Qi Mingxia, Mei Fei, Wang Hui, Sun Ming, Wang Gejiao, Yu Ziniu, Je Yeonho, Li Mingshun
State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Hongshan District, Wuhan 430070, P.R. China.
J Microbiol Biotechnol. 2015 Feb;25(2):152-61. doi: 10.4014/jmb.1406.06036.
CodY is a highly conserved protein in low G+C gram-positive bacteria that regulates genes involved in sporulation and stationary-phase adaptation. Bacillus thuringiensis is a grampositive bacterium that forms spores and parasporal crystals during the stationary phase. To our knowledge, the regulatory mechanism of CodY in B. thuringiensis is unknown. To study the function of CodY protein in B. thuringiensis, BMB171codY(-) was constructed in a BMB171 strain. A shuttle vector containing the ORF of cry1Ac10 was transformed into BMB171 and BMB171codY(-), named BMB171cry1Ac and BMB171codY(-)cry1Ac, respectively. Some morphological and physiological changes of codY mutant BMB171codY(-)cry1Ac were observed. A comparative proteomic analysis was conducted for both BMB171codY(-)cry1Ac and BMB171cry1Ac through two-dimensional gel electrophoresis and MALDI-TOF-MS/MS analysis. The results showed that the proteins regulated by CodY are involved in microbial metabolism, including branched-chain amino acid metabolism, carbohydrate metabolism, fatty acid metabolism, and energy metabolism. Furthermore, we found CodY to be involved in sporulation, biosynthesis of poly-β-hydroxybutyrate, growth, genetic competence, and translation. According to the analysis of differentially expressed proteins, and physiological characterization of the codY mutant, we performed bacterial one-hybrid and electrophoretic mobility shift assay experiments and confirmed the direct regulation of genes by CodY, specifically those involved in metabolism of branched-chain amino acids, ribosomal recycling factor FRR, and the late competence protein ComER. Our data establish the foundation for in-depth study of the regulation of CodY in B. thuringiensis, and also offer a potential biocatalyst for functions of CodY in other bacteria.
CodY是低G+C含量革兰氏阳性菌中一种高度保守的蛋白质,可调控参与芽孢形成和稳定期适应的基因。苏云金芽孢杆菌是一种革兰氏阳性菌,在稳定期形成芽孢和伴孢晶体。据我们所知,CodY在苏云金芽孢杆菌中的调控机制尚不清楚。为了研究CodY蛋白在苏云金芽孢杆菌中的功能,在BMB171菌株中构建了BMB171codY(-)。将含有cry1Ac10开放阅读框的穿梭载体分别转化到BMB171和BMB171codY(-)中,命名为BMB171cry1Ac和BMB171codY(-)cry1Ac。观察到codY突变体BMB171codY(-)cry1Ac的一些形态和生理变化。通过二维凝胶电泳和MALDI-TOF-MS/MS分析对BMB171codY(-)cry1Ac和BMB171cry1Ac进行了比较蛋白质组学分析。结果表明,受CodY调控的蛋白质参与微生物代谢,包括支链氨基酸代谢、碳水化合物代谢、脂肪酸代谢和能量代谢。此外,我们发现CodY参与芽孢形成、聚-β-羟基丁酸的生物合成、生长、遗传感受态和翻译。根据差异表达蛋白的分析以及codY突变体的生理特征,我们进行了细菌单杂交和电泳迁移率变动分析实验,并证实了CodY对基因的直接调控,特别是那些参与支链氨基酸代谢、核糖体循环因子FRR和晚期感受态蛋白ComER的基因。我们的数据为深入研究苏云金芽孢杆菌中CodY的调控奠定了基础,也为CodY在其他细菌中的功能提供了潜在的生物催化剂。