Impact Factor 4.298

The 1st most cited journal in Plant Sciences

This article is part of the Research Topic

Root Apex Zones: From Growth to Behaviour

Original Research ARTICLE

Front. Plant Sci., 18 February 2016 | https://doi.org/10.3389/fpls.2016.00079

MES Buffer Affects Arabidopsis Root Apex Zonation and Root Growth by Suppressing Superoxide Generation in Root Apex

  • 1Institute of Cellular and Molecular Botany, University of Bonn, Bonn, Germany
  • 2Department of Biological Sciences, Tokyo Metropolitan University, Tokyo, Japan

In plants, growth of roots and root hairs is regulated by the fine cellular control of pH and reactive oxygen species (ROS). MES, 2-(N-morpholino)ethanesulfonic acid as one of the Good’s buffers has broadly been used for buffering medium, and it is thought to suit for plant growth with the concentration at 0.1% (w/v) because the buffer capacity of MES ranging pH 5.5–7.0 (for Arabidopsis, pH 5.8). However, many reports have shown that, in nature, roots require different pH values on the surface of specific root apex zones, namely meristem, transition zone, and elongation zone. Despite the fact that roots always grow on a media containing buffer molecule, little is known about impact of MES on root growth. Here, we have checked the effects of different concentrations of MES buffer using growing roots of Arabidopsis thaliana. Our results show that 1% of MES significantly inhibited root growth, the number of root hairs and length of meristem, whereas 0.1% promoted root growth and root apex area (region spanning from the root tip up to the transition zone). Furthermore, superoxide generation in root apex disappeared at 1% of MES. These results suggest that MES disturbs normal root morphogenesis by changing the ROS homeostasis in root apex.

Introduction

Good et al. (1966) selected and reported buffers with less toxicity and less reactivity to biological compounds. Since then, these buffers were introduced to enormous amount of laboratory-based experiments. Since eighties of the last century, many studies using plant hydroponic culture have been reporting the availability of MES molecule for buffering pH in liquid culture media. Imsande and Ralston (1981) demonstrated that 1–2 mM of MES solution has an excellent buffering capacity and it shows neither inhibition of nodulation nor lowering of nitrogen fixation in soybean hydroponic culture. Bugbee and Salisbury (1985) reported that MES did not significantly decrease growth as measured by the seven growth parameters in any of the five species. 5 mM of MES was shown no impact on growth or uptake of most nutrients. Potassium uptake was even enhanced by the MES buffer in non-nodulated seedlings of soybean (Schuttler, 1987).

MES, 2-(N-morpholino)ethanesulfonic acid, is one of broadly used Good’s buffers. This is broadly used to regulate pH value for plants culture medium, reagent solution, and physiological experiments. Since the pKa value of MES is 6.15 at 20°C, it is thought to be suitable for plant growth in terms of nutrient uptake, e.g., for Arabidopsis at pH 5.8. Besides MES, HEPES, PIPES and MOPS are also well-known Good’s buffers as synthetic zwitterionic buffers utilizes for culture of living organisms both for animals and plants.

Meanwhile, some studies have been reporting considerable problems caused by a chemical reaction between buffer molecules and other compounds in the media. In the presence of high concentrations of MES and PIPES, the polymerization of purified tubulin was observed using electron microscope (Waxman et al., 1981). For plant experiments, MES was reported to lower nitrogen fixation and plant growth in white clover (Rys and Phung, 1985). Medeiros et al. (1993) reported that 2 mM MES in hydroponic culture reduced shoot and root dry matter yields in maize (Zea mays L.) and increased accumulation of N, Ca, Mg, Mn, and Zn in shoot. Miyasaka et al. (1988) reported that Mg, Mn, and Zn uptake was decreased in winter wheat. MES was reported to perturb normal growth of cucumber in hydroponic condition, because MES oxidizes Mn2+ to Mn3+ and precipitates it from the nutrient solution, and thus nutrient uptake was inhibited due to this direct chemical reaction (Stahl et al., 1999). Importantly, 4 mM MES cannot maintain pH value for long period in hydroponic condition. The pH was decreased from 6.5 to 4.0 just for 5 days (Nicholas and James, 1993). It was also reported that MES inhibits the adventitious root formation from apple stem disks at 10 mM of concentration (De Klerk et al., 2008).

