首页> 外文期刊>Current Microbiology: An International Journal >Improvement of Manganese Peroxidase Production by the Hyper Lignin-Degrading Fungus Phanerochaete sordida YK-624 by Recombinant Expression of the 5-Aminolevulinic Acid Synthase Gene
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Improvement of Manganese Peroxidase Production by the Hyper Lignin-Degrading Fungus Phanerochaete sordida YK-624 by Recombinant Expression of the 5-Aminolevulinic Acid Synthase Gene

机译:通过5-氨基乙酰丙酸合酶基因的重组表达改善木质素过度降解真菌Phanerochaete sordida YK-624产生的锰过氧化物酶

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摘要

The manganese peroxidase (MnP) gene (mnp4) promoter of Phanerochaete sordida YK-624 was used to drive expression of 5-aminolevulinic acid synthase (als), which is a key heme biosynthesis enzyme. The expression plasmid pMnP4pro-als was transformed into P. sordida YK-624 uracil auxotrophic mutant UV-64, and 14 recombinant als expressing-transformants were generated. Average cumulative MnP activities in the transformants were 1.18-fold higher than that of control transformants. In particular, transformants A-14 and A-61 showed significantly higher MnP activity (approximately 2.8-fold) than wild type. RT-PCR analysis indicated that the increased MnP activity was caused by elevated recombinant als expression. These results suggest that the production of MnP is improved by high expression of als.
机译:Phanerochaete sordida YK-624的锰过氧化物酶(MnP)基因(mnp4)启动子用于驱动5-氨基乙酰丙酸合酶(als)的表达,这是一种关键的血红素生物合成酶。将表达质粒pMnP4pro-als转化到P.srdida YK-624尿嘧啶营养缺陷型突变体UV-64中,并产生14个重组als表达转化子。转化子中的平均累积MnP活性是对照转化子的1.18倍。特别地,转化体A-14和A-61显示出比野生型显着更高的MnP活性(约2.8倍)。 RT-PCR分析表明,MnP活性增加是由重组als表达升高引起的。这些结果表明,通过als的高表达改善了MnP的产生。

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