Construction of an efficient expression system for Agrobacterium tumefaciens based on the coliphage T5 promoter

被引:32
作者
Wang, YL
Mukhopadhyay, A
Howitz, VR
Binns, AN
Lynn, DG
机构
[1] Univ Chicago, Dept Chem, Chicago, IL 60637 USA
[2] Cedar Crest Muhlenberg Coll, Allentown, PA 18104 USA
[3] Univ Penn, Inst Plant Sci, Philadelphia, PA 19104 USA
关键词
signal transduction; virA; virG; vir gene induction;
D O I
10.1016/S0378-1119(99)00541-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A versatile expression Vector utilizing a promoter of coliphage T5, P-N25 (Gentz and Bujard, 1985. J. Bacteriol. 164, 70-77) and a derivative of the IncW broad-host-range plasmid pJB20 (Beaupre et al., 1997. J. Bacteriol. 179, 78-89) has been developed. This vector successfully expresses virulence proteins of Agrobacterium tumefaciens encoded by virG and a mutant allele of virA, virA (Delta 1-284, G665D) in Escherichia coli as well as in A. tumefaciens. The signal transduction proteins VirA (Delta 1-284, G665D) and virG are fully functional when expressed in Agrobacterium, and the P-N25 driven expression overrides the complex transcriptional regulation present with the native promoters. This expression system will enable a more detailed analysis of the activation events in signal transduction in A. trumefaciens, and we expect it to be useful in other prokaryotes. (C) 2000 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:105 / 114
页数:10
相关论文
共 34 条
[1]  
Ausubel F.M., 1991, CURRENT PROTOCOLS MO
[2]   ACTIVITY OF THE HYBRID TRP-LAC(TAC) PROMOTER OF ESCHERICHIA-COLI IN PSEUDOMONAS-PUTIDA - CONSTRUCTION OF BROAD-HOST-RANGE, CONTROLLED-EXPRESSION VECTORS [J].
BAGDASARIAN, MM ;
AMANN, E ;
LURZ, R ;
RUCKERT, B ;
BAGDASARIAN, M .
GENE, 1983, 26 (2-3) :273-282
[3]   Interactions between VirB9 and VirB10 membrane proteins involved in movement of DNA from Agrobacterium tumefaciens into plant cells [J].
Beaupre, CE ;
Bohne, J ;
Dale, EM ;
Binns, AN .
JOURNAL OF BACTERIOLOGY, 1997, 179 (01) :78-89
[4]   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
[5]  
BUJARD H, 1987, METHOD ENZYMOL, V155, P416
[6]  
CANGELOSI GA, 1990, P NATL ACAD SCI USA, V87, P708
[7]   FUNCTIONAL ROLES ASSIGNED TO THE PERIPLASMIC, LINKER, AND RECEIVER DOMAINS OF THE AGROBACTERIUM-TUMEFACIENS VIRA PROTEIN [J].
CHANG, CH ;
WINANS, SC .
JOURNAL OF BACTERIOLOGY, 1992, 174 (21) :7033-7039
[8]   CONTROLLED EXPRESSION OF THE TRANSCRIPTIONAL ACTIVATOR GENE VIRG IN AGROBACTERIUM-TUMEFACIENS BY USING THE ESCHERICHIA-COLI LAC PROMOTER [J].
CHEN, CY ;
WINANS, SC .
JOURNAL OF BACTERIOLOGY, 1991, 173 (03) :1139-1144
[9]   DESIGN AND DEVELOPMENT OF AMPLIFIABLE BROAD-HOST-RANGE CLONING VECTORS - ANALYSIS OF THE VIR REGION OF AGROBACTERIUM-TUMEFACIENS PLASMID PTIC58 [J].
CLOSE, TJ ;
ZAITLIN, D ;
KADO, CI .
PLASMID, 1984, 12 (02) :111-118
[10]   GENETIC-ANALYSIS OF CROWN GALL - FINE-STRUCTURE MAP OF THE T-DNA BY SITE-DIRECTED MUTAGENESIS [J].
GARFINKEL, DJ ;
SIMPSON, RB ;
REAM, LW ;
WHITE, FF ;
GORDON, MP ;
NESTER, EW .
CELL, 1981, 27 (01) :143-153