Original Research ARTICLE
Earthworm Grazed-Trichoderma harzianum Biofortified Spent Mushroom Substrates Modulate Accumulation of Natural Antioxidants and Bio-Fortification of Mineral Nutrients in Tomato
- 1Plant-Microbe Interaction and Rhizosphere Biology Lab, ICAR-National Bureau of Agriculturally Important Microorganisms (ICAR-NBAIM), Maunath Bhanjan, India
- 2Department of Biosciences, Faculty of Science, Integral University, Lucknow, India
- 3Department of Mycology and Plant Pathology (Krishi Vigyan Kendra), Institute of Agricultural Sciences, Banaras Hindu University, Varanasi, India
- 4Department of Mycology and Plant Pathology, Institute of Agricultural Sciences, Banaras Hindu University, Varanasi, India
- 5Division of Soil Biology, ICAR-Indian Institute of Soil Science, Bhopal, India
- 6Department of Botany, Faculty of Science, Banaras Hindu University, Varanasi, India
- 7Pilgram Marpeck School of STEM, Truett McConnel University, Cleveland, GA, United States
- 8Department of Animal Biotechnology, Konkuk University, Seoul, South Korea
The present investigation was aimed at evaluating the impact of earthworm grazed and Trichoderma harzianum biofortified spent mushroom substrate (SMS) on natural antioxidant and nutritional properties of tomato. Results of the investigation reveal that earthworm grazing and T. harzianum bio-fortification led to significant improvement in the physico-chemical properties of fresh SMS and its application increased the accumulation of natural antioxidants and mineral content in tomato as compared to either T. harzianum biofortified SMS or fresh SMS. In particular, the earthworm grazed, T. harzianum biofortified SMS (EGTHB-SMS) was found to inhibit lipid peroxidation and protein oxidation with significant increase in total polyphenol and flavonoid content in tomato. Further, it increased Fe2+/Fe3+ chelating activity, superoxide anion radical scavenging activity compared to other treatments. The results thus suggest an augmented elicitation of natural antioxidant properties in tomato treated with EGTHB-SMS, resulting in a higher radical scavenging activity, that is highly desirable for human health. In addition, the use of SMS to enhance the nutritional value of tomato fruits becomes an environment friendly approach in sustainable crop production.
People are increasingly becoming more conscious about their health and more attention is being paid to the nutritional value of human diet with an eye on role of mineral nutrients and antioxidants in health. Several epidemiological studies have reported that high intake of green vegetables, fruits and pulses is associated with reduced risk of a number of chronic diseases (Singh et al., 2010) due to imbalance in the antioxidant and prooxidant homeostasis in human body (Nautiyal et al., 2008). Such conditions dominate either due to increased generation of free radicals (FRs) caused by excessive oxidative stress or due to poor scavenging/quenching of FRs in the body (Bhanja et al., 2009; Ahmad et al., 2016). Free radicals are chemically unstable compounds that results in damage to lipid cells, proteins and DNA (Ahmad et al., 2016). Reactive oxygen species (ROS) are produced intra-cellularly through multiple mechanisms and depending on the cell and tissue types, the major sources being the ‘professional’ producers of ROS NADPH oxidase (NOX) complexes in cell membranes, mitochondria, peroxisomes, and endoplasmic reticulum (Singh et al., 2009b; Singh et al., 2010). Biological systems have several antioxidant defense mechanisms that prevent the destructive effects of ROS and FRs such as antioxidative compounds and enzymes (Nautiyal et al., 2008; Ahmad et al., 2016). In aerobic organisms, the major target sites for ROS and FRs are the cellular membrane lipids, proteins and DNA and they cause alterations in membrane structure and its function (Ahmad et al., 2016). A wide range of antioxidants, both natural and synthetic have been used as external supplements in the regular diet that could influence and suppress/slow down the processes including lipid oxidation, binding of transitional metal ion catalysts, decomposition of peroxides, etc. Increase in FR scavenging through simple or complex cellular mechanisms both in living organisms as well as in the food industry has been well documented (Prakash et al., 2007b; Singh et al., 2009b, 2010). Due to the apparent toxicity of synthetic antioxidants, currently, the interest of the society in natural antioxidants is increasing day by day (Huang and Wang, 2004).
Tomato (Solanum lycopersicum) is one of the most important vegetable crops consumed across the various climatic regions of the world. Tomato and its products serve as rich sources of dietary bioactive molecules such as lycopene, beta-carotene, phytoene, phytofluene, folic acid, flavonoids and vitamin C (George et al., 2004; Hyman et al., 2004). These bioactive compounds are well-studied for their health protective abilities especially against cardiovascular diseases, coronary heart diseases and various types of cancer. Similarly, Trichoderma harzianum (avirulent, plant beneficial fungus) is a common soil inhabitant broadly distributed in terrestrial ecosystems (Harman et al., 2004) and plays many important roles in diverse natural environments. Although the fungus absorbs nutrition from dead organic materials as a saprophyte, majority of its population is concentrated in nutrient rich niches like the rhizosphere. In agriculture, T. harzianum is primarily known for its biocontrol activities against soilborne phytopathogens but other multifarious activities have also been recorded by various researchers. Therefore, the ability of the fungus to colonize roots of crop plants is of a great advantage when it is used as a nutrient mobilizer, plant growth promoter and biological control agent (Harman et al., 2004; Sarma et al., 2015). The ability to colonize root and endophytic behavior of Trichoderma spp. in plant roots are proven and it was found that Trichoderma responds chemotropically to roots. The response of root cells to colonization by fungi may have profound implications in the performance of these organisms as plant growth promoting as well as biocontrol agents of soilborne plant pathogens (Harman et al., 2004). There are strains of T. harzianum which improve nutrient uptake and translocation in plants, resulting in enhanced nutritional value of the produce there from Glick (1995), Berg (2009).
