Pugsley A P
J Bacteriol. 1984 May;158(2):523-9. doi: 10.1128/jb.158.2.523-529.1984.
Colicin N was identified as the 39,000-molecular-weight protein encoded by the 4,900-base-pair, multiple copy number, amplifiable plasmid ColN -284. Its production was controlled by the SOS regulatory circuit and by catabolite repression. Colicin accumulated intracellularly to ca. 10(6) molecules per cell after growth for 2 to 3 h in medium containing 0.5 microgram of mitomycin C per ml and was then released as the cells underwent partial lysis. Strains carrying pColN -284 and its derivatives exhibited low-level immunity to colicin N and were fully sensitive to all other colicins tested. Regions of the plasmid responsible for colicin N activity (cna), for mitomycin-induced lysis ( cnl ), and for colicin N immunity ( cni ) were localized and characterized by cloning, transposon Tn5 and hydroxylamine mutagenesis, and restriction endonuclease deletion and mapping analysis. The results are discussed in terms of both the organization of the cna, cnl , and cni genes and the respective role of cnl expression and colicin N production in mitomycin sensitivity, colicin export, and induced partial lysis of ColN + cells.
大肠杆菌素N被鉴定为一种分子量为39,000的蛋白质,由4,900个碱基对、多拷贝数、可扩增的质粒ColN -284编码。其产生受SOS调节回路和分解代谢物阻遏的控制。在含有每毫升0.5微克丝裂霉素C的培养基中生长2至3小时后,大肠杆菌素在细胞内积累至约每细胞10⁶个分子,然后随着细胞发生部分裂解而释放。携带pColN -284及其衍生物的菌株对大肠杆菌素N表现出低水平的免疫性,并且对所有其他测试的大肠杆菌素完全敏感。通过克隆、转座子Tn5和羟胺诱变以及限制性内切酶缺失和图谱分析,对负责大肠杆菌素N活性(cna)、丝裂霉素诱导的裂解(cnl)和大肠杆菌素N免疫性(cni)的质粒区域进行了定位和表征。从cna、cnl和cni基因的组织以及cnl表达和大肠杆菌素N产生在丝裂霉素敏感性、大肠杆菌素输出和ColN⁺细胞诱导的部分裂解中的各自作用方面对结果进行了讨论。