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首页> 外文期刊>Applied and Environmental Microbiology >Butanol-Ethanol Dehydrogenase and Butanol-Ethanol-Isopropanol Dehydrogenase: Different Alcohol Dehydrogenases in Two Strains of Clostridium beijerinckii (Clostridium butylicum)
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Butanol-Ethanol Dehydrogenase and Butanol-Ethanol-Isopropanol Dehydrogenase: Different Alcohol Dehydrogenases in Two Strains of Clostridium beijerinckii (Clostridium butylicum)

机译:丁醇-乙醇脱氢酶和丁醇-乙醇-异丙醇脱氢酶:两株拜氏梭状芽胞杆菌(丁酸梭状芽孢杆菌)中不同的醇脱氢酶

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Alcohol-producing strains of Clostridium beijerinckii (Clostridium butylicum) produce, besides acetone, either n-butanol and ethanol or n-butanol, ethanol, and isopropanol as their characteristic products. Alcohol dehydrogenase has been isolated from a strain (NRRL B593) of C. beijerinckii producing isopropanol and from a strain (NRRL B592) not producing isopropanol. Butanol-ethanol dehydrogenase activities were present in both strains, but isopropanol dehydrogenase activity was present only in the isopropanol-producing strain. The butanol-ethanol dehydrogenase of strain NRRL B592 had Mr 66,000 and a Km of 6 μM for butyraldehyde. In contrast, the butanol-ethanol-isopropanol dehydrogenase of strain NRRL B593 had a Mr 100,000 and Kms of 9.5 and 1.0 mM for butyraldehyde and acetone, respectively. In a purification by four different types of separatory methods (DEAE-cellulose, hydroxyapatite, Sephacryl S-300, and Matrex Gel Red A), butanol-ethanol-isopropanol dehydrogenase activities of strain NRRL B593 were purified up to 200-fold (10 to 30% yield), and these activities were not separated. Gel electrophoresis followed by activity stain also revealed distinct mobilities for the butanol-ethanol dehydrogenase of strain NRRL B592 and the butanol-ethanol-isopropanol dehydrogenase of strain NRRL B593. In cell extracts from both strains, a higher alcohol dehydrogenase activity was measured with NADP(H) than with NAD(H). The 150- to 200-fold-purified alcohol dehydrogenase from strain NRRL B593 did not show any NAD(H)-linked activities. The Km for NADPH was 31 μM (with butyraldehyde as cosubstrate) and 18 μM (with acetone as cosubstrate) for the alcohol dehydrogenase of strain NRRL B593. This study showed that the alcohol dehydrogenases from two strains of C. beijerinckii differed significantly.
机译:除丙酮外,产酒精的拜氏梭状芽胞杆菌(丁酸梭菌)菌株还产生正丁醇和乙醇或正丁醇,乙醇和异丙醇作为特征产物。从产生异丙醇的拜氏梭菌菌株(NRRL B593)和不产生异丙醇的菌株(NRRL B592)中分离了醇脱氢酶。在两个菌株中均存在丁醇-乙醇脱氢酶活性,但是仅在产生异丙醇的菌株中存在异丙醇脱氢酶活性。 NRRL B592菌株的丁醇-乙醇脱氢酶的Mr为66,000,丁醛的Km为6μM。相反,菌株NRRL B593的丁醇-乙醇-异丙醇脱氢酶的丁醛和丙酮的Mr 100,000和Kms分别为9.5和1.0 mM。在通过四种不同类型的分离方法(DEAE-纤维素,羟基磷灰石,Sephacryl S-300和Matrex Gel Red A)纯化中,NRRL B593菌株的丁醇-乙醇-异丙醇脱氢酶活性被纯化至200倍(10倍于30%的收率),并且这些活动未分离。凝胶电泳和随后的活性染色也揭示了NRRL B592菌株的丁醇-乙醇脱氢酶和NRRL B593菌株的丁醇-乙醇-异丙醇脱氢酶的独特迁移率。在两种菌株的细胞提取物中,使用NADP(H)测得的酒精脱氢酶活性均高于使用NAD(H)测得的酒精脱氢酶活性。 NRRL B593菌株的150至200倍纯化的醇脱氢酶未显示任何NAD(H)连接的活性。对于NADPH菌株NRRL B593的醇脱氢酶,Km为31μM(以丁醛为底物)和18μM(以丙酮为底物)。这项研究表明,来自两株拜氏梭菌的醇脱氢酶差异显着。

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