In addition to compounds prepared in media such as nutrients, there are numerous biomolecules in living organisms which interact with these buffers. Reactive oxygen species (ROS) and reactive nitrogen species (RNS) are considered as important primary signaling molecules playing a role in the propagation of cellular physiological information. As an interaction with RNS, Lomonosova et al. (1998) found out the production of hydrogen peroxide in the presence of peroxynitrite (ONOO; one of RNS) and HEPES buffer. HEPES was also shown to consume superoxide (one of ROS) and nitric oxide (NO) (Keynes et al., 2003). Very intriguingly, the combination of HEPES and riboflavin, often added as vitamin, in the culture medium drastically reduced NO content under the laboratory light environment (Keynes et al., 2003). Light-activated riboflavin accelerated the reaction mediated by HEPES (Keynes et al., 2003). In fact, piperazine ring-based buffers such as HEPES and PIPES have the ability to form radicals (Grady et al., 1988). These findings suggest that such buffers potentially interferes cellular ROS/RNS homeostasis. In this respect, a biochemical study demonstrated that a normal peroxidase activity for oxidizing phenolics was strongly interfered in the presence of MES at concentrations of 5 mM in the solution, due to the replacement of target substrate with MES molecule (Baker et al., 2007).

Surprisingly, 2.5–10 mM (ca. 0.05–0.2% w/v) of MES has been used as a proper concentration for culture media since Arabidopsis has been introduced as model plant several decades ago. It implies that plant peroxidase, one of main functions is to compose cell wall, might be affected as roots always contact to buffer-containing media. Roots require precise control of pH value and ROS homeostasis for their normal morphogenesis in different specific zones (namely; root tip, meristematic zone, transition zone, and elongation zone). Therefore, the effect of buffer, which potentially modifies the culture environments, must be assessed. Here, we observed the followings using roots of Arabidopsis seedlings, (1) MES enhanced the root growth as well as the number of root hairs at 0.01% (w/v) and 0.1%, whereas 1% inhibited, (2) MES enhanced the root waving phenotype, (3) MES promoted the enlargement of meristem at 0.1%, (4) 1% MES depleted apical root meristems. Less superoxide accumulation at the root apices was found in the MES-exposed roots when compared to the control roots.

Materials and Methods

Plant Growth Condition

Seeds of Arabidopsis thaliana were sterilized with 2% NaClO (ROTH, Karlsruhe, Germany) containing 0.1% Triton-X (ROTH, Karlsruhe, Germany) for 5 min. These seeds were washed in water for four times. Seeds were planted on 1/2 MS media (Duchefa, Haarlem, The Netherlands) containing 1% (w/v) sucrose (pH 5.8 with KOH) solidified with 0.4% (w/v) phytagel (Sigma, Steinheim, Germany). Each concentration of MES (Duchefa, Haarlem, The Netherlands) was added to 1/2 MS media before autoclaved. The petri dishes were incubated at 4°C for 1 day for imbibition and were put vertically at 23–25°C in 16 h light/8 h dark (light intensity: ∼120 μmol/s/m2, humidity: ∼50%). At the time point of 3 and 6 days, pictures of the seedlings were taken with EOS Kiss X7 (Canon, Tokyo). Root lengths were measured by ImageJ software (ver. 1.43u for Mac OSX1). The number of waves were counted and compared in 6 day-old roots grown in different MES concentrations.

Microscopic Observation

Images of root hairs were taken through 0.8× objective lens of a stereomicroscope Leica MZFLIII (Solms, Germany). Images of root apices were taken through 10× objective lens of a light microscope Leica DM750 (Solms, Germany). Root hairs and distances between root tip to root growth were measured by ImageJ software.

Histochemical NBT Staining for Superoxide Detection

To detect the presence of superoxide in root apex grown in different concentrations of MES, 6 day-old seedlings were incubated for 5 min in the staining solution of 300 μM nitroblue tetrazolium salt (NBT; Fluka, Germany) dissolved in 0.1 M Tris-HCl, 0.1 M NaCl, 0.05 M MgCl2 (pH = 9.5). Seedlings were then observed and imaged under a light stereomicroscope.

