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微小青霉葡聚糖酶编码基因的克隆及其在毕赤酵母中的表达。

Cloning of the Penicillium minioluteum gene encoding dextranase and its expression in Pichia pastoris.

作者信息

Roca H, Garcia B, Rodriguez E, Mateu D, Coroas L, Cremata J, Garcia R, Pons T, Delgado J

机构信息

Bioindustry Division, Centre for Genetic Engineering and Biotechnology, Havana, Cuba.

出版信息

Yeast. 1996 Sep 30;12(12):1187-200. doi: 10.1002/(SICI)1097-0061(19960930)12:12%3C1187::AID-YEA986%3E3.0.CO;2-U.

Abstract

The DEX gene encoding an extracellular dextranase was isolated from the genomic DNA library of Penicillium minioluteum by hybridization using the dextranase cDNA as a probe. Comparison of the gene and cDNA sequences revealed that the DEX gene does not contain introns. Amino acid sequences comparison of P. minioluteum dextranase with other reported dextranases reveals a significant homology (29% identity) with a dextranase from Arthrobacter sp. CB-8. The DEX gene fragment encoding a mature protein of 574 amino acids was expressed in the methylotrophic yeast Pichia pastoris by using the SUC2 gene signal sequence from Saccharomyces cerevisiae under control of the alcohol oxidase-1 (AOX1) promoter. Over 3.2 g/l of enzymatically active dextranase was secreted into the medium after induction by methanol. The yeast product was indistinguishable from the native enzyme in specific activity and the N-terminus of both proteins were identical.

摘要

以葡聚糖酶cDNA为探针,通过杂交从微小青霉基因组DNA文库中分离出编码细胞外葡聚糖酶的DEX基因。基因和cDNA序列比较表明,DEX基因不含内含子。微小青霉葡聚糖酶与其他已报道葡聚糖酶的氨基酸序列比较显示,与节杆菌属CB - 8的一种葡聚糖酶有显著同源性(同一性为29%)。编码574个氨基酸成熟蛋白的DEX基因片段,在醇氧化酶-1(AOX1)启动子控制下,利用来自酿酒酵母的SUC2基因信号序列,在甲基营养型酵母毕赤酵母中表达。甲醇诱导后,超过3.2 g/l的具有酶活性的葡聚糖酶分泌到培养基中。酵母产物与天然酶的比活性无法区分,且两种蛋白质的N端相同。

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