期刊文献+

突变生物合成在微生物药物领域的研究进展 被引量:3

Review on mutational biosynthesis in microbial medicinal fields
下载PDF
导出
摘要 突变生物合成作为产生抗生素衍生物的重要手段,自20世纪70年代兴起以来,发挥了巨大作用,已开发出许多至今在临床上仍广泛使用的抗生素品种。随着基因技术的发展,突变生物合成技术可直接对次级代谢途径中一特定酶基因进行改造获得突变株,大大提高了工作效率和准确性。本文综述了突变生物合成技术在微生物药物领域的应用,特别是结合基因技术进行突变生物合成研究的新进展。 Mutational biosynthesis since its rising in 1970's, as a tool for the formation of antibiotic structural analogues, has played an important role and developed some novel derivatives which are still widely used in the clinic today. With the advance of gene engineering, mutants can be obtained by direct gene modification to certain enzyme in secondary metabolism pathway and efficiency is greatly promoted. In this paper, the progress, especially combining gene engineering of mutational biosynthesis is reviewed.
出处 《中国抗生素杂志》 CAS CSCD 北大核心 2007年第2期65-72,94,共9页 Chinese Journal of Antibiotics
关键词 突变生物合成 突变合成元 阻断突变株 抗生素 Mutational biosynthesis (MBS) Mutasynthon Blocked mutant Antibiotics
  • 相关文献

参考文献33

  • 1Rinehart K L. Mutasynthesis of new antibiotics [J]. Pure Appl Chem, 1977,49(9) : 1361
  • 2Daum S J, Lemke J R. Mutational biosynthesis of new antibiotics [J]. Annu Rev Microbiol,1979,33:241
  • 3Takeda K, Kinumaki A, Yukiolto, et al. Mutational biosynthesis of butirosin analogs [J]. J Antibiot, 1978,31 (10):1023
  • 4范铭琦,赵敏.氨基糖苷类抗生素产生菌的代谢调控与菌种选育[J].中国抗生素杂志,2005,30(9):576-580. 被引量:6
  • 5程杉,夏焕章.氨基糖苷类抗生素生物合成基因研究进展[J].沈阳药科大学学报,2003,20(1):60-64. 被引量:11
  • 6Delzer J, Rathmann R, Mullerr H, et al. New nikkomyeins by mutasynthesis and directed fermentation [J]. J Antlbiot, 1984,37 (1) : 80
  • 7Bormann C, Kalmanczhelyi A, Sussmuth R, et al. Production of nikkomyclns Bx and Bz by mutasynthesls with genetically engineered Streptomyces tendae Til901 [J]. J Antibiot,1999,52(2):102
  • 8Galm U, Heller S, Shapiro S, et al. Antimlcrobial and DNA gyrase inhibitory activities of novel cloroblocin derlvatives produced by mutasynthesis[J]. Antimlcrob Agents Chemother , 2004,48 (4): 1:307
  • 9Pojer F, Heide L, Shu-Ming Li, et al. Molecular cloning and sequence analysis of the clorobiocin biosynthetic gene cluster: new insights into the biosynthesis of aminocoumarin antibiotics [J]. J Microbiol,2002,148(12):3901
  • 10Pelzer S, Stissmuth R, Heckmann D, et al. Identification and analysis of the balhimycin biosynthetic gene cluster and its use for manipulating glycopeptide biosynthesis in Amycolatopsis mediterranei DSM5908 [J]. Antimicrob Agents Chemother, 1999,43(7) : 1565

