The role of the trehalose system in regulating the maltose regulon of Escherichia coli

被引:25
作者
Decker, K [1 ]
Gerhardt, F [1 ]
Boos, W [1 ]
机构
[1] Univ Konstanz, Dept Biol, D-78457 Constance, Germany
关键词
D O I
10.1046/j.1365-2958.1999.01395.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
The maltose regulon consists of 10 genes encoding an ABC transporter for maltose and maltodextrins as well as enzymes necessary for their degradation. MalK, the energy-transducing subunit of the transport system, acts phenotypically as a repressor of MalT, the transcriptional activator of the mal genes. Using MacConkey maltose indicator plates we isolated an insertion mutation that strongly reduced the repressing effect of overproduced MalK. The insertion had occurred in treR encoding the repressor of the trehalose system. The loss of TreR function led to derepression of treB encoding an enzymeII(Tre) of the PTS for trehalose and of treC encoding TreC, the cytoplasmic trehalose-6-phosphate hydrolase. Further analysis revealed that maltose can enter the cell by facilitated diffusion through enzymeII(Tre), thus causing induction of the maltose system. In addition, derepression of TreC by itself caused induction of the maltose system, and a mutant lacking TreC was reduced in the uninduced level of mal gene expression indicating synthesis of endogenous inducer by TreC. Extracts containing TreC transformed [C-14]-maltose into another C-14-labelled compound (preliminarily identified as maltose 1-phosphate) that is likely to be an alternative inducer of the maltose system.
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收藏
页码:777 / 788
页数:12
相关论文
共 47 条
[1]   TIGHTLY REGULATED TAC PROMOTER VECTORS USEFUL FOR THE EXPRESSION OF UNFUSED AND FUSED PROTEINS IN ESCHERICHIA-COLI [J].
AMANN, E ;
OCHS, B ;
ABEL, KJ .
GENE, 1988, 69 (02) :301-315
[2]   POSITIVE SELECTION FOR LOSS OF TETRACYCLINE RESISTANCE [J].
BOCHNER, BR ;
HUANG, HC ;
SCHIEVEN, GL ;
AMES, BN .
JOURNAL OF BACTERIOLOGY, 1980, 143 (02) :926-933
[3]   CONSTRUCTION AND CHARACTERIZATION OF NEW CLONING VEHICLES .2. MULTIPURPOSE CLONING SYSTEM [J].
BOLIVAR, F ;
RODRIGUEZ, RL ;
GREENE, PJ ;
BETLACH, MC ;
HEYNEKER, HL ;
BOYER, HW ;
CROSA, JH ;
FALKOW, S .
GENE, 1977, 2 (02) :95-113
[4]   Maltose/maltodextrin system of Escherichia coli:: Transport, metabolism, and regulation [J].
Boos, W ;
Shuman, H .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1998, 62 (01) :204-+
[5]   TRANSPOSABLE-LAMBDA PLACMU BACTERIOPHAGES FOR CREATING LACZ OPERON FUSIONS AND KANAMYCIN RESISTANCE INSERTIONS IN ESCHERICHIA-COLI [J].
BREMER, E ;
SILHAVY, TJ ;
WEINSTOCK, GM .
JOURNAL OF BACTERIOLOGY, 1985, 162 (03) :1092-1099
[6]   OSMOREGULATION OF THE MALTOSE REGULON IN ESCHERICHIA-COLI [J].
BUKAU, B ;
EHRMANN, M ;
BOOS, W .
JOURNAL OF BACTERIOLOGY, 1986, 166 (03) :884-891
[7]   TRANSPOSITION AND FUSION OF LAC GENES TO SELECTED PROMOTERS IN ESCHERICHIA-COLI USING BACTERIOPHAGE-LAMBDA AND BACTERIOPHAGE-MU [J].
CASADABAN, MJ .
JOURNAL OF MOLECULAR BIOLOGY, 1976, 104 (03) :541-555
[8]   CONSTRUCTION AND CHARACTERIZATION OF AMPLIFIABLE MULTICOPY DNA CLONING VEHICLES DERIVED FROM P15A CRYPTIC MINIPLASMID [J].
CHANG, ACY ;
COHEN, SN .
JOURNAL OF BACTERIOLOGY, 1978, 134 (03) :1141-1156
[10]   ACTION OF CAP ON THE MALT PROMOTER INVITRO [J].
CHAPON, C ;
KOLB, A .
JOURNAL OF BACTERIOLOGY, 1983, 156 (03) :1135-1143