Statistical Analysis

All numerical data obtained here were analyzed and tested in appropriate statistical methods. Tukey’s HSD (honestly significant difference) was applied to test a level of significance at p < 0.05 using R software (R for Mac OS X Cocoa2).

Results

Effect of MES Buffer on Root Growth

Arabidopsis Col-0 seeds were germinated and grown on the media containing four different concentrations of MES (0, 0.01, 0.1, and 1%). The MES-containing media at this range of concentration showed no effect on seed germination (data not shown). The root length was then measured at the time point of 3 and 6 days after germination.

Three days after germination, the average of root lengths showed significant different among 0, 0.01, 0.1, and 1% MES treatments. As Figure 1B shows, 0.01 and 0.1% of MES promoted the growth whereas 1% of concentration inhibited. Similarly, 6 days after germination, both 0.01 and 0.1% of MES still promoted the root growth (Figures 1A,C). These data indicates low MES concentration (in the range from 0.01 to 0.1%) in 1/2 MS phytagel enhances root growth from early developmental stage of seedlings, however, 1% MES inhibited. In addition to the growth, we observed the effect of MES on root growth behavior, so-called waving phenotype, which is known to reflect a root tropic growth affected by several physical factors such as gravity, light, touch etc. (Okada and Shimura, 1990; Simmons et al., 1995). Therefore, the frequency of root waving on each MES containing plate was also assessed. In the result, waving frequency was enhanced as MES concentration increased (Figures 1A,D).

FIGURE 1
www.frontiersin.org

FIGURE 1. Root growth and morphology in different concentrations of MES. (A) Appearances of seedlings at 6-day old. The seeds were germinated on 1/2 MS medium containing each concentration of MES. Black marks indicate positions of root apices at 3-day old. (B) Root lengths at 3-day after germination on each concentration of MES. Error bars indicate standard deviation of the mean (n = 62–72). (C) Root lengths at 6-day after germination old on each concentration of MES. Error bars indicate standard deviation of the mean (n = 34–65). (D) The number of waves of the roots. Error bars indicate standard deviation of the mean (n = 17). (E) Root hair formation affected by MES. Lengths of root hairs were measured at position where long root hairs emerge, because the distance from the tip varies under different MES treatments. Five root hairs were measured from five seedlings. Error bars indicate standard deviation of the mean (n = 25). Different letters indicate significant difference (Tukey’s HSD test, P < 0.05).

As we described in the introduction part, pH and ROS have an important role for root growth. The formation of root hair also requires fine control of those parameters. Here the impacts of MES on root hairs in 6 days after germination seedlings were compared. Images of roots were taken through 0.8× objective lens of a stereomicroscope. As Figure 1E shows, 1% of MES drastically inhibited normal root hair formation. Lengths of five root hairs from five different roots (n = 25) in each treatment were measured and averaged. In the result, MES increased the length of root hairs when it is at 0.01% (p < 0.05) compared to control, but not at 0.1%. Interestingly, 1% MES strongly suppresses the formation (Figure 1E). The total number of root hairs did not show significant differences among four MES concentrations (data not shown).

Root Morphology in Apex Region in the Presence of MES

As we observed, the presence of MES changed the root growth and its tropic behavior. Next, we have focused on root apex region in roots grown in different MES concentrations. This region is known to play an important role for polar auxin transport, which controls root tropic behaviors, and it is most sensitive part of roots to external environments. Figure 2A shows a scheme of root apices. Cells with asterisks indicate the typical cells in the transition zone. In this study, we have defined borders between transition zone and elongation zone as following morphological category: the cell lengths obtain values which are two times higher as the cell widths (Baluška et al., 2010). Arrows in Figure 2B indicate positions of the border between transition zone and elongation zone. A dashed horizontal line indicates the position of root tips. As depicted in Figures 2B,C, the treatment of MES resulted in altering the size of root apex region including transition zone. MES at 0.1% concentration significantly enlarged the size of area, whereas 1% minified. We observed that only the number of cells in root apex region (from the root tip to the elongation zone) was affected by MES exposure, not cell size, namely 10–15 μm of longitudinal cell length (growth direction) in the region was observed in all MES treatments. Interestingly, the abnormality in cell shape in root apex was observed in 1% MES growth condition (also shown Figure 3). It suggests that high MES condition might interfere with the overall root morphogenesis similarly to root hair formation (Figure 1E)

