Cao Lianbin, Lu Mingguo, Zhao Mengrui, Zhang Yifan, Nong Yiping, Hu Mengxue, Wang Ya, Li Tongbiao, Chen Fujia, Wang Mingcheng, Liu Junhe, Li Enzhong, Sun Hongmei
School of Biological and Food Engineering, Huanghuai University, Zhumadian, Henan, China.
Front Microbiol. 2023 May 26;14:1161303. doi: 10.3389/fmicb.2023.1161303. eCollection 2023.
A facultative exoelectrogen, strain Clb-11, was isolated from polluted river water. This strain could generate electricity in microbial fuel cells (MFCs) with carboxymethyl cellulose (CMC) as the carbon source, and the maximum output power density was 12.17 ± 2.74 mW·m. In addition, Clb-11 could secrete extracellular chromate reductase or extracellular electron mediator to reduce Cr(VI) to Cr(III). When the Cr(VI) concentration was less than 0.5 mM in Luria-Bertani (LB) medium, Cr(VI) could be completely reduced by Clb-11. However, the Clb-11 cells swelled significantly in the presence of Cr(VI). We employed transcriptome sequencing analysis to identify genes involved in different Cr(VI) stress responses in Clb-11. The results indicate that 99 genes were continuously upregulated while 78 genes were continuously downregulated as the Cr(VI) concentration increased in the growth medium. These genes were mostly associated with DNA replication and repair, biosynthesis of secondary metabolites, ABC transporters, amino sugar and nucleotide sugar metabolism, and carbon metabolism. The swelling of Clb-11 cells might have been related to the upregulation of the genes , , , , , and , which encode acetyl-CoA C-acetyltransferase, myo-inositol-1-phosphate synthase, phosphoenolpyruvate-glycerone phosphotransferase, and acetyl-CoA/propionyl-CoA carboxylase, respectively. Interestingly, the genes and related to electron transport were continuously downregulated as the Cr(VI) concentration increased. Our results provide clues to the molecular mechanism of Cr(VI) reduction by microorganisms in MFCs systems.
从受污染的河水中分离出一株兼性产电菌Clb-11。该菌株能够在以羧甲基纤维素(CMC)为碳源的微生物燃料电池(MFC)中发电,最大输出功率密度为12.17±2.74 mW·m 。此外,Clb-11能够分泌细胞外铬酸盐还原酶或细胞外电子介质,将Cr(VI)还原为Cr(III)。当Luria-Bertani(LB)培养基中Cr(VI)浓度低于0.5 mM时,Clb-11能够将Cr(VI)完全还原。然而,在Cr(VI)存在的情况下,Clb-11细胞显著肿胀。我们采用转录组测序分析来鉴定Clb-11中参与不同Cr(VI)应激反应的基因。结果表明,随着生长培养基中Cr(VI)浓度的增加,99个基因持续上调,78个基因持续下调。这些基因大多与DNA复制和修复、次级代谢产物生物合成、ABC转运蛋白、氨基糖和核苷酸糖代谢以及碳代谢有关。Clb-11细胞的肿胀可能与分别编码乙酰辅酶A C-乙酰转移酶、肌醇-1-磷酸合酶、磷酸烯醇丙酮酸-甘油磷酸转移酶和乙酰辅酶A/丙酰辅酶A羧化酶的基因 、 、 、 、 和 的上调有关。有趣的是,随着Cr(VI)浓度的增加,与电子传递相关的基因 和 持续下调。我们的结果为MFCs系统中微生物还原Cr(VI)的分子机制提供了线索。