remobilization when required (). Nevertheless under Zn deficiency, production of citrate increased in roots of Si-treated cucumber plants which could improve Zn distribution as described before for Fe-deficient plants (). However, further research efforts coupled with advanced methodological approaches are required to evaluate the potential of Si in alleviation of micronutrient deficiency in crop plants.
From Soil to Plant: Silicon uptake and Transport Mechanisms
Plants accumulate silica to 0.1–15% of their dry weight. The degree of accumulation depends on uptake and transport mechanisms which differ significantly between species (Takahashi et al., 1990; Ma et al., 2001). Strong genotypic differences are reported even within species. Following the discovery of Si transporters in rice, over 500 plant species have been studied for their Si uptake and transport mechanisms and were placed into different categories depending on their silica contents (Ma and Takahashi, 2002). Among them, monocots such as rice, wheat, maize and barley are categorized as Si accumulators due their very high silica contents (10–15%) (; Ma and Yamaji, 2015). Interestingly other monocots including also distinct members of the orders of Poales and Aricales and most dicots accumulate less than 0.5% Si in dry mass (Neumann, 2003; Ma et al., 2008). Thus at least for Si-accumulators the Si uptake exceeds that of macronutrients essential for plant growth and development.
Silicic acid (H4SiO4) dissolved in the soil solution is taken up by plant roots as an uncharged monomeric molecule below pH 9 and subsequently transported through the roots either actively in an energy-dependent process or passively (energy-independent process) which occur against and down an (electro-)chemical potential gradient, respectively. The active mode of uptake is mostly dominant in certain monocots such as rice, wheat, maize and barley (Takahashi et al., 1990; Ma et al., 2001, 2006, 2007a, 2011; Mitani et al., 2009) and is characterized by the presence of influx and efflux transporters regulating optimum supply of Si to different plant tissues. For example in rice, a channel type influx transporter named Lsi1 (Low Si 1) mediates passive transport of Si across the plasma membrane between the external solution and the plant cells (Figure 2A). Lsi1 displays high sequence similarity with nodulin-26 like intrinsic proteins (NIP), a subfamily of plant aquaporins and is mainly localized in mature plant roots at the distal side of both exodermis and endodermis, where apoplastic barriers decrease free diffusion or mass flow (Ma et al., 2006) (Figure 2A). Although Lsi1 is a bidirectional passive channel, it functions as an influx transporter of Si in plant, because it cooperates with the efflux Si transporter named Lsi2 which is driven by the proton gradient across the plasma membrane (Ma and Yamaji, 2015). In contrast to Lsi1, Lsi2 facilitates active transport of Si out of the plant cells and is localized to the proximal sides of exodermis and endodermis and belongs to a family of putative anion transporters (Ma et al., 2007b). Therefore once absorbed by plant roots, subsequent silica transport from root cortex to stele is carried out by high affinity efflux transporter called Lsi2 (Low Si2). Subsequently, Si as silicic acid is transported to the shoots via the transpiration stream in xylem. A transporter responsible for xylem loading of Si has not been identified yet. However, a transporter named Lsi6 (Low Si6) was localized at the adaxial side of xylem parenchyma cells of leaf blades and leaf sheaths and found responsible for xylem un-loading (Yamaji et al., 2008). It also mediates preferential distribution of silicic acid to panicles by controlling inter-vascular transport in nodes (Yamaji and Ma, 2009). Until recently, many plant species such as rice, maize, barley, and wheat, and also recently some dicots like soybean and pumpkin have been studied and identified with efficient Si uptake and transport system (Mitani et al., 2009, 2011a,b; ; Montpetit et al., 2012; ). Plants with active uptake mechanism significantly decrease the free silica concentration of the soil solution. And in most of them, a major proportion of absorbed silica is translocated to above ground plant tissues where inorganic amorphous oxides of silica cristallize upon loss of water and accumulate extracellularly or intracellularly in plant body as solid silica bodies, silica cells or phytoliths [phyto means plant and Greek word lithos means rock] (Ma and Yamaji, 2006) (Figure 2B). According to an estimate, as much as 90% of total Si uptake are deposited in the cell wall of hulls and leaf epidermal cells and constitute up to 10% of dry weight in grass shoots (Yoshida, 1965; Ma and Takahashi, 2002; Raven, 2003). Other cellular compartments such as short and long cells of leaf epidermis, bulliform cells and dumbbell-shaped cells also contain silica. Intracellular accumulation of silica in cell cytoplasm and vacuole is generally stable even after plant decomposition and are found abundantly in soils with variable but distinct shapes like boats, bowls, dumbells, saddels etc. (Piperno, 1988; Lins et al., 2002) (Figure 2B).
FIGURE 2
Silicon in Plants: the Stress Reliever
Until the advent of accumulating dioxygen about two billion years ago, the evidence of life involvement in the processing of silicic acid to biogenic forms such as phytoliths is totally lacking. However, today, plants and other biological organisms are known to incorporate silica in amounts of gigatons per year (Piperno, 1988). Biological membranes display a basal permeability to silicic acid (permeability coefficient ∼10-10 m s-1; Raven, 2001). Silicic acid moves across the membranes by dissolving in the lipid phase of the membrane in a process called ‘lipid solution’ transport (Raven, 2001). As a small, uncharged, monomeric molecule, silicic acid closely mimics water in its movement into and out of biota (). However, the uptake and distribution of silicic acid by plants is increased many folds by the presence of different type of influx and efflux transporters (Ma and Yamaji, 2015). As pointed out above, absolute requirement and essentiality of Si for plants is still debated despite its extraordinary abundance in the earth and high biological availability. Most current knowledge about the utility of Si comes from biosilicifier species, in which silicic acid is deposited as amorphous silica (Perry, 2009). In general, biochemical functions of Si for plants can be attributed to aqueous silicic acid and physical functions to silica accumulated in solid form such as phytoliths.
Insight into Si functions in plant biology emerges from agricultural experiments conducted on higher plants, where Si supplementation significantly ameliorated a range of biotic and abiotic stress symptoms (Figure 1c). Therefore, use of silicate-containing fertilizers in agricultural crop production system is increasingly practiced to improve plant performance by alleviating stresses (). It should be noted that Si-free growth of plants is difficult to realize due to Si contaminations in glassware, water and chemicals. Thus most studies compare highly Si-depleted growth conditions with Si-enriched conditions.
Biotic Stresses
Silicon alleviates detrimental effects of biotic stresses through a range of mechanisms, including the production of anti-bacterial and antifungal compounds as a broad response against pathogen attack (). For instance, Si-induced resistance to powdery mildew in wheat and to blast in rice is attributed to enhanced production of antifungal compounds called phytoalexins (Rodrigues et al., 2003; Remus-Borel et al., 2005). Additionally, deposition of silica at the site of attack also reduces fungal and pathogen damage, owing to surface hardness which deters pathogen penetration (Piperno, 1988). reported that application of Si in bitter gourd, a moderate Si-accumulator, reduced the spread of root rot pathogen, but not in tomato, a low Si-accumulator. This indicates that fitness benefits involving Si vary between plant groups depending on Si-uptake and deposition mechanisms, potentially giving some plants an adaptive advantage in a diverse system.
