A multiplasmid approach to preparing large libraries of polyketides

被引:129
作者
Xue, Q
Ashley, G
Hutchinson, CR
Santi, DV
机构
[1] Kosan Biosci, Hayward, CA 94545 USA
[2] Univ Wisconsin, Sch Pharm, Madison, WI 53706 USA
[3] Univ Wisconsin, Dept Bacteriol, Madison, WI 53706 USA
关键词
D O I
10.1073/pnas.96.21.11740
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A three-plasmid system for heterologous expression of 6-deoxy-erythronolide B synthase (DEBS) has been developed to facilitate combinatorial biosynthesis of polyketides made by type I modular polyketide synthases (PKSs), The eryA PKS genes encoding the three DEBS subunits were individually cloned into three compatible Streptomyces vectors carrying mutually selectable antibiotic resistance markers, A strain of Streptomyces lividans transformed with all three plasmids produced 6-deoxyerythronolide B at a level similar to that of a strain transformed with a single plasmid containing all three genes. The utility of this system in combinatorial biosynthesis was demonstrated through production of a library of modified polyketide macrolactones by using versions of each plasmid constructed to contain defined mutations. Combinations of these vector sets were introduced into S. lividans, resulting in strains producing a wide range of 6-deoxyerythronolide B analogs, This method can be extended to any modular PKS and has the potential to produce thousands of novel natural products, including ones derived from further modification of the PKS products by tailoring enzymes.
引用
收藏
页码:11740 / 11745
页数:6
相关论文
共 28 条
  • [1] Biosynthesis of the ansamycin antibiotic rifamycin: deductions from the molecular analysis of the rif biosynthetic gene cluster of Amycolatopsis mediterranei S699
    August, PR
    Tang, L
    Yoon, YJ
    Ning, S
    Muller, R
    Yu, TW
    Taylor, M
    Hoffmann, D
    Kim, CG
    Zhang, XH
    Hutchinson, CR
    Floss, HG
    [J]. CHEMISTRY & BIOLOGY, 1998, 5 (02): : 69 - 79
  • [2] PLASMID CLONING VECTORS FOR THE CONJUGAL TRANSFER OF DNA FROM ESCHERICHIA-COLI TO STREPTOMYCES SPP
    BIERMAN, M
    LOGAN, R
    OBRIEN, K
    SENO, ET
    RAO, RN
    SCHONER, BE
    [J]. GENE, 1992, 116 (01) : 43 - 49
  • [3] AN UNUSUALLY LARGE MULTIFUNCTIONAL POLYPEPTIDE IN THE ERYTHROMYCIN-PRODUCING POLYKETIDE SYNTHASE OF SACCHAROPOLYSPORA-ERYTHRAEA
    CORTES, J
    HAYDOCK, SF
    ROBERTS, GA
    BEVITT, DJ
    LEADLAY, PF
    [J]. NATURE, 1990, 348 (6297) : 176 - 178
  • [4] MODULAR ORGANIZATION OF GENES REQUIRED FOR COMPLEX POLYKETIDE BIOSYNTHESIS
    DONADIO, S
    STAVER, MJ
    MCALPINE, JB
    SWANSON, SJ
    KATZ, L
    [J]. SCIENCE, 1991, 252 (5006) : 675 - 679
  • [5] Coordinate transcription and physical linkage of domains in surfactin synthetase are not essential for proper assembly and activity of the multienzyme complex
    Guenzi, E
    Galli, G
    Grgurina, I
    Pace, E
    Ferranti, P
    Grandi, G
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (23) : 14403 - 14410
  • [6] Hopwood D.A., 1985, GENETIC MANIPULATION
  • [7] Precursor-directed biosynthesis of erythromycin analogs by an engineered polyketide synthase
    Jacobsen, JR
    Hutchinson, CR
    Cane, DE
    Khosla, C
    [J]. SCIENCE, 1997, 277 (5324) : 367 - 369
  • [8] ENGINEERED BIOSYNTHESIS OF A COMPLETE MACROLACTONE IN A HETEROLOGOUS HOST
    KAO, CM
    KATZ, L
    KHOSLA, C
    [J]. SCIENCE, 1994, 265 (5171) : 509 - 512
  • [9] Evidence for two catalytically independent clusters of active sites in a functional modular polyketide synthase
    Kao, CM
    Pieper, R
    Cane, DE
    Khosla, C
    [J]. BIOCHEMISTRY, 1996, 35 (38) : 12363 - 12368
  • [10] MANIPULATION OF MACROLIDE RING SIZE BY DIRECTED MUTAGENESIS OF A MODULAR POLYKETIDE SYNTHASE
    KAO, CM
    LUO, GL
    KATZ, L
    CANE, DE
    KHOSLA, C
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (35) : 9105 - 9106