Glycosyltransferase Slr1064 regulates carbon metabolism by modulating the levels of UDP‐GlcNAc in Synechocystis sp. PCC 6803

Author:

Han Yuling12,Ge Haitao3,Xu Congzhuo1,Zeng Gang4,Li Zhen5ORCID,Huang Xiahe3,Zhang Yuanya3,Liu Zhipeng1ORCID,Wang Yingchun3ORCID,Fang Longfa1ORCID

Affiliation:

1. State Key Laboratory of Herbage Improvement and Grassland Agro‐Ecosystems, College of Pastoral Agriculture Science and Technology Lanzhou University Lanzhou China

2. Tropical Crops Genetic Resources Institute Chinese Academy of Tropical Agricultural Sciences Haikou 571101 China

3. State Key Laboratory of Molecular Developmental Biology, Innovation Academy for Seed Design, CAS, Institute of Genetics and Developmental Biology Chinese Academy of Sciences Beijing 100049 China

4. Zunyi Normal College Zunyi 100049 China

5. National Engineering Laboratory for VOCs Pollution Control Material & Technology University of Chinese Academy of Sciences Beijing 100049 China

Abstract

Summary Glycosyltransferases (GTs) are enzymes that transfer sugars to various targets. They play important roles in diverse biological processes, including photosynthesis, cell motility, exopolysaccharide biosynthesis, and lipid metabolism; however, their involvement in regulating carbon metabolism in Synechocystis sp. PCC 6803 has not been reported. We identified a novel GT protein, Slr1064, involved in carbon metabolism. The effect of slr1064 deletion on the growth of Synechocystis cells and functional mechanisms of Slr1064 on carbon metabolism were thoroughly investigated through physiological, biochemistry, proteomic, and metabolic analyses. We found that this GT, which is mainly distributed in the membrane compartment, is essential for the growth of Synechocystis under heterotrophic and mixotrophic conditions, but not under autotrophic conditions. The deletion of slr1064 hampers the turnover rate of Gap2 under mixotrophic conditions and disrupts the assembly of the PRK/GAPDH/CP12 complex under dark culture conditions. Additionally, UDP‐GlcNAc, the pivotal metabolite responsible for the O‐GlcNAc modification of GAPDH, is downregulated in the Δslr1064. Our work provides new insights into the role of GTs in carbon metabolism in Synechocystis and elucidate the mechanism by which carbon metabolism is regulated in this important model organism.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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