Spent mushroom substrate (SMS) is a by-product of mushroom industry, rich in organic matter and other essential nutrients for plant growth. Annually, mushroom industries release more than 50 million tons of SMS as waste material (Fox and Chorover, 1999) which is vastly under utilized. A larger portion of SMS is carelessly disposed outside the production unit itself begetting a number of environmental issues. Piling-up of SMS may cause various environmental problems/pollution which further leads to groundwater contamination and production of greenhouse gasses such as carbon dioxide and nitrous oxide causing global warming and loss of essential plant nutrients (Beyer, 1996). In recent years, attention has been made toward more amicable ways of SMS disposal. These surplus residues can be recycled for sustaining soil health and enhancing crop productivity because the SMS is rich source of organic matter and mineral nutrients. Some of the researchers used SMS as organic amendment in various vegetable and high value crops and reported positive effect on crop yield (Beyer, 1996; Ahlawat et al., 2006). Earthworm grazing is a biooxidation process accelerating the stabilization of organic matter involving the joint action with microorganisms which are responsible for the physico-biochemical degradation of organic matter present in the waste. Earthworms are the important drivers of the process, conditioning the substrate and altering physico-biological activities (Aira et al., 2002; Domınguez, 2004). Further, earthworm has indirect effects on the structure and activities of microbial communities present in the waste through stimulation of microbial populations, inoculum dispersal, litter comminution, grazing, gut passage and aggregate formation (Anderson, 1987; Aira et al., 2002). Earthworms are involved in the fragmentation and ingestion of fresh organic matter, providing a greater surface area for the microbial colonization, and thereby drastically altering biological activity (Lores et al., 2006). Earthworms also have a great impact on nutrient mineralization and transformation during vermicomposting through modifications of the environmental conditions in the organic wastes and their interactions with microbes which favor the nitrogen transformation by rapid conversion of ammonia-nitrogen into nitrates (Aira et al., 2008; Domınguez et al., 2010). It increases the macro- and micronutrients, plant growth hormones auxins, gibberellins and cytokinins (Krishnamoorthy and Vajrabhiah, 1986), humic acids (Atiyeh et al., 2002) and enzymes in the decomposed organic manures (Sarma et al., 2010) which not only enhance plant growth but also hold nutrients for longer periods (Ndegwa and Thompson, 2001; Singh et al., 2013a). But so far no attempt seems to be made on value addition of SMS using T. harzianum and its synergistic effect with earthworm (Eisenia fetida). Moreover, the effect of earthworm grazed and T. harzianum bio-fortified SMS on nutritional quality and natural antioxidant properties of tomato is also an unexplored area. Recognizing the importance of nutritional value of tomato in terms of antioxidant properties and other mineral nutrients and their role in human health, the present study was undertaken with the objectives to study (1) the effect of earthworm grazing and T. harzianum bio-fortification on value addition of SMS, and (2) the impact of earthworm grazed and T. harzianum bio-fortified SMS on natural antioxidant and other nutritional properties of tomato.
Materials and Methods
Source of Reagents and Media
Culture media were procured from HiMedia, India, whereas, chemical reagents including standards were procured from Sigma–Aldrich, India. Bovine serum albumin (BSA), lycopene, β-carotene, organic solvents and other chemicals and analytical grade solvents were purchased from Merck Biosciences, India.
Fungal Strain, Earthworm (Eisenia fetida) and Culture Condition
The test fungal strain, T. harzianum UBSTH-501 (GenBank Accession No: MG972984) was obtained from Plant-Microbe Interaction and Rhizosphere Biology Lab, ICAR-National Bureau of Agriculturally Important Microorganisms (ICAR-NBAIM), Kushmaur, Maunath Bhanjan, India and maintained on potato dextrose agar (PDA) by sub-culturing at 25 ± 2°C at 15 days interval. Earthworms (E. fetida) were obtained from Dr. M. C. Manna, Division of Soil Biology, ICAR-Indian Institute of Soil Science, Bhopal, India.
In Planta Study
The effects of earthworm grazed, T. harzianum biofortified SMS on nutritional quality of tomato were evaluated under nethouse conditions at ICAR-NBAIM, India. The treatments were: T1- Control (without SMS), T2- Fresh SMS, T3-earthworm grazed SMS, T4- T. harzianum biofortified SMS and T5- earthworm grazed, T. harzianum biofortified SMS. Experiments were arranged in a completely randomized block design under nethouse conditions and each treatment consisted of five replications.
Preparation of Earthworm Grazed and T. harzianum Bio-Fortified SMS
Fresh SMS of white button mushroom (Agaricus bisporus) was collected from Department of Mycology and Plant Pathology, Institute of Agricultural Sciences, Banaras Hindu University, Varanasi, India. It was subsequently air-dried under shade, sieved (2 mm pore size) and filled into Vermi-bed of the dimensions of 5 × 3 × 2 ft. Grain-based bioformulation of T. harzianum was prepared following the procedure described by Singh et al. (2012). T. harzianum bio-fortified SMS was prepared as per the methods/steps described in Figure 1. Physico-chemical properties of fresh SMS, earthworm grazed SMS, T. harzianum biofortified SMS and earthworm grazed and T. harzianum biofortified SMS were analyzed. At the time of application, the population of T. harzianum in earthworm grazed and T. harzianum biofortified and only T. harzianum biofortified SMS were 3.20 × 106 and 2.25 × 106 cfu g−1, respectively.
FIGURE 1. Flow diagram showing a newly developed technique for preparation of earthworm grazed and Trichoderma harzianum UBSTH-501 biofortified SMS.
Planting Material and Growth Condition
Tomato seedlings (cv. Dev, Nunhems Pvt. Ltd., India) were grown in sterile potting mixture adopting standard horticultural practices at ICAR-NBAIM, Maunath Bhanjan, India. Forty-five days old tomato plants were uprooted gently without much disturbance to the roots and transplanted into pots in nethouse. The experiments were conducted during November to February with the range of relative humidity being 80–85% under 11/13 h light/dark photoperiod.
Soil Collection, Preparation and Analysis
Soil was collected from an agricultural farm, Indian Institute of Seed Science (formerly known as Directorate of Seed Research), Kushmaur, Maunath Bhanjan, India. Such soil was further processed for the study by sieving (2 mm pore size) and air drying. After processing, the soil was mixed with vermicompost in a 4:1 ratio (w/w) and chemical fertilizers, viz. diammonium phosphate, urea and muriate of potash at 174, 326, and 100 kg per hectare, respectively, followed by its sterilization by autoclaving at 121°C for 60 min twice at 12 h interval and storage in the same position. The physico-chemical properties of experimental soil were analyzed after 5 days of sterilization (Table 1).
Forty-five days old tomato plants were transplanted into pots each containing 200 g of fresh and bio-fortified SMS. The SMS was thoroughly mixed in the pots containing experimental soil (5 kg) and a single plant was transplanted into each pot. SMS free soil served as the negative control and soil with fresh SMS was taken as positive control. Further, two blocks were randomly arranged to replicate the five treatments and each treatment with five replicates (pots) was randomly arranged within each block.
Estimation of Natural Antioxidants and Nutritional Quality of Ripe Tomato Fruits
Five ripe tomato fruits were randomly picked from each treatment for further analysis. The contents of total carbohydrate, soluble sugar, protein and lutein zeaxanthin were determined according to Sadasivam and Manickam (1996), whereas vitamin A (as retinal) and ascorbic acid were quantified according to Thimmaiah (2012). Lycopene and β-carotene content in ripe tomato fruits were measured according to Hyman et al. (2004). N content in the ripe fruits was quantified by Kjeldahl method, whereas the composition of minerals and micronutrients was determined according to Sahu (2011).
A modified thiobarbituric acid-reactive species (TBARS) assay of Ohkawa et al. (1979) was used to measure lipid peroxidation with slight modifications (Singh et al., 2010). Similarly, protein oxidation was estimated according to the methods of Singh et al. (2009b) with slight modifications (Singh et al., 2010). The contents of total polyphenols and flavonoids were determined according to Singh et al. (2009a). The ferrous and ferric ion chelating properties and superoxide anion radical scavenging ability of ripe tomato extract were determined according to Singh et al. (2010). β-carotene bleaching assay was performed by the auto-oxidation of β-carotene and linoleic acid coupled reaction method according to Singh et al. (2010). Peroxidase and catalase activities were measured according to Thimmaiah (2012). A unit of catalase is defined as the quantity of enzyme necessary to decompose 1 μM of H2O2 per minute at 25°C, whereas 1 unit of peroxidase is equal to 0.1 of absorbance. Superoxide dismutase activity of tomato extracts was determined following the method of Sadasivam and Manickam (1996). The effect of T. harzianum biofortified SMS on number of fruit per plants and yield was measured after final harvest of fruits. For this purpose, five plants were randomly selected from each treatments and first picking was done after 75 days of transplanting. A total of five picking was done at 10 days interval and finally average number of fruits per plants and yield (kg per plant) were calculated.