FIGURE 2
www.frontiersin.org

FIGURE 2. Comparison of the root apex lengths. (A) A scheme of the root apex. Cells with asterisks indicate the typical cells in transition zone. In this study, we define the border between transition zone and elongation zone as following morphological category: the cell lengths obtain values which are two times higher as the cell widths (Baluška et al., 2010). (B) Microscope images of the root apices. Tips of black triangulates indicate positions of the end of transition zone. A dashed horizontal line indicates the position of root apices. (C) Lengths of the root apices (from the root tip to the end of the transition zone). Error bars indicate standard deviations of the mean (n = 9–11). Different letters indicate significant difference (Tukey’s HSD test, P < 0.05).

FIGURE 3
www.frontiersin.org

FIGURE 3. Light Stereomicroscope pictures of NBT staining for superoxide detection. Seedlings were grown in different concentrations of MES for 6 days. These were incubated for 5 min in NBT. The representative picture is shown here (n = 5).

Superoxide Localization in Root Apex

As we have described in the introduction part, MES was reported to interact or interfere with biological redox machineries. Many studies have already revealed that proper control of redox homeostasis or ROS signaling are ultimately essential for root growth and root tropisms. Here we tried to detect the distribution of superoxide in roots of Arabidopsis using a histochemical staining method, NBT staining. When NBT compound reacts with superoxide, formazan visualized as blue precipitation in cells is immediately formed. Superoxide is known as one of ROS existing in apex region, which controls cell proliferation (Tsukagoshi et al., 2010). As shown in Figure 3, NBT staining pattern in root apex region was observed in control, 0.01 and 0.1% MES condition. However, it completely disappeared in the 1% MES growth condition. It means that superoxide required for normal root growth in apex region is continuously diminished by 1% MES in growth media during culture on a plate for 6 days.

Discussion

MES Effect to pH and ROS Homeostasis

Because of the pKa value in acidic region, MES compound has been used for pH buffer by adding to plant culture media in terms of nutrient uptake. In Arabidopsis research, MES was also introduced to buffer pH value in agar-solidified plate culture. In this study, we have demonstrated that the effect of MES on Arabidopsis root growth, morphogenesis and tropic behavior. Furthermore, staining superoxide in root apex indicated that MES strongly interferes with ROS homeostasis at 1% of MES, but not at 0.1%, which has an important role for root growth.

Foreman et al. (2003) demonstrated that superoxide produced by plasma membrane-associated NADPH oxidase is necessary for intracellular Ca2+ elevation leading to root hair formation and cell expansion. The treatment of diphenylene iodonium (DPI), inhibitor for flavo-proteins including NADPH oxidase, resulted in suppressing ROS accumulation and lacking root hairs (phenocopy of rhd2 mutants; Foreman et al., 2003). The inhibitory effect of 1% of MES on root growth and root hair formation can be concluded as the result of disruption of superoxide production (Figure 3).

Besides ROS homeostasis, pH is also important factor for cell expansion and root growth regulation. It was already reported that root hair formation requires acidification of cell wall (Bibikova et al., 1998), interplay between extracellular pH and ROS production (Monshausen et al., 2007). Therefore, the interruption of root hair initiation observed here might be interpreted due to a high buffering capacity of MES at 1% concentration in the phytagel media. On the other hand, 0.01 and 0.1% MES treatment significantly enhanced root growth (Figures 1A–C), and 0.1% MES enhanced root hair length (Figure 1E) compared to control conditions. This is probably because of modest buffering ability at this range of concentrations (0.01–0.1%) support continuous acidification required for root hair tip growth as well as for the root growth.

