全部

1·Chemical modification studies showed that the sulfhydryl, guanido, amino, carboxyl and indolyl groups may participate in the active center of the enzyme.

化学修饰实验发现：巯基、胍基、氨基、羧基和吲哚基可能参与酶活性中心的组成。

2·Modification of histidine residue did not change the activity of enzyme and its fluorescence emission peak intensity.

组氨酸残基被修饰后酶活力基本不变，酶的荧光强度也不改变。

3·Modification of histidine residue did not change the activity of the enzyme and its fluorescence emission peak intensity.

组氨酸残基被修饰后酶活力基本不变，酶的荧光强度也不改变。

4·The surface modification of polymeric materials by plasma technique were discussed. The recent advances in the preparation of immobilized enzyme carriers by plasma technique were reviewed.

本文阐述了等离子体的发生及其引起材料表面改性的主要特点。就近年来，国内外运用等离子体技术制备固定化酶载体的方法及应用情况作了综述。

5·Several surface modification methods and enzyme immobilization methods were designed and tried to search for the best surface modification method and the best enzyme immobilization method.

为寻找最佳的电极表面修饰方法及酶固定化方法，设计并实验了几种不同的电极表面修饰方法及酶固定化方法。

6·Enzyme technology has been used in oil and fats research for years, such as enzyme degumming for oils, enzyme modification for lecithins and biodiesel productions.

酶反应技术在油脂研究中已经得到了一定的应用，如酶法脱胶、 磷脂酶法改性、 生物燃料的研究等等。

7·Amino acid analysis showed that the inactivation of the enzyme was due to the modification of the arginyl residue by butanedione( Table3).

氨基酸分析表明，酶的失活是因为丁二酮修饰了精氨酸残基。

8·As an artificial enzyme, it can be optimized by changing the diphenylmethane units or bridging chains or by chemical modification of hydrophobic cavities to form new host compounds.

作为人工模拟酶，通过改变氮杂环蕃化合物的形状以及引入活性基团，形成不同包结性能的主体化合物。

9·The enzyme was not effected by NEM, IAA or NAI modification suggesting that thiol group or tyrosine residues were non-essential for enzyme activity.

在一定条件下，当巯基及酪氨酸残基分别被NEM、IAA及NAI修饰后，酶活力不受影响，说明这些基团与活力无关。

10·Modification of the substrate by an enzyme can then be monitored electrochemically by means of the redox-active group.

随后可以通过氧化还原活性基团电化学监测酶对底物的修饰。