Effect of Earthworm Grazed and T. harzianum Bio-Fortified SMS on Physico-Biochemical Properties of Soil
The effects of earthworm grazed and T. harzianum bio-fortified SMS on physico-biochemical properties of soil were analyzed at the end of the experiment. Soil samples (200 g) were collected from each treatment and stored at 4°C till analysis. Soil pH and EC were measured in 1:2.5 soil-water mixture. Soil organic carbon was measured by using modified Walkley-Black method. However, bulk density, particle density CaCO3, available micronutrients (N, P, K, and S) and available micronutrients (Fe, Mn, Cu, Zn, B, and Mo) in the soil samples were analyzed by following the standard procedures described by Sahu (2011).
In vitro laboratory experiments were performed in a completely randomized design and the nethouse experiments were conducted in a completely randomized block design. Laboratory experiments were repeated three times, whereas nethouse experiments were repeated twice in five replications each. Data were subjected to analysis of variance (ANOVA) and Duncan’s Multiple Range Test using SPSS software Version 16.0 program. Data were compared with DMRT at p≤ 0.05. Graphs and figures were drawn using the statistical package Origin Version 8.0.
Effect of Earthworm Grazing and T. harzianum Bio-Fortification on Nutritional Value of SMS
Results showed that earthworm grazing and T. harzianum bio-fortification alone or in combination significantly increased the biochemical and nutritional properties of fresh SMS (Table 2). The physico-chemical properties in terms of pH, EC, bulk and particle density showed significant improvement in EGTHB-SMS and only T. harzianum biofortified SMS (THB-SMS) over the earthworm grazed SMS (EG-SMS) and fresh SMS. However, marginal increase was recorded with respect to nitrogen content, whereas phosphorus and potassium content were significantly higher in EGTHB-SMS (1.79 and 285.50, respectively) over only THB-SMS (1.65 and 256.25, respectively), EG-SMS (1.25 and 241.50, respectively) and fresh SMS (1.18 and 231.0, respectively). Similar trend was recorded in case of calcium content (Table 2). Further, results of the investigation reveal the fact that T. harzianum biofortification and earthworm grazing significantly decrease the sodium, chloride and nitrate content, and simultaneously increased porosity and moisture content in the biofortified SMS as compared to other treatments (Table 2).
TABLE 2. Effect of solid-state cultivation of Trichoderma harzianum UBSTH-501 and earthworm (Eisenia fetida) grazing on physico-chemical properties of spent button mushroom substrate.
Effect on Accumulation of Total Carbohydrate, Soluble Sugar, Proteins and Lutein Zeaxanthin Content
Plants treated with T. harzianum bio-fortified SMS showed higher accumulation of total carbohydrate, soluble sugar, proteins and lutein zeaxanthin in the ripe tomato fruits. The accumulation of total carbohydrate was significantly higher in the tomato fruits obtained from the plants treated with EGTHB-SMS (53.90 μg g−1 fresh wt.) when compared to only THB-SMS (46.92 μg g−1 fresh wt.), EG-SMS (42.35 μg g−1 fresh wt.), fresh SMS treated (41.04 μg g−1 fresh wt.) and control plants (35.67 μg g−1 fresh wt.) (Figure 2A). Similarly, significant increase in total soluble sugar content in ripe fruits was recorded in plants treated with EGTHB-SMS (48.67 μg g−1 fresh wt.) followed by only THB-SMS (39.56 μg g−1 fresh wt.), EG-SMS (32.45 μg g−1 fresh wt.), fresh SMS (30.92 μg g−1 fresh wt.) compared to the untreated control plants (26.33 μg g−1 fresh wt.) under nethouse conditions (Figure 2B). Similarly, the total protein content (Figure 2C) and lutein zeaxanthin content (Figure 2D) in ripe fresh tomato fruits were also significantly higher when treated with EGTHB-SMS compared to the other treatments under investigation.
FIGURE 2. Effect of solid state cultivated T. harzianum UBSTH-501 on nutritional quality of tomato at harvest, (A) total carbohydrate, (B) total soluble sugar, (C) protein content, and (D) lutein zeaxanthin content. Treatments: 1- Control (untreated), 2- Fresh SMS, 3- Earthworm grazed SMS, 4- T. harzianum UBSTH-501 biofortified SMS, and 5- Earthworm grazed and T. harzianum UBSTH-501 biofortified SMS. Data are means (n = 5) and vertical bars represent standard error of means. Different letters above columns show significant difference in randomized block design test at p < 0.05 under Duncan’s multiple range test.
Effect on Accumulation of Vitamin A, β-Carotene, Lycopene and Ascorbic Acid
In the present study, EGTHB-SMS recorded considerable increase in synthesis and accumulation of vitamin A, β-carotene, lycopene and ascorbic acid in ripe tomato fruits under nethouse experiments. Quantitative estimation showed that vitamin A in tomato fruits was significantly higher in the plants inoculated with EGTHB-SMS (8.33 μg g−1 fresh wt.) compared to other treatments (Figure 3A). Similarly, the highest β-carotene content was also recorded in tomato treated with EGTHB-SMS (7.01 μg g−1 fresh wt.) compared to only THB-SMS treated (6.50 μg g−1 fresh wt.), EG-SMS (5.75 μg g−1 fresh wt.), fresh SMS (5.54 μg g−1 fresh wt.) and untreated control plants (4.49 μg g−1 fresh wt.) (Figure 3B). Further, more or less similar trend was observed with lycopene (Figure 3C) and ascorbic acid content in ripe tomato fruits (Figure 3D).
FIGURE 3. Effect of solid state cultivated T. harzianum UBSTH-501 on antioxidant compound in ripe tomato fruits at harvest. (A) Vitamin A (as retinal), (B) β-carotene content, (C) lycopene content, and (D) ascorbic acid content. Treatments: 1- Control (untreated), 2- Fresh SMS, 3- Earthworm grazed SMS, 4- T. harzianum UBSTH-501 biofortified SMS, and 5- Earthworm grazed and T. harzianum UBSTH-501 biofortified SMS. Data are means (n = 5) and vertical bars represent standard error of means. Different letters above columns show significant difference in randomized block design test at p < 0.05 under Duncan’s multiple range test.
