Improvement of acetoin reductase activity enhances bacitracin production by Bacillus licheniformis

被引:12
作者
Wang, Zhi [1 ]
Wang, Yong [1 ]
Xie, Fuli [2 ]
Chen, Shouwen [2 ]
Li, Junhui [3 ]
Li, Dongsheng [1 ]
Chen, Xiong [1 ]
机构
[1] Hubei Univ Technol, Minist Educ, Hubei Collaborat Innovat Ctr Ind Fermentat, Key Lab Fermentat Engn, Wuhan 430068, Peoples R China
[2] Huazhong Agr Univ, Lifecome Bioengn Inst, Coll Life Sci & Technol, State Key Lab Agr Microbiol, Wuhan 430071, Peoples R China
[3] Lifecome Biochem Co Ltd, Pucheng 353400, Peoples R China
关键词
NADH oxidation; Acetoin reductase; Fermentation; Bacitracin; ESCHERICHIA-COLI; TRANSCRIPTIONAL LEVEL; TORULOPSIS-GLABRATA; SUBTILIS; METABOLISM; EXPRESSION; PATHWAY; GROWTH; GENES;
D O I
10.1016/j.procbio.2014.08.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bacitracin fermentation by Bacillus licheniformis in this work showed three characteristics: (1) the extracellular propionate, butyrate, acetoin and 2,3-butanediol accumulates under conditions of low dissolved oxygen (zero after 4h cultivation), reaching a total content of approximately 11.1 g/L; (2) cell growth occurs quickly subsequent to cell autolysis and the second growth; and (3) there is a low content of 2,3-butanediol, a reduced product of acetoin catalyzed by acetoin reductase, in the culture process. In this study, addition of MnCl2 (0.3 mg/L) to the production medium increased the acetoin reductase activity, redirected the NADH oxidation partly from the propionate- and butyrate-production pathways to the 2,3-butanediol synthesis pathway, reduced the intracellular NADH/NAD(+) ratio, and facilitated cell growth, ultimately achieving a 11.6% increase in bacitracin production (1076 U/mL) versus the control. The results provide useful information regarding large-scale bacitracin production by B. licheniformis. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2039 / 2043
页数:5
相关论文
共 26 条
  • [1] Aftab MN, 2012, BRAZ J MICROBIOL, V43, P78, DOI 10.1590/S1517-83822012000100009
  • [2] Supplementations of ornithine and KNO3 enhanced bacitracin production by Bacillus licheniformis LC-11
    Chen, Xiong
    Xie, Fuli
    Zeng, Xinnian
    Li, Dongsheng
    Chen, Shouwen
    Li, Junhui
    Wang, Zhi
    [J]. ANNALS OF MICROBIOLOGY, 2014, 64 (02) : 509 - 514
  • [3] Comparative growth analysis of the facultative anaerobes Bacillus subtilis, Bacillus licheniformis, and Escherichia coli
    Clements, LD
    Miller, BS
    Streips, UN
    [J]. SYSTEMATIC AND APPLIED MICROBIOLOGY, 2002, 25 (02) : 284 - 286
  • [4] Jamil B, 2007, PAK J PHARM SCI, V20, P26
  • [5] Function, structure and regulation of the vacuolar (H+)-ATPases
    Jefferies, Kevin C.
    Cipriano, Daniel J.
    Forgac, Michael
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2008, 476 (01) : 33 - 42
  • [6] The glycolytic flux in Escherichia coli is controlled by the demand for ATP
    Koebmann, BJ
    Westerhoff, HV
    Snoep, JL
    Nilsson, D
    Jensen, PR
    [J]. JOURNAL OF BACTERIOLOGY, 2002, 184 (14) : 3909 - 3916
  • [7] The bacitracin biosynthesis operon of Bacillus licheniformis ATCC 10716: molecular characterization of three multi-modular peptide synthetases
    Konz, D
    Klens, A
    Schorgendorfer, K
    Marahiel, MA
    [J]. CHEMISTRY & BIOLOGY, 1997, 4 (12): : 927 - 937
  • [8] Genome Sequences of Two Thermophilic Bacillus licheniformis Strains, Efficient Producers of Platform Chemical 2,3-Butanediol
    Li, Lixiang
    Su, Fei
    Wang, Yu
    Zhang, Lijie
    Liu, Cuicui
    Li, Jingwen
    Ma, Cuiqing
    Xu, Ping
    [J]. JOURNAL OF BACTERIOLOGY, 2012, 194 (15) : 4133 - 4134
  • [9] Metabolic engineering of aerobic succinate prod-action systems in Escherichia coli to improve process productivity and achieve the maximum theoretical succinate yield
    Lin, H
    Bennett, GN
    San, KY
    [J]. METABOLIC ENGINEERING, 2005, 7 (02) : 116 - 127
  • [10] Enhancement of pyruvate productivity in Torulopsis glabrata:: Increase of NAD+ availability
    Liu, Liming
    Li, Yin
    Shi, Zhongping
    Du, Guocheng
    Chen, Jian
    [J]. JOURNAL OF BIOTECHNOLOGY, 2006, 126 (02) : 173 - 185