mutase

英式音标：['mju:teɪs]

美式音标：['mjuteɪs]

词汇分类：生物化学基础词汇,神经系统（百歌医学单词USMLE）,医学英语词汇大集合

词义：

n.

变位酶；

英英释义

Mutase

A mutase is an enzyme of the isomerase class that catalyzes the shifting of a functional group from one position to another within the same molecule. Examples of this are bisphosphoglycerate mutase, which appears in red blood cells and phosphoglycerate mutase, which acts in glycolysis.

以上来源于:Wikipedia

用法：

权威例句

Inhibitors of UDP-galactopyranose mutase thwart mycobacterial growth

Mitochondrial superoxide simutase. Site of synthesis and intramitochondrial localization.

Crystal structure of the monofunctional chorismate mutase from Bacillus subtilis

Glutamate mutase from Clostridium cochlearium: the structure of a coenzyme B12-dependent enzyme provides new mechanistic insights

Extracellular superoxide dismutase and other superoxide dimutase isoenzymes in tissues from nine mammalian species.

Isolation of a cDNA encoding the muscle-specific subunit of human phosphoglycerate mutase.

Structure of the gene encoding the muscle-specific subunit of human phosphoglycerate mutase

Crystal structures of the monofunctional chorismate mutase from Bacillus subtilis and its complex with a transition state analog.

Cloning and characterization of an esophageal-gland-specific chorismate mutase from the phytoparasitic nematode Meloidogyne javanica.

How coenzyme B12 radicals are generated: the crystal structure of methylmalonyl-coenzyme A mutase at 2 A resolution.

造句：

1. T-protein from Escherichia coli consists of three domains: chorismate mutase, prephenate dehydrogenase and a regulatory domain.

大肠杆菌 T 蛋白含有三个结构域：分支酸变位酶、预苯酸脱氢酶和调节结构域。

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2. T-protein from Escherichia coli consists of three domains:chorismate mutase, prephenate dehydrogenase and a regulatory domain.

大肠杆菌T蛋白含有三个结构域：分支酸变位酶、预苯酸脱氢酶和调节结构域。

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3. Methylmalonic acidemia is an inherited metabolic disorder, which is caused by deficiency of methylmalonyl-coenzyme a mutase or its cofactor adenosylcobalamin.

甲基丙二酸血症是由于甲基丙二酰辅酶A变位酶或其辅酶腺苷钴胺素缺陷所致的一种遗传性代谢疾病。

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4. Methylmalonic acidemia is an inherited metabolic disorder, which is caused by deficiency of methylmalonyl-coenzyme a mutase or its cofactor adenosylcobalamin.

甲基丙二酸血症是由于甲基丙二酰辅酶A变位酶或其辅酶腺苷钴胺素缺陷所致的一种遗传性代谢疾病。

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5. aldehyde mutase

醛变位酶

-- 来源 -- 英汉 - 翻译参考[网络]