Polyene macrolide antibiotic biosynthesis

被引:0
作者
Aparicio, JF
Mendes, MV
Antón, N
Recio, E
Martín, JF
机构
[1] Inst Biotechnol INBIOTEC, Leon 24006, Spain
[2] Univ Leon, Fac Biol, Area Microbiol, E-24071 Leon, Spain
关键词
polyene; polyketicle synthase; macrolide; antifungal;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Polyenes constitute a large class of natural metabolites produced by giant multifunctional enzymes in a process resembling fatty acid biosynthesis. Like fatty acids, polyene macrolides and other polyketides are assembled by decarboxylative condensations of simple carboxylic acids. But while fatty acid intermediates are fully reduced, polyene macrolide intermediates suffer the suppression of reduction or dehydration reactions at given biosynthetic steps. In the last years, much progress has been made in our understanding of the linear and modular organization of the gene clusters, and the enzymes encoded by them, responsible for the biosynthesis of these macrocyclic metabolites. This know-how about the rules that govern polyene chain growth has provided the basis for the first rational manipulations of these fascinating systems for the production of engineered derivatives and promises a new era of novel polyene development, which will hopefully yield new molecules with improved pharmacological properties.
引用
收藏
页码:1645 / 1656
页数:12
相关论文
共 122 条
[21]   Biosynthesis of the polyene antifungal antibiotic nystatin in Streptomyces noursei ATCC 11455:: analysis of the gene cluster and deduction of the biosynthetic pathway [J].
Brautaset, T ;
Sekurova, ON ;
Sletta, H ;
Ellingsen, TE ;
Strom, AR ;
Valla, S ;
Zotchev, SB .
CHEMISTRY & BIOLOGY, 2000, 7 (06) :395-403
[22]   Hexaene derivatives of nystatin produced as a result of an induced rearrangement within the nysC polyketide synthase gene in S. noursei ATCC 11455 [J].
Brautaset, T ;
Bruheim, P ;
Sletta, H ;
Hagen, L ;
Ellingsen, TE ;
Strom, AR ;
Valla, S ;
Zotchev, SB .
CHEMISTRY & BIOLOGY, 2002, 9 (03) :367-373
[23]   Amphotericin biosynthesis in Streptomyces nodosus:: deductions from analysis of polyketide synthase and late genes [J].
Caffrey, P ;
Lynch, S ;
Flood, E ;
Finnan, S ;
Oliynyk, M .
CHEMISTRY & BIOLOGY, 2001, 8 (07) :713-723
[24]  
CALNE RY, 1989, LANCET, V2, P227
[25]   The candicidin gene cluster from Streptomyces griseus IMRU 3570 [J].
Campelo, AB ;
Gil, JA .
MICROBIOLOGY-SGM, 2002, 148 :51-59
[26]   The parallel and convergent universes of polyketide synthases and nonribosomal peptide synthetases [J].
Cane, DE ;
Walsh, CT .
CHEMISTRY & BIOLOGY, 1999, 6 (12) :R319-R325
[27]   Biochemistry - Harnessing the biosynthetic code: Combinations, permutations, and mutations [J].
Cane, DE ;
Walsh, CT ;
Khosla, C .
SCIENCE, 1998, 282 (5386) :63-68
[28]   Antifungal drug resistance to azoles and polyenes [J].
Canuto, MM ;
Gutierrez, F .
LANCET INFECTIOUS DISEASES, 2002, 2 (09) :550-563
[29]   INCREASED CALCIUM PERMEABILITY IS NOT RESPONSIBLE FOR THE RAPID LETHAL EFFECTS OF AMPHOTERICIN-B ON LEISHMANIA SP [J].
COHEN, BE ;
BENAIM, G ;
RUIZ, MC ;
MICHELANGELI, F .
FEBS LETTERS, 1990, 259 (02) :286-288
[30]   Amphotericin B toxicity and lethality: a tale of two channels [J].
Cohen, BE .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1998, 162 (1-2) :95-106