Effect on Accumulation of Mineral Content in Ripe Tomato Fruits
The present study reveals a significant increase in mineral contents of ripe tomato fruits when inoculated with EGTHB-SMS compared to the only THB-SMS, EG-SMS, fresh SMS and control plants (Figure 4). Results of the investigation also establish that in ripe fruits from tomato plants inoculated with EGTHB-SMS induced 1.5–2 times more uptake and accumulation of nitrogen, phosphorus, potassium and calcium compared to those from plants treated with only THB-SMS, EG-SMS and fresh SMS (Figures 4A–D, respectively). Also, a similar trend was recorded for the magnesium and iron content of the ripe tomato fruits (Figures 4E,F). Again, maximum zinc, manganese and sodium content was recorded in tomato fruits from plants treated with EGTHB-SMS followed by only THB-SMS, fresh SMS and EG-SMS treated plants (Figures 4G–I, respectively), whereas minimum mineral content was recorded in control plants (Figure 4).
FIGURE 4. Effect of solid state cultivated T. harzianum UBSTH-501 on mineral content in ripe tomato fruits at harvest. (A) N content, (B) P content, (C) K content, (D) Ca content, (E) Mg content, (F) Fe content, (G) Zn content, (H) Mn content, and (I) Na content. Treatments: 1- Control (untreated), 2- Fresh SMS, 3- Earthworm grazed SMS, 4- T. harzianum UBSTH-501 biofortified SMS, and 5- Earthworm grazed and T. harzianum UBSTH-501 biofortified SMS. Data are means (n = 5) and vertical bars represent standard error of means. Different letters above columns show significant difference in randomized block design test at p < 0.05 under Duncan’s multiple range test.
Effect on Accumulation of Natural Antioxidants and Enzymatic Activities
In the present study, antioxidant activity was measured by different methods, namely presence of lipid peroxidation and protein oxidation assay, total polyphenols and flavonoids, ferrous and ferric ion chelating activity, superoxide anion radical scavenging activity, β-carotene bleaching assay and antioxidant enzymatic activity.
Effect on Lipid Peroxidation and Protein Oxidation
The activity of extracts to scavenge HO⋅ was also measured by protein oxidation method; extract obtained from plants treated with EGTHB-SMS inhibited the degree of lipid peroxidation and protein oxidation significantly (p < 0.01). Maximum inhibition in lipid peroxidation (34.34%) and protein oxidation (33.66%) was recorded in the fresh extract obtained from EGTHB-SMS treated plants followed by those treated with only THB-SMS, EG-SMS and fresh SMS treated plants at 10 mg ml−1 (Figures 5A,B). However, minimum inhibition of the mentioned processes was recorded in control plants. Further, the reference compound quercetin exhibited better inhibitory effects on lipid peroxidation and protein oxidation than other treatments (Figure 5).
FIGURE 5. Effect of solid state cultivated T. harzianum UBSTH-501 on (A) lipid peroxidation and (B) protein oxidation in ripe tomato fruits at harvest. Treatments: 1- Control (untreated), 2- Fresh SMS, 3- Earthworm grazed SMS, 4- T. harzianum UBSTH-501 biofortified SMS, 5- Earthworm grazed and T. harzianum UBSTH-501 biofortified SMS and 6- Reference compound quercetin. Data are means (n = 5) and vertical bars represent standard error of means. Different letters above columns show significant difference in randomized block design test at p < 0.05 under Duncan’s multiple range test.
Total Polyphenol and Flavonoid Content
It was observed that total polyphenol and flavonoid content of ripe tomato fruits increased significantly in plants treated with EGTHB-SMS (125.19 mg of gallic acid equivalents g−1 of extract and 62.97 mg of quercetin equivalents g−1 of extract) as compared to the plants treated with only THB-SMS (95.23 mg of gallic acid equivalents g−1 of extract and 59.82 mg of quercetin equivalents g−1 of extract), EG-SMS (82.50 mg of gallic acid equivalents g−1 of extract and 49.52 mg of quercetin equivalents g−1 of extract) and fresh SMS (81.55 mg of gallic acid equivalents g−1 of extract and 46.33 mg of quercetin equivalents g−1 of extract). Minimum polyphenol and flavonoid content was recorded in ripe fruits obtained from control plants (65.66 mg of gallic acid equivalents g−1 of extract and 32.59 mg of quercetin equivalents g−1 of extract) (Figures 6A,B, respectively).
FIGURE 6. Effect of solid state cultivated T. harzianum UBSTH-501 on antioxidant enzymatic activities in ripe tomato fruits at harvest (A) Total polyphenol content, (B) total flavonoid content, (C) ferrous ion chelating activity, (D) ferric ion chelating activity, (E) superoxide anion radical scavenging activity, (F) β-carotene bleaching assay, (G) peroxidase activity, (H) catalase activity, and (I) superoxide dismutase activity. Treatments: 1- Control (untreated), 2- Fresh SMS, 3- Earthworm grazed SMS, 4- T. harzianum UBSTH-501 biofortified SMS, and 5- Earthworm grazed and T. harzianum UBSTH-501 biofortified SMS. Data are means (n = 5) and vertical bars represent standard error of means. Different letters above columns show significant difference in randomized block design test at p < 0.05 under Duncan’s multiple range test.
Ferrous and Ferric Ion Chelating Activity
In the current study, further investigations were done on the role of the ripe tomato fruit extract on Fe2+ and Fe3+chelation, because these are the most effective pro-oxidants that are present in the food system (Halliwell et al., 1987). Maximum chelating effects on Fe2+ and Fe3+ ions (27.65 and 40.70%, respectively) were observed in the extracts of ripe fruits from plants treated with EGTHB-SMS followed by THB-SMS, EG-SMS and fresh SMS. However, minimum Fe2+ and Fe3+ ions chelation (12.40 and 19.65%, respectively) was recorded in the extracts of ripe fruits obtained from control plants at 10 mg ml−1 under nethouse conditions (Figures 6C,D).
Effects on Superoxide Anion Radical Scavenging Activity and β-Carotene Bleaching Assay
The extract of fruits from plants treated with EGTHB-SMS was found to be the most potent superoxide scavenger (41.23%) compared to that of fruits from only THB-SMS (36.59%), EG-SMS (30.25%), fresh SMS (28.92%) and control (21.67%) plants (Figure 6E).
Auto-oxidation of β-carotene (β-carotene chelating assay) was used to evaluate the antioxidant activity of the ripe tomato fruit extracts. Results showed that extract taken from plants treated with EGTHB-SMS exhibited higher antioxidant activities (57.89%) compared to that from plants treated with THB-SMS (57.32%), EG-SMS (50.22%) and fresh SMS (49.67%), whereas extract of fruits from control plants was found to be least antioxidative (42.91%) on the selected parameter (Figure 6F).
Antioxidant Enzymatic Activity
Earthworm grazed, T. harzianum biofortified SMS treated tomato exhibited higher antioxidant activities. The results exhibited more or less similar pattern for antioxidant enzymes activity in ripe tomato fruit extract as recorded for mineral content (Figures 6G–I). Figure 6G reflects higher peroxidase activity in ripe fruits from plants treated with EGTHB-SMS (130.49 unit mg−1 min−1 fresh wt.) compared to other treatments. As revealed in Figure 6H, the activity of catalase showed similar behavior, responding significantly to the different treatments. The superoxide dismutase (SOD) activity was highest in ripe fruits taken from plants treated with EGTHB-SMS (4.21 unit mg−1 min−1 fresh wt.) compared to plants treated with only THB-SMS (3.89 unit mg−1 min−1 fresh wt.), EG-SMS (3.00 unit mg−1 min−1 fresh wt.) and fresh SMS (3.25 unit mg−1 min−1 fresh wt.). However, least SOD activity was recorded in the extract of fruits taken from control plants grown under nethouse conditions (Figure 6I).
