The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/plants11212927/s1 , Figure S1: WinRhizo analyzed root lengths and root and shoot biomass; Figure S2: Root sampling and bacterial colonization confirmation; Figure S3: Sample root images generated by the GrowScreen-Agar II; Figure S4: Agar plates for GrowScreen-Agar II; Figure S5: Magazines for GrowScreen-Agar II; Figure S6: Imaging station of GrowScreen-Agar II; Table S1: Mean values and standard error of different root type morphological traits; Table S2: Mean values and standard error of different root system traits describing distribution and spread.
Open resource ↗lines:106-120Paper record
Plant Growth Promotion and Heat Stress Amelioration in Arabidopsis Inoculated with Paraburkholderia phytofirmans PsJN Rhizobacteria Quantified with the GrowScreen-Agar II Phenotyping Platform
Plants · 30 Oct 2022 · 10.3390/plants11212927
Abstract
High temperatures inhibit plant growth. A proposed strategy for improving plant productivity under elevated temperatures is the use of plant growth-promoting rhizobacteria (PGPR). While the effects of PGPR on plant shoots have been extensively explored, roots—particularly their spatial and temporal dynamics—have been hard to study, due to their below-ground nature. Here, we characterized the time- and tissue-specific morphological changes in bacterized plants using a novel non-invasive high-resolution plant phenotyping and imaging platform—GrowScreen-Agar II. The platform uses custom-made agar plates, which allow air exchange to occur with the agar medium and enable the shoot to grow outside the compartment. The platform provides light protection to the roots, the exposure of it to the shoots, and the non-invasive phenotyping of both organs. Arabidopsis thaliana, co-cultivated with Paraburkholderia phytofirmans PsJN at elevated and ambient temperatures, showed increased lengths, growth rates, and numbers of roots. However, the magnitude and direction of the growth promotion varied depending on root type, timing, and temperature. The root length and distribution per depth and according to time was also influenced by bacterization and the temperature. The shoot biomass increased at the later stages under ambient temperature in the bacterized plants. The study offers insights into the timing of the tissue-specific, PsJN-induced morphological changes and should facilitate future molecular and biochemical studies on plant–microbe–environment interactions.
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