Deposition and concentration of silica bodies in plant tissues such as wood, leaves and seed coats increase strength and rigidity of cell walls and provide resistance against herbivory attack, owing to their ability to wear down tooth enamel and ultimately compromised growth and reproduction of herbivore due to reduced nutrient and carbohydrate acquisition. Therefore silicate fertilization correlates with efficient defense mechanisms against feeding guilds by reducing palatability and digestibility of plants tissues (Skinner and Jahren, 2004; MacFadden, 2005). reported that leaf silicification is induced upon herbivory attack, with response patterns that were specific to herbivore type and the amount of damage sustained. For example, in areas under intensive grazing, silicification of grasses was reported to be greater (McNaughton et al., 1985).
Abiotic Stresses
Silicon application also counteracts various kind of abiotic stresses including physical stress (drought, lodging, low and high temperature, UV light) and chemical stress (heavy metal and salinity) (Ma et al., 2006; Liang et al., 2007; Li et al., 2008) (Figure 1c). As described above, strengthened physical defense is attributed to presence of silicified structures called phytoliths or silica bodies. Increased thickness of leaf surfaces due to silica deposition underneath the cuticle reduces water loss by transpiration under drought stress (). Similarly, silica bodies accumulating in cell vacuoles reduce crop damage due to lodging, or improve light capture characteristics by keeping leaf blades erect, thus aiding photosynthetic process (Ma et al., 2011). In addition, silica bodies reduce leaf heat-load through efficient far-infrared thermal emission of silica providing a passive cooling mechanism under conditions of high solar irradiation (Wang et al., 2005).
The presence of silicic acid in dissolved form increases plant tolerance against salinity and metal ions such as Zn, Al, Mn, and Cd and is accompanied by increased activities of enzymatic antioxidants such as superoxide dismutase (SOD) and catalase, and non-enzymatic antioxidant (ascorbate) and reduced rate of lipid peroxidation (Neumann and zur Nieden, 2001; Zhu et al., 2004; Shi et al., 2005; Moussa, 2006). It should be noted that these observations describe secondary effects of the beneficial action of Si but unlikely address the primary mechanisms. Likewise, increased deposition of Si in plant roots reduces apoplastic flow and uptake of toxic metals (Ma et al., 2011).
The results summarized so far indicate that optimizing silica content in plants might be a promising strategy to increase general tolerance against multiple biotic and abiotic stresses. Frequently, the studies provide convincing but more descriptive evidence for the beneficial effect of Si and assess accompanying phenomena such as strengthened antioxidant defense and lowered oxidative damage. However, the molecular mechanisms of Si-dependent fortification against the stresses await elucidation, e.g., Si-dependent regulation of intracellular ion homeostasis or elevated chaperone levels. Future studies should take advantage of available genome-wide methods such as transcriptomics and proteomics to address changes in an untargeted manner and kinetically dissect first transcriptional responses and subsequently identify involved primary signaling and important metabolic pathways in combinatory stress experiments.
Potential of Phytoliths for Carbon Sequestration
The industrial and technical revolution seriously threatens stability of the global climate due to increasing load of the atmosphere with CO2 and global warming. Plants play a fundamental role in the regulation of atmospheric CO2, and studies have established a significant relationship between silicate weathering and CO2 consumption (Li et al., 2011; Song et al., 2011). The high nutrient requirement of vascular plants is covered by active mobilization of nutrient reserves. This is achieved by root-induced acidification, activation of chelation mechanisms and shifts in ion exchange equilibria. All these processes alter the soil physical properties and cause a continued soil development which accelerates the process of silicate weathering. As a result, CO2 is consumed in a reaction where silicic acid is released during the breakdown of calcium and magnesium containing silicate minerals (Struyf et al., 2009). reported that annually 0.104 Gt carbon is consumed during the process of silicate weathering which indicates a crucial role of plants in the terrestrial biogeochemical cycles of Si with significant implications on the global carbon cycle (Serna and Fenoll, 2003). Inside the plant body, silicic acid is polymerized to form silica bodies/phytoliths which encapsulate carbon macromolecules and cellular organelles such as plastids and mitochondria. These phytoliths are entrapped within cell vacuole (Piperno, 1988; Raven et al., 1999; Ma, 2003; Neumann, 2003; ). Phytolith morphologies can be diagnostic of plant species (Piperno, 1988) and usually consist of 66–91% silica, but also 1–6% occluded carbon, iron and aluminum (Wilding, 1967; Parr et al., 2010). After decay of the organic plant matter, phytoliths are released into the soil and may remain stable for many years, thereby increasing the chemical and physical protection of organic carbon. However, these properties greatly vary with phytolith composition, soil chemistry, and climatic factors (; ). According to an estimate, phytoliths mediate carbon sequestration of Si-accumulating crop species and bamboo in the range of approximately 1.5 billion ton-equivalents-CO2 per year, which equates to sequestering 11% of the current increase in atmospheric CO2 (Parr et al., 2010).
Silicon in Humans
In recent years, research focuses on the effects of silica on human health, in contrast to prior research which focused solely on nutritional significance of Si for plant growth and development. Plant-based foods, however, are the major contributor to dietary silica, or Si. This includes cereal grains and grain products, vegetables and beverages (Table 1; detail discussed in the next section) (Pennington, 1991; Powell et al., 2005). Circumstantial evidence for the essentiality of Si in animals, the presence of silica in most cells and in primitive organisms such as bacteria, viruses, and fungi suggest that silica may have a desirable or even an essential role in all organisms (Schwarz and Milne, 1972; Iler, 1979). Si is actively up-taken and transported by diatoms, algae, and sponges and is essential for their survival and replication (Werner, 1977; Iler, 1979). In 1972, Si deprivation experiments by Carlisle and in parallel Schwarz and Milne on growing chicks and rats suggested that dietary Si is essential for the normal growth of chicks and rats. Si deficiency in their diet caused abnormal tissue growth, particularly of collagenous tissues such as skull and peripheral bones, joints, hair, and skin. Both studies suggest that silica may also be essential for higher animals, including humans. They mark the beginning of bio-Si research and its significance for human health, especially in orthopedics (; Kokubo et al., 2004; Jugdaohsingh, 2007). Globally, osteoporosis is a growing health problem which is caused by low mass and increased fragility of bones, and leads to severe disabilities and elevates mortality rates. Annual costs of treating osteoporosis exceeds one billion pounds in countries like UK and requires cogent, long-term preventive strategy (; McClung, 2003). Subsequently, many human nutritionists focused on the understanding of dietary importance of Si on bone health. Relevant data on Si sources for human intake and associated health-associated benefits are compiled in the next sections.
Table 1
Dietary Si sources and their contribution for human intake.
NA, no data available.
