Roles of VioG and VioQ in the incorporation and modification of the capreomycidine residue in the peptide antibiotic viomycin

被引:21
作者
Fei, Xiaobo
Yin, Xihou
Zhang, Ling
Zabriskie, T. Mark [1 ]
机构
[1] Oregon State Univ, Mol & Cellular Biol Program, Corvallis, OR 97331 USA
[2] Oregon State Univ, Dept Pharmaceut Sci, Corvallis, OR 97331 USA
来源
JOURNAL OF NATURAL PRODUCTS | 2007年 / 70卷 / 04期
关键词
D O I
10.1021/np060605u
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The nonproteinogenic amino acid capreomycidine is the signature residue found in the tuberactinomycin family of antitubercular peptide antibiotics and an important element of the pharmacophore. Recombinant VioG, a single-module peptide synthetase from the viomycin gene cluster cloned from Streptomyces vinaceus (ATCC11861), specifically activates capreomycidine for incorporation into viomycin (tuberactinomycin B). Insertional disruption of the putative hydroxylase gene vioQ resulted in a mutant that accumulated tuberactinomycin O, suggesting that hydroxylation at C-5 of the capreomycidine residue is a post-assembly event. The inactivated chromosomal copy of vioQ could be complemented with a wild-type copy of the gene to restore viomycin production.
引用
收藏
页码:618 / 622
页数:5
相关论文
共 30 条
[1]  
[Anonymous], 1983, COLD SPRING HARBOR L
[2]   PLASMID CLONING VECTORS FOR THE CONJUGAL TRANSFER OF DNA FROM ESCHERICHIA-COLI TO STREPTOMYCES SPP [J].
BIERMAN, M ;
LOGAN, R ;
OBRIEN, K ;
SENO, ET ;
RAO, RN ;
SCHONER, BE .
GENE, 1992, 116 (01) :43-49
[3]   Predictive, structure-based model of amino acid recognition by nonribosomal peptide synthetase adenylation domains [J].
Challis, GL ;
Ravel, J ;
Townsend, CA .
CHEMISTRY & BIOLOGY, 2000, 7 (03) :211-224
[4]   BIOSYNTHESIS OF CAPREOMYCIN .1. INCORPORATION OF ARGININE [J].
GOULD, SJ ;
MINOTT, DA .
JOURNAL OF ORGANIC CHEMISTRY, 1992, 57 (19) :5214-5217
[5]   Investigating β-hydroxyenduracididine formation in the biosynthesis of the mannopeptimycins [J].
Haltli, B ;
Tan, Y ;
Magarvey, NA ;
Wagenaar, M ;
Yin, XH ;
Greenstein, M ;
Hucul, JA ;
Zabriskie, TM .
CHEMISTRY & BIOLOGY, 2005, 12 (11) :1163-1168
[6]   THE CHEMISTRY OF VIOMYCIN [J].
HASKELL, TH ;
FUSARI, SA ;
FROHARDT, RP ;
BARTZ, QR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1952, 74 (03) :599-602
[7]   Mannopeptimycins, novel antibacterial glycopeptides from Streptomyces hygroscopicus, LL-AC98 [J].
He, HY ;
Williamson, RT ;
Shen, B ;
Graziani, EI ;
Yang, HY ;
Sakya, SM ;
Petersen, PJ ;
Carter, GT .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (33) :9729-9736
[8]  
HERR EB, 1962, ANTIMICROB AGENTS CH, P201
[9]   ENDURACIDIN A NEW ANTIBIOTIC .V. STRUCTURES OF NEW BASIC AMINO ACIDS ENDURACIDIDINE AND ALLOENDURACIDIDINE [J].
HORII, S ;
KAMEDA, Y .
JOURNAL OF ANTIBIOTICS, 1968, 21 (11) :665-+
[10]   STUDIES ON TUBERACTINOMYCIN .3. ISOLATION AND CHARACTERIZATION OF 2 MINOR COMPONENTS, TUBERACTINOMYCIN-B AND TUBERACTINOMYCIN-O [J].
IZUMI, R ;
TAKE, T ;
ANDO, T ;
NODA, T ;
NAGATA, A .
JOURNAL OF ANTIBIOTICS, 1972, 25 (04) :201-&