Isolation and characterization of the new Klebsiella pneumoniae J2B strain showing improved growth characteristics with reduced lipopolysaccharide formation

被引:30
作者
Arasu, Mariadhas Valan [1 ]
Kumar, Vinod [1 ]
Ashok, Somasundar [1 ]
Song, Hyohak [2 ]
Rathnasingh, Chelladurai [2 ]
Lee, Hee Jong [2 ]
Seung, Doyoung [2 ]
Park, Sunghoon [1 ]
机构
[1] Pusan Natl Univ, Dept Chem & Biomol Engn, Pusan 609735, South Korea
[2] GS Caltex Corp, Ctr Res & Dev, Taejon 305380, South Korea
关键词
Klebsiella pneumoniae J2B; Klebsiella pneumoniae DSMZ2026; 1,3-propanediol; growth; lipopolysaccharides; ESCHERICHIA-COLI; 3-HYDROXYPROPIONIC ACID; GLYCEROL METABOLISM; GENE-PRODUCTS; 1,3-PROPANEDIOL; FERMENTATION; BIOFILM; PATHWAY; CULTURE;
D O I
10.1007/s12257-011-0513-9
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Klebsiella pneumoniae is a suitable biocatalyst for the production of 1,3-propanediol (1,3-PDO) and 3-hydroxypropionic acid (3-HP) from glycerol. However, its commercial applications have been impeded due to its poor growth characteristics and the excessive production of lipopolysaccharide (LPS). To overcome these limitations, a new K. pneumoniae J2B (KpJ2B) strain was isolated from municipal waste anaerobic digester samples. The shake flask cultivation of this new strain under aerobic conditions showed a specific growth rate of 0.92/h, which is 1.13 times higher than that achieved using the well studied K. pneumoniae DSMZ2026 (KpDSMZ). When the new strain was grown in a bioreactor under aerobic conditions using a fed-batch mode for 36 h, the biomass concentration (4.03 g/L CDW) and productivity (0.15 g/L/h) were almost 2.2 times higher than the corresponding values with KpDSMZ. Growth was accompanied by the production of 1,3-PDO (186 mM), lactic acid (235 mM), ethanol (170 mM), and acetic acid (92.2 mM) at significant levels, indicating the resistance of the strain to the inhibitory effects of these metabolites. A comparison of the SEM images and 2-keto-3-deoxyoctonate content (KpJ2B, 1.4 mu g/g CDW; KpDSMZ, 1.9 mu g/g CDW) confirmed the lower LPS content in the KpJ2B strain. Furthermore, this new isolate exhibited higher sensitivity towards a range of antibiotics and better sedimentation properties than the KpDSMZ strain. This suggests that KpJ2B is an attractive strain for industrial applications.
引用
收藏
页码:1134 / 1143
页数:10
相关论文
共 26 条
  • [1] Ahrens K, 1998, BIOTECHNOL BIOENG, V59, P544, DOI 10.1002/(SICI)1097-0290(19980905)59:5<544::AID-BIT3>3.0.CO
  • [2] 2-A
  • [3] Relationship between the physiology of Enterobacter agglomerans CNCM 1210 grown anaerobically on glycerol and the culture conditions
    Barbirato, F
    Bories, A
    [J]. RESEARCH IN MICROBIOLOGY, 1997, 148 (06) : 475 - 484
  • [4] BAUER AW, 1966, AM J CLIN PATHOL, V45, P493
  • [5] Microbial production of 1,3-propanediol
    Biebl, H
    Menzel, K
    Zeng, AP
    Deckwer, WD
    [J]. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1999, 52 (03) : 289 - 297
  • [6] Comparative analyses of secondary gene products of 3-deoxy-D-manno-oct-2-ulosonic acid transferases from Chlamydiaceae in Escherichia coli K-12
    Brabetz, W
    Lindner, B
    Brade, H
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 2000, 267 (17): : 5458 - 5465
  • [7] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [8] Roles of Capsule and Lipopolysaccharide O Antigen in Interactions of Human Monocyte-Derived Dendritic Cells and Klebsiella pneumoniae
    Evrard, B.
    Balestrino, D.
    Dosgilbert, A.
    Bouya-Gachancard, J. -L. J.
    Charbonnel, N.
    Forestier, C.
    Tridon, A.
    [J]. INFECTION AND IMMUNITY, 2010, 78 (01) : 210 - 219
  • [9] PSEUDOMONAS-AERUGINOSA BIOFILM AS A DIFFUSION BARRIER TO PIPERACILLIN
    HOYLE, BD
    ALCANTARA, J
    COSTERTON, JW
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (09) : 2054 - 2056
  • [10] Dissolved-oxygen-stat Fed-batch Fermentation of 1,3-Dihydroxyacetone from Glycerol by Gluconobacter oxydans ZJB09112
    Hu, Zhong-Ce
    Zheng, Yu-Guo
    Shen, Yin-Chu
    [J]. BIOTECHNOLOGY AND BIOPROCESS ENGINEERING, 2010, 15 (04) : 651 - 656