An Improved Binary Vector and Escherichia coli Strain for Agrobacterium tumefaciens-Mediated Plant Transformation

被引:6
作者
Watson, Michael R. [1 ,2 ]
Lin, Yu-fei [1 ,2 ]
Hollwey, Elizabeth [1 ,2 ]
Dodds, Rachel E. [1 ,2 ]
Meyer, Peter [1 ,2 ]
McDowall, Kenneth J. [3 ,4 ]
机构
[1] Univ Leeds, Fac Biol Sci, Ctr Plant Sci, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Leeds, Fac Biol Sci, Sch Biol, Leeds LS2 9JT, W Yorkshire, England
[3] Univ Leeds, Fac Biol Sci, Sch Mol & Cellular Biol, Leeds LS2 9JT, W Yorkshire, England
[4] Univ Leeds, Astbury Ctr Struct Mol Biol, Leeds LS2 9JT, W Yorkshire, England
来源
G3-GENES GENOMES GENETICS | 2016年 / 6卷 / 07期
基金
英国生物技术与生命科学研究理事会;
关键词
Agrobacterium; plant transformation; pGreen; E; coli; growth defects; PLASMID COPY NUMBER; RNA-POLYMERASE; TI-PLASMID; GENE; EXPRESSION; PCNB; DNA; PROTEIN; REPLICATION; DEGRADATION;
D O I
10.1534/g3.116.029405
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The plasmid vector pGreenII is widely used to produce plant transformants via a process that involves propagation in Escherichia coli. However, we show here that pGreenII-based constructs can be unstable in E. coli as a consequence of them hampering cell division and promoting cell death. In addition, we describe a new version of pGreenII that does not cause these effects, thereby removing the selective pressure for mutation, and a new strain of E. coli that better tolerates existing pGreenII-based constructs without reducing plasmid yield. The adoption of the new derivative of pGreenII and the E. coli strain, which we have named pViridis and MW906, respectively, should help to ensure the integrity of genes destined for study in plants while they are propagated and manipulated in E. coli. The mechanism by which pGreenII perturbs E. coli growth appears to be dysregulation within the ColE1 origin of replication.
引用
收藏
页码:2195 / 2201
页数:7
相关论文
共 42 条
  • [31] Sambrook J, 2001, MOL CLONING LAB MANU, DOI DOI 10.1086/394015
  • [32] A plant tumor of bacterial origin
    Smith, EF
    Townsend, CO
    [J]. SCIENCE, 1907, 25 : 671 - 673
  • [33] STUDIER FW, 1990, METHOD ENZYMOL, V185, P60
  • [34] USE OF BACTERIOPHAGE-T7 RNA-POLYMERASE TO DIRECT SELECTIVE HIGH-LEVEL EXPRESSION OF CLONED GENES
    STUDIER, FW
    MOFFATT, BA
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1986, 189 (01) : 113 - 130
  • [35] Szybalski W., 1977, DNA INSERTION ELEMEN, P583
  • [36] INTEGRATION AND ORGANIZATION OF TI PLASMID SEQUENCES IN CROWN GALL TUMORS
    THOMASHOW, MF
    NUTTER, R
    MONTOYA, AL
    GORDON, MP
    NESTER, EW
    [J]. CELL, 1980, 19 (03) : 729 - 739
  • [37] LARGE PLASMID IN AGROBACTERIUM-TUMEFACIENS ESSENTIAL FOR CROWN GALL-INDUCING ABILITY
    VAN LAREBEKE, N
    ENGLER, G
    HOLSTERS, M
    VAN DEN ELSACKER, S
    ZAENEN, I
    SCHILPEROORT, RA
    SCHELL, J
    [J]. NATURE, 1974, 252 (5479) : 169 - 170
  • [38] Transmission of Epi-Alleles with MET1-Dependent Dense Methylation in Arabidopsis thaliana
    Watson, Michael
    Hawkes, Emily
    Meyer, Peter
    [J]. PLOS ONE, 2014, 9 (08):
  • [39] A CRISPR/Cas9 toolkit for multiplex genome editing in plants
    Xing, Hui-Li
    Dong, Li
    Wang, Zhi-Ping
    Zhang, Hai-Yan
    Han, Chun-Yan
    Liu, Bing
    Wang, Xue-Chen
    Chen, Qi-Jun
    [J]. BMC PLANT BIOLOGY, 2014, 14
  • [40] THE ESCHERICHIA-COLI PCNB GENE PROMOTES ADENYLYLATION OF ANTISENSE RNAI OF COLE1-TYPE PLASMIDS IN-VIVO AND DEGRADATION OF RNAI DECAY INTERMEDIATES
    XU, FF
    LINCHAO, S
    COHEN, SN
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (14) : 6756 - 6760