INVIVO EXPRESSION OF THE PSEUDOMONAS-STUTZERI MALTOTETRAOSE-FORMING AMYLASE GENE (AMYP)

被引:6
作者
FUJITA, M
FUTAI, M
AMEMURA, A
机构
[1] FUKUYAMA UNIV,FAC ENGN,DEPT BIOTECHNOL,HIGASHIMURA CHO,FUKUYAMA,HIROSHIMA 72902,JAPAN
[2] OSAKA UNIV,INST SCI & IND RES,IBARAKI,OSAKA 567,JAPAN
关键词
D O I
10.1128/jb.172.3.1595-1599.1990
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Northern hybridization and S1 nuclease mapping revealed that the amyP gene coding for maltotetraose-forming amylase of Pseudomonas stutzeri MO-19 is transcribed as a monocistronic mRNA of 2.0 kilobases and that the transcription start site is located 81 base pairs upstream from the first nucleotide of the initiation codon. The amyP gene was expressed weakly in Escherichia coli, and transcription started 49 base pairs downstream of the P. stutzeri MO-19 transcription start site. Synthesis of the amylase in P. stutzeri MO-19 was induced by the addition of maltose to the culture medium and was repressed by the addition of glucose. The induction by maltose was shown to be the result of transcriptional induction of the amyP gene. In contrast, glucose did not repress transcription initiation of amyP, indicating that it controls synthesis of the enzyme, probably at the posttranscriptional level.
引用
收藏
页码:1595 / 1599
页数:5
相关论文
共 19 条
[1]  
AIBA H, 1981, J BIOL CHEM, V256, P1905
[2]  
BIRNBOIM HC, 1979, NUCLEIC ACIDS RES, V7, P1513
[3]   INTERACTIONS OF BACTERIOPHAGE AND HOST MACROMOLECULES IN THE GROWTH OF BACTERIOPHAGE-LAMBDA [J].
FRIEDMAN, DI ;
OLSON, ER ;
GEORGOPOULOS, C ;
TILLY, K ;
HERSKOWITZ, I ;
BANUETT, F .
MICROBIOLOGICAL REVIEWS, 1984, 48 (04) :299-325
[4]   TRANSCRIPTION OF THE ISOAMYLASE GENE (IAM) IN PSEUDOMONAS-AMYLODERAMOSA SB-15 [J].
FUJITA, M ;
AMEMURA, A ;
FUTAI, M .
JOURNAL OF BACTERIOLOGY, 1989, 171 (08) :4320-4325
[5]   CLONING AND NUCLEOTIDE-SEQUENCE OF THE GENE (AMYP) FOR MALTOTETRAOSE-FORMING AMYLASE FROM PSEUDOMONAS-STUTZERI MO-19 [J].
FUJITA, M ;
TORIGOE, K ;
NAKADA, T ;
TSUSAKI, K ;
KUBOTA, M ;
SAKAI, S ;
TSUJISAKA, Y .
JOURNAL OF BACTERIOLOGY, 1989, 171 (03) :1333-1339
[6]   PRODUCTS OF NITROGEN REGULATORY GENES NTRA AND NTRC OF ENTERIC BACTERIA ACTIVATE GLNA TRANSCRIPTION INVITRO - EVIDENCE THAT THE NTRA PRODUCT IS A SIGMA-FACTOR [J].
HIRSCHMAN, J ;
WONG, PK ;
SEI, K ;
KEENER, J ;
KUSTU, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (22) :7525-7529
[7]   TRANSCRIPTION OF GLNA BY PURIFIED ESCHERICHIA-COLI COMPONENTS - CORE RNA-POLYMERASE AND THE PRODUCTS OF GLNF, GLNG, AND GLNL [J].
HUNT, TP ;
MAGASANIK, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (24) :8453-8457
[8]   EXPRESSION OF THE REGULATORY GENE XYLS ON THE TOL PLASMID IS POSITIVELY CONTROLLED BY THE XYLR GENE-PRODUCT [J].
INOUYE, S ;
NAKAZAWA, A ;
NAKAZAWA, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (15) :5182-5186
[9]   MOLECULAR-CLONING OF REGULATORY GENE XYLR AND OPERATOR-PROMOTER REGIONS OF THE XYLABC AND XYLDEGF OPERONS OF THE TOL PLASMID [J].
INOUYE, S ;
NAKAZAWA, A ;
NAKAZAWA, T .
JOURNAL OF BACTERIOLOGY, 1983, 155 (03) :1192-1199
[10]  
Maniatis T., 1982, MOL CLONING