MES Impacts on Transition Zone and Tropism of Roots

In this study, we found out that 0.1% MES increased the area of apex region including from root tip to the border between transition zone and elongation zone (Figure 2). With stereomicroscope, the increase of cell numbers in this root apex region was observed. Transition zone of the root apex plays an important role for all root tropic behaviors based on polar auxin transport, which is accomplished via endocytic vesicle recycling as found in cells of this region (Baluška et al., 2010). As we have observed, the enlargement of the region in the presence of 0.1% MES (Figure 2) enhances waving phenotype of growing roots (Figure 1D). This root waving phenotype is known as a result of root tropic response of physical contact to agar surface (Okada and Shimura, 1990; Simmons et al., 1995). It was also reported that this phenotype became stronger if roots grown in light condition (Okada and Shimura, 1990). In addition, root growth pattern (waving and skewing) was also reported to change by the hardness of agar medium. 1.5% agar medium show stronger slanted-growth than 0.8% or 3% (Rutherford and Masson, 1996). Huang et al. (1995) showed that the rigidity of phytagel was altered by pH or the concentrations of nutrient components in media. Since root growth patterns depend on environmental factors (e.g., light and gravity) as well as physical contacts to media, high buffer contents are possibly changing physical properties of agar, affecting root growth on solidified plates. Very interestingly, the size of root apex correlates with the waving frequency (Figures 1D and 2), suggesting that the MES-induced enlargement of this root apex region results in changing root tropic behavior.

Tsukagoshi et al. (2010) reported that UPBEAT1, a transcription factor, regulates the expression of peroxidase in root apex, determining the borderline between transition zone and elongation zone. There are two different ROS types present in these two root apex zones playing distinct roles, hydrogen peroxide in elongation zone and superoxide in transition zone is for cell differentiation and is for cell proliferation, respectively. In response to environmental conditions, roots regulate mode of growth by modulating the position of this borderline via UPBEAT1 regulation.

Possible reasons for MES-altered the area of transition zone can be considered as follows. (1) Indirect effect due to MES buffering ability. Similar to ROS in roots, pH must also be controlled in different zones in roots (He et al., 2015). Therefore, roots changed the morphology as a result of an attempt to recover pH homeostasis or escape from such a situation. (2) Direct interaction of MES with peroxidases. It was already reported in a biochemical study as aforementioned. Because of the molecular structure of MES, it interferes with peroxidase activities oxidizing phenolic compounds (Baker et al., 2007). Peroxidases in root apex region might be affected in the presence of MES. It was reported that the appropriate control of ROS homeostasis by cell wall peroxidase is essential to regulate root cell elongation (Liszkay et al., 2004). As Figure 3 shows, since superoxide in transition zone was completely disappeared at 1% concentration, it is likely that MES disturbs ROS-generating pathway, possibly via enzymes (peroxidases) or direct scavenging. A schematic summary is shown in Figure 4.

FIGURE 4
www.frontiersin.org

FIGURE 4. A schematic diagram of MES effects on root growth. MES disturbs ROS-generating pathway in the root apex, possibly via enzymes (e.g., peroxidases), affecting the root apex zonation. The ROS (O2) is involved in root hair formation, root growth and root tropisms.

MES for Laboratory-based Experiments

In addition to extracellular interaction of MES and biological compounds, it is likely that MES compound is also taken up by roots and transported to other tissues in plant body such as leaves. This suggests that incorporated MES molecule in cellular space might cause lasting reactions interfering with many extracellular and intracellular signaling molecules. For example, HEPES buffer, structurally analogous to MES, drastically consumes endogenous NO in the presence of riboflavin under laboratory light condition (Keynes et al., 2003). Culturing plants under light in a growth chamber needs great caution if growth media contain such buffers. Impacts of light on growing Arabidopsis roots have been reported recently. Under illuminated condition, roots alter their physiological conditions, growth rate, tropisms (Yokawa et al., 2011, 2013, 2014; Wan et al., 2012; Kagenishi et al., 2015; Mo et al., 2015; Novák et al., 2015). Importantly, roots are evolutionarily optimized to grow in darkness in nature. Light activates root photoreceptors, or probably other light-absorbing compounds in root cells. In this regard, light may even bring unexpected results through a reaction with buffer compounds inside or outside of root cells as already discussed above (Keynes et al., 2003). Moreover, as we have noted in the introduction part, 4 mM of MES (approximately 0.1%) could not maintain pH value for 5 days in liquid media. The pH was gradually decreased from 6.5 to 4.0. Potential problems with MES were pointed out previous study (Nicholas and James, 1993). All this suggests that the long-term experiments (longer than a day), that require fine pH control in liquid or solidified media, must be interpreted with a great care.