Dietary Silicon Sources Reveal Major Contribution of Plants
Ubiquitous presence of Si in soil and plants provide the major dietary source of silica to the human body (Figure 1d). Si is the most abundant trace element in humans after Fe and Zn (; Solomons, 1984; Wedepohl, 1995). The water soluble forms of silica such as orthosilicic acid is the main source for absorbed Si in humans and is associated with several health benefits related to structure and function of blood vessels, bones, kidney, liver, skin, and tendons etc. (Reffitt et al., 2003; Powell et al., 2005; Jugdaohsingh, 2007; Nielsen, 2014) (Figure 1e). As in plants, Si nutrition imparts several growth benefits particularly under stress conditions, but its biological role still remains an enigma. Si is still not considered as essential element despite accumulating evidence revealing a strong link between Si deficiency and bone deformities, reduced collagen contents, joint problems and improper mineral balance in femur and vertebrae (; Schwarz and Milne, 1972; Seaborn and Nielsen, 2002). Major dietary Si requirement of human body is fulfilled by cereals such as rice, wheat, oat and barley (30%), followed by fruits (particularly banana and apple), vegetables (e.g., potato, beet roots, carrot, green beans, and reddish), beverages (alcoholic, hot, and cold combined) and some nuts and dried fruits such as raisins etc. (Pennington, 1991; Jugdaohsingh, 2007). Collectively, these foods provide >75% of the dietary Si intake (McNaughton et al., 2005). However, it is noteworthy that refinement of grains remove Si during the process but silica-derived food additives can replace the stripped Si and increase the content (Pennington, 1991). However, grain products such as breakfast cereals, rice, cake, biscuits, pasta, flour, and bread etc., are still high dietary sources of Si (Varo et al., 1980a,b,c; Pennington, 1991; Powell et al., 2005; Table 1). Other sources of Si include animal and fish meat, milk, eggs (Nielsen, 1974; Nuurtamo et al., 1980; Varo et al., 1980c; ), drinking water, fruit juices, alcoholic beverages, and even many pharmaceutical products such as capsules, gels, solutions, and tablets contain Si as supplement such as aluminum and magnesium silicates (Lomer et al., 2004; Powell et al., 2005). Several other products of daily use such as tooth paste, cosmetics, creams, and shampoos also contain Si but rather in inactive form. In some other cases, exposure to Si via dust and soil adhered to vegetables also fulfill silica requirement, but to minor extent due to low digestibility (Jugdaohsingh, 1999; Jugdaohsingh et al., 2002). As reported above, seed grains of cereals contain very high levels of silica, e.g., breakfast cereals and beer prepared from barley malt (Pennington, 1991; Sripanyakorn et al., 2004). But silica levels in dietary products decrease during industrial processing and along with the increasing trend to growing vegetables in hydroponic media omitting Si addition (; Sripanyakorn et al., 2004). Similarly, Si levels in drinking water vary with water source geology and water treatment processes reduce soluble Si contents (Perry and Keeling-Tucker, 1998). Daily Si intake can be categorized based on several reports from different regions of the world which results in the ranking of USA < other Western countries < Japan < China < India (Teraoka et al., 1981; ; ; Jugdaohsingh et al., 2002). The very high silica intake per person and day in India might be due to the predominant rice diet which greatly depends on personal dietary habits.
Significance of Silica in Human Nutrition
In the last four decades, numerous studies have reported the beneficial effects of Si for human health (Figure 1e). It is estimated that human daily intake of Si as silicic acid ranges from 9 to 14 mg, while intakes near 25 mg/d might promote bone health. Initial experiments about nutritional significance of Si for human health were performed by Schiano et al. (1979), who found a significant increase in trabecular bone volume by using monomethyl trisilanol as an external silica source. Recent epidemiological experiments have reported that Si is involved in several biochemical functions including bone and connective tissue metabolism. Si is necessary for biosynthesis of collagen and glycosaminoglycan which are required for organic bone matrix formation (; ). Evidence of dietary silica intake and its subsequent absorption, transport, retention, and excretion indicates that Si levels are well regulated in humans. Jugdaohsingh et al. (2002) reported that use of silica enriched food and drinks increases its absorption as well as consumption by human body. About 41% of the absorbed silica from food is excreted in urine while its concentration in the blood serum remains constant (10–31 μg/dL). Over a range of dietary intake the major part is retained in connective tissues, including bone, skin, trachea, and tendon, with another fraction being transferred to the brain (; Jugdaohsingh, 2007; Robberecht et al., 2009). Prolonged intake of diets low in silica causes skull and bone disabilities in humans (). Likewise, low Si levels in drinking water increase the risk of cognitive impairment due to high aluminum (Al) intake (Jacqmin-Gadda et al., 1996). Silicic acid forms complexes with aluminum hydroxide. The resulting aluminosilicates decrease the availability of free Al, hence prevents the occurrence of neurodegeneration in the brain (). In order to prevent risks of developing Al-induced Alzheimer’s disease, use of silica rich water with concentrations ≥11 mg/L is recommended (). The presence of Si increases the absorption and utilization of other mineral elements such as magnesium and copper (; Kikunaga et al., 1991). Additionally, suggested that Si plays a role in regulating the cell cycle of lymphocytes which ultimately affect the immune and inflammatory response. As in plants, Si is involved in signal transduction because it binds to hydroxyl groups of proteins (Rezanka and Sigler, 2007). It may be assumed that similar mechanisms of action improve mental health, immune and inflammatory response, and gene expression of factors involved in osteoblastogenesis and osteoclastogenesis.
Conclusion and Future Prospects
The beneficial action of Si on cell physiology and stress acclimation-related processes is well established. Independent principle mechanisms likely contribute to the positive effects of Si: (i) Si at high concentrations changes physicochemical properties which affect solubility, binding and sequestration of other elements ex planta and in planta. Examples of this kind of effect have been described above. The challenge is to transfer and predict such processes for the cellular environment. More detailed subcellular compartmentation analyses combined with modeling of speciation may provide access to better understanding such processes. (ii) Si may bind to proteins such as effector proteins and receptors or compete with other binding processes in the cell or on the cell surface. The proof of concept comes from synthetic 12-mer peptides that could be selected from a phage display screening and efficiently bound to silicon surfaces (). Likewise the existence of Si transporters demonstrates specificity of silica recognition and transport (Ma et al., 2006, 2007b; Yamaji et al., 2008). Thus it appears timely to initiated Si metallomics screenings to identify high affinity Si binding entities and to analyze the role of identified candidates. (iii) Interference of Si with other cell processes by virtue of its high concentrations but with low affinity unlikely will be accessible by proteomic search for Si binding partners. Identification of indirect effects using omics technologies such as RNA profiling may be expected to provide circumstantial evidence for involved processes. Here a new type of experiment needs to be considered where stressed plants are supplemented with beneficial Si. The kinetics of the cell and tissue recovery responses at high time resolution may provide novel insight and dissect the order of involved processes. In rice addition of Si to Cd-stressed plants revealed full recovery of the stressed plant and separated fast and slow processes proving the potential of kinetic recovery experiments. These three strategies should also be employed for animal and human cell lines and experimental systems with vertebrates in order to improve our understanding of Si-dependent signaling and regulation in vertebrates.
Further, the increasing evidence of significance of silica nutrition for human health, mainly contributed by plant-based foods, suggests timely initiation of new concept of Si-bio-fortification of crop plants. Despite being among the most abundant elements on earth, silicates do not provide bioavailable dietary Si. In fact, phytolithic silica occurring in plants is often associated with polysaccharide/carbohydrate components of the cell wall and is only absorbed at 1–20% depending on the food source (Martin, 2007). Further, high levels of Si are found in unrefined grains such as wheat, oat, rice, and barley bran (Jugdaohsingh, 2007). Therefore, in order to improve the silica contents in the edible plant parts (Si-biofortification), two strategic approaches are proposed, namely (i) increasing silica bioavailability by reducing the anti-nutritional factors and favoring or increasing expression of nutritional factors. In recent years, the scientific community has published several studies related to the possibility of enriching micronutrients in the plant, using soil-less system as a tool for biofortification; (ii) enhancing nutritional quality of plant-based foods by applying molecular breeding tools as a strategy for modifying the content of silica in the edible parts of the plant.
