Journal
ALGAL RESEARCH-BIOMASS BIOFUELS AND BIOPRODUCTS
Volume 11, Issue -, Pages 194-203Publisher
ELSEVIER
DOI: 10.1016/j.algal.2015.06.022
Keywords
N-2-fixing cyanobacteria; Glycinebetaine; Intracellular cation; Nitrate assimilation; Photosynthesis; Respiration; Salinity
Categories
Funding
- Department of Biotechnology, New Delhi [BT/PR12805/AGR/21/328/2009]
- CSIR, New Delhi
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To find out the physiologic mechanisms contributing to increased tolerance to salinity by glycinebetaine in diazoptrophic cyanobacteria, methyl transferase gene ApGSMT-DMT catalyzing glycinebetaine synthesis in Aphanothece halophytica was transferred into N-2-fixing filamentous cyanobacteria Anabaena PCC7120 and Anabaena doliolum. The transformants synthesized/accumulated significant amount of glycinebetaine. Under salt-stress (0.1 M NaCl), the transformants were more efficient in reducing nitrate and its incorporation into amino compounds compared to wild-types indicating that glycinebetaine not only shielded the enzymes from deleterious effect of salt but enhanced their activities. High photosynthetic rate of ApGSMT-DMT transformants under salt-stress exhibited haloprotection of the photosynthetic machinery, while reduced respiration revealed efficient use of photosynthates. Salinity reduced the electron flow activity of PS II causing damage to cytochrome b(6)-f complex, which was overcome to an extent by glycinebetaine. The observed limited electrons transport from PSII to PSI under salinity favored additional excitation of PSI resulting in increased electron transport activity of PSI. Salinity reduced the intracellular K+/Na+ and Ca2+/Na+ ratios, while transformants showed the highest K+/Na+ ratio. This attempt to develop salt tolerant N-2-fixers can increase the nitrogen availability under saline conditions, and opens the way to transform symbiotic and free-living N-2-fixers to increase the salt tolerance and productivity. (C) 2015 Elsevier B.V. All rights reserved.
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