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基因amyE(TV1)在枯草芽孢杆菌中编码来自普通嗜热放线菌94 - 2A的一种非生糖α淀粉酶。

The gene amyE(TV1) codes for a nonglucogenic alpha-amylase from Thermoactinomyces vulgaris 94-2A in Bacillus subtilis.

作者信息

Hofemeister B, König S, Hoang V, Engel J, Mayer G, Hansen G, Hofemeister J

机构信息

Institut für Pflanzengenetik und Kulturpflanzenforschung, Gatersleben, Germany.

出版信息

Appl Environ Microbiol. 1994 Sep;60(9):3381-9. doi: 10.1128/aem.60.9.3381-3389.1994.

Abstract

We isolated the gene amyE(TV1) from Thermoactinomyces vulgaris 94-2A encoding a nonglucogenic alpha-amylase (AmyTV1). A chromosomal DNA fragment of 2,247 bp contained an open reading frame of 483 codons, which was expressed in Escherichia coli and Bacillus subtilis. The deduced amino acid sequence of the AmyTV1 protein was confirmed by sequencing of several peptides derived from the enzyme isolated from a T. vulgaris 94-2A culture. The amino acid sequence was aligned with several known alpha-amylase sequences. We found 83% homology with the 48-kDa alpha-amylase part of the Bacillus polymyxa beta-alpha-amylase polyprotein and 50% homology with Taka amylase A of Aspergillus oryzae but only 45% homology with another T. vulgaris amylase (neopullulanase, TVA II) recently cloned from strain R-47. The putative promoter region was characterized with primer extension and deletion experiments and by expression studies with B. subtilis. Multiple promoter sites (P3, P2, and P1) were found; P1 alone drives about 1/10 of the AmyTV1 expression directed by the native tandem configuration P3P2P1. The expression levels in B. subtilis could be enhanced by fusion of the amyE(TV1) coding region to the promoter of the Bacillus amyloliquefaciens alpha-amylase gene.

摘要

我们从嗜热放线菌94-2A中分离出编码非生糖α-淀粉酶(AmyTV1)的基因amyE(TV1)。一个2247 bp的染色体DNA片段包含一个483个密码子的开放阅读框,该片段在大肠杆菌和枯草芽孢杆菌中表达。通过对从嗜热放线菌94-2A培养物中分离出的该酶的几个肽段进行测序,证实了AmyTV1蛋白推导的氨基酸序列。将该氨基酸序列与几个已知的α-淀粉酶序列进行比对。我们发现它与多粘芽孢杆菌β-α-淀粉酶多蛋白的48 kDaα-淀粉酶部分有83%的同源性,与米曲霉的Taka淀粉酶A有50%的同源性,但与最近从R-47菌株克隆的另一种嗜热放线菌淀粉酶(新普鲁兰酶,TVA II)只有45%的同源性。通过引物延伸和缺失实验以及枯草芽孢杆菌的表达研究对推定的启动子区域进行了表征。发现了多个启动子位点(P3、P2和P1);单独的P1驱动的AmyTV1表达约为天然串联结构P3P2P1所指导表达的1/10。通过将amyE(TV1)编码区与解淀粉芽孢杆菌α-淀粉酶基因的启动子融合,可以提高枯草芽孢杆菌中的表达水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/932e/201813/1eb9fb71bc34/aem00026-0360-a.jpg

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