Effect on Fruit Yield
Results showed that plants treated with EGTHB-SMS produced significantly higher number of fruits per plants and yield (25.75 and 1.69 kg/plant, respectively) as compared to other treatments including plants treated with only THB-SMS (21.67 and 1.55 kg/plant, respectively), EG-SMS (18.15 and 1.45 kg/plant, respectively), fresh SMS (18.35 and 1.45 kg/plant, respectively) and control (14.52 and 1.25 kg/plant, respectively) under nethouse conditions after final harvest. However, lowest fruit yield was recorded in untreated control plants (Figure 7).
FIGURE 7. Effect of solid state cultivated T. harzianum UBSTH-501 on number of fruits per plant and yield of tomato at harvest. Treatments: 1- Control (untreated), 2- Fresh SMS, 3- Earthworm grazed SMS, 4- T. harzianum UBSTH-501 biofortified SMS, and 5- Earthworm grazed and T. harzianum UBSTH-501 biofortified SMS. Data are means (n = 5) and vertical bars represent standard error of means. Different letters above columns show significant difference in randomized block design test at p < 0.05 under Duncan’s multiple range test.
Effect of Bio-Fortified SMS on Physico-Biochemical Properties of Soil
Results showed that amendment of fresh and biofortified SMS significantly affect the biochemical properties of the soil (Table 3). A significant increase in the soil organic carbon, organic matter and available macronutrients (N, P, K, and S) was recorded in the soil amended with earthworm grazed-T. harzianum biofortified SMS as compared to other treatments and initial value as presented in Table 1. Further, maximum available Fe, Mn, Zn, and Mo was recorded in the soil treated with earthworm grazed-T. harzianum biofortified SMS other treatments (Table 3). However, minimum CaCO3 was found in the soil amended with earthworm grazed-T. harzianum biofortified SMS.
TABLE 3. Effect of earthworm grazed and T. harzianum bio-fortified spent mushroom substrate on the physico-biochemical properties of post-harvested soil.
Natural antioxidants and their role of in human health maintenance is a complex process and understanding these complex processes is the key to recognize cell responses against damage by free radicals. Free radicals (syn. reactive oxygen species-ROS) are produced in the cells as a by-product of normal metabolism and/or as a result of biotic and abiotic stresses (Sardesai, 1995). A promineprominent role of antioxidants in the reduction of ROS in the stressed tissues has already been established and reported by several workers (Halliwell, 1996; Devasagayam et al., 2004; Singh et al., 2010). ROS/FRs are normally neutralized by efficient systems in the body itself that include the antioxidant enzymes (peroxidase, catalase, SOD and glutathione peroxidase) and the nutrient-derived antioxidant small molecules such as lycopene, vitamin A, vitamin E, vitamin C, β-carotenes, polyphenolics, flavonoids, glutathione, etc. (Sardesai, 1995; Halliwell, 1996, 1997; Devasagayam et al., 2004). Since ancient era, fresh fruits, vegetables and herbal medicines have been the rich source of antioxidants in traditional human diet that protect tissues from the damage caused by free radicals (Sardesai, 1995; Sen and Chakraborty, 2011). In the present study, it has been demonstrated that application of T. harzianum biofortified SMS modulates accumulation of natural antioxidants and bio-fortification of mineral nutrients in tomato (S. lycopersicum) fruits rendering them more valuable as a food. Tomato constitutes an important source of antioxidants in Indian diet (George et al., 2004). The antioxidant activity of ripe tomato fruits has been tested using a wide variety of methods. Antioxidant activity is the capacity to prevent auto-oxidation of FR-mediated oxidation of the substrates when present at low concentration (Halliwell, 1992; Deepa et al., 2006; Bhanja et al., 2009). All these assays have been frequently used to assess antioxidant activity in the substrates (Deepa et al., 2006; Bhanja et al., 2009; Singh et al., 2010). Results from the present study involving earthworm grazing and T. harzianum biofortification of fresh SMS increases its physico-chemical and nutritional properties to significant extents. The nutritional quality of fresh SMS was even higher when the fresh SMS was co-inoculated with T. harzianum and earthworm in an additive manner as compared to only T. harzianum biofortified and earthworm grazed SMS. Results showed that optimized composting system with appropriate microorganisms and earthworm, E. fetida proved highly efficient in transforming SMS into odorless, porous and homogenized biofortified SMS. The improvement in nutritional quality of SMS may be attributed to accelerated mineralisation of the organic matter by T. harzianum and further enrichment by the earthworm feeding of biofortified SMS (Jordan et al., 2008). Further, several reports showed that earthworm grazing enhances physical property of the organic waste (Lalander et al., 2015). Recycling of these organics in agriculture after bio-fortification and earthworm grazing has several benefits such as improving soil carbon content and sustaining soil health that eventually lead to better crop produce and enhanced productivity (Lau et al., 2003; Jordan et al., 2008; Jonathan et al., 2011). In the current study, it was observed that application of EGTHB-SMS significantly increased the total carbohydrate, soluble sugar, proteins and lutein zeaxanthin in ripe tomato extract. Carbohydrate, sugars and proteins are the primary building blocks for any living cell (Singh et al., 2009a). The biofortified SMS carries substantial amount of essential plant nutrients, organics and enzymes which, on one hand, are useful for the better crop growth leading to improvement in the yield and returns thereby and on the other, help improve the nutritional quality of the produce (Lau et al., 2003; Jordan et al., 2008; Jonathan et al., 2011; Lalander et al., 2015).
Further application of biofortified SMS increases the antioxidant compounds namely lycopene and β-carotene in the ripe tomato fruits. There is an increase in concentration of β-carotene as the lycopene content increases, but the degree of increase is not similar. In ripe fresh tomato fruits, significant positive correlation has been found between lycopene and β-carotene content. Tomato lycopene and β-carotene have more bioactivity and bioavailability and also β-carotene is the precursor of vitamin A. Significant variation in concentrations of these compounds in different treatments might be due to the effect of solid-state cultivated T. harzianum and bioactive compounds present in the biofortified SMS. Organically cultivated fruits and vegetables generally tend to have higher concentrations of various essential nutrients like iron, phosphorous, potassium, vitamin C and several antioxidants compared to their conventionally grown counterparts (Barron, 2010; Montalba et al., 2010). The present investigation also validates the positive effects of T. harzianum enriched SMS on yield and quality of tomato fruits. While investigating the impact of nitrogen and bioinoculant Bacillus licheniformis, Ochoa-Velasco et al. (2016) have reported a positive effect of application of B. licheniformis on vitamin C and lycopene content in tomato. Similarly, enhancement in quality parameters of tomato due to the application of bio-augmented compost with effective microorganisms was reported by Verma et al. (2015). Currently, increased attention is being paid to evaluate the role of antioxidants in human diet and health (Singh et al., 2013c). Increase in lycopene, β-carotene, ascorbic acid and other antioxidant compounds in tomato under the influence of T. harzianum could help in improving dietary antioxidants and lowering cholesterol and oxidative burst effects, thereby aiding the prevention of several chronic diseases (Singh et al., 2013c) by better scavenging/quenching activities in the body (Bhanja et al., 2009; Singh et al., 2009a).