A word of caution is needed, when just looking on a single trait like Si accumulation in context of improvement of Si nutrition in food and feed: Si transporters facilitate arsenite transport (Moore et al., 2011). Arsenite accumulation is not a preferable trait due to its toxicity to animals and humans. Si transporters are receiving attention since downregulation of Lsi transporters might be exploited as strategy to reduce As accumulation in rice (Moore et al., 2011). This example shows the delicate balance in nutrient homeostasis, here between Si enrichment and As avoidance, and that any change in single components intended to improve performance should be considered for possible side effects under other environmental conditions.
Statements
Acknowledgments
The financial support by Higher Education Commission (HEC) of Pakistan and German Academic Exchange Service (DAAD) during the study period is gratefully acknowledged. We acknowledge the financial support of the German Research Foundation (DFG) and the Open Access Publication Fund of Bielefeld University for the article processing charge.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
References
1
AlexandreA.MeunierJ. D.ColinF.KoudJ. M. (1997). Plant impact on the biogeochemical cycle of silicon and related weathering processes.Geochim. Cosmochim. Acta61677–682. 10.1016/S0016-7037(97)00001-X
2
AnusuyaA.BapuraoS.ParanjapeP. K. (1996). Fluoride and silicon intake in normal and endemic fluorotic areas.J. Trace Elements Med. Biol.10149–155. 10.1016/S0946-672X(96)80025-3
3
Basile-DoelschI.MeunierJ. D.ParronC. (2005). Another continental pool in the terrestrial silicon cycle.Nature433399–402. 10.1038/nature03217
4
BienfaitH. F.VandenbrielW.MeslandmulN. T. (1985). Free space iron pools in roots generation and mobilization.Plant Physiol.78596–600. 10.1104/pp.78.3.596
5
BityutskiiN.PavlovicJ.YakkonenK.MaksimoviV.NikolicM. (2014). Contrasting effect of silicon on iron, zinc and manganese status and accumulation of metal mobilizing compounds in micronutrient-deficient cucumber.Plant Physiol. Biochem.74205–211. 10.1016/j.plaphy.2013.11.015
6
BleckerS. W.McCulleyR. L.ChadwickO. A.KellyE. F. (2006). Biologic cycling of silica across a grassland bioclimosequence.Global Biogeochem. Cycles201–11. 10.1029/2006GB002690
7
BowenH. J. M.PeggsA. (2006). Determination of the silicon content of food.J. Sci. Food Agric.351225–1229. 10.1002/jsfa.2740351114
8
BrenchleyW. E.MaskellE. J.KatherineW. (2008). The inter-relation between silicon and other elements in plant nutrition.Ann. Appl. Biol.1445–82. 10.1111/j.1744-7348.1927.tb07005.x
9
BriatJ. F.Fobis-LoisyI.GrignonN.LobreauxS.PascalN.SavinoG.et al (1995). Cellular and molecular aspects of iron metabolism in plants.Biol. Cell8469–81. 10.1016/0248-4900(96)81320-7
10
CarlisleE. M. (1972). Silicon: an essential element for the chick.Science178619–621. 10.1126/science.178.4061.619
11
CarlisleE. M. (1981). Silicon: a requirement in bone formation independent of vitamin D1.Calcif. Tissue Int.3327–34. 10.1007/BF02409409
12
CarlisleE. M. (1988). Silicon as a trace nutrient.Sci. Total Environ.7395–106. 10.1016/0048-9697(88)90190-8
13
CarlisleE. M. (1997). “Silicon,” inHandbook of Nutritionally Essential MineralsedsO’DellB. L.SundeR. A. (New York, NY: Marcel Dekker) 603–618.
14
CarterJ. A. (2009). Atmospheric carbon isotope signatures in phytolith-occluded carbon.Q. Int.19320–29. 10.1016/j.quaint.2007.11.013
15
ChenF.ColeP.WenL. (1994). Estimates of trace element intakes in Chinese farmers.Commun. Int. Nutr.124196–201.
16
CheongY. W. Y.ChanP. Y. (1973). Incorporation of P32 in phosphate esters of the sugar cane plant and the effect of Si and Al on the distribution of these esters.Plant Soil38113–123. 10.1007/BF00011221
17
CherifM.AsselinA.BelangerR. R. (1994). Defence responses induced by soluble silicon in cucumber roots infected by Pythium spp.Phytopathology84236–242. 10.1094/Phyto-84-236
18
ChibaY.MitaniN.YamajiN.MaJ. F. (2009). HvLsi1 is a silicon influx transporter in barley.Plant J.57810–818. 10.1111/j.1365-313X.2008.03728.x
19
ChristodoulouC.CooperC. (2003). What is osteoporosis?Postgrad. Med. J.79133–138. 10.1136/pmj.79.929.133
20
CidM. S.DetlingJ. K.BrizuelaM. A.WhickerA. D. (1989). Patterns in grass silicification: response to grazing history and defoliation.Oecologia80268–271. 10.1007/BF00380162
21
CornelisJ. T.DelvauxB.GeorgR. B.LucasY.RangerJ.OpfergeltS. (2011). Tracing the origin of dissolved silicon transferred from various soil-plant systems towards rivers: a review.Biogeoscience889–112. 10.5194/bg-8-89-2011
22
CurrieH. A.PerryC. C. (2007). Silica in plants: biological, biochemical and chemical studies.Ann. Bot.1001383–1389. 10.1093/aob/mcm247
23
da CunhaK. P. V.do NascimentoC. W. A.da SilvaA. J. (2008). Silicon alleviates the toxicity of cadmium and zinc for maize (Zea mays L.) grown on a contaminated soil.J. Plant Nutr. Soil Sci.171849–853. 10.1002/jpln.200800147
24
DatnoffL. E.SnyderG. H.KorndörferG. H. (2001). Silicon in Agriculture.Amsterdam: Elsevier.
25
DeshmukhR.VivancosJ.GuerinV.SonahH.Labbe´C.BelzileF.et al (2013). Identification and functional characterization of silicon transporters in soybean using comparative genomics of major intrinsic proteins in Arabidopsis and rice.Plant Mol. Biol.83303–315. 10.1007/s11103-013-0087-3
26
DesplanquesV.CaryL.MouretJ. C.TrolardF.BourriéG.GraubyO.et al (2006). Silicon transfers in a rice field in Camargue (France).J. Geochem. Explor.88190–193. 10.1016/j.gexplo.2005.08.036
27
DietzelM. (2002). “Interaction of polysilicic and monosilicic acid with mineral surfaces,” inWater–Rock InteractionedsStoberI.BucherK. (Dordrecht: Kluwer) 207–235.
28
DobbieJ. W.SmithM. J. (1982). The silicon content of body fluids.Scott. Med. J.2717–19.
29
DomingoJ. L.GómezM.ColominaM. T. (2011). Oral silicon supplementation: an effective therapy preventing oral aluminum absorption and retention in mammals.Nutr. Rev.6941–51. 10.1111/j.1753-4887.2010.00360.x
30
DraycottA. P. (2006). Sugar Beet. World Agriculture Series.Oxford: Blackwell Publishing.
