Highly efficient production of enzymes of an extreme thermophile, Thermus thermophilus: A practical method to overexpress GC-rich genes in Escherichia coli

被引:10
作者
Ishida, M
Yoshida, M
Oshima, T
机构
[1] TOKYO INST TECHNOL,RESOURCES UTILIZAT RES LAB,MIDORI KU,YOKOHAMA,KANAGAWA 227,JAPAN
[2] TOKYO UNIV PHARM & LIFE SCI,DEPT MOL BIOL,HACHIOJI,TOKYO 19203,JAPAN
关键词
Thermus thermophilus; GC-rich gene; 3-isopropylmalate dehydrogenase; phosphofructokinase; overproduction; leader open reading frame (ORF); gene overlapping;
D O I
10.1007/s007920050029
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 GC-rich leuB gene (coding for 3-isopropylmalate dehydrogenase) of Thermus thermophilus is scarcely expressed in Escherichia coli. unless a leader open reading frame (ORF) is provided. We conducted experiments on nonexpressible plasmids and obtained a modified plasmid showing greatly enhanced expression: the degree of expression from the plasmid was higher than that from any other plasmid so far constructed. Sequence analysis of the plasmid showed that a 258-bp leader ORF overlapped with the initiation codon of leuB was newly formed as a consequence of the insertion of a 0.5-kb BamHI fragment derived from the E. coli chromosome. The degree of expression from the plasmid was further improved by shortening the leader ORF to 36 bp without changing the overlapping portion, and the flanking sequence between the promoter and the leader ORF was removed. The expression in E. coli of the pfk1 gene (coding for phosphofructokinase) of T. thermophilus was improved by the construction of a structure similar to that which enhanced the expression of the leuB gene. Based on the results, a practical method for the overexpression of GC-rich genes in E. coli is proposed.
引用
收藏
页码:157 / 162
页数:6
相关论文
共 22 条
[1]  
ALMOND J, 1985, BASIC CLONING TECHNI
[2]   LYSIS GENE OF BACTERIOPHAGE-MS2 IS ACTIVATED BY TRANSLATION TERMINATION AT THE OVERLAPPING COAT GENE [J].
BERKHOUT, B ;
SCHMIDT, BF ;
VANSTRIEN, A ;
VANBOOM, J ;
VANWESTRENEN, J ;
VANDUIN, J .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 195 (03) :517-524
[3]   PRIMARY CHARACTERIZATION OF THE PROTEIN PRODUCTS OF THE ESCHERICHIA-COLI OMPR LOCUS - STRUCTURE AND REGULATION OF SYNTHESIS OF THE OMPR AND ENVZ PROTEINS [J].
COMEAU, DE ;
IKENAKA, K ;
TSUNG, K ;
INOUYE, M .
JOURNAL OF BACTERIOLOGY, 1985, 164 (02) :578-584
[4]   DNA-SEQUENCE AND CODING PROPERTIES OF MUTD(DNAQ) A DOMINANT ESCHERICHIA-COLI MUTATOR GENE [J].
COX, EC ;
HORNER, DL .
JOURNAL OF MOLECULAR BIOLOGY, 1986, 190 (01) :113-117
[5]   GENE SEQUENCE AND PREDICTED AMINO-ACID-SEQUENCE OF THE MOTA PROTEIN, A MEMBRANE-ASSOCIATED PROTEIN REQUIRED FOR FLAGELLAR ROTATION IN ESCHERICHIA-COLI [J].
DEAN, GE ;
MACNAB, RM ;
STADER, J ;
MATSUMURA, P ;
BURKS, C .
JOURNAL OF BACTERIOLOGY, 1984, 159 (03) :991-999
[6]  
GOLD L, 1987, ESCHERICHIA COLI SAL
[7]   OVEREXPRESSION OF GENES OF AN EXTREME THERMOPHILE, THERMUS-THERMOPHILUS, IN ESCHERICHIA-COLI-CELLS [J].
ISHIDA, M ;
OSHIMA, T .
JOURNAL OF BACTERIOLOGY, 1994, 176 (09) :2767-2770
[8]  
Ishida M, 1996, FEMS MICROBIOL LETT, V135, P137
[9]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[10]   STRUCTURE AND EXPRESSION OF THE OMPB OPERON, THE REGULATORY LOCUS FOR THE OUTER-MEMBRANE PORIN REGULON IN SALMONELLA-TYPHIMURIUM LT-2 [J].
LILJESTROM, P ;
LAAMANEN, I ;
PALVA, ET .
JOURNAL OF MOLECULAR BIOLOGY, 1988, 201 (04) :663-673