Cloning and functional analysis of a phosphopantetheinyl transferase superfamily gene associated with jadomycin biosynthesis in Streptomyces venezuelae ISP5230

被引:34
作者
Wang, LR [1 ]
McVey, J [1 ]
Vining, LC [1 ]
机构
[1] Dalhousie Univ, Dept Biol, Halifax, NS B3H 4J1, Canada
来源
MICROBIOLOGY-SGM | 2001年 / 147卷
关键词
phosphopantetheinyl transferase gene; jad genes; polyketide antibiotic; acyl carrier protein synthase;
D O I
10.1099/00221287-147-6-1535
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Sequence analysis of a Xhol/Sacl fragment of chromosomal DNA downstream of jadL in the Streptomyces venezuelae ISP5230 gene cluster for jadomycin biosynthesis detected a partial ORF similar in its deduced amino acid sequence to the hetl product involved in synthesizing a regulator of heterocyst spacing in Anabaena, By probing a phage library of S, venezuelae DNA with the Xhol/Sad fragment, the authors identified and isolated a hybridizing clone. The nucleotide sequence of its DNA contained three complete ORFs (jadM, N and X) and one incomplete ORF (jadO), The jadM ORF lay immediately downstream of, and partially overlapped, jadL, It contained 786 nucleotides encoding an amino acid sequence like those of enzymes in the phosphopantetheinyl transferase family. The jadN ORF contained 1794 nucleotides and encoded an amino acid sequence resembling acyl-CoA decarboxylases. thus suggesting a role in polyketide condensation reactions. The jadX ORF was not identified, but the partial jadO showed marked similarities in its deduced amino acid sequence to NDP-hexose-2,3-dehydratases, indicating a role in forming the sugar component of jadomycin B, Expression of jadM in Escherichia coli and examination of the product by SDS-PAGE established that the ORF encoded a 29.1 kDa protein, corresponding in size to the 262 amino acid polypeptide deduced from the jadM sequence. Evidence from a Northern hybridization indicated that jadM expression is correlated with jadomycin B synthesis, Cultures of S, venezuelae ISP5230 disrupted in jadM produced only 2-5 % of the wild-type titre of jadomycin B, but grew well and produced chloramphenicol normally. The authors conclude that jadM encodes a holo-ACP synthase needed primarily for jadomycin B biosynthesis.
引用
收藏
页码:1535 / 1545
页数:11
相关论文
共 48 条
[1]   ANALYSIS OF A HET(-) MUTATION IN ANABAENA SP STRAIN PCC-7120 IMPLICATES A SECONDARY METABOLITE IN THE REGULATION OF HETEROCYST SPACING [J].
BLACK, TA ;
WOLK, CP .
JOURNAL OF BACTERIOLOGY, 1994, 176 (08) :2282-2292
[2]   INDUCTION OF SURFACTIN PRODUCTION IN BACILLUS-SUBTILIS BY GSP, A GENE LOCATED UPSTREAM OF THE GRAMICIDIN-S OPERON IN BACILLUS-BREVIS [J].
BORCHERT, S ;
STACHELHAUS, T ;
MARAHIEL, MA .
JOURNAL OF BACTERIOLOGY, 1994, 176 (08) :2458-2462
[3]   Utilization of enzymatically phosphopantetheinylated acyl carrier proteins and acetyl-acyl carrier proteins by the actinorhodin polyketide synthase [J].
Carreras, CW ;
Gehring, AM ;
Walsh, CT ;
Khosla, C .
BIOCHEMISTRY, 1997, 36 (39) :11757-11761
[4]  
CHANG Z, 1999, THESIS DALHOUSIE U
[5]   Post-translational modification of heterologously expressed Streptomyces type II polyketide synthase acyl carrier proteins [J].
Cox, RJ ;
Hitchman, TS ;
Byrom, KJ ;
Findlow, ISC ;
Tanner, JA ;
Crosby, J ;
Simpson, TJ .
FEBS LETTERS, 1997, 405 (03) :267-272
[6]   PRODUCTION OF A NOVEL POLYKETIDE ANTIBIOTIC, JADOMYCIN-B, BY STREPTOMYCES-VENEZUELAE FOLLOWING HEAT-SHOCK [J].
DOULL, JL ;
AYER, SW ;
SINGH, AK ;
THIBAULT, P .
JOURNAL OF ANTIBIOTICS, 1993, 46 (05) :869-871
[7]  
DOULL JL, 1986, J GEN MICROBIOL, V132, P1327
[8]   CONDITIONS FOR THE PRODUCTION OF JADOMYCIN-B BY STREPTOMYCES-VENEZUELAE ISP5230 - EFFECTS OF HEAT-SHOCK, ETHANOL TREATMENT AND PHAGE INFECTION [J].
DOULL, JL ;
SINGH, AK ;
HOARE, M ;
AYER, SW .
JOURNAL OF INDUSTRIAL MICROBIOLOGY, 1994, 13 (02) :120-125
[9]   Lysine biosynthesis in Saccharomyces cerevisiae:: Mechanism of α-aminoadipate reductase (Lys2) involves posttranslational phosphopantetheinylation by Lys5 [J].
Ehmann, DE ;
Gehring, AM ;
Walsh, CT .
BIOCHEMISTRY, 1999, 38 (19) :6171-6177
[10]  
FACEY S, 1994, THESIS HOHENHEIM U