Protocol: Optimising hydroponic growth systems for nutritional and physiological analysis of Arabidopsis thaliana and other plants

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Abstract

Background: Hydroponic growth systems are a convenient platform for studying whole plant physiology. However, we found through trialling systems as they are described in the literature that our experiments were frequently confounded by factors that affected plant growth, including algal contamination and hypoxia. We also found the way in which the plants were grown made them poorly amenable to a number of common physiological assays.Results: The drivers for the development of this hydroponic system were: 1) the exclusion of light from the growth solution; 2) to simplify the handling of individual plants, and 3) the growth of the plant to allow easy implementation of multiple assays. These aims were all met by the use of pierced lids of black microcentrifuge tubes. Seed was germinated on a lid filled with an agar-containing germination media immersed in the same solution. Following germination, the liquid growth media was exchanged with the experimental solution, and after 14-21 days seedlings were transferred to larger tanks with aerated solution where they remained until experimentation. We provide details of the protocol including composition of the basal growth solution, and separate solutions with altered calcium, magnesium, potassium or sodium supply whilst maintaining the activity of the majority of other ions. We demonstrate the adaptability of this system for: gas exchange measurement on single leaves and whole plants; qRT-PCR to probe the transcriptional response of roots or shoots to altered nutrient composition in the growth solution (we demonstrate this using high and low calcium supply); producing highly competent mesophyll protoplasts; and, accelerating the screening of Arabidopsis transformants. This system is also ideal for manipulating plants for micropipette techniques such as electrophysiology or SiCSA.Conclusions: We present an optimised plant hydroponic culture system that can be quickly and cheaply constructed, and produces plants with similar growth kinetics to soil-grown plants, but with the advantage of being a versatile platform for a myriad of physiological and molecular biological measurements on all plant tissues at all developmental stages. We present 'tips and tricks' for the easy adoption of this hydroponic culture system. © 2013 Conn et al.; licensee BioMed Central Ltd.

Figures

  • Table 1 Advantages and disadvantages between geoponics, agar plates and three distinct aggregate hydroponics methods for cultivating arabidopsis plants
  • Figure 1 Simplified Arabidopsis hydroponics growth method. Flow chart outlining the timeline and key steps in the process. Timing (in bold) on right of arrows indicate time between steps (d: days). Images on right-hand panel showing setup of seed germination and representative images of seedlings and mature plants, including view of roots contained within centrifuge tubes of 5-week old plant. Also refer to protocol, and Additional file 2 and online tutorial video (http://www.youtube.com/watch?v=c9neVLaS63c) for more detailed descriptions of the equipment set-up.
  • Figure 2 Comparisons of Arabidopsis shoot growth kinetics and protoplast transformation efficiency between soil and hydroponics system. A) Shoot biomass during vegetative growth phase of Arabidopsis Col-0 is equivalent between soil-grown and hydroponically-grown plants under short-day photoperiod (8 h:16 h) until seven weeks post-germination. Mean ± SD (n = 6 plants per timepoint, per condition). No significant differences were found between growth conditions at each timepoint using a t-test (P < 0.01). B) Transfection efficiency of Arabidopsis mesophyll protoplasts were determined by fluorescence microscopy comparing two quantities (5 μg and 10 μg) of two sGFP-expressing plasmids under a single CaMV 35S promoter, pHBT-sGFP(S65T)-NOS (GenBank accession number: EF090408) [25] and pGWB406 (GenBank accession number: AB294430) [37] of 4.2 kb and 12.4 kb, respectively as per Conn et al. [20]. For each condition n = 5 independent transformations, each with cell counts > 100 protoplasts. Data presented as the proportion of GFP-expressing cells; Mean + SEM. Asterisks indicate significant difference between soil and hydroponics derived protoplasts within each condition (P < 0.01).
  • Table 2 Comparative ionomics of soil-grown and hydroponically-grown plants
  • Figure 3 Calcium-dependent transcriptional responses of Arabidopsis on RNA isolated from the (A) shoots and (B) roots (above and below the h under three different Ca activities (aCa LCS = 0.025mM; aCa BNS = 1 mM; aC per tissue. Mean + SD. Asterisk indicates significant expression difference fr with primers listed in Additional file 3.
  • Figure 4 Gas exchange measurements for Arabidopsis Col-0 measured using the LiCOR extended reach chamber or whole plant chamber whilst growing in hydroponics. A Transpiration or B Net CO2 assimilation/photosynthesis measured using 6-week old plants growing the basal nutrient solution. Individual plants were exposed to light intensity of ~350 μmol m-2 s-1 at least 30 min prior to the start of measurement. The rosette was allowed to acclimatise inside the Arabidopsis whole rosette or extended reach chamber for at least 10 min before gas exchange data were recorded with reference CO2 concentration set at 500 μmol mol-1, flow rate at 500 μmol s-1 (for the whole plant chamber) or 100 μmol s-1 (for the extended reach chamber) light intensity at 350 μmol photons m-2 s-1 and relative humidity at 56%. Data shown as Mean + SEM of fifteen biological replicates. No significant differences were found between each dataset using a t-test (P < 0.01).

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Conn, S. J., Hocking, B., Dayod, M., Xu, B., Athman, A., Henderson, S., … Gilliham, M. (2013). Protocol: Optimising hydroponic growth systems for nutritional and physiological analysis of Arabidopsis thaliana and other plants. Plant Methods, 9(1). https://doi.org/10.1186/1746-4811-9-4

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