31
EmerickR.Kayongo-MaleH. (1990). Silicon facilitation of copper utilization in the rat.J. Nutr. Biochem.1487–492. 10.1016/0955-2863(90)90086-Z
32
EnejiA. E.InanagaS.MuranakaS.LiJ.HattoriT.AnP.et al (2008). Growth and nutrient use in four grasses under drought stress as mediated by silicon fertilizers.J. Plant Nutr.31355–365. 10.1080/01904160801894913
33
EpsteinE. (1994). The anomaly of silicon in plant biology.Proc. Natl. Acad. Sci. U.S.A.9111–17. 10.1073/pnas.91.1.11
34
EpsteinE. (1999). Silicon.Ann. Rev. Plant Physiol. Plant Mol. Biol.50641–664. 10.1146/annurev.arplant.50.1.641
35
EpsteinE. (2009). Silicon: its manifold roles in plants.Ann. Appl. Biol.155155–160. 10.1111/j.1744-7348.2009.00343.x
36
EstephanE.SaabM. B.AgarwalV.CuisinierF. J. G.LarroqueC.GergelyC. (2011). Peptides for the biofunctionalization of silicon for use in optical sensing with porous silicon microcavities.Adv. Funct. Mater.212003–2011. 10.1002/adfm.201002742
37
ExleyC. (2009). “Silicon in life: whither biological silicification?,” inBiosilica in Evolution, Morphogenesis, and Nano-biotechnologyedsMuellerW. E. G.GrachevM. A. (Berlin: Springer) 173–184.
38
FarmerV.DelbosE.MillerJ. D. (2005). The role of phytolith formation and dissolution in controlling concentrations of silica in soil solutions and streams.Geoderma12771–79. 10.1016/j.geoderma.2004.11.014
39
FarooqM. A.SaqibZ. A.AkhtarJ. (2015). Silicon-mediated oxidative stress tolerance and genetic variability in rice (Oryza sativa L.) grown under combined stress of salinity and boron toxicity.Turk. J. Agric. For.39718–729. 10.3906/tar-1410-26
40
FischerR. A. (1929). A preliminary note on the effect of sodium silicate in increasing the yield of barley.J. Agric. Sci19132–139. 10.1017/S0021859600011217
41
FuY. K.ShenH.WuW. M.CaiK. Z. (2012). Silicon mediated amelioration of Fe toxicity in rice (Oryza sativa L.) roots.Pedosphere22795–802. 10.1016/S1002-0160(12)60065-4
42
GaillardetJ.DupreB.LouvatP.AllegreC. J. (1999). Global silicate weathering and CO2 consumption rates deduced from the chemistry of large rivers.Chem. Geol.1593–30. 10.1016/S0009-2541(99)00031-5
43
Gillette-GuyonnetS.AndrieuS.NourhashemiF.de La GuéronnièreV.GranjeanH.VellasB. (2005). Cognitive impairment and composition of drinking water in women: findings of the EPIDOS study.Am. J. Clin. Nutr.81897–902.
44
GonzaloM. J.LucenaJ. J.Hernández-ApaolazaL. (2013). Effect of silicon addition on soybean (Glycine max) and cucumber (Cucumis sativus) plants grown under iron deficiency.Plant Physiol. Biochem.70455–461. 10.1016/j.plaphy.2013.06.007
45
GrebennikovE. P.SorokaV. R.SabadashE. V. (1964). Trace elements in human and animal milk.Fed. Proc. Transl. Suppl.23:T461.
46
GuH. H.ZhanS. S.WangS. Z.TangY. T.ChaneyR. L.FangX. H.et al (2012). Silicon-mediated amelioration of zinc toxicity in rice (Oryza sativa L.) seedlings.Plant Soil350193–204. 10.1007/s11104-011-0894-8
47
GuntzerF.KellerC.MeunierJ. D. (2012). Benefits of plant silicon for crops: a review.Agron. Sustain. Dev.32201–213. 10.1007/s13593.011-0039.8
48
HaghiriR. (1964). Strontium-90 accumulation by some vegetable crops.Ohio J. Sci.64371–374.
49
HeineG.TikumG.HorstW. J. (2007). The effect of silicon on the infection by and spread of Pythium aphanidermatum in single roots of tomato and bitter gourd.J. Exp. Bot.58569–577. 10.1093/jxb/erl232
50
HenchL. L.WilsonJ. (1986). “Biocompatibility of silicates for medical use,” inSilicon BiochemistryedsEveredD.ConnorM. O. (Chichester: John Wiley and Sons Ltd.) 231–246.
51
HenrotteJ. G.VizaD.VichJ. M.GueyneJ. (1988). Le role régulateur du silicium dans ladivision cellulaire.C. R. Acad. Sci. Ser. 3306525–528.
52
HodsonM. J.EvansD. E. (1995). Aluminium/silicon interactions in higher plants.J. Exp. Bot.46161–171. 10.1093/jxb/46.2.161
53
HodsonM. J.WhiteP. J.MeadA.BroadleyM. R. (2005). Phylogenetic variation in the silicon composition of plants.Annal. Bot.961027–1046. 10.1093/aob/mci255
54
HottM.PollakC. D.ModrowskiD.MarieP. J. (1993). Short-term effects of organic silicon on trabecular bone in mature ovariectomised rats.Calcif. Tissue Int.53174–179. 10.1007/BF01321834
55
IlerR. K. (1979). The Chemistry of Silica: Solubility, Polymerization, Colloidal and Surface Properties, and Biochemistry.Newyork, NY: John Wiley & Sons.
56
Jacqmin-GaddaH.CommengesD.LetenneurL.DartiguesJ. F. (1996). Silica and aluminum in drinking water and cognitive impairment in the elderly.Epidemology7281–285. 10.1097/00001648-199605000-00011
57
JonesL. H. P.HandreckK. A. (1967). Silica in soils, plants, and animals.Adv. Agron.19104–149.
58
JugdaohsinghR. (1999). Soluble Silica and Aluminium Bioavailability.Ph.D. thesis. University of LondonLondon.
59
JugdaohsinghR. (2007). Silicon and bone health.J. Nutr. Health Aging.1199–110.
60
JugdaohsinghR.AndersonS. H.TuckerK. L. (2002). Dietary silicon intake and absorption.Am. J. Clin. Nutr.75887–893.
61
JugdaohsinghR.ReffittD. M.OldhamC. (2000). Oligomeric but not monomeric silica prevents aluminium absorption in human.Am. J. Clin. Nutr.71944–949.
62
KaufmannK. (1993). Silica: The Forgotten Nutrient.New York, NY: Alive Books.
63
KiddP. S.LluganyM.PoschenriederC.Gunse´B.Barcelo´J. (2001). The role of root exudates in aluminum resistance and silicon-induced amelioration of aluminum toxicity in three varieties of maize (Zea mays L.).J. Exp. Bot.521339–1352. 10.1093/jexbot/52.359.1339
64
KikunagaS.KitanoT.KikukawaT.TakahashiM. (1991). Effects of fluoride and silicon on distribution of minerals in the magnesium-deficient rat.Maguneshumu10181–191.
