首页> 外文会议>International symposium on bioanalytical chemistry >PURIFICATION OF A CLONED ENZYME-FUNGI NITRIC OXIDE REDUCTASE (FUSARIUM OXYSPORUM P-450 NOR)
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PURIFICATION OF A CLONED ENZYME-FUNGI NITRIC OXIDE REDUCTASE (FUSARIUM OXYSPORUM P-450 NOR)

机译:纯化克隆酶 - 真菌一氧化氮还原酶(牡蛎P-450也不是)

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Denitrification activities were considered to be characteristic of prokaryotes, but in resent years it was found that several fungi could form nitrous oxide(N_2O)from nitrate or nitrite. A unique cytochrome P-450 is involved in fungal denitrification, acting as a nitric oxide reductase (P - 450nor). P-450nor shows several interesting properties. It catalyzes the reduction of NO to N_2O in the presence of NADH wthout mediation by any other proteinaceous components ,and seems to receive electrons directly from NADH. We successfully cloned Fungus (Fusarium oxysporum)P - 450nor cDNA, and expressed in quantity by a expression vector-pCW in E. coli. The cloned enzyme-F. P-450nor was purified with DEAE -cellulose and FPLC system.
机译:反硝化活性被认为是原核生物的特征,但在怨恨年份中发现,几个真菌可以从硝酸盐或亚硝酸盐形成氧化二氮(N_2O)。独特的细胞色素P-450涉及真菌脱氮,作用作一氧化氮还原酶(P - 450nor)。 P-450nor显示了几个有趣的属性。它催化在NADH WHOUT中调解的情况下通过任何其他蛋白质组分的存在,并且似乎直接从NADH接收电子。我们成功地克隆了真菌(牡蛎)p-450nor cDNA,并通过大肠杆菌中的表达载体-CCW表达数量。克隆的酶-f。用DEAE - 纤维素和FPLC系统纯化P-450nor。

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