Synechocystis sp. PCC 6803 is a widely used model cyanobacterium, whose substrains can vary on both genotype and phenotype levels. Previously described phenotypic variations include ability of mixotrophic growth, ability of movement on agar plates and variations in pigments composition or cell size. In this study, we report for the first time significant variation among Synechocystis substrains in complex cellular traits such as growth rate, photosynthesis efficiency, cellular dry weight and cellular composition (including protein or carbohydrates content). We also confirmed previously reported differences in cell size. Synechocystis cultures were cultivated in controlled environment of flat panel photobioreactors under red, blue and white light of intensities up to 790 μmol(photons) m-2 s-1, temperatures 23°C–60°C, input CO2 concentrations ranging from 400 to 15 000 ppm and in BG11 cultivation medium with and without addition of NaCl. Three Synechocystis substrains were used for the comparative experiments: GT-L, GT-B (Brno, CZ) and PCC-B (Brno, CZ). Growth rates of Synechocystis GT-B were inhibited under high intensities of red light (585–670 nm), and growth rates of both substrains GT-B and PCC-B were inhibited under photons of wavelengths 485–585 nm and 670–700 nm. Synechocystis GT-B was more sensitive to low temperatures than the other two tested substrains, and Synechocystis GT-L was sensitive to the presence of NaCl in the cultivation media. The results suggest that stress sensitivity of commonly used Synechocystis substrains can strongly vary, similarly as glucose tolerance or motility as reported previously. Our study further supports the previous statement that emphasizes importance of proper Synechocystis substrains selection and awareness of phenotypical differences among Synechocystis substrains which is crucial for comparative and reproducible research. This is highly relevant for studies related to stress physiology and development of sustainable biotechnological applications.
The paper deals with the differences in sensitivity of Antarctic lichen to photoinhibition. Thalli of Usnea antarctica were collected at the James Ross Island, Antarctica (57°52´57´´W, 63°48´02´´S) and transferred in dry state to the Czech Republic. After rewetting in a laboratory, they were exposed to 2 high light treatments: short-term (30 min), and long-term (6 h). In short-term treatment, the sample were exposed to 1000 and 2000 µmol m -2 s -1 of photosynthetically active radiation (PAR). In long-term experiment, PAR of 300, 600, and 1000 µmol m -2 s -1 were used. Photosynthetic efficiency of U. antarctica thalli was monitored by chlorophyll fluorescence parameters, potential (F V /F M ) and actual ( PSII ) quantum yield of photochemical processes in photosystem II in particular. In short-term treatments, the F 0 , F V and F M signals, as well as the values of F V /F M , and PSII showed light-induced decrease, however substantial recovery after consequent 30 min. in dark. Longer exposition (60 min) to high light led to more pronounced decrease in chlorophyll fluorescence than after 30 min treatment, however dark recovery was faster in the thalli treated before for longer time (60 min). Long-term treatment by high light caused gradual decrease in F V /F M and PSII with the time of exposition. The extent of the decrease was found light dose-dependent. The time course was biphasic for F V /F M but not for PSII . The study showed that wet thalli of Usnea antarctica had high capacity of photoprotective mechanisms to cope well either with short-or long-term high light stress. This might be of particular importance in the field at the James Ross Island, particularly at the begining of growing season when melting water is available and, simultaneously, high light stress may happen on fully sunny days.
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The authors thank the CzechPolar project for research infrastructure and the PASSEB project for funding traveling to coordination meetings of team members.
The authors are grateful to CzechPolar project for the infrastructure provided during field collection of samples in Antarctica and laboratory measurements.
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