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利用实时直接分析(DART)质谱法研究家蚕组织中的丙氨酸转氨酶活性。

The Study of Alanine Transaminase Activity in Tissues of Silkworm () via Direct Analysis in Real-Time (DART) Mass Spectrometry.

机构信息

College of Biotechnology, Jiangsu University of Science and Technology, Zhenjiang 212100, China.

College of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang 212100, China.

出版信息

Molecules. 2023 May 16;28(10):4131. doi: 10.3390/molecules28104131.

Abstract

Alanine transaminase (ALT) is an important amino acid-metabolizing enzyme in silkworm L., and is mainly involved in transferring glutamate to alanine (serving as an essential precursor in silk protein synthesis) through transamination. Therefore, it is generally believed that silk protein synthesis in the silk gland and the cocoon quantity increase with the increase in ALT activity to a certain extent. Here, a novel analytical method was developed to determine the ALT activity in several key tissues of L. including the posterior silk gland, midgut, fat body, middle silk gland, trachea and hemolymph, by combining the direct-analysis-in-real-time (DART) ion source with a triple-quadrupole mass spectrometer. In addition, a traditional ALT activity assay, the Reitman-Frankel method, was also used to measure ALT activity for comparison. The ALT activity results obtained via the DART-MS method are in good agreement with those obtained via the Reitman-Frankel method. However, the present DART-MS method provides a more convenient, rapid and environmentally friendly quantitative method for ALT measurement. Especially, this method can also monitor ALT activity in different tissues of L. in real time.

摘要

丙氨酸氨基转移酶(ALT)是家蚕 L. 中一种重要的氨基酸代谢酶,主要通过转氨基作用将谷氨酸转移到丙氨酸(作为丝蛋白合成的必需前体)。因此,一般认为丝腺中丝蛋白的合成和茧量的增加在一定程度上与 ALT 活性的增加有关。本研究采用直接实时分析(DART)离子源与三重四极杆质谱联用的方法,建立了一种测定家蚕 L. 后丝腺、中肠、脂肪体、中丝腺、气管和血液等几个关键组织中 ALT 活性的新方法,并与传统的 Reitman-Frankel 法进行了比较。DART-MS 法测定的 ALT 活性与 Reitman-Frankel 法测定的结果基本一致,但本研究建立的 DART-MS 方法为 ALT 的定量分析提供了一种更方便、快速、环保的方法,尤其可以实时监测家蚕不同组织中的 ALT 活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7279/10223717/672acd02c9f9/molecules-28-04131-g001.jpg

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