Bacillus subtilis 168 contains two differentially regulated genes encoding L-asparaginase

被引:69
作者
Fisher, SH [1 ]
Wray, LV [1 ]
机构
[1] Boston Univ, Sch Med, Dept Microbiol, Boston, MA 02118 USA
关键词
D O I
10.1128/JB.184.8.2148-2154.2002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Expression of the two Bacillus subtilis genes encoding L-asparaginase is controlled by independent regulatory factors. The ansZ gene (formerly yccC) was shown by mutational analysis to encode a functional L-asparaginase, the expression of which is activated during nitrogen-limited growth by the TnrA transcription factor. Gel mobility shift and DNase I footprinting experiments indicate that TnrA regulates ansZ expression by binding to a DNA site located upstream of the ansZ promoter. The expression of the ansA gene, which encodes the second L-asparaginase, was found to be induced by asparagine. The ansA repressor, AnsR, was shown to negatively regulate its own expression.
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页码:2148 / 2154
页数:7
相关论文
共 37 条
[1]   REGULATION OF HISTIDINE AND PROLINE DEGRADATION ENZYMES BY AMINO-ACID AVAILABILITY IN BACILLUS-SUBTILIS [J].
ATKINSON, MR ;
WRAY, LV ;
FISHER, SH .
JOURNAL OF BACTERIOLOGY, 1990, 172 (09) :4758-4765
[2]   IDENTIFICATION OF GENES AND GENE-PRODUCTS WHOSE EXPRESSION IS ACTIVATED DURING NITROGEN-LIMITED GROWTH IN BACILLUS-SUBTILIS [J].
ATKINSON, MR ;
FISHER, SH .
JOURNAL OF BACTERIOLOGY, 1991, 173 (01) :23-27
[3]   Role of TnrA in nitrogen source-dependent repression of Bacillus subtilis glutamate synthase gene expression [J].
Belitsky, BR ;
Wray, LV ;
Fisher, SH ;
Bohannon, DE ;
Sonenshein, AL .
JOURNAL OF BACTERIOLOGY, 2000, 182 (21) :5939-5947
[4]   Computerized genetic map of Bacillus subtilis [J].
Biaudet, V ;
Samson, F ;
Anagnostopoulos, C ;
Ehrlich, SD ;
Bessieres, P .
MICROBIOLOGY-SGM, 1996, 142 :2669-2729
[5]   L-ASPARAGINASE-II OF ESCHERICHIA-COLI K-12 - CLONING, MAPPING AND SEQUENCING OF THE ANSB GENE [J].
BONTHRON, DT .
GENE, 1990, 91 (01) :101-105
[6]   A sigma(E)-dependent operon subject to catabolite repression during sporulation in Bacillus subtilis [J].
Bryan, EM ;
Beall, BW ;
Moran, CP .
JOURNAL OF BACTERIOLOGY, 1996, 178 (16) :4778-4786
[7]   THE PMTL NIC-CLONING VECTORS .1. IMPROVED PUC POLYLINKER REGIONS TO FACILITATE THE USE OF SONICATED DNA FOR NUCLEOTIDE SEQUENCING [J].
CHAMBERS, SP ;
PRIOR, SE ;
BARSTOW, DA ;
MINTON, NP .
GENE, 1988, 68 (01) :139-149
[8]   CONSTRUCTION AND PROPERTIES OF A NEW INSERTION VECTOR, PJDC9, THAT IS PROTECTED BY TRANSCRIPTIONAL TERMINATORS AND USEFUL FOR CLONING OF DNA FROM STREPTOCOCCUS-PNEUMONIAE [J].
CHEN, JD ;
MORRISON, DA .
GENE, 1988, 64 (01) :155-164
[9]  
DUNLOP PC, 1978, J BIOL CHEM, V253, P1297
[10]   REGULATION OF GLUTAMINE-SYNTHETASE IN STREPTOMYCES-COELICOLOR [J].
FISHER, SH ;
WRAY, LV .
JOURNAL OF BACTERIOLOGY, 1989, 171 (05) :2378-2383