65
KnightC. T. G.KinradeS. D. (2001). “A primer on the aqueous chemistry of silicon,” inSilicon in AgricultureedsDatnoffL. E.SnyderG. H.KorndoerferG. H. (Amsterdam: Elsevier Science) 57–84.
66
KokuboT.KimH. M.KawachitaM.NakamuraT. (2004). Bioactive metals: preparation and properties.J. Mater. Sci. Mater. Med.1599–107. 10.1023/B:JMSM.0000011809.36275.0c
67
KovdaV. A. (1973). The Bases of Learning About Soils.Moscow: Nayka.
68
LiD. D.LermanA.MackenzieF. T. (2011). Human perturbations on the global biogeochemical cycles of coupled Si–C and responses of terrestrial processes and the coastal ocean.Appl. Geochem.26289–291. 10.1016/j.apgeochem.2011.03.084
69
LiJ.LeisnerM.FrantzJ. (2008). Alleviation of copper toxicity in Arabidopsis thaliana by silicon addition to hydroponic solutions.J. Am. Soc. Hortic. Sci.133670–677.
70
LiY. C.SummerM. E.MillerW. P.AlvaA. K. (1996). Mechanism of silicon induced alleviation of aluminum phytotoxicity.J. Plant Nutr.191075–1087. 10.1080/01904169609365181
71
LiangY. C.SunW. C.ZhuY. G.ChristieP. (2007). Mechanisms of silicon-mediated alleviation of abiotic stresses in higher plants: a review.Environ. Pollut.147422–428. 10.1016/j.envpol.2006.06.008
72
LiangY. C.WongJ. W. C.WeiL. (2005). Silicon-mediated enhancement of cadmium tolerance in maize (Zea mays L.) grown in cadmium contaminated soil.Chemosphere58475–483. 10.1016/j.chemosphere.2004.09.034
73
LinsU.BarrosC. F.da CunhaM.MiguensF. C. (2002). Structure, morphology and composition of silicon biocomposites in the palm tree Syagrus coronate (Mart.) Becc.Protoplasma22089–96. 10.1007/s00709-002-0036-5
74
LomerM. C. E.HutchinsonC.VolkertS. (2004). Dietary sources of inorganic micro-particles and their intake in healthy subjects and patients with Crohn’s disease.Br. J. Nutr.92947–955. 10.1079/BJN20041276
75
LuH. P.ZhuangP.LiZ. A.TaiY. P.ZouB.LiY. W.et al (2014). Contrasting effects of silicates on cadmium uptake by three dicotyledonous crops grown in contaminated soil.Environ. Sci. Pollut. Res.219921–9930. 10.1007/s11356-014-2947-z
76
MaJ. F. (2003). “Functions of silicon in higher plants,” inSilicon Biomineralizationed.MüllerW. E. G. (Berlin: Springer Verlag) 127–148.
77
MaJ. F. (2004). Role of silicon in enhancing the resistance of plants to biotic and abiotic stresses.Soil Sci. Plant Nutr.5011–18. 10.1080/00380768.2004.10408447
78
MaJ. F.MiyakY.TakahashiE. (2001). “Silicon as a beneficial element for crop plants,” inSilicon in AgricultureedsDatnoffL. E.SnyderG. H.KorndoerferG. H. (Amsterdam: Elsevier Science) 17–39.
79
MaJ. F.TakahashiE. (2002). Soil, Fertilizer and Plant Silicon Research in Japan.Amsterdam: Elsevier Science.
80
MaJ. F.TamaiK.YamajiN.MitaniN.KonishiS.KatsuharaM.et al (2006). A silicon transporter in rice.Nature440688–691. 10.1038/nature04590
81
MaJ. F.YamajiN. (2006). Silicon uptake and accumulation in higher plants.Trends Plant Sci.11392–397. 10.1016/j.tplants.2006.06.007
82
MaJ. F.YamajiN. (2015). A cooperative system of silicon transport in plants.Trends Plant Sci.20435–442. 10.1016/j.tplants.2015.04.007
83
MaJ. F.YamajiN.MitaniN.XuX.SuY.McGrathS. P.et al (2008). Transporters of arsenite in rice and their role in arsenic accumulation in rice grain.Proc. Natl. Acad. Sci. U.S.A.1059931–9935. 10.1073/pnas.0802361105
84
MaJ. F.YamajiN.Mitani-UenoN. (2011). Transport of silicon from roots to panicles in plants.Proc. Jpn. Acad. Ser. B Phys. Biol. Sci.87377–385. 10.2183/pjab.87.377
85
MaJ. F.YamajiN.TamaiK.MitaniN. (2007a). Genotypic difference in silicon uptake and expression of silicon transporter genes in rice.Plant Physiol.145919–924. 10.1104/pp.107.107599
86
MaJ. F.YamajiN.MitaniN.TamaiK.KonishiS.FujiwaraT.et al (2007b). An efflux transporter of silicon in rice.Nature448209–212. 10.1038/nature05964
87
MacFaddenB. J. (2005). “Terrestrial mammalian herbivore response to declining levels of atmospheric CO2 during the cenozoic: evidence from North American fossil horses (family Equidae),” inA History of Atmospheric CO2 and its effects on Plants, Animals, and EcosystemsedsCerlingT. E.DearingM. D. (New York, NY: Springer) 273–292.
88
MarschnerH. (1995). Mineral Nutrition of Higher Plants.London: Academic Press.
89
MartinK. R. (2007). The chemistry of silica and its potential health benefits.J. Nutr. Health Aging1194–98.
90
McClungM. R. (2003). Pathogenesis of osteoporotic hip fractures.Clin. Cornerstone222–29. 10.1016/S1098-3597(03)90044-5
91
McNaughtonS. A.Bolton-SmithC.MishraG. D.JugdaosinghR.PowellJ. J. (2005). Dietary silicon intake in post-menopausal women.Br. J. Nutr.94813–817. 10.1079/BJN20051548
92
McNaughtonS. A.TarrantsJ. L.McNaughtonM. M.DavisR. D. (1985). Silica as a defence against herbivory and a growth promoter in African grasses.Ecology66528–535. 10.2307/1940401
93
MitaniN.ChibaY.YamajiN.MaJ. F. (2009). Identification of maize and barley Lsi2-like silicon efflux transporters reveal a distinct silicon uptake system from that in rice.Plant Cell212133–2142. 10.1105/tpc.109.067884
94
MitaniN.YamajiN.AgoY.IwasakiK.MaJ. F. (2011a). Isolation and functional characterization of an influx silicon transporter in two pumpkin cultivars contrasting in silicon accumulation.Plant J.66231–240. 10.1111/j.1365-313X.2011.04483
95
MitaniN.YamajiN.MaJ. F. (2011b). Silicon efflux transporters isolated from two pumpkin cultivars contrasting in Si uptake.Plant Signal. Behav.6991–994. 10.4161/psb.6.7.15462
96
MiyakeY.TakahashiE. (1983). Effect of silicon on the growth of solution-cultured cucumber plant.Soil Sci. Plant Nutr.2971–83. 10.1080/00380768.1983.10432407
97
MontpetitJ.VivancosJ.MitaniN.YamajiN.Remus-BorelW.BelzileF.et al (2012). Cloning, functional characterization and heterologous expression of TaLsi1, a wheat silicon transporter gene.Plant Mol. Biol.7935–46. 10.1007/s11103-012-9892-3
98
MooreK. L.SchröderM.WuZ.MartinB. G. H.HawesC. R.McGrathS. P.et al (2011). High-resolution secondary ion mass spectrometry reveals the contrasting subcellular distribution of arsenic and silicon in rice roots.Plant Physiol.156913–924. 10.1104/pp.111.173088
99
MoussaH. R. (2006). Influence of exogenous application of silicon on physiological response of salt stressed maize (Zea mays L.).Int. J. Agric. Biol.8293–297.