Moreover, lipid peroxidation by ROS/FRs may lead to the formation of toxic by-products/compounds such as malondialdehyde and 4-hydroxynonenal which can attack on membrane, DNA, inducing mutagenicity and carcinogenicity (Nautiyal et al., 2008; Singh et al., 2009a; Ademoyegun et al., 2011). The ability of any external agent to inhibit the oxidation process is often used to evaluate its antioxidant activity. In the present investigation, we used rat liver homogenate assay to investigate, whether the fresh extract of ripe tomato was able to protect the lipids from oxidation provoked by FeSO4-based HO⋅. In the light of the above findings, the most probable reason for fresh tomato extracts as FRs and/or ROS-scavengers might be the enhanced concentration of antioxidant compounds in the extract that have been reported to inhibit lipid peroxidation and protein oxidation by quenching FRs (Yang et al., 2000; Lee et al., 2008; Singh et al., 2009b, 2010). On the other hand, results also register the fact that plants treated with EGTHB-SMS accumulate more isoflavonoids and phenolics in the ripe tomato fruits. These are also powerful protecting agents against the lethal effects of oxidative damage and protect macromolecules by chelating redox-active transition metal ions (Bhanja et al., 2009; Singh et al., 2010). The present investigation indicates synergistic action of phenolic compounds in scavenging ROS, repairing protein and lipid peroxidation and metal chelation (Prakash et al., 2007a; Lee et al., 2008; Moktan et al., 2008; Singh et al., 2010).
The antioxidant efficiency of phenolic compounds has been related to the number of OH⋅ groups in their structures and also to their hydrogen radical donating abilities (Lemanska et al., 2001; Altunkaya et al., 2009). This observation is in agreement with the findings of other investigators (Lin et al., 2006; Lee et al., 2008; Singh et al., 2010). Higher polyphenolics in the extract might be due to T. harzianum-mediated formation or mobilization of free phenolic and flavonoid molecules in the tomato fruits from site of synthesis (Singh et al., 2010; Ahmad et al., 2016; Altunkaya et al., 2016). We further investigated the role of the ripe tomato fruit extract on Fe2+ and Fe3+chelation, because these are the most effective pro-oxidants that are present in the food system (Halliwell et al., 1987). The results also reveal that the tomato extracts showed a marked capacity for iron binding which might be helping in the lipid peroxidation and protein protection under stressed condition. The reducing capacity of a compound Fe3+ complex to the ferrous form may serve as a significant indicator of its antioxidant capacity (Roy and Rice-Evans, 1994). The existence of reductions is the key of the reducing power, which exhibit their antioxidant activities by breaking the free radical chain by donating a hydrogen atom (Schally and Nagy, 1999). The reduction of the Fe3+/ferric cyanide complex to the ferrous form occurs due to the presence of resultants in the solution. Chelating agents have been reported to be effective as secondary antioxidants as they reduce the redox potential, thereby stabilizing the oxidized form of the metal ions (Halliwell et al., 1987; Prakash et al., 2007b; Singh et al., 2009a, 2010). Superoxide ions directly and/or indirectly initiate oxidation of biomolecules such as nucleic acids, proteins, lipids and carbohydrates as a result of superoxide and hydrogen peroxide serving as precursors of singlet oxygen and HO⋅ (Singh et al., 2010). The present study also revealed that high flavonoid content in the extract leads to scavenging of superoxide radicals. This result is in agreement with the earlier findings of Singh et al. (2009a). Our results also indicate better O2⋅− scavenging abilities in the extracts of plants treated with EGTHB-SMS than the control, and it might be due to formation of a glycones from glycosides of total phenolic and flavonoid and activation of superoxide dismutase (SOD) activity in the tomato fruits from T. harzianum treated plants. Furthermore, tomato is reported to contain sufficient amount of polyphenols (Singh et al., 2010, 2013b; Altunkaya et al., 2016), which are naturally occurring antioxidants, that possess an O2⋅− scavenging effect similar to flavonoids (Singh et al., 2010; Ahmad et al., 2016).
The antioxidant activity assayed was the ability to inhibit the peroxidation of lipids. The higher antioxidant activity of extracts might be due to the inhibition of chain reaction, decomposing peroxides, preventing continued hydrogen abstraction and also attributed to the presence of antioxidant enzymes and phytochemicals, such as phenolics and isoflavones, ascorbic acid etc. (Singh et al., 2010). Our findings demonstrate a direct correlation between antioxidant activities and levels of enzymatic activity and are in agreement with the findings of some previous studies (Yang et al., 2008; Gao et al., 2010; Singh et al., 2013b,c). Further, the increase in the tomato yield is directly related to the higher nutritional content, enzymes and other plant growth promoting substrates present in the EGTHB-SMS. Furthermore, soil physico-biochemical properties were significantly affected by the application of biofortified SMS. Previous studies showed that application of organic matter significantly increases the soil biological properties (Sahu, 2011; Singh et al., 2013a; Lim et al., 2015). However, the available macro- and micronutrients in vermicompost are generally higher than in traditional compost produced from the same raw material (Lim et al., 2015). The biofortification further increases the quality of the compost and ultimately, influences the plant growth and quality of end products (Pramanik et al., 2007; Singh et al., 2008, 2013a). Additional indirect mechanisms include enhancement in the population of other beneficial microbes in the rhizosphere, enhanced nutrient use efficiency, and modulation of host physio-biological pathways leading to better plant growth and productivity (Ahlawat et al., 2006).
The demand for organically grown fruits and vegetables has been growing steadily over the past few decades due to the awareness developed among people for a healthy lifestyle. Addition of organic manure and bioinoculants enhances the nutrient mobilization by the plants and helps them defend against various stresses by enhanced production of antioxidant enzymes and phenolics. The study describes the multifarious effects of EGTHB-SMS in tomato plants that significantly increase various attributes in the tomato fruits. Further, it was noted that EGTHB-SMS was found to be more potential in enhancing natural antioxidants, mineral nutrients and enzymes in the fruits. Encouraging results were also obtained with increase in nutritional quality of ripe tomato fruits (mineral nutrients and natural antioxidant properties) modulated by the application of EGTHB-SMS. Results of the investigation suggest that application of EGTHB-SMS in tomato not only helps in increasing yield and enhancing the nutritional value of ripe fruits but also reduces the risk of environmental pollution caused by piling and rather unsafe disposal of SMS.
