WHOLE-CELL GENERATION OF LANTIBIOTIC VARIANTS

被引:23
作者
Cortes, Jesus [1 ]
Appleyard, Antony N. [1 ]
Dawson, Michael J. [1 ]
机构
[1] Novacta Biosyst Ltd, Welwyn Garden City, Herts, England
来源
COMPLEX ENZYMES IN MICROBIAL NATURAL PRODUCT BIOSYNTHESIS, PART A: OVERVIEW ARTICLES AND PEPTIDES | 2009年 / 458卷
关键词
SITE-DIRECTED MUTAGENESIS; LACTOCOCCUS-LACTIS; EXPRESSION SYSTEM; GENE REPLACEMENT; POSTTRANSLATIONAL MODIFICATION; OXIDATIVE DECARBOXYLATION; CHEMICAL DERIVATIZATION; FUNCTIONAL-ANALYSIS; BACILLUS-SUBTILIS; NUKACIN ISK-1;
D O I
10.1016/S0076-6879(09)04822-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The generation of modified lantibiotics in whole cells has proved to be of value for the investigation of the specificity of the lantibiotic-processing enzymes and their tolerance to mutations in the primary sequence of lantibiotics. The development of methods to produce new lantibiotic variants has also enabled the investigation of the structure-activity relationships of these compounds and hence an evaluation of this hitherto underexploited class of natural products as a source of potential therapeutic drug candidates. We report the methods and strategies that have been used to engineer new lantibiotic variants and practical methods to analyze libraries of new compounds with a view toward optimizing drug properties.
引用
收藏
页码:559 / 574
页数:16
相关论文
共 47 条
[1]   Lysine-oriented charges trigger the membrane binding and activity of nukacin ISK-1 [J].
Asaduzzaman, Sikder M. ;
Nagao, Jun-ichi ;
Aso, Yuji ;
Nakayama, Jiro ;
Sonomoto, Kenji .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2006, 72 (09) :6012-6017
[2]  
Aso Y, 2004, J BIOSCI BIOENG, V98, P429, DOI 10.1263/jbb.98.429
[3]   GENETIC-ANALYSIS OF EPIDERMIN BIOSYNTHETIC GENES AND EPIDERMIN-NEGATIVE MUTANTS OF STAPHYLOCOCCUS-EPIDERMIDIS [J].
AUGUSTIN, J ;
ROSENSTEIN, R ;
WIELAND, B ;
SCHNEIDER, U ;
SCHNELL, N ;
ENGELKE, G ;
ENTIAN, KD ;
GOTZ, F .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 204 (03) :1149-1154
[4]   CONSTRUCTION OF AN EXPRESSION SYSTEM FOR ENGINEERING OF THE LANTIBIOTIC PEP5 [J].
BIERBAUM, G ;
REIS, M ;
SZEKAT, C ;
SAHL, HG .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1994, 60 (12) :4332-4338
[5]   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
[6]  
Bruckner R, 1997, FEMS MICROBIOL LETT, V151, P1
[7]   Determining the structure and mode of action of microbisporicin, a potent lantibiotic active against multiresistant pathogens [J].
Castiglione, Franca ;
Lazzarini, Ameriga ;
Carrano, Lucia ;
Corti, Emiliana ;
Ciciliato, Ismaela ;
Gastaldo, Luciano ;
Candiani, Paolo ;
Losi, Daniele ;
Marinelli, Flavia ;
Selva, Enrico ;
Parenti, Francesco .
CHEMISTRY & BIOLOGY, 2008, 15 (01) :22-31
[8]   Biosynthesis and mode of action of lantibiotics [J].
Chatterjee, C ;
Paul, M ;
Xie, LL ;
van der Donk, WA .
CHEMICAL REVIEWS, 2005, 105 (02) :633-683
[9]   Lacticin 481 synthetase phosphorylates its substrate during lantibiotic production [J].
Chatterjee, C ;
Miller, LM ;
Leung, YL ;
Xie, LL ;
Yi, MS ;
Kelleher, NL ;
van der Donk, WA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (44) :15332-15333
[10]  
Chen P, 1998, APPL ENVIRON MICROB, V64, P2335