Regulation of pepc gene expression in Anabaena sp. PCC 7120 and its effects on cyclic electron flow around photosystem I and tolerances to environmental stresses

Since pepc gene encoding phosphoenolpyruvate carboxylase (PEPCase) has been cloned from Anabaena sp. PCC 7120 and other cyanobacteria, the effects of pepc gene expression on photosynthesis have not been reported yet. In this study, we constructed mutants containing either upregu-lated (forward) or d...

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Published inJournal of integrative plant biology Vol. 57; no. 5; pp. 468 - 476
Main Authors Jia, Xiao‐Hui, Zhang, Peng‐Peng, Shi, Ding‐Ji, Mi, Hua‐Ling, Zhu, Jia‐Cheng, Huang, Xi‐Wen, He, Pei‐Min
Format Journal Article
LanguageEnglish
Published China (Republic : 1949- ) Blackwell Pub 01.05.2015
Blackwell Publishing Ltd
Key Laboratory of Exploration and Utilization of Aquatic Genetic Resources, Shanghai 0cean University, Ministry of Education Shanghai, Shanghai 201306, China%Department of Biological Sciences, Louisiana State University, LA 70803, USA%National Key Laboratory of Plant Molecular Genetics, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, the Chinese Academy of Sciences, Shanghai 200032, China
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Summary:Since pepc gene encoding phosphoenolpyruvate carboxylase (PEPCase) has been cloned from Anabaena sp. PCC 7120 and other cyanobacteria, the effects of pepc gene expression on photosynthesis have not been reported yet. In this study, we constructed mutants containing either upregu-lated (forward) or downregulated (reverse) pepc gene in Anabaena sp. PCC 7120. Results from real‐time quantitative polymerase chain reaction (RT‐qPCR), Western blot and enzymatic analysis showed that PEPCase activity was signifi-cantly reduced in the reverse mutant compared with the wild type, and that of the forward mutant was obviously increased. Interestingly, the net photosynthesis in both the reverse mutant and the forward mutant were higher than that of the wild type, but dark respiration was decreased only in the reverse mutant. The absorbance changes of P700 upon saturation pulse showed the photosystem I (PSI) activity was inhibited, as reflected by Y(I), and Y(NA) was elevated, and dark reduction of P700t was stimulated, indicating enhanced cyclic electron flow (CEF) around PSI in the reverse mutant. Additional y, the reverse mutant photosynthesis was higher than that of the wild type in low temperature, low and high pH, and high salinity, and this implies increased tolerance in the reverse mutant through downregulated pepc gene.
Bibliography:Since pepc gene encoding phosphoenolpyruvate carboxylase (PEPCase) has been cloned from Anabaena sp. PCC 7120 and other cyanobacteria, the effects of pepc gene expression on photosynthesis have not been reported yet. In this study, we constructed mutants containing either upregu-lated (forward) or downregulated (reverse) pepc gene in Anabaena sp. PCC 7120. Results from real‐time quantitative polymerase chain reaction (RT‐qPCR), Western blot and enzymatic analysis showed that PEPCase activity was signifi-cantly reduced in the reverse mutant compared with the wild type, and that of the forward mutant was obviously increased. Interestingly, the net photosynthesis in both the reverse mutant and the forward mutant were higher than that of the wild type, but dark respiration was decreased only in the reverse mutant. The absorbance changes of P700 upon saturation pulse showed the photosystem I (PSI) activity was inhibited, as reflected by Y(I), and Y(NA) was elevated, and dark reduction of P700t was stimulated, indicating enhanced cyclic electron flow (CEF) around PSI in the reverse mutant. Additional y, the reverse mutant photosynthesis was higher than that of the wild type in low temperature, low and high pH, and high salinity, and this implies increased tolerance in the reverse mutant through downregulated pepc gene.
Anabaena sp. PCC 7120; cyclic electron flow; pepc gene;photosynthesis; tolerance
11-5067/Q
http://dx.doi.org/10.1111/jipb.12241
istex:7A3796349D564DFF5FC44AABAC7E8763F8221A0B
National High-tech R&D Program - No. 2009AA064401; No. 2014AA093506
ArticleID:JIPB12241
ark:/67375/WNG-3PVRNQMG-2
National Administration Project from Chinese Ministry of Environmental Protection
Shanghai Universities First-class Disciplines Project of Fisheries
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1672-9072
1744-7909
DOI:10.1111/jipb.12241