Science & Technology Department of Sichuan Province, Chengdu, Sichuan, China.
State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
Proteomics. 2024 Sep;24(18):e2300222. doi: 10.1002/pmic.202300222. Epub 2024 Apr 5.
The group 2 σ factor for RNA polymerase SigE plays important role in regulating central carbon metabolism in cyanobacteria. However, the regulation of SigE for these pathways at a proteome level remains unknown. Using a sigE-deficient strain (ΔsigE) of Synechocystis sp. PCC 6803 and quantitative proteomics, we found that SigE depletion induces differential protein expression for sugar catabolic pathways including glycolysis, oxidative pentose phosphate (OPP) pathway, and glycogen catabolism. Two glycogen debranching enzyme homologues Slr1857 and Slr0237 are found differentially expressed in ΔsigE. Glycogen determination indicated that Δslr0237 accumulated glycogen under photomixotrophic condition but was unable to utilize these reserves in the dark, whereas Δslr1857 accumulates and utilizes glycogen in a similar way as the WT strain does in the same condition. These results suggest that Slr0237 plays the major role as the glycogen debranching enzyme in Synechocystis.
RNA 聚合酶 SigE 的组 2σ 因子在调节蓝藻的中心碳代谢中起着重要作用。然而,SigE 对这些途径的蛋白质组水平的调节仍然未知。利用 Synechocystis sp. PCC 6803 的 sigE 缺陷株(ΔsigE)和定量蛋白质组学,我们发现 SigE 耗竭诱导糖分解代谢途径(包括糖酵解、氧化戊糖磷酸(OPP)途径和糖原分解代谢)的差异蛋白表达。发现两种糖原分支酶同源物 Slr1857 和 Slr0237 在 ΔsigE 中差异表达。糖原测定表明,Δslr0237 在光混合营养条件下积累糖原,但在黑暗中无法利用这些储备,而 Δslr1857 以与 WT 菌株在相同条件下相似的方式积累和利用糖原。这些结果表明 Slr0237 在 Synechocystis 中作为糖原分支酶发挥主要作用。