ISOLATION AND PROPERTIES OF A PLASMID WHICH EXPRESSES THE E-COLI SU+7 AMBER SUPPRESSOR TRANSFER-RNA GENE

被引:17
作者
YARUS, M
机构
[1] Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, 80302, Colorado
来源
MOLECULAR & GENERAL GENETICS | 1979年 / 170卷 / 03期
关键词
D O I
10.1007/BF00267062
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 gene of the amber suppressor tRNA derived from tRNATry, Su+7, has been inserted into a col E1-derived vehicle by selecting for its expression. Despite selection for a suppressor phenotype, and the plasmid's stable presence at ca. 180 copies/cell during balanced growth, the level of mature tRNA maintained by the gene is less than that of the normal haploid tRNATry locus in the bacterial chromosome. Transfer RNA genes, both the plasmid Su+7 gene and chromosomal tRNA's are expressed during inhibition of protein synthesis. During, e.g. chloramphenicol inhibition, Su-7 and Su+7 tRNA can be elevated similarly in the plasmid-containing cell; Su+7 reaches levels of molecules/cell which ordinarily characterize a major tRNA. The recombinant plasmid, but not the cloning vehicle alone, has a more general effect on tRNA levels; accumulation of tRNA from three chromosomal tRNA loci including tRNATry, continues during extensive isoleucine limitation. The plasmid therefore contains a locus which probably alters the relaxedstringent circuit, whose effects is disseminated to at least 3 widely separated loci. © 1979 Springer-Verlag.
引用
收藏
页码:291 / 298
页数:8
相关论文
共 31 条
[1]   RECALIBRATED LINKAGE MAP OF ESCHERICHIA-COLI K-12 [J].
BACHMANN, BJ ;
LOW, KB ;
TAYLOR, AL .
BACTERIOLOGICAL REVIEWS, 1976, 40 (01) :116-167
[3]   NONCHROMOSOMAL ANTIBIOTIC RESISTANCE IN BACTERIA - GENETIC TRANSFORMATION OF ESCHERICHIA-COLI BY R-FACTOR DNA [J].
COHEN, SN ;
CHANG, ACY ;
HSU, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1972, 69 (08) :2110-&
[4]   CHROMOSOME REPLICATION AND DIVISION CYCLE OF ESCHERICHIA COLI B/R [J].
COOPER, S ;
HELMSTETTER, CE .
JOURNAL OF MOLECULAR BIOLOGY, 1968, 31 (03) :519-+
[5]   LIGATION OF ECORI ENDONUCLEASE-GENERATED DNA FRAGMENTS INTO LINEAR AND CIRCULAR STRUCTURES [J].
DUGAICZYK, A ;
BOYER, HW ;
GOODMAN, HM .
JOURNAL OF MOLECULAR BIOLOGY, 1975, 96 (01) :171-&
[6]  
GALLANT J, 1976, PROTEIN SYNTHESIS SE, V2, P309
[7]   SEPARATION OF SOLUBLE RIBONUCLEIC ACIDS ON BENZOYLATED DIETHYLAMINOETHYLCELLULOSE [J].
GILLAM, I ;
MILLWARD, S ;
BLEW, D ;
VONTIGER.M ;
WIMMER, E ;
TENER, GM .
BIOCHEMISTRY, 1967, 6 (10) :3043-&
[8]  
GREENE PJ, 1974, DNA REPLICATION, P87
[9]   LOCATION IN BACTERIOPHAGE-LAMBDA DNA OF CLEAVAGE SITES OF SITE-SPECIFIC ENDONUCLEASE FROM BACILLUS-AMYLOLIQUEFACIENS H [J].
HAGGERTY, DM ;
SCHLEIF, RF .
JOURNAL OF VIROLOGY, 1976, 18 (02) :659-663
[10]   PLASMID COLE1 AS A MOLECULAR VEHICLE FOR CLONING AND AMPLIFICATION OF DNA [J].
HERSHFIE.V ;
BOYER, HW ;
YANOFSKY, C ;
LOVETT, MA ;
HELINSKI, DR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1974, 71 (09) :3455-3459