Growth conditions, buffers, other supplemental compounds such as riboflavin (vitamins) have been chosen to grow Arabidopsis as a model plant for laboratory-based experiments, we must take into account such artificial environments for further root research.

Author Contributions

All authors conceived of the research. TK and KY designed the experiments, TK conducted the experiments and analyses of data. And all authors prepared and revised 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.

Acknowledgments

KY was supported by the JSPS (Japanese Society for the Promotion of Science) Postdoctoral Fellowship. This work was supported in part by JSPS KAKENHI, Grant-in-Aid for JSPS fellows, No. 261654.

Footnotes

  1. ^ http://imagej.nih.gov/ij/
  2. ^ http://www.R-project.org

References

Baker, J., Mock, N., Roberts, D., Deahl, K., Hapeman, C., Schmidt, W., et al. (2007). Interference by Mes [2-(4-morpholino) ethanesulfonic acid] and related buffers with phenolic oxidation by peroxidase. Free Radic. Biol. Med. 43, 1322–1327. doi: 10.1016/j.freeradbiomed.2007.07.020

PubMed Abstract | CrossRef Full Text | Google Scholar

Baluška, F., Mancuso, S., Volkmann, D., and Barlow, P. W. (2010). Root apex transition zone: a signalling-response nexus in the root. Trends Plant Sci. 15, 402–408. doi: 10.1016/j.tplants.2010.04.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Bibikova, T. N., Jacob, T., Dahse, I., and Gilroy, S. (1998). Localized changes in apoplastic and cytoplasmic pH are associated with root hair development in Arabidopsis thaliana. Development 125, 2925–2934.

PubMed Abstract | Google Scholar

Bugbee, B. G., and Salisbury, F. B. (1985). An evaluation of MES (2(N-Morpholino) ethanesulfonic acid) and amberlite IRC-50 as pH buffers for nutrient solution studies. J. Plant Nutr. 8, 567–583. doi: 10.1080/01904168509363369

PubMed Abstract | CrossRef Full Text | Google Scholar

De Klerk, G. -J., Hanecakova, J., and Jásik, J. (2008). Effect of medium-pH and MES on adventitious root formation from stem disks of apple. Plant Cell Tiss. Organ. Cult. 95, 285–292. doi: 10.1007/s11240-008-9442-5

CrossRef Full Text | Google Scholar

Foreman, J., Demidchik, V., Bothwell, J. H., Mylona, P., Miedema, H., Torres, M., et al. (2003). Reactive oxygen species produced by NADPH oxidase regulate plant cell growth. Nature 422, 442–446. doi: 10.1038/nature01485

PubMed Abstract | CrossRef Full Text | Google Scholar

Good, N. E., Winget, G. D., Winter, W., Connolly, T. N., Izawa, S., and Singh, R. M. (1966). Hydrogen ion buffers for biological research. Biochemistry 5, 467–477. doi: 10.1021/bi00866a011

CrossRef Full Text | Google Scholar

Grady, J. K, Chasteen, N. D., and Harris, D. C. (1988). Radicals from “Good’s” buffers. Anal. Biochem. 173, 111–115. doi: 10.1016/0003-2697(88)90167-4

CrossRef Full Text | Google Scholar

He, Y., Wu, J., Lv, B., Li, J., Gao, Z., Xu, W., et al. (2015). Involvement of 14-3-3 protein GRF9 in root growth and response under polyethylene glycol-induced water stress. J. Exp. Bot. 66, 2271–2281. doi: 10.1093/jxb/erv149

