Roca H, Garcia B, Rodriguez E, Mateu D, Coroas L, Cremata J, Garcia R, Pons T, Delgado J
Bioindustry Division, Centre for Genetic Engineering and Biotechnology, Havana, Cuba.
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.
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.
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。