100
NaeemA.GhafoorA.FarooqM. (2014). Suppression of cadmium concentration in wheat grains by silicon is related to its application rate and cadmium accumulating abilities of cultivars.J. Sci. Food Agric.952467–2472. 10.1002/jsfa.6976
101
NeumannD. (2003). Silicon in plants.Prog. Mol. Subcell. Biol.33149–160. 10.1007/978-3-642-55486-5_6
102
NeumannD.zur NiedenU. (2001). Silicon and heavy metal tolerance of higher plants.Phytochemistry56685–692. 10.1016/S0031-9422(00)00472-6
103
NielsenF. H. (1974). “Newer” trace elements in human nutrition.Food Tech.2838–44.
104
NielsenF. H. (2014). Update on the possible nutritional importance of silicon.J. Trace Elem. Med. Biol.28379–382. 10.1016/j.jtemb.2014.06.024
105
NuurtamoM.VaroP.SaariE.KoivistionenP. (1980). Mineral element composition of Finnish foods. V. Meat and meat products.Acta Agric. Scand. Suppl.2257–76.
106
ParrJ. F.SullivanL. A.ChenB.YeG. (2010). Carbon bio-sequestration within the phytoliths of economic bamboo species.Global Change Biol.162661–2667. 10.1111/j.1365-2486.2009.02118.x
107
PavlovicJ.SamardzicJ.MaksimovicV.TimotijevicG.StevicN.LaursenK. H.et al (2013). Silicon alleviates iron deficiency in cucumber by promoting mobilization of iron in the root apoplast.New Phytol.1981096–1107. 10.1111/nph.12213
108
PenningtonJ. A. T. (1991). Silicon in foods and diets.Food Addit. Contam.897–118. 10.1080/02652039109373959
109
PerryC. C. (2009). “An overview of silica in biology: its chemistry and recent technological advances,” inBiosilica in Evolution, Morphogenesis, and Nano-biotechnologyedsMuellerW. E. G.GrachevM. A. (Berlin: Springer) 295–314.
110
PerryC. C.Keeling-TuckerT. (1998). Aspects of the bioinorganic chemistry of silicon in conjunction with the biometals calcium, iron and aluminium.J. Inorg. Biochem.69181–191. 10.1016/S0162-0134(97)10017-4
111
PipernoD. R. (1988). Phytolith Analysis: An Archeological and Geological Perspective.Waltham, MA: Academic Press.
112
PipernoD. R.SuesH. D. (2005). Paleontology: dinosaurs dined on grass.Science3101126–1128. 10.1126/science.1121020
113
PontigoS.RiberaA.GianfredaL.de la Luz MoraM.NikolicM.CartesP. (2015). Silicon in vascular plants: uptake, transport and its influence on mineral stress under acidic conditions.Planta24223–37. 10.1007/s00425-015-2333-1
114
PowellJ. J.McNaughtonS. A.JugdaosinghR.AndersonS. H. C.DearJ.KhotF.et al (2005). A provisional database for the silicon content of foods in the United Kingdom.Br. J. Nutr.94804–812. 10.1079/BJN20051542
115
RafiM. M.EpsteinE. (1999). Silicon absorption by wheat (Triticum aestivum L.).Plant Soil211223–230. 10.1023/A:1004600611582
116
RainsD. W.EpsteinE.ZasoskiR. J.AslamM. (2006). Active silicon uptake by wheat.Plant Soil280223–228. 10.1007/s11104-005-3082-x
117
RavenJ. A. (2001). “Silicon transport at the cell and tissue level,” inSilicon in AgricultureedsDatnoffL. E.SynderG. H.KorndoerferG. H. (Amsterdam: Elsevier) 41–51.
118
RavenJ. A. (2003). Cycling silicon–the role of accumulation in plants.New Phytol.158419–421. 10.1046/j.1469-8137.2003.00778.x
119
RavenP. H.EvertR. F.EichhornS. E. (1999). Biology of Plants.New York, NY: Freeman.
120
ReffittD. M.OgstonN.JugdaosinghR.CheungH. F.EvansB. A.ThompsonR. P.et al (2003). Orthosilicic acid stimulates collagen type 1 synthesis and osteoblastic differentiation in human osteoblast-like cells in vitro.Bone32127–135. 10.1016/S8756-3282(02)00950-X
121
Rellán-AlvarezR.Giner-Martínez-SierraJ.OrdunaJ.OreraI.Rodríguez-CastrillónJ. A.Garcia-AlonsoJ. I.et al (2010). Identification of a tri-iron(III), tri-citrate complex in the xylem sap of iron deficient tomato resupplied with iron: new insights into plant iron long distance transport.Plant Cell Physiol.5191–102. 10.1093/pcp/pcp170
122
Remus-BorelW.MenzierJ. G.BelangerR. R. (2005). Silicon induces antifungal compounds in powdery mildew-infected wheat.Physiol. Mol. Plant Pathol.66108–115. 10.1016/j.pmpp.2005.05.006
123
RezankaT.SiglerK. (2007). Biologically active compounds of semi-metals.Phytochemistry69585–606. 10.1016/j.phytochem.2007.09.018
124
RezankaT.SiglerK. (2008). Biologically active compounds of semi metals.Stud. Nat. Prod. Chem.35835–921. 10.1016/S1572-5995(08)80018-X
125
RobberechtH.Van-CauwenberghR.Van-VlaslaerV.HermansN. (2009). Dietary silicon intake in Belgium: sources, availability from foods, and human serum levels.Sci. Total Environ.4074777–4782. 10.1016/j.scitotenv.2009.05.019
126
RodriguesF. A.BenhamouN.DatnoffL. E.JonesJ. B.BelangerR. R. (2003). Ultrastructural and cytochemical aspects of silicon-mediated rice blast resistance.Phytopathology93535–546. 10.1094/PHYTO.2003.93.5.535
127
RogallaH.RomheldV. (2002). Role of leaf apoplast in silicon mediated manganese tolerance of Cucumis sativus L.Plant Cell Environ.25549–555. 10.1046/j.1365-3040.2002.00835.x
128
SauerD.SacconeL.ConleyD. J.HermannL.SommerM. (2006). Review of methodologies for extracting plant-available and amorphous Si from soils and aquatic sediments.Biogeochemistry8089–108. 10.1007/s10533-005-5879-3
129
SavantN. K.SynderG. H.DatnoffL. E. (1997). Silicon management and sustainable rice production.Adv. Agron.58151–191. 10.1016/S0065-2113(08)60255-2
130
SchianoA.EisingerF.DetolleP.LaponcheA. M.BrisouB.EisingerJ. (1979). Silicium, tissu osseux et immunité.Rev. Rhum.46483–486.