PubMed Abstract | CrossRef Full Text | Google Scholar

Huang, L.-C., Kohashi, C., Vangundy, R., and Murashige, T. (1995). Effects of common components on hardness of culture media prepared with gelrite. In Vitro Cell. Dev. 31, 84–89. doi: 10.1007/BF02632242

CrossRef Full Text | Google Scholar

Imsande, J., and Ralston, E. J. (1981). Hydroponic growth and the nondestructive assay for dinitrogen fixation. Plant physiol. 68, 1380–1384. doi: 10.1104/pp.68.6.1380

PubMed Abstract | CrossRef Full Text | Google Scholar

Kagenishi, T., Yokawa, K., and Baluška, F. (2015). Dynamic regulation of endocytic vesicle recycling and PIN2 localization in Arabidopsis roots under varying light qualities. Environ. Control Biol. (in press).

Google Scholar

Keynes, R. G., Griffiths, C., and Garthwaite, J. (2003). Superoxide-dependent consumption of nitric oxide in biological media may confound in vitro experiments. Biochem. J. 369, 399–406. doi: 10.1042/BJ20020933

PubMed Abstract | CrossRef Full Text | Google Scholar

Liszkay, A., van der Zalm, E., and Schopfer, P. (2004). Production of reactive oxygen intermediates (O2-, H2O2, and OH) by maize roots and their role in wall loosening and elongation growth. Plant Physiol. 136, 3114–3123. doi: 10.1104/pp.104.044784

PubMed Abstract | CrossRef Full Text | Google Scholar

Lomonosova, E. E., Kirsch, M., Rauen, U., and Groot, H. (1998). The critical role of Hepes in SIN-1 cytotoxicity, peroxynitrite versus hydrogen peroxide. Free Radic. Biol. Med. 24, 522–528. doi: 10.1016/S0891-5849(97)00295-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Medeiros, C., Clark, R. B., and Ellis, J. R. (1993). Effects of mes [2(n-morpholino)-ethanesulfonic acid] and ph on mineral nutrient uptake by mycorrhizal and nonmycorrhizal maize. J. Plant Nutr. 16, 2255–2272. doi: 10.1080/01904169309364684

CrossRef Full Text | Google Scholar

Miyasaka, S. C., Checkai, R. T., Grunes, D. L., and Norvell, W. A. (1988). Methods for Controlling pH in hydroponic culture of winter wheat forage. Agron. J. 80, 213–220. doi: 10.2134/agronj1988.00021962008000020015x

CrossRef Full Text | Google Scholar

Mo, M., Yokawa, K., Baluška, F., and Wan, Y. (2015). How and why do root apices sense light under the soil surface? Front. Plant Sci. 6:775. doi: 10.3389/fpls.2015.00775

PubMed Abstract | CrossRef Full Text | Google Scholar

Monshausen, G. B., Bibikova, T. N., Messerli, M. A., Shi, C., and Gilroy, S. (2007). Oscillations in extracellular pH and reactive oxygen species modulate tip growth of Arabidopsis root hairs. Proc. Natl. Acad. Sci. U.S.A. 104, 20996–21001. doi: 10.1073/pnas.0708586104

PubMed Abstract | CrossRef Full Text | Google Scholar

Nicholas, J. C., and Harper, J. E. (1993). Effect of MES [2 (N-morpholino) ethanesulfonic acid] and amberlite IRC-50 resin on nutrient pH control and soybean growth. J. Plant Nutr. 16, 895–909. doi: 10.1080/01904169309364582

CrossRef Full Text | Google Scholar

Novák, J., Černý, M., Pavlč, J., Zemánková, J., Skalák, J., Plaèková, L., et al. (2015). Roles of proteome dynamics and cytokinin signaling in root to hypocotyl ratio changes induced by shading roots of Arabidopsis seedlings. Plant Cell Physiol. 56, 1006–1018. doi: 10.1093/pcp/pcv026

PubMed Abstract | CrossRef Full Text | Google Scholar

Okada, K., and Shimura, Y. (1990). Reversible root tip rotation in Arabidopsis seedlings induced by obstacle-touching stimulus. Science 250, 274–276. doi: 10.1126/science.250.4978.274