二级参考文献47

  • 1陈林,刘家健.氨基糖苷类抗生素的新研究动向[J].国外医药(抗生素分册),2005,26(2):86-91. 被引量:3
  • 2赵敏,范瑾,胡小玲,谢凤龙,刘军,汪洁,杨晓伟.庆大霉素C_(1a)单组份产生菌─—棘孢小单孢菌JIM-202的筛选和研究[J].中国抗生素杂志,1997,22(1):12-15. 被引量:13
  • 3Skinner D, Morgenstem M, Fedechko R, et al. Cloning and sequencing of a cluster of genes encoding branched-chain α-keto acid dehydrogenase from Strcptomyces averrnitilis and the production of a functional E1 [αβ] component in Escherichia coli. J Bacteriol,1995, 177, 183-190.
  • 4Denoya C, Fedechko R, Hafner E, et al. A second branched-chain α-keto acid dehydrogenase gene cluster (bkdFGH) from Streptomyces avermitilis : its relationship to avermectin biosynthesis and the construetion of a bkdF mutant suitable for the production of novel antiparasitic avermectins. J Bacteriol, 1995, 177, 3504 - 3511.
  • 5Zhu H J, Zheng Y H. Study on C5-O-methyltransferase gene cloning, sequencing and replacement. J Chin J Antibiotics, 2003, 28 ( 1 ) : 1-5.
  • 6Sambrook J, Fritsch E F, Maniatis T. Molecular Cloning : A laboratory Manual. 2^nd ed. New York: Cold Spring Harbor Laboratory Press, 1989.
  • 7Tobias K, Bibb M J, Mark J B, et al. Practical Streptomyces Genetic. Norwich: The John Innes Foundation, 2000.
  • 8MacNeil T, Gewain K, MacNeil D. Deletion analysis of the avermectin biosynthetic genes of Streptomyces avermitilis by gene cluster displacement. J Bacteriol, 1993, 175:2552 - 2563.
  • 9Ikeda H, Nonomiya T, Omura S. Organization of biosynthetic gene cluster for avermectin in Streptomyces avermitilis : analysis of enzymatic domains in four polyketide synthases. Journal of Industrial Microbiology & Biotechnology, 2001, 27, 170 - 176.
  • 10Skinner D, Morgenstern M, Fedechko R, et al. Cloning and sequencing of a cluster of genes encoding branched-chain α-keto acid dehydrogenase from Streptomyces avermitilis and the production of a functional E1[αβ] component in Escherichia coli. J Bacteri

共引文献22

同被引文献23

  • 1张竹霞,吕荣文,张珂珂,高昆玉.水合肼还原芳硝基物的研究[J].精细化工,2001,18(4):239-242. 被引量:54
  • 2房春林,杨光友,古小彬.多拉菌素的研究进展[J].中国畜牧兽医,2006,33(5):55-57. 被引量:18
  • 3Burg R W, Miller B M, Baker E E, et al. Avermectins, new family of potent anthelmintic agents: producing organism and fermentation. Antimicorb Agents Chemother,1979, 15:361.
  • 4Claudio D D, Ronald W F, Edmund W H, et al. A second branched-chain alpha-keto acid dehydrogenase gene cluster (bkdFGH) from Streptomyces avermitilis: its relationship to avermectin biosynthesis and construction of a bkdF mutant suitable for production of novel antiparasit[c avermectins. J. Bacteriol, 1995, 177 : 3504 - 3511.
  • 5Cropp T A, Dennis J W, Reynolds K A. Identification of a cyclohexylcarbonyl CoA biosynthetie gene cluster and application in the production of doramectin. Nature, 2000, 18 : 980 - 983.
  • 6Hanahan D. Studies on transformation of Escherichia coli with plasmids. J Mot Biol,1983,166:557.
  • 7Bierman M, Logan R, O'Brien K. Plasmid cloning vectors for the conjugal transfer of DNA from Escherichia coli to Streptomyces spp. Gene, 1992, 116:43 - 49.
  • 8Sambrook J, Fritsch E F, Maniatis T. Molecular Cloning. A Laboratory Manual. 2^nd ed. New York: Cold Spring Harbor laboratory Press, 1989.
  • 9MacNeil D J, Klapko L M. Transformation of Streptomyces avermitilis by plasmid DNA. J Ind Microbiol, 1987,2:209 -218.
  • 10Ikeda H, Kotaki H, Tanaka H, et al. Involvement of glucose catabolism in avcrmectin production by Streptomyces avermitilis. Antimicrob Agents Chemother, 1988,32:282 - 284.

引证文献3

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部