131
SchwarzK.MilneD. B. (1972). Growth promoting effect of silicon in rats.Nature239333–334. 10.1038/239333a0
132
SeabornC. D.NielsenF. H. (2002). Silicon deprivation decreases collagen formation inwounds and bone, and ornithine transaminase enzyme activity in liver.Biol. Trace Elem. Res.89251–261. 10.1385/BTER:89:3:251
133
SernaL.FenollC. (2003). Cycling silicon–the role of accumulation in plants.New Phytol.158419–430. 10.1046/j.1469-8137.2003.00778.x
134
ShiX.ChaochunZ.WangH.ZhangF. (2005). Effect of Si on the distribution of Cd in rice seedlings.Plant Soil27253–60. 10.1007/s11104-004-3920-2
135
SkinnerH. C. W.JahrenA. H. (2004). “Biomineralization,” inBiogeochemistry Vol. 8, Treatise on Geochemistryed.SchlesingerW. H. (Amsterdam: Elsevier Science Ltd.) 117–184.
136
SkjemstadJ. O.FitzpatrickR. W.ZarcinasB. A.ThompsonC. H. (1992). Genesis of Podzols on coastal dunes in southern Queensland: II. Geochemistry and forms of elements as deduced from various soil extraction procedures.Aust. J. Soil Sci.30615–644. 10.1071/SR9920615
137
SolomonsN. W. (1984). “The other trace minerals: manganese, molybdenum, vanadium, nickle, silicon and arsenic,” inAbsorption and Malabsorption of Mineral NutrientsedsSolomonsN. W.RosenbergI. H. (New York, NY: Alan R. Liss. Inc.) 269–295.
138
SongZ.ZhaoS.ZhangY.HuG.CaoZ.WongM. (2011). Plant impact on CO2 consumption by silicate weathering: the role of bamboo.Bot. Rev.77208–213. 10.1007/s12229-011-9077-9
139
SripanyakornS.JugdaohsinghR.ElliottH. (2004). The silicon content of beer and its bioavailability in healthy volunteers.Br. J. Nutr.91403–409. 10.1079/BJN20031082
140
StruyfE.SmisA.Van DammeS.MeireP.ConleyD. J. (2009). The global biogeochemical silicon cycle.Silicon1207–213. 10.1007/s12663-010-9035-x
141
SummerfieldM. A. (1983). “Silcrete,” inChemical Sediments and GeomorphologyedsGoudieA. S.PyeK. (London: Academic Press) 59–93.
142
TakahashiE.MaJ. F.MiyakeY. (1990). The possibility of silicon as an essential element for higher plants.Comments Agric. Food Chem.299–122. 10.1016/j.bbagen.2013.11.021
143
TeraokaH.MoriiF.KobayashiJ. (1981). Contents of 24 elements in foods and the estimated daily intakes.Eiyo Shokuryo34221–224. 10.4327/jsnfs1949.34.3_221
144
VaroP.NuurtamoM.SaariE.KoivistoinenP. (1980a). Mineral element composition of finnish foods. IV. Flours and bakery products.Acta Agric. Scand. Suppl.2237–55.
145
VaroP.LahelmaO.NuurtamoM.SaariE.KoivstoinenP. (1980b). Mineral element composition of Finnish foods. VII. Potato, vegetables, fruits, berries, nuts and mushrooms.Acta Agric. Scand. Suppl.2289–113.
146
VaroP.NuurtamoM.SaariE.KoivistoinenP. (1980c). Mineral element composition of finnish foods. VIII. Dairy products, eggs and margarine.Acta Agric. Scand. Suppl.22115–126.
147
WangL.NieQ.LiM.ZhangF.ZhuangJ.YangW.et al (2005). Biosilicified structures for cooling plant leaves: a mechanism of highly efficient mid infrared thermal emission.Appl. Phys. Lett.87:195105.
148
WatersB. M.UauyC.DubcovskyJ.GrusakM. A. (2009). Wheat (Triticum aestivum) NAM proteins regulate the translocation of iron, zinc, and nitrogen compounds from vegetative tissues to grain.J. Exp. Bot.604263–4274. 10.1093/jxb/erp257
149
WeastR. C.AstleM. J. (1983). Handbook of Chemistry and Physics.Florida: CRC Press.
150
WedepohlK. H. (1995). The composition of the continental crust.Geochim. Cosmochim. Acta591217–1232. 10.1016/0016-7037(95)00038-2
151
WernerD. (1977). “Silicate metabolism,” inThe Biology of Diatomsed.WernerD. (Oxford: Blackwell scientific publications) 140–141.
152
WhittonJ. S.WellsN. (1978). Analyses of 27 Elements in Plants Grown in a Pot Trial on Soils Mixed with Auckland Sewage Sludge.New Zealand Soil Bureau Scientific Report 33. Wellington: Department of Scientific and Industrial Research.
153
WieseH.NikolicM.RoemheldV. (2007). “Silicon in plant nutirion. Effect of zinc, manganese and boron leaf concentrations and compartmentation,” inThe Apoplast of Higher Plants: Compartment of Storage, Transport and ReactionsedsSattelmacherB.HorstW. J. (Dordrecht: Springer) 33–47.
154
WildingL. P. (1967). Radiocarbon dating of biogenetic opal.Science15666–67. 10.1126/science.156.3771.66
155
WuJ.-W.ShiY.ZhuY.-X.WangY.-C.GongH.-J. (2013). Mechanisms of enhanced heavy metal tolerance in plants by silicon: a review.Pedosphere23815–825. 10.1016/S1002-0160(13)60073-9
156
YamajiN.MaJ. F. (2009). A transporter at the node responsible for intervascular transfer of silicon in rice.Plant Cell212878–2883. 10.1105/tpc.109.069831
157
YamajiN.MitaniN.MaJ. F. (2008). A transporter regulating silicon distribution in rice shoots.Plant Cell201381–1389. 10.1105/tpc.108.059311
158
YoshidaS. (1965). Chemical aspects of the role of silicon in physiology of the rice plant.Bull. Natl. Inst. Agric. Sci. Ser. B151–58.
159
ZhuY.GongH. (2014). Beneficial effects of silicon on salt and drought tolerance in plants.Agron. Sust. Dev.34455–472. 10.1007/s13593-013-0194-1
160
ZhuZ.WeiG.LiJ.QianQ.YuJ. (2004). Silicon alleviates salt stress and increases antioxidant enzymes activity in leaves of salt-stressed cucumber (Cucumis sativus L.).Plant Sci.167527–533. 10.1016/j.plantsci.2004.04.020
Summary
Keywords
silicon, dietary sources, human exposure, health benefits, plant nutrition, stress tolerance
Citation
Farooq MA and Dietz K-J (2015) Silicon as Versatile Player in Plant and Human Biology: Overlooked and Poorly Understood. Front. Plant Sci. 6:994. doi: 10.3389/fpls.2015.00994
Received
18 August 2015
Accepted
29 October 2015
Published
12 November 2015
Volume
6 - 2015
Edited by
Karl H. Muehling, Christian-Albrechts-Universität zu Kiel, Germany
Reviewed by
Michael Frei, Rheinische Friedrich-Wilhelms-Universität Bonn, Germany; Naoki Yamaji, Okayama University, Japan
Updates
Copyright
© 2015 Farooq and Dietz.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Karl-Josef Dietz, karl-josef.dietz@uni-bielefeld.de
This article was submitted to Plant Nutrition, a section of the journal Frontiers in Plant Science
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.