PubMed Abstract | CrossRef Full Text | Google Scholar

Rutherford, R., and Masson, P. H. (1996). Arabidopsis thaliana sku mutant seedlings show exaggerated surface- dependent alteration in root growth vector. Plant Physiol. 111, 987–988. doi: 10.1104/pp.111.4.987

PubMed Abstract | CrossRef Full Text | Google Scholar

Rys, G. J., and Phung, T. (1985). Nutrient solution pH control using dipolar buffers in studies of Trifolium repens L. nitrogen nutrition. J. Exp. Bot. 36, 426–431. doi: 10.1093/jxb/36.3.426

CrossRef Full Text | Google Scholar

Schuttler, P. L. (1987). Early Macronutrient Uptake, and Partitioning. in Glycine max L. Merr. ph. D. thesis, Oregon State University, Corvallis, OR.

Google Scholar

Simmons, C., Söll, D., and Migliaccio, F. (1995). Circumnutation and gravitropism cause root waving in Arabidopsis thaliana. J. Exp. Bot. 46, 143–150. doi: 10.1093/jxb/46.1.143

CrossRef Full Text | Google Scholar

Stahl, R., Grossl, P., and Bugbee, B. (1999). Effect of 2(N-morpholino)ethanesulfonic acid (MES) on the growth and tissue composition of cucumber. J. Plant Nutr. 22, 315–330. doi: 10.1080/01904169909365629

CrossRef Full Text | Google Scholar

Tsukagoshi, H., Busch, W., and Benfey, P. N. (2010). Transcriptional regulation of ROS controls transition from proliferation to differentiation in the root. Cell 143, 606–616. doi: 10.1016/j.cell.2010.10.020

PubMed Abstract | CrossRef Full Text | Google Scholar

Wan, Y., Jasik, J., Wang, L., Hao, H., Volkmann, D., Menzel, D., et al. (2012). The signal transducer NPH3 integrates the phototropin1 photosensor with PIN2-based polar auxin transport in Arabidopsis root phototropism. Plant Cell 24, 551–565. doi: 10.1105/tpc.111.094284

PubMed Abstract | CrossRef Full Text | Google Scholar

Waxman, P. G., Campo, A. A., Love, M. C., and Hamel, E. (1981). Induction of polymerization of purified tubulin by sulfonate buffers. Eur. J. Biochem. 120, 129–136. doi: 10.1111/j.1432-1033.1981.tb05679.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Yokawa, K., Fasano, R., Kagenishi, T., and Baluška, F. (2014). Light as stress factor to plant roots - case of root halotropism. Front. Plant Sci. 5:718. doi: 10.3389/fpls.2014.00718

PubMed Abstract | CrossRef Full Text | Google Scholar

Yokawa, K., Kagenishi, T., and Baluška, F. (2013). Root photomorphogenesis in laboratory-maintained Arabidopsis seedlings. Trends Plant Sci. 18, 117–119. doi: 10.1016/j.tplants.2013.01.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Yokawa, K., Kagenishi, T., Kawano, T., Mancuso, S., and Baluška, F. (2011). Illumination of Arabidopsis roots induces immediate burst of ROS production. Plant Signal. Behav. 6, 1460–1464. doi: 10.4161/psb.6.10.18165

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: root, 2-(N-morpholino)ethanesulfonic acid, Arabidopsis, ROS, transition zone, root hair

Citation: Kagenishi T, Yokawa K and Baluška F (2016) MES Buffer Affects Arabidopsis Root Apex Zonation and Root Growth by Suppressing Superoxide Generation in Root Apex. Front. Plant Sci. 7:79. doi: 10.3389/fpls.2016.00079

Received: 25 August 2015; Accepted: 16 January 2016;
Published: 18 February 2016.

Edited by:

Kimberly Lynne Gallagher, University of Pennsylvania, USA

Reviewed by:

José R. Dinneny, Carnegie Institution for Science, USA
Yoselin Benitez-Alfonso, University of Leeds, UK

Copyright © 2016 Kagenishi, Yokawa and Baluška. 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: František Baluška, baluska@uni-bonn.de