UBS, DM, JPR, BKS, AKS, RC, MCM, and DP were involved in conceiving the idea and designing the work. UBS, DM, WK, SS, NK, MI, MCM, and RC conducted the actual research work. UBS, DM, WK, SS, NK, JPR, BKS, AKS, RC, MCM, and DP wrote the paper. However, J-WO contributed to the general designing and also in revising the MS during the review process. All authors were contributed to interpretation of results and discussion and approved the final version of the manuscript.
Conflict of Interest Statement
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.
We would like to express our special thanks to Dr. Pratap Singh, Department of Plant Physiology and Dr. Alok Jha, Centre of Food Science and Technology, Institute of Agricultural Sciences, BHU, Varanasi for providing experimental support to carry out a part of this research work. We wish to thank Dr. A. K. Saxena, ICAR-NBAIM, Kushmaur, Maunath Bhanjan for technical assistance in writing and preparation of the manuscript. We also thank Dr. H. B. Singh, Department of Mycology and Plant Pathology, Institute of Agricultural Sciences, BHU, Varanasi for technical assistance in planning the experiments.
Ademoyegun, O. T., Fariyike, T. A., and Aminu-Taiwo, R. B. (2011). Effects of poultry dropping on the biologically active compounds in Capsicum annuum L. (var. Nsukka yellow). Agric. Biol. J. N. Am. 2, 665–672. doi: 10.5251/abjna.2011.2.4.665.672
Ahlawat, O. P., Dev, R., Sagar, M. P., Gupta, P., and Vijay, B. (2006). Effect of recomposted spent mushroom substrate on yield and quality of cauliflower (Brassica oleracea L. var. botrytis). Mushroom Res. 15, 149–152.
Ahmad, N., Zuo, Y., Lu, X., Anwar, F., and Hameed, S. (2016). Characterization of free and conjugated phenolic compounds in fruits of selected wild plants. Food Chem. 190, 80–89. doi: 10.1016/j.foodchem.2015.05.077
Aira, M., Sampedro, L., Monroy, F., and Domınguez, J. (2008). Detritivorous earthworms directly modify the structure, thus altering the functioning of a microdecomposer food web. Soil Biol. Biochem. 40, 2511–2516. doi: 10.1016/j.soilbio.2008.06.010
Altunkaya, A., Becker, E. M., Gokmen, V., and Skibsted, L. H. (2009). Effect of various inhibitors on enzymatic browning, antioxidant activity and total phenol content of fresh lettuce. Food Chem. 115, 163–168. doi: 10.1016/j.foodchem.2008.11.082
Altunkaya, A., Gokmen, V., and Skibsted, L. H. (2016). pH dependent antioxidant activities of lettuce (L. sativa) and synergism with added phenolic antioxidants. Food Chem. 190, 25–32. doi: 10.1016/j.foodchem.2015.05.069
Anderson, J. M. (1987). “Interactions between invertebrates and microorganisms: noise or necessity for soil processes,” in Ecology of Microbial Communities, eds J. M. Anderson, A. D. M. Rayner, and D. W. H. Walton (Cambridge: Cambridge University Press), 125–145.
Atiyeh, R. M., Lee, S., Edwards, C. A., Arancon, N. Q., and Metzger, J. D. (2002). The influence of humic acids derived from organic wastes on plant growth. Bioresour. Technol. 84, 7–14. doi: 10.1016/S0960-8524(02)00017-2
Berg, G. (2009). Plant–microbe interactions promoting plant growth and health: perspectives for controlled use of microorganisms in agriculture. Appl. Microbiol. Biotechnol. 84, 11–18. doi: 10.1007/s00253-009-2092-7
Bhanja, T., Kumari, A., and Banerjee, R. (2009). Enrichment of phenolics and free radical scavenging property of wheat koji prepared with two filamentous fungi. Bioresour. Technol. 100, 2861–2866. doi: 10.1016/j.biortech.2008.12.055
Devasagayam, T. P., Tilak, J. C., Boloor, K. K., Sane, K. S., Ghaskadbi, S. S., and Lele, R. D. (2004). Free radicals and antioxidants in human health: current status and future prospects. J. Assoc. Physicians India 52, 794–804.
Gao, D., Du, L., Yang, J., Wu, W. M., and Hong Ling, H. (2010). A critical review of the application of white rot fungus to environmental pollution control. Crit. Rev. Biotechnol. 30, 70–77. doi: 10.3109/07388550903427272
Halliwell, B., Gutteridge, J. M. C., and Aruoma, O. I. (1987). The deoxyribose method: a simple test tube assay for the determination of rate constants for the reaction of hydroxyl radicals. Anal. Biochem. 165, 215–219. doi: 10.1016/0003-2697(87)90222-3
Hyman, J. R., Gaus, J., and Foolad, M. R. (2004). A rapid and accurate method for estimating tomato lycopene content by measuring chromaticity values of fruit puree. J. Am. Soc. Hortic. Sci. 129, 717–723.
Jonathan, S. G., Lawal, M. M., and Oyetunji, O. J. (2011). Effect of spent mushroom compost of Pleurotus pulmonarius on growth performance of four Nigerian vegetables. Mycobiology 39, 164–169. doi: 10.5941/MYCO.2011.39.3.164
Krishnamoorthy, R. V., and Vajrabhiah, S. N. (1986). Biological activity of earthworm casts: an assessment of plant growth promoter levels in casts. Proc. Natl. Acad. Sci. U.S.A. 95, 341–351. doi: 10.1007/BF03179368
Lalander, C. H., Komakech, A. J., and Vinnerås, B. (2015). Vermicomposting as manure management strategy for urbansmall-holder animal farms – Kampala case study. Waste Manag. 39, 96–103. doi: 10.1016/j.wasman.2015.02.009
Lemanska, K., Szymusiak, H., Tyrakowska, B., Zielinski, R., Soffers, A. E. M. F., and Rietjens, I. M. C. M. (2001). The influence of pH on antioxidant properties and the mechanism of antioxidant action of hydroxyflavones. Free Radic. Biol. Med. 31, 869–881. doi: 10.1016/S0891-5849(01)00638-4
Lim, S. L., Wu, T. Y., Lim, P. N., and Shak, K. P. Y. (2015). The use of vermicompost in organic farming: overview, effects on soil and economics. J. Sci. Food Agric. 95, 1143–1156. doi: 10.1002/jsfa.6849
Lores, M., Gomez-Brandon, M., Perez-Dıaz, D., and Domınguez, J. (2006). Using FAME profiles for the characterization of animal wastes and vermicomposts. Soil Biol. Biochem. 38, 2993–2996. doi: 10.1016/j.soilbio.2006.05.001
Montalba, R., Arriagada, C., Alvear, M., and Zuniga, G. E. (2010). Effects of conventional and organic nitrogen fertilizers on soil microbial activity, mycorrhizal colonization, leaf antioxidant content, and Fusarium wilt in high bush blue berry (Vaccinium corymbosum L.). Sci. Hortic. 125, 775–778. doi: 10.1016/j.scienta.2010.04.046
Nautiyal, C. S., Govindarajan, R., Lavania, M., and Pushpangadan, P. (2008). Novel mechanism of modulating natural antioxidants in functional foods: involvement of plant growth promoting rhizobacteria NRRL B-30488. J. Agric. Food Chem. 56, 4474–4481. doi: 10.1021/jf073258i
Ndegwa, P. M., and Thompson, S. A. (2001). Integrating composting and vermicomposting in the treatment and bioconversion of biosolids. Bioresour. Technol. 76, 107–112. doi: 10.1016/S0960-8524(00)00104-8
Ochoa-Velasco, C. E., Valadez-Blanco, R., Salas-Coronado, R., Sustaita-Rivera, F., Hernández-Carlos, B., García-Ortega, S., et al. (2016). Effect of nitrogen fertilization and Bacillus licheniformis biofertilizer addition on the antioxidants compounds and antioxidant activity of greenhouse cultivated tomato fruits (Solanum lycopersicum L. var. Sheva). Sci. Hortic. 201, 338–345. doi: 10.1016/j.scienta.2016.02.015
Prakash, D., Singh, B. N., and Upadhyay, G. (2007a). Antioxidant and free radical scavenging activities of phenols from onion (Allium cepa). Food Chem. 102, 1389–1393. doi: 10.1016/j.foodchem.2006.06.063
Prakash, D., Upadhyay, G., Singh, B. N., and Singh, H. B. (2007b). Antioxidant and free radical scavenging activities of seeds and agri-wastes of some varieties of soybean (Glycine max). Food Chem. 104, 783–790. doi: 10.1016/j.foodchem.2006.12.029
Pramanik, P., Ghosh, G. K., Ghosal, P. K., and Banik, P. (2007). Changes in organic-C, N, P and K and enzyme activities in vermicompost of biodegradable organic wastes under liming and microbial inoculants. Bioresour. Technol. 98, 2485–2494. doi: 10.1016/j.biortech.2006.09.017
Sarma, B. K., Singh, P., Pandey, S. K., and Singh, H. B. (2010). “Vermicompost as modulator of plant growth and disease suppression,” in Vermitechnology II. Dynamic Soil, Dynamic Plant, Vol. 4, ed. N. Karmegam (Varanasi: Banaras Hindu University), 58–66.
