SCI和EI收录∣中国化工学会会刊

中国化学工程学报 ›› 2022, Vol. 46 ›› Issue (6): 84-93.DOI: 10.1016/j.cjche.2021.04.024

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Identification of a sensor histidine kinase (BfcK) controlling biofilm formation in Clostridium acetobutylicum

Dong Liu1,2, Shikai Ge1, Zhenyu Wang1, Mengting Li2, Wei Zhuang1, Pengpeng Yang1, Yong Chen1,2, Hanjie Ying1,2   

  1. 1 State Key Laboratory of Materials-Oriented Chemical Engineering, College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing 211816, China;
    2 School of Chemical Engineering and Energy, Zhengzhou University, Zhengzhou 450001, China
  • 收稿日期:2021-01-27 修回日期:2021-03-23 出版日期:2022-06-28 发布日期:2022-07-20
  • 通讯作者: Yong Chen,E-mail:chenyong1982@njtech.edu.cn;Hanjie Ying,E-mail:Yinghanjie@njtech.edu.cn
  • 基金资助:
    The authors thank Prof. Nigel P. Minton from the University of Nottingham for kindly providing the ClosTron plasmids, and Prof. Sheng Yang from Shanghai Institutes for Biological Sciences for kindly providing pSY8 plasmid. This work was supported by the Key Program of the National Natural Science Foundation of China (Grant No. 21636003), the Outstanding Youth Foundation of Jiangsu (Grant No. SBK2017010373), the National Key Research and Development Program of China (Grant No. 2019YFD1101204), and the Jiangsu Synergetic Innovation Center for Advanced Bio-Manufacture. Dong Liu is supported by the Jiangsu Qinglan Talent Program.

Identification of a sensor histidine kinase (BfcK) controlling biofilm formation in Clostridium acetobutylicum

Dong Liu1,2, Shikai Ge1, Zhenyu Wang1, Mengting Li2, Wei Zhuang1, Pengpeng Yang1, Yong Chen1,2, Hanjie Ying1,2   

  1. 1 State Key Laboratory of Materials-Oriented Chemical Engineering, College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing 211816, China;
    2 School of Chemical Engineering and Energy, Zhengzhou University, Zhengzhou 450001, China
  • Received:2021-01-27 Revised:2021-03-23 Online:2022-06-28 Published:2022-07-20
  • Contact: Yong Chen,E-mail:chenyong1982@njtech.edu.cn;Hanjie Ying,E-mail:Yinghanjie@njtech.edu.cn
  • Supported by:
    The authors thank Prof. Nigel P. Minton from the University of Nottingham for kindly providing the ClosTron plasmids, and Prof. Sheng Yang from Shanghai Institutes for Biological Sciences for kindly providing pSY8 plasmid. This work was supported by the Key Program of the National Natural Science Foundation of China (Grant No. 21636003), the Outstanding Youth Foundation of Jiangsu (Grant No. SBK2017010373), the National Key Research and Development Program of China (Grant No. 2019YFD1101204), and the Jiangsu Synergetic Innovation Center for Advanced Bio-Manufacture. Dong Liu is supported by the Jiangsu Qinglan Talent Program.

摘要: Clostridium acetobutylicum has been extensively exploited to produce biofuels and solvents and its biofilm could dramatically improve the productivities. However, genetic control of C. acetobutylicum biofilm has not been dissected so far. Here, to identify potential genes controlling C. acetobutylicum biofilm formation, over 40 gene candidates associated with extracellular matrix, cell surface, cell signaling or gene transcription, were tried to be disrupted to examine their individual impact. A total of 25 disruptants were finally obtained over years of attempts, for which biofilm and relevant phenotypes were characterized. Most of these disruptants formed robust biofilm still, or suffered both growth and biofilm defect. Only a strain with a disrupted histidine kinase gene (CA_C2730, designated bfcK in this study) abolished biofilm formation without impairing cell growth or solvent production. Further analysis revealed that bfcK could control flagellar biogenesis and cell motility at protein levels. The bfcK also appeared to repress the phosphorylation of a serine/threonine protein kinase (encoded by CA_C0404) that might negatively regulate biofilm formation. Based on these findings, possible bfcK-mediated mechanisms for biofilm formation were proposed. This is a big step toward understanding the biofilm formation in C. acetobutylicum and will help further engineering of its biofilm-based industrial processes.

关键词: Clostridium acetobutylicum, Biofilm, Histidine kinases, CA_C2730, Phosphoproteomics, Flagellar motility

Abstract: Clostridium acetobutylicum has been extensively exploited to produce biofuels and solvents and its biofilm could dramatically improve the productivities. However, genetic control of C. acetobutylicum biofilm has not been dissected so far. Here, to identify potential genes controlling C. acetobutylicum biofilm formation, over 40 gene candidates associated with extracellular matrix, cell surface, cell signaling or gene transcription, were tried to be disrupted to examine their individual impact. A total of 25 disruptants were finally obtained over years of attempts, for which biofilm and relevant phenotypes were characterized. Most of these disruptants formed robust biofilm still, or suffered both growth and biofilm defect. Only a strain with a disrupted histidine kinase gene (CA_C2730, designated bfcK in this study) abolished biofilm formation without impairing cell growth or solvent production. Further analysis revealed that bfcK could control flagellar biogenesis and cell motility at protein levels. The bfcK also appeared to repress the phosphorylation of a serine/threonine protein kinase (encoded by CA_C0404) that might negatively regulate biofilm formation. Based on these findings, possible bfcK-mediated mechanisms for biofilm formation were proposed. This is a big step toward understanding the biofilm formation in C. acetobutylicum and will help further engineering of its biofilm-based industrial processes.

Key words: Clostridium acetobutylicum, Biofilm, Histidine kinases, CA_C2730, Phosphoproteomics, Flagellar motility