TN5 INSERTIONS IN THE AGROCIN-84 PLASMID - THE CONJUGAL NATURE OF PAGK84 AND THE LOCATIONS OF DETERMINANTS FOR TRANSFER AND AGROCIN-84 PRODUCTION

被引:51
作者
FARRAND, SK
SLOTA, JE
SHIM, JS
KERR, A
机构
[1] LOYOLA UNIV, STRITCH SCH MED, DEPT MICROBIOL, MAYWOOD, IL 60153 USA
[2] UNIV ADELAIDE, WAITE AGR RES INST, DEPT PLANT PATHOL, GLEN OSMOND, SA 5064, AUSTRALIA
关键词
D O I
10.1016/0147-619X(85)90063-0
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The kanamycin-resistance transposon Tn5 was randomly introduced into pAgK84, a 47.7-kb [kilobase] plasmid coding for agrocin 84 production in Agrobacterium. Using such marked plasmids, pAgK84 was found to be conjugal. It could be transferred to several Agrobacterium strains including those harboring octopine- or nopaline-type Ti plasmids. Its presence has no effect on Ti plasmid functions such as opine utilization and tumorigenicity, but it does confer agrocin 84 immunity upon previuosly sensitive strains. The plasmid could also be conjugally transferred to a Nod+ Fix+ strain of Rhizobium meliloti. The production of agrocin 84 is expressed in all Agrobacterium and Rhizobium transconjugants tested. The agrocin plasmid could not be introduced into restrictionless Escherichia coli or Pseudomonas aeruginosa recipients by conjugation or transformation. The sites of 92 independent Tn5 insertions were mapped on pAgK84. These insertions are dispersed over the entire length of the plasmid. Analysis of the sites and effects of the Tn5 insertions has allowed one to construct a functional map of pAgK84. Forty-three of these insertions, spanning a 20-kb segment of the plasmid, abolished or greatly reduced the production of agrocin 84. The presence of 2 insertions within this segment having an effect on agrocin production suggest that at least 3 regions of the plasmid are involved in agrocin 84 biosynthesis. Fourteen of the Tn5 insertion derivatives are no longer conjugally transferable. These insertions all map to a single region of the plasmid and define .apprx. 3.5-kb as being associated with transfer functions.
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页码:106 / 117
页数:12
相关论文
共 40 条
[1]  
ALCONERO R, 1980, Plant Disease, V64, P835, DOI 10.1094/PD-64-835
[2]   SPECIFIC-PURPOSE PLASMID CLONING VECTORS .2. BROAD HOST RANGE, HIGH COPY NUMBER, RSF1010-DERIVED VECTORS, AND A HOST-VECTOR SYSTEM FOR GENE CLONING IN PSEUDOMONAS [J].
BAGDASARIAN, M ;
LURZ, R ;
RUCKERT, B ;
FRANKLIN, FCH ;
BAGDASARIAN, MM ;
FREY, J ;
TIMMIS, KN .
GENE, 1981, 16 (1-3) :237-247
[3]  
BARTH PT, 1979, PLASMIDS MED ENV COM, P399
[4]  
BAZZI C, 1982, PHYTOPATHOL Z, V103, P280
[5]   TRANSFER OF DRUG-RESISTANCE TRANSPOSON TN5 TO RHIZOBIUM [J].
BERINGER, JE ;
BEYNON, JL ;
BUCHANANWOLLASTON, AV ;
JOHNSTON, AWB .
NATURE, 1978, 276 (5688) :633-634
[6]   A PHYSICAL AND GENETIC-MAP OF THE INCN PLASMID R46 [J].
BROWN, AMC ;
WILLETTS, NS .
PLASMID, 1981, 5 (02) :188-201
[7]   IDENTIFICATION AND CHARACTERIZATION OF LARGE PLASMIDS IN RHIZOBIUM-MELILOTI USING AGAROSE-GEL ELECTROPHORESIS [J].
CASSE, F ;
BOUCHER, C ;
JULLIOT, JS ;
MICHEL, M ;
DENARIE, J .
JOURNAL OF GENERAL MICROBIOLOGY, 1979, 113 (AUG) :229-242
[8]   STABLE INCORPORATION OF PLASMID DNA INTO HIGHER PLANT-CELLS - MOLECULAR-BASIS OF CROWN GALL TUMORIGENESIS [J].
CHILTON, MD ;
DRUMMOND, MH ;
MERLO, DJ ;
SCIAKY, D ;
MONTOYA, AL ;
GORDON, MP ;
NESTER, EW .
CELL, 1977, 11 (02) :263-271
[9]  
Ellis J. G., 1979, SOIL BORNE PLANT PAT, P579
[10]   ISOLATION AND PROPERTIES OF TRANSFER REGULATORY MUTANTS OF THE NOPALINE TI-PLASMID PTIC58 [J].
ELLIS, JG ;
MURPHY, PJ ;
KERR, A .
MOLECULAR & GENERAL GENETICS, 1982, 186 (02) :275-281