首页> 外文期刊>FEMS Microbiology Letters >Expression of a laccase cDNA from Trametes sp AH28-2 in Pichia pastoris and mutagenesis of transformants by nitrogen ion implantation
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Expression of a laccase cDNA from Trametes sp AH28-2 in Pichia pastoris and mutagenesis of transformants by nitrogen ion implantation

机译:Trametes sp AH28-2漆酶cDNA在毕赤酵母中的表达及氮离子注入诱变转化子。

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摘要

A laccase cDNA from Trametes sp. AH28-2 was expressed in Pichia pastoris, with the highest expression level of 4.0 mg L-1 (1360 U mg(-1)). The apparent K-m (24.6 mu M) for ABTS (2,2'-azinobis [3-ethylbenzothia-zoline-6-sulfonic acid]) and the carbohydrate content of the recombinant laccase A (rLacA) are approximately identical to those of the native LacA (nLacA). However, the two enzymes differed in the pH optimum when both ABTS and guaiacol served as substrates. The optimum pH for enzyme stability is 5.5 for rLacA. Thermal stability was also investigated. The mutagenesis of rLacA utilizing low-energy nitrogen ion implantation resulted in the isolation of a yeast clone that produced 7.7 mg L-1 (1085 U mg(-1)) of laccase, 92.5% more than the nonirradiated control (4.0 mg L-1). Compared with rLacA, the mutant LacA (mLacA) with five amino-acid residue changes in the coding sequence showed a slight change in its catalytic ability but superior thermal stability.
机译:Trametes sp。的漆酶cDNA。 AH28-2在毕赤酵母中表达,最高表达水平为4.0 mg L-1(1360 U mg(-1))。 ABTS(2,2'-azinobis [3-乙基苯并噻唑-唑啉-6-磺酸])的表观Km(24.6μM)和重组漆酶A(rLacA)的碳水化合物含量与天然LacA(nLacA)。但是,当ABTS和愈创木酚均作为底物时,两种酶的最适pH值不同。对于rLacA,酶稳定性的最佳pH为5.5。还研究了热稳定性。利用低能氮离子植入对rLacA进行诱变导致分离出酵母克隆,该克隆产生了7.7 mg L-1(1085 U mg(-1))的漆酶,比未辐照的对照(4.0 mg L-)高92.5%。 1)。与rLacA相比,突变的LacA(mLacA)在编码序列中有五个氨基酸残基变化,显示出其催化能力略有变化,但具有出色的热稳定性。

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