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牛肠激酶催化亚基在丝状真菌黑曲霉中的表达。

Expression of catalytic subunit of bovine enterokinase in the filamentous fungus Aspergillus niger.

作者信息

Svetina M, Krasevec N, Gaberc-Porekar V, Komel R

机构信息

National Institute of Chemistry, and Laboratory for Biosynthesis and Biotransformation, Ljubljana, Slovenia.

出版信息

J Biotechnol. 2000 Jan 21;76(2-3):245-51. doi: 10.1016/s0168-1656(99)00191-1.

Abstract

The cDNA encoding for catalytic subunit of bovine enterokinase (EK(L)), to which the sequence for Kex2 protease cleavage site was inserted, was expressed in the protease deficient filamentous fungus Aspergillus niger AB1.13. Fungal transformants were obtained in which expression of the glucoamylase fusion gene resulted in secretion of the protein into growth medium. Fusion polypeptide was processed to mature EK(L) by endogenous Kex-2 like protease cleavage during secretory pathway. The highest quantity of EK(L), up to 5 mg l(-1), was obtained in soya milk medium. The secreted EK(L) was easily purified from other proteins found in A. niger culture supernatant, using ion exchange and affinity chromatography. The yield of the purified and highly active EK(L) was 1.9 mg l(-1) of culture.

摘要

编码牛肠激酶催化亚基(EK(L))的cDNA,其中插入了Kex2蛋白酶切割位点序列,在蛋白酶缺陷型丝状真菌黑曲霉AB1.13中表达。获得了真菌转化体,其中糖化淀粉酶融合基因的表达导致蛋白质分泌到生长培养基中。融合多肽在分泌途径中通过内源性Kex-2样蛋白酶切割加工成成熟的EK(L)。在豆浆培养基中获得了最高量的EK(L),高达5 mg l(-1)。使用离子交换和亲和色谱法,分泌的EK(L)很容易从黑曲霉培养上清液中发现的其他蛋白质中纯化出来。纯化后的高活性EK(L)产量为每升培养物1.9 mg。

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