The expression of the trpD, trpC and trpBA genes of Streptomyces coelicolor A3(2) is regulated by growth rate and growth phase but not by feedback repression

被引:20
作者
Hu, DSJ [1 ]
Hood, DW [1 ]
Heidstra, R [1 ]
Hodgson, DA [1 ]
机构
[1] Univ Warwick, Dept Biol Sci, Coventry CV4 7AL, W Midlands, England
关键词
D O I
10.1046/j.1365-2958.1999.01407.x
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
Transformation of tryptophan auxotrophs of Streptomyces coelicolor A3(2) and subsequent analysis have allowed the identification of four tryptophan biosynthetic genes. Subcloning, complementation of trp strains, nucleotide sequencing of 5.1 kb and 1.95 kb of DNA and subsequent homology comparisons identified the trpC, trpB and trpA genes and trpD gene respectively. The arrangement of genes in the trpCBA cluster is unusual in that trpC is separated by a small open reading frame, trpX, from the potentially translationally coupled trpB and trpA genes, Sequence analysis of the trpD gene revealed the presence of a large mRNA loop structure directly upstream of the trpD-coding region. S1 nuclease mapping studies of trpCXBA have revealed two major potential transcription start points, one just upstream of the trpC gene and the other located upstream of the trpX gene, S1 nuclease mapping of the trpD region revealed four fragment end-points. Quantitative S1 nuclease protection assays and a promoterless catechol dioxygenase reporter gene have revealed that the expression of all these genes is growth phase dependent and growth rate dependent, expression being maximal during early exponential phase and dropping off sharply in late exponential phase. This growth phase-dependent and growth rate-dependent regulation is the first reported in streptomycete primary metabolism.
引用
收藏
页码:869 / 880
页数:12
相关论文
共 34 条
[1]   PREDICTION OF RNA SECONDARY STRUCTURE, INCLUDING PSEUDOKNOTTING, BY COMPUTER-SIMULATION [J].
ABRAHAMS, JP ;
VANDENBERG, M ;
VANBATENBURG, E ;
PLEIJ, C .
NUCLEIC ACIDS RESEARCH, 1990, 18 (10) :3035-3044
[2]  
BABITZKE P, 1994, J BIOL CHEM, V269, P16597
[3]   TRYPTOPHAN BIOSYNTHESIS GENES IN LACTOCOCCUS-LACTIS SUBSP LACTIS [J].
BARDOWSKI, J ;
EHRLICH, SD ;
CHOPIN, A .
JOURNAL OF BACTERIOLOGY, 1992, 174 (20) :6563-6570
[4]   THE RELATIONSHIP BETWEEN BASE COMPOSITION AND CODON USAGE IN BACTERIAL GENES AND ITS USE FOR THE SIMPLE AND RELIABLE IDENTIFICATION OF PROTEIN-CODING SEQUENCES [J].
BIBB, MJ ;
FINDLAY, PR ;
JOHNSON, MW .
GENE, 1984, 30 (1-3) :157-166
[5]   SEQUENCE OF THE PSEUDOMONAS-AERUGINOSA TRPI ACTIVATOR GENE AND RELATEDNESS OF TRPI TO OTHER PROCARYOTIC REGULATORY GENES [J].
CHANG, M ;
HADERO, A ;
CRAWFORD, IP .
JOURNAL OF BACTERIOLOGY, 1989, 171 (01) :172-183
[6]   Accumulation of glycosphingolipids in human atherosclerotic plaque and unaffected aorta tissues [J].
Chatterjee, SB ;
Dey, S ;
Shi, WY ;
Thomas, K ;
Hutchins, GM .
GLYCOBIOLOGY, 1997, 7 (01) :57-65
[7]   Physical identification of a chromosomal locus encoding biosynthetic genes for the lipopeptide calcium-dependent antibiotic (CDA) of Streptomyces coelicolor A3(2) [J].
Chong, PP ;
Podmore, SM ;
Kieser, HM ;
Redenbach, M ;
Turgay, K ;
Marahiel, M ;
Hopwood, DA ;
Smith, CP .
MICROBIOLOGY-UK, 1998, 144 :193-199
[8]   STREPTOMYCES PROMOTER-PROBE PLASMIDS THAT UTILIZE THE XYLE GENE OF PSEUDOMONAS-PUTIDA [J].
CLAYTON, TM ;
BIBB, MJ .
NUCLEIC ACIDS RESEARCH, 1990, 18 (04) :1077-1077
[9]   Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence [J].
Cole, ST ;
Brosch, R ;
Parkhill, J ;
Garnier, T ;
Churcher, C ;
Harris, D ;
Gordon, SV ;
Eiglmeier, K ;
Gas, S ;
Barry, CE ;
Tekaia, F ;
Badcock, K ;
Basham, D ;
Brown, D ;
Chillingworth, T ;
Connor, R ;
Davies, R ;
Devlin, K ;
Feltwell, T ;
Gentles, S ;
Hamlin, N ;
Holroyd, S ;
Hornby, T ;
Jagels, K ;
Krogh, A ;
McLean, J ;
Moule, S ;
Murphy, L ;
Oliver, K ;
Osborne, J ;
Quail, MA ;
Rajandream, MA ;
Rogers, J ;
Rutter, S ;
Seeger, K ;
Skelton, J ;
Squares, R ;
Squares, S ;
Sulston, JE ;
Taylor, K ;
Whitehead, S ;
Barrell, BG .
NATURE, 1998, 393 (6685) :537-+
[10]  
DOOLITTLE WF, 1992, PROKARYOTIC STRUCTUR, P1