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具有更高去除高硝酸盐负荷效率的重组产酸克雷伯菌菌株。

Recombinant klebsiella oxytoca strains with improved efficiency in removal of high nitrate loads.

作者信息

Pinar G, Ramos JL

机构信息

Department of Biochemistry and Molecular and Cellular Biology of Plants, Estacion Experimental del Zaidin-Consejo Superior de Investigaciones Cientificas, 18008 Granada, Spain.

出版信息

Appl Environ Microbiol. 1998 Dec;64(12):5016-9. doi: 10.1128/AEM.64.12.5016-5019.1998.

Abstract

Klebsiella oxytoca CECT 4460 removes high nitrate loads from industrial wastewaters without accumulation of nitrite under optimal culture conditions; however, under nonoptimal conditions nitrite accumulates. This situation reflects an in vivo-limited functioning of nitrite reductase in this strain. As a way to overcome this limitation, an increase in the nitrite reductase gene dose in K. oxytoca CECT 4460 was considered. To achieve this, we cloned and transferred into this strain the Klebsiella pneumoniae nasB gene, which encodes assimilatory nitrite reductase (Lin et al., J. Bacteriol. 176:2551-2559, 1994). The delivery vector was either the wide-host-range plasmid pUPE2, in which the nasB gene is expressed from the Escherichia coli Plac promoter, or a mini-Tn5-Km vector, which upon random insertion in the host chromosome allowed expression of the nasB gene from an unidentified chromosomal host promoter. The effect of the increase in the dose of the nasB gene in K. oxytoca CECT 4460 on the accumulation of nitrite in the culture medium was tested in two recombinant strains. The results obtained showed that K. oxytoca CECT 4460 bearing pUPE2 accumulated 88% less nitrite than the wild-type strain, while the recombinant strain bearing the K. pneumoniae nasB gene in the host chromosome showed a 25% lower level of nitrite accumulation in the culture medium than that of the wild type.

摘要

在最佳培养条件下,产酸克雷伯菌CECT 4460能去除工业废水中的高硝酸盐负荷且不会积累亚硝酸盐;然而,在非最佳条件下会积累亚硝酸盐。这种情况反映出该菌株中亚硝酸盐还原酶在体内的功能受限。作为克服这一限制的一种方法,考虑增加产酸克雷伯菌CECT 4460中亚硝酸盐还原酶基因的剂量。为实现这一点,我们克隆了肺炎克雷伯菌的nasB基因并将其转入该菌株,该基因编码同化型亚硝酸盐还原酶(Lin等人,《细菌学杂志》176:2551 - 2559,1994年)。递送载体要么是广宿主范围质粒pUPE2,其中nasB基因由大肠杆菌Plac启动子表达,要么是mini - Tn5 - Km载体,它随机插入宿主染色体后可从一个未确定的染色体宿主启动子表达nasB基因。在两个重组菌株中测试了产酸克雷伯菌CECT 4460中nasB基因剂量增加对培养基中亚硝酸盐积累的影响。所得结果表明,携带pUPE2的产酸克雷伯菌CECT 4460积累的亚硝酸盐比野生型菌株少88%,而宿主染色体中携带肺炎克雷伯菌nasB基因的重组菌株在培养基中的亚硝酸盐积累水平比野生型低25%。

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