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费氏中华根瘤菌两个组氨酸利用基因在恶臭假单胞菌中的克隆与表达

Cloning and expression in Pseudomonas putida of two of the histidine utilization genes from Rhizobium fredii.

作者信息

Burke R R, Heard D D, Nieuwkoop A J

机构信息

School of Health Sciences, Grand Valley State University, Allendale, MI 49401-9403, USA.

出版信息

Curr Microbiol. 1997 Jan;34(1):55-60. doi: 10.1007/s002849900144.

Abstract

Two of the genes encoding histidine utilization (hut) in Rhizobium fredii strain HH303 have been cloned in Pseudomonas putida and partially characterized. Molecular cloning of the genes was achieved by mobilizing an R. fredii cosmid library into a mutant strain of P. putida containing a Tn5 element in its histidase (hutH) gene. A number of overlapping clones were identified, all of which contain a 7.1-kbp HindIII fragment. The origin of this 7.1-kbp fragment from the chromosome of R. fredii was confirmed by Southern blotting and hybridization studies. In addition, this fragment and the two adjacent HindIII fragments of 9 and 12 kbp respectively were subcloned into pBluescript KS+ and further characterized. Although the R. fredii clones expressed histidase in Pseudomonas, they did not in Escherichia coli, suggesting that E. coli is not a suitable cloning host for Rhizobia genes.

摘要

费氏中华根瘤菌HH303中两个编码组氨酸利用(hut)的基因已在恶臭假单胞菌中克隆并进行了部分特性分析。通过将费氏中华根瘤菌黏粒文库导入其组氨酸酶(hutH)基因中含有Tn5元件的恶臭假单胞菌突变株,实现了这些基因的分子克隆。鉴定出了多个重叠克隆,所有克隆均包含一个7.1kbp的HindIII片段。通过Southern印迹和杂交研究证实了该7.1kbp片段源自费氏中华根瘤菌的染色体。此外,该片段以及分别相邻的9kbp和12kbp的两个HindIII片段被亚克隆到pBluescript KS+中并进一步进行特性分析。尽管费氏中华根瘤菌克隆在假单胞菌中表达组氨酸酶,但在大肠杆菌中却不表达,这表明大肠杆菌不是根瘤菌基因合适的克隆宿主。

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