首页> 外文期刊>Biotechnology Letters >Molecular cloning and sequence analysis of a mannitol dehydrogenase gene and isolation of mdh promoter from Candida magnoliae.
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Molecular cloning and sequence analysis of a mannitol dehydrogenase gene and isolation of mdh promoter from Candida magnoliae.

机译:甘露醇脱氢酶基因的分子克隆和序列分析以及从白色假丝酵母中分离mdh启动子。

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摘要

The mdh gene encodes mannitol dehydrogenase (MDH), which catalyzes the conversion of fructose into mannitol. The putative mdh gene of Candida magnoliae was isolated by PCR using the primers deduced from the N-terminal amino acid sequences of an intact MDH and its tryptic peptides, cloned in E. coli, and sequenced. The mdh gene consisted of 852 bp encoding for 283 amino acids. Analysis of the amino acid sequence revealed that MDH consisted of typical NADPH-dependent short chain dehydrogenases/reductases. To develop a strong promoter to induce expression of the foreign genes in C. magnolia, the putative promoter was isolated. The reporter protein, GFP, was well-expressed under the control of the putative mdh promoter of 153 bp in C. magnoliae. (c)Springer Science+Business Media B.V. 2010.
机译:mdh基因编码甘露醇脱氢酶(MDH),可催化果糖转化为甘露醇。通过使用从完整MDH及其胰蛋白酶肽的N末端氨基酸序列推导的引物,通过PCR分离出大假念珠菌的推定mdh基因,并将其克隆到大肠杆菌中并进行测序。 mdh基因由852 bp编码,编码283个氨基酸。氨基酸序列分析表明,MDH由典型的NADPH依赖性短链脱氢酶/还原酶组成。为了开发强启动子以诱导玉兰假单胞菌中外源基因的表达,分离了假定的启动子。在假定的153个bp的mdh启动子的控制下,报道蛋白GFP在玉兰假单胞菌中得到了良好的表达。 (c)Springer Science + Business Media B.V. 2010。

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