Evolution of Streptomyces pristinaespiralis for resistance and production of pristinamycin by genome shuffling

被引:57
作者
Xu, Bo [1 ,2 ]
Jin, Zhihua [1 ,2 ]
Wang, Hengzheng [1 ]
Jin, Qingchao [1 ]
Jin, Xin [1 ]
Cen, Peilin [2 ]
机构
[1] Zhejiang Univ, Ningbo Inst Technol, Dept Biochem & Pharmaceut Engn, Ningbo 315100, Zhejiang, Peoples R China
[2] Zhejiang Univ, Inst Bioengn, Coll Mat Sci & Chem Engn, Hangzhou 310027, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
genome shuffling; protoplast fusion; pristinamycin; Streptomyces pristinaespiralis; pristinamycin resistant recombinant;
D O I
10.1007/s00253-008-1540-0
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
Improvement of pristinamycin production by Streptomyces pristinaespiralis was performed by using recursive protoplast fusion and selection for improved resistance to the product antibiotic in a genome shuffling format. A 100-mu g/ml pristinamycin resistant recombinant, G 4-17, was obtained after four rounds of protoplast fusion, and its production of pristinamycin reached 0.89 g/l, which was increased by 89.4% and 145.9% in comparison with that of the highest parent strain M-156 and the original strain CGMCC 0957, respectively. The subculture experiments indicated that the hereditary character of high producing S. pristinaespiralis G 4-17 was stable. It is concluded that genome shuffling improves the production of pristinamycin by enhancing product-resistance in a stepwise manner. Pristinamycin fermentation experiments by recombinant G 4-17 were carried out in a 5-l fermentor, and its production of pristinamycin reached 0.90 g/l after 60 h of fermentation.
引用
收藏
页码:261 / 267
页数:7
相关论文
共 26 条
[1]   RP 59500 - A PROPOSED MECHANISM FOR ITS BACTERICIDAL ACTIVITY [J].
AUMERCIER, M ;
BOUHALLAB, S ;
CAPMAU, ML ;
LEGOFFIC, F .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1992, 30 :9-14
[2]  
Chen JM, 1991, ANAL ANTIBIOTIC IND, P109
[3]   MOLECULAR MECHANISM OF ACTION OF VIRGINIAMYCIN-LIKE ANTIBIOTICS (SYNERGIMYCINS) ON PROTEIN-SYNTHESIS IN BACTERIAL CELL-FREE SYSTEMS [J].
COCITO, C ;
CHINALI, G .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1985, 16 :35-52
[4]   Intracellular ph determination of pristinamycin-producing Streptomyces pristinaespiralis by image analysis [J].
Corvini, PFX ;
Gautier, H ;
Rondags, E ;
Vivier, H ;
Goergen, JL ;
Germain, P .
MICROBIOLOGY-SGM, 2000, 146 :2671-2678
[5]   Intracellular pH of Streptomyces pristinaespiralis is correlated to the sequential use of carbon sources during the pristinamycins-producing process [J].
Corvini, PFX ;
Delaunay, S ;
Maujean, F ;
Rondags, E ;
Vivier, H ;
Goergen, JL ;
Germain, P .
ENZYME AND MICROBIAL TECHNOLOGY, 2004, 34 (02) :101-107
[6]   Genome shuffling improves degradation of the anthropogenic pesticide pentachlorophenol by Sphingobium chlorophenolicum ATCC 39723 [J].
Dai, MH ;
Copley, SD .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (04) :2391-2397
[7]   Genome shuffling of Streptomyces sp U121 for improved production of hydroxycitric acid [J].
Hida, Hiroyuki ;
Yamada, Takashi ;
Yamada, Yasuhiro .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2007, 73 (06) :1387-1393
[8]  
Hopwood DA, 1985, GENETIC MANIPULATION, P356
[9]   Acquisition of certain streptomycin-resistant (str) mutations enhances antibiotic production in bacteria [J].
Hosoya, Y ;
Okamoto, S ;
Muramatsu, H ;
Ochi, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (08) :2041-2047
[10]   SECONDARY AMINOGLYCOSIDE RESISTANCE IN AMINOGLYCOSIDE-PRODUCING STRAINS OF STREPTOMYCES [J].
HOTTA, K ;
ISHIKAWA, J ;
OGATA, T ;
MIZUNO, S .
GENE, 1992, 115 (1-2) :113-117