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新型质粒 DNA 改变与恶臭假单胞菌 R5-3 芳烃利用相关。

Novel Alterations in Plasmid DNA Associated with Aromatic Hydrocarbon Utilization by Pseudomonas putida R5-3.

机构信息

Department of Plant Pathology, University of California, Riverside, California 92521.

出版信息

Appl Environ Microbiol. 1989 Jun;55(6):1523-30. doi: 10.1128/aem.55.6.1523-1530.1989.

Abstract

Subcultures of Pseudomonas putida R5-3 altered their plasmid DNA content in specific ways depending on the particular aromatic hydrocarbon utilized as the sole carbon source. Two indigenous plasmids, 115 and 95 kilobases (kb) in size, were observed in R5-3A, which was derived from R5-3 by growth on minimal medium containing p-methylbenzoate as the sole carbon source. When R5-3A was transferred to medium containing m-xylene or toluene, derivative strains were obtained in which the 95-kb plasmid was lost and a new plasmid of 50 or 60 kb appeared. Reversion to the original plasmid profile of R5-3A was observed when xylene- or toluene-grown cells were returned to medium containing p-methylbenzoate. Restriction enzyme analysis and Southern blot hybridizations of total plasmid DNA indicated deletions and rearrangements of DNA restriction fragments in the derivatives maintained on m-xylene and toluene when compared with the original R5-3A. In the derivatives which retrieved the original plasmid profile, the restriction enzyme fragment pattern was identical to that in the original R5-3A, in that the fragments which were missing after growth on m-xylene or toluene were again present. Southern blot hybridizations revealed that part of the plasmid DNA lost from the original plasmid profile was integrated into the chromosomal DNA of xylene-grown R5-3B and that these plasmid fragments were associated with aromatic hydrocarbon metabolism. Hybridization with pathway-specific DNA fragments from the TOL plasmid pWWO indicated that this 95-kb plasmid contains DNA homologous to the meta-fission pathway genes.

摘要

恶臭假单胞菌 R5-3 的亚群根据其利用的特定芳香烃作为唯一碳源,以特定的方式改变其质粒 DNA 含量。在 R5-3A 中观察到两种本土质粒,大小分别为 115 和 95 千碱基(kb),R5-3A 是由 R5-3 通过在含有对甲基苯甲酸作为唯一碳源的最小培养基上生长而衍生出来的。当 R5-3A 被转移到含有间二甲苯或甲苯的培养基中时,会获得衍生菌株,其中 95-kb 质粒丢失,出现一个新的 50 或 60-kb 质粒。当细胞从间二甲苯或甲苯生长的培养基中返回含有对甲基苯甲酸的培养基时,观察到 R5-3A 的原始质粒图谱的回复。与原始 R5-3A 相比,在间二甲苯和甲苯上维持的衍生物中,总质粒 DNA 的限制性内切酶分析和 Southern 印迹杂交表明 DNA 限制片段的缺失和重排。在恢复原始质粒图谱的衍生物中,限制性内切酶片段模式与原始 R5-3A 相同,即在间二甲苯或甲苯生长后丢失的片段再次出现。Southern 印迹杂交显示,从原始质粒图谱中丢失的部分质粒 DNA 已整合到二甲苯生长的 R5-3B 的染色体 DNA 中,并且这些质粒片段与芳香烃代谢有关。与 TOL 质粒 pWWO 的途径特异性 DNA 片段杂交表明,该 95-kb 质粒含有与 meta-fission 途径基因同源的 DNA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bcd/202898/d59cbdbb484c/aem00099-0213-a.jpg

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