Sarma, B. K., Yadav, S. K., Singh, S., and Singh, H. B. (2015). Microbial consortium-mediated plant defense against phytopathogens: readdressing for enhancing efficacy. Soil Biol. Biochem. 87, 25–33. doi: 10.1016/j.soilbio.2015.04.001
Sen, S., and Chakraborty, R. (2011). “The role of antioxidants in human health,” in Oxidative Stress: Diagnostics, Prevention, and Therapy. ACS Symposium Series, Vol. 1083, (Washington, DC: American Chemical Society), 1–37. doi: 10.1021/bk-2011-1083.ch001
Singh, A., Jain, A., Sarma, B. K., Abhilash, P. C., and Singh, H. B. (2013a). Solid waste management of temple floral offerings by vermicomposting using Eisenia fetida. Waste Manag. 33, 1113–1118. doi: 10.1016/j.wasman.2013.01.022
Singh, A., Sarma, B. K., Upadhyay, R. S., and Singh, H. B. (2013b). Compatible rhizosphere microbes mediated alleviation of biotic stress in chickpea through enhanced antioxidant and phenylpropanoid activities. Microbiol. Res. 168, 33–40. doi: 10.1016/j.micres.2012.07.001
Singh, B. N., Singh, B. R., Singh, R. L., Prakash, D., Sarma, B. K., and Singh, H. B. (2009a). Antioxidant and anti-quorum sensing activities of green pod of Acacia nilotica L. Food Chem. Toxicol. 47, 778–786. doi: 10.1016/j.fct.2009.01.009
Singh, B. N., Singh, B. R., Singh, R. L., Prakash, D., Singh, D. P., Sarma, B. K., et al. (2009b). Polyphenolics from various extracts/fractions of red onion (Allium cepa) peel with potential antioxidants and antimutagenic activities. Food Chem. Toxicol. 47, 1161–1167. doi: 10.1016/j.fct.2009.02.004
Singh, H. B., Singh, B. N., Singh, S. P., and Nautiyal, C. S. (2010). Solid-state cultivation of Trichoderma harzianum NBRI-1055 for modulating natural antioxidants in soybean seed matrix. Bioresour. Technol. 101, 6444–6453. doi: 10.1016/j.biortech.2010.03.057
Singh, R., Sharma, R. R., Kumar, S., Gupta, R. K., and Patil, R. T. (2008). Vermicompost substitution influences growth, physiological disorders, fruit yield and quality of strawberry (Fragaria ananassa Duch.). Bioresour. Technol. 99, 8507–8511. doi: 10.1016/j.biortech.2008.03.034
Singh, U. B., Sahu, A., Sahu, N., Singh, B. P., Singh, R. K., Renu, S. D. P., et al. (2013c). Can endophytic Arthrobotrys oligospora modulate accumulation of defence related biomolecules and induced systemic resistance in tomato (Lycopersicon esculentum Mill.) against root knot disease caused by Meloidogyne incognita. Appl. Soil Ecol. 63, 45–56. doi: 10.1016/j.apsoil.2012.08.007
Singh, U. B., Sahu, A., Singh, R. K., Singh Dhananjaya, P., Meena, et al. (2012). Evaluation of biocontrol potential of Arthrobotrys oligospora against Meloidogyne graminicola and Rhizoctonia solani in rice (Oryza sativa L.). Biol. Control 60, 262–270. doi: 10.1016/j.biocontrol.2011.10.006
Verma, S., Sharma, A., Kumar, R., Kaur, C., Arora, A., Shah, R., et al. (2015). Improvement of antioxidant and defense properties of tomato (var. Pusa Rohini) by application of bioaugmented compost. Saudi J. Biol. Sci. 22, 256–264. doi: 10.1016/j.sjbs.2014.11.003
Keywords: Trichoderma harzianum, solid-state cultivation, spent mushroom substrate, antioxidants, ROS, lipid peroxidation, protein oxidation
Citation: Singh UB, Malviya D, Khan W, Singh S, Karthikeyan N, Imran M, Rai JP, Sarma BK, Manna MC, Chaurasia R, Sharma AK, Paul D and Oh J-W (2018) Earthworm Grazed-Trichoderma harzianum Biofortified Spent Mushroom Substrates Modulate Accumulation of Natural Antioxidants and Bio-Fortification of Mineral Nutrients in Tomato. Front. Plant Sci. 9:1017. doi: 10.3389/fpls.2018.01017
Received: 28 March 2018; Accepted: 22 June 2018;
Published: 17 July 2018.
Edited by:Youssef Rouphael, Università degli Studi di Napoli Federico II, Italy
Reviewed by:Alessandra Salvioli, Università degli Studi di Torino, Italy
László Kredics, University of Szeged, Hungary
Copyright © 2018 Singh, Malviya, Khan, Singh, Karthikeyan, Imran, Rai, Sarma, Manna, Chaurasia, Sharma, Paul and Oh. 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) and the copyright owner(s) 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: Jae-Wook Oh, firstname.lastname@example.org
†These authors have contributed equally to this work.