A NusG-like transcription anti-terminator is involved in the biosynthesis of the polyketide antibiotic TA of Myxococcus xanthus

被引:18
作者
Paitan, Y
Orr, E
Ron, EZ
Rosenberg, E [1 ]
机构
[1] Tel Aviv Univ, George S Wise Fac Life Sci, Dept Mol Microbiol & Biotechnol, Ramat Aviv, Israel
[2] Univ Leicester, Dept Genet, Leicester LE1 7RH, Leics, England
基金
英国惠康基金;
关键词
Myxococcus xanthus; antibiotic biosynthesis; type I polyketide synthase; polyketide; NusG; transcription anti-termination;
D O I
10.1111/j.1574-6968.1999.tb13377.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The antibiotic TA of Myxococcus xanthus is synthesized through a type I polyketide synthase mechanism. Previous studies have indicated that several genes essential for TA production are clustered within a 40-kb region and are transcriptionally co-regulated. In this study, we report the genetic analysis of the first gene in the TA gene cluster, identified as a NusG-like transcription anti-terminator. Functional analysis of this NusG-like anti-terminator gene by specific gene disruption confirms that it is essential for TA production bur not for normal growth and development. (C) 1999 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:221 / 227
页数:7
相关论文
共 30 条
[1]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]   NUSG IS REQUIRED TO OVERCOME A KINETIC LIMITATION TO RHO-FUNCTION AT AN INTRAGENIC TERMINATOR [J].
BURNS, CM ;
RICHARDSON, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (11) :4738-4742
[3]   ESCHERICHIA-COLI NUSG PROTEIN STIMULATES TRANSCRIPTION ELONGATION RATES IN-VIVO AND IN-VITRO [J].
BUROVA, E ;
HUNG, SC ;
SAGITOV, V ;
STITT, BL ;
GOTTESMAN, ME .
JOURNAL OF BACTERIOLOGY, 1995, 177 (05) :1388-1392
[4]   AMINO-ACID PRECURSORS OF MYXOCOCCUS-XANTHUS ANTIBIOTIC-TA [J].
FYTLOVITCH, S ;
NATHAN, PD ;
ZAFRIRI, D ;
ROSENBERG, E .
JOURNAL OF ANTIBIOTICS, 1983, 36 (11) :1525-1530
[5]   TRANSCRIPTIONAL ANTITERMINATION [J].
GREENBLATT, J ;
NODWELL, JR ;
MASON, SW .
NATURE, 1993, 364 (6436) :401-406
[6]   GENETIC SUPPRESSION AND PHENOTYPIC MASKING OF A MYXOCOCCUS-XANTHUS FRZF(-) DEFECT [J].
KASHEFI, K ;
HARTZELL, PL .
MOLECULAR MICROBIOLOGY, 1995, 15 (03) :483-494
[7]   CONSTRUCTION OF TN5 LAC, A TRANSPOSON THAT FUSES LACZ EXPRESSION TO EXOGENOUS PROMOTERS, AND ITS INTRODUCTION INTO MYXOCOCCUS-XANTHUS [J].
KROOS, L ;
KAISER, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (18) :5816-5820
[8]   A GLOBAL ANALYSIS OF DEVELOPMENTALLY REGULATED GENES IN MYXOCOCCUS-XANTHUS [J].
KROOS, L ;
KUSPA, A ;
KAISER, D .
DEVELOPMENTAL BIOLOGY, 1986, 117 (01) :252-266
[9]   KOW: A novel motif linking a bacterial transcription factor with ribosomal proteins [J].
Kyrpides, NC ;
Woese, CR ;
Ouzounis, CA .
TRENDS IN BIOCHEMICAL SCIENCES, 1996, 21 (11) :425-426
[10]  
LI J, 1992, J BIOL CHEM, V267, P6012