Ramos-Díaz M A, Ramos J L
Department of Biochemistry and Molecular and Cellular Biology of Plants, Estación Experimental del Zaidín, Consejo Superior de Investigaciones Científicas, 18008 Granada, Spain.
J Bacteriol. 1998 Dec;180(23):6352-63. doi: 10.1128/JB.180.23.6352-6363.1998.
A combined physical and genetic map of the Pseudomonas putida KT2440 genome was constructed from data obtained by pulsed-field gel electrophoresis techniques (PFGE) and Southern hybridization. Circular genome size was estimated at 6.0 Mb by adding the sizes of 19 SwaI, 9 PmeI, 6 PacI, and 6 I-CeuI fragments. A complete physical map was achieved by combining the results of (i) analysis of PFGE of the DNA fragments resulting from digestion of the whole genome with PmeI, SwaI, I-CeuI, and PacI as well as double digestion with combinations of these enzymes and (ii) Southern hybridization analysis of the whole wild-type genome digested with different enzymes and hybridized against a series of probes obtained as cloned genes from different pseudomonads of rRNA group I and Escherichia coli, as P. putida DNA obtained by PCR amplification based on sequences deposited at the GenBank database, and by labeling of macrorestriction fragments of the P. putida genome eluted from agarose gels. As an alternative, 10 random mini-Tn5-Km mutants of P. putida KT2440 were used as a source of DNA, and the band carrying the mini-Tn5 in each mutant was identified after PFGE of a series of complete chromosomal digestions and hybridization with the kanamycin resistance gene of the mini-Tn5 as a probe. We established a circular genome map with an average resolution of 160 kb. Among the 63 genes located on the genetic map were key markers such as oriC, 6 rrn loci (rnnA to -F), recA, ftsZ, rpoS, rpoD, rpoN, and gyrB; auxotrophic markers; and catabolic genes for the metabolism of aromatic compounds. The genetic map of P. putida KT2440 was compared to those of Pseudomonas aeruginosa PAO1 and Pseudomonas fluorescens SBW25. The chromosomal backbone revealed some similarity in gene clustering among the three pseudomonads but differences in physical organization, probably as a result of intraspecific rearrangements.
利用脉冲场凝胶电泳技术(PFGE)和Southern杂交获得的数据,构建了恶臭假单胞菌KT2440基因组的物理图谱与遗传图谱的组合。通过将19个SwaI、9个PmeI、6个PacI和6个I-CeuI片段的大小相加,估计环状基因组大小为6.0 Mb。通过结合以下结果构建了完整的物理图谱:(i)对用PmeI、SwaI、I-CeuI和PacI消化全基因组产生的DNA片段进行PFGE分析,以及用这些酶的组合进行双酶切分析;(ii)对用不同酶消化的野生型全基因组进行Southern杂交分析,并与一系列从rRNA I组的不同假单胞菌和大肠杆菌中作为克隆基因获得的探针杂交;以GenBank数据库中保存的序列为基础,通过PCR扩增获得的恶臭假单胞菌DNA;以及对从琼脂糖凝胶上洗脱的恶臭假单胞菌基因组的大限制性片段进行标记。作为一种替代方法,使用恶臭假单胞菌KT2440的10个随机mini-Tn5-Km突变体作为DNA来源,在对一系列完整的染色体消化产物进行PFGE并以mini-Tn5的卡那霉素抗性基因作为探针进行杂交后,鉴定每个突变体中携带mini-Tn5的条带。我们建立了平均分辨率为160 kb的环状基因组图谱。位于遗传图谱上的63个基因中包括关键标记物,如oriC、6个rrn位点(rrnA至-F)、recA、ftsZ、rpoS、rpoD、rpoN和gyrB;营养缺陷型标记物;以及芳香族化合物代谢的分解代谢基因。将恶臭假单胞菌KT2440的遗传图谱与铜绿假单胞菌PAO1和荧光假单胞菌SBW25的遗传图谱进行了比较。染色体骨架显示这三种假单胞菌在基因聚类方面存在一些相似性,但在物理组织上存在差异,这可能是种内重排的结果。