PATHWAY ENGINEERING IN SECONDARY METABOLITE-PRODUCING ACTINOMYCETES

被引:64
作者
PIEPERSBERG, W
机构
[1] Department of Microbiology, BUGH Wuppertal, D-42097, Wuppertal
关键词
ACTINOMYCETES; SECONDARY METABOLISM; ANTIBIOTICS; PATHWAY ENGINEERING; (6-DEOXY-)HEXOSE METABOLISM; POLYKETIDES; PEPTIDES;
D O I
10.3109/07388554409079835
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
Actinomycetes represent the microbial group richest in production of variable secondary metabolites. These mostly bioactive molecules are the end products of complex multistep biosynthetic pathways. Recent progress in the molecular genetics and biochemistry of the biosynthetic capacities of actinomycetes enables first attempts to redesign these pathways in a directed fashion. However, in contrast to several examples of designed biochemical improvement of primary metabolic processes in microorganisms, none of the products or strains derived from pathway engineering in actinomycetes discussed herein have reached pilot or production scale. The main reasons for this slow progress are the complicated pathways themselves, their complex regulation during the actinomycete cell cycle, and their uniqueness, as most pathways and products are specific for a strain rather than for a given species or larger taxonomic group. However, the modular use of a minimum of very similar enzymes and their conversion of similar intermediates to form the building blocks for the production of a maximum of divergent end products gives hope for the future application of these genetic models for the redesign of complex pathways for modified or new natural products. Several strategies that can be followed to reach this aim are discussed, mainly for the variable 6-deoxyhexose metabolism as an ubiquitously applicable example.
引用
收藏
页码:251 / 285
页数:35
相关论文
共 128 条
[1]   PENICILLIN AND CEPHALOSPORIN BIOSYNTHETIC GENES - STRUCTURE, ORGANIZATION, REGULATION, AND EVOLUTION [J].
AHARONOWITZ, Y ;
COHEN, G ;
MARTIN, JF .
ANNUAL REVIEW OF MICROBIOLOGY, 1992, 46 :461-495
[2]  
ANDERSON JM, 1989, J BIOL CHEM, V264, P12238
[3]   A NEW AMINOGLYCOSIDE ANTIBIOTIC, SUBSTANCE AC4437 [J].
AWATA, M ;
MUTO, N ;
HAYASHI, M ;
YAGINUMA, S .
JOURNAL OF ANTIBIOTICS, 1986, 39 (05) :724-726
[4]  
BAECKER PA, 1983, J BIOL CHEM, V258, P5084
[5]   BIOSYNTHESIS OF ANTHRAQUINONES BY INTERSPECIES CLONING OF ACTINORHODIN BIOSYNTHESIS GENES IN STREPTOMYCETES - CLARIFICATION OF ACTINORHODIN GENE FUNCTIONS [J].
BARTEL, PL ;
ZHU, CB ;
LAMPEL, JS ;
DOSCH, DC ;
CONNORS, NC ;
STROHL, WR ;
BEALE, JM ;
FLOSS, HG .
JOURNAL OF BACTERIOLOGY, 1990, 172 (09) :4816-4826
[6]  
BECKMANN R, 1993, INDUSTRIAL MICROORGANISMS: BASIC AND APPLIED MOLECULAR GENETICS, P177
[7]   SECONDARY METABOLITES AS CHEMICAL SIGNALS FOR CELLULAR-DIFFERENTIATION [J].
BEPPU, T .
GENE, 1992, 115 (1-2) :159-165
[8]   THE RELATIONSHIP BETWEEN BASE COMPOSITION AND CODON USAGE IN BACTERIAL GENES AND ITS USE FOR THE SIMPLE AND RELIABLE IDENTIFICATION OF PROTEIN-CODING SEQUENCES [J].
BIBB, MJ ;
FINDLAY, PR ;
JOHNSON, MW .
GENE, 1984, 30 (1-3) :157-166
[9]   BIOSYNTHESIS OF THE LINCOMYCINS .1. STUDIES USING STABLE ISOTOPES ON THE BIOSYNTHESIS OF THE PROPYL-L-HYGRIC AND ETHYL-L-HYGRIC ACID MOIETIES OF LINCOMYCIN-A AND LINCOMYCIN-B [J].
BRAHME, NM ;
GONZALEZ, JE ;
ROLLS, JP ;
HESSLER, EJ ;
MIZSAK, S ;
HURLEY, LH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1984, 106 (25) :7873-7878
[10]   BIOSYNTHESIS OF THE LINCOMYCINS .2. STUDIES USING STABLE ISOTOPES ON THE BIOSYNTHESIS OF METHYLTHIOLINCOSAMINIDE MOIETY OF LINCOMYCIN-A [J].
BRAHME, NM ;
GONZALEZ, JE ;
MIZSAK, S ;
ROLLS, JR ;
HESSLER, EJ ;
HURLEY, LH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1984, 106 (25) :7878-7883