McEvoy J L, Murata H, Chatterjee A K
Department of Plant Pathology, University of Missouri, Columbia 65211.
J Bacteriol. 1990 Jun;172(6):3284-9. doi: 10.1128/jb.172.6.3284-3289.1990.
recA-mediated production of pectin lyase (PNL) and the bacteriocin carotovoricin occurs in Erwinia carotovora subsp. carotovora 71 when this organism is subjected to agents that damage or inhibit the synthesis of DNA. The structural gene pnlA was isolated from a strain 71 cosmid gene library following mobilization of the cosmids into a moderate PNL producer, strain 193. The cosmid complemented pnl::Tn5 but not ctv::Tn5 mutations. A constitutive level of PNL activity was detected in RecA+ and RecA- Escherichia coli strains carrying the pnlA+ gene on the high-copy-number plasmid pBluescript SK-. Mappings of Mu dI1734 (Km lac'ZYA) insertions in pnlA and unidirectional deletion analyses allowed localization of the gene to approximately 1.4 kilobases of DNA. A typical pnlA-lacZ transcriptional fusion was inducible in a RecA+ but not a RecA- derivative of strain 71. In contrast, the pnlA-lacZ fusion was not inducible in a RecA+ E. coli strain. DNA sequences homologous to pnlA were detected in E. carotovora subsp. carotovora and E. carotovora subsp. atroseptica strains and in one of four Erwinia rhapontici strains but not in Erwinia chrysanthemi.
当胡萝卜软腐欧文氏菌胡萝卜软腐亚种71受到损害或抑制DNA合成的因子作用时,recA介导的果胶裂解酶(PNL)和细菌素胡萝卜软腐欧文氏菌素的产生就会发生。在将黏粒转移到中度PNL产生菌193株后,从71株黏粒基因文库中分离出结构基因pnlA。该黏粒可互补pnl::Tn5突变,但不能互补ctv::Tn5突变。在携带高拷贝数质粒pBluescript SK-上的pnlA+基因的RecA+和RecA-大肠杆菌菌株中检测到组成型水平的PNL活性。通过对pnlA中Mu dI1734(Km lac'ZYA)插入的定位和单向缺失分析,可将该基因定位到约1.4千碱基的DNA上。典型的pnlA-lacZ转录融合在71株的RecA+衍生物中可诱导,但在RecA-衍生物中不可诱导。相比之下,pnlA-lacZ融合在RecA+大肠杆菌菌株中不可诱导。在胡萝卜软腐欧文氏菌胡萝卜软腐亚种和胡萝卜软腐欧文氏菌黑腐亚种菌株以及四个大黄欧文氏菌菌株中的一个中检测到与pnlA同源的DNA序列,但在菊欧文氏菌中未检测到。