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卷曲分枝杆菌对正丙胺、异丙胺和1,3 -丙二胺的代谢

Metabolism of n-propylamine, isopropylamine, and 1,3-propane diamine by Mycobacterium convolutum.

作者信息

Cerniglia C E, Perry J J

出版信息

J Bacteriol. 1975 Oct;124(1):285-9. doi: 10.1128/jb.124.1.285-289.1975.

Abstract

Mycobacterium convolutum strain NPA-1 can utilize n-propylamine (NPA), isopropylamine (IPA), and 1,3-propane diamine (PD) as sole source of carbon, nitrogen, and energy. Enzyme assays, fatty acid profiles, and 14CO2 incorporation experiments indicate that NPA is deaminated to propionate and further metabolized via the methylmalonyl succinate pathway, and IPA and PD were metabolized (after deamination) through a C2 + C1 cleavage. An inducible amine dehydrogenase was present in cell extracts after growth on the three amines. Polyacrylamide gel electrophoresis of cell extracts from NPA- and IPA-grown cells yielded one major band of amine dehydrogenase activity. When extracts of NPA-grown cells were assayed with NPA, IPA, or PD as substrate, the relative position of the major band on gel electrophoresis was equivalent. Similar results were obtained with extracts prepared from IPA-grown cells. Sephadex G-100 chromatography also indicated one major peak of activity. This suggests that one enzyme of broad specificity is involved in deamination of IPA, NPA, and PD. IPA-grown cells utilized NPA readily, whereas NPA-grown cells could not utilize IPA without lag. Since amine dehydrogenase activity was present in extracts of cells after growth on either substrate, this lag was probably due to the inability to transport IPA without an induction period. The molecular weight of the amine dehydrogenase was approximately 38,500 as determined by gel filtration.

摘要

卷曲分枝杆菌菌株NPA-1能够利用正丙胺(NPA)、异丙胺(IPA)和1,3-丙二胺(PD)作为唯一的碳、氮和能量来源。酶活性测定、脂肪酸谱分析以及14CO2掺入实验表明,NPA被脱氨基生成丙酸盐,并通过甲基丙二酸琥珀酸途径进一步代谢,而IPA和PD(脱氨基后)通过C2 + C1裂解进行代谢。在三种胺上生长后,细胞提取物中存在一种可诱导的胺脱氢酶。对在NPA和IPA上生长的细胞提取物进行聚丙烯酰胺凝胶电泳,产生了一条主要的胺脱氢酶活性带。当用NPA、IPA或PD作为底物对NPA生长的细胞提取物进行测定时,凝胶电泳上主要条带的相对位置是相同的。用IPA生长的细胞提取物也得到了类似的结果。葡聚糖G-100柱层析也显示出一个主要的活性峰。这表明一种具有广泛特异性的酶参与了IPA、NPA和PD的脱氨基作用。在IPA上生长的细胞很容易利用NPA,而在NPA上生长的细胞在没有延迟期的情况下不能利用IPA。由于在任何一种底物上生长后的细胞提取物中都存在胺脱氢酶活性,这种延迟可能是由于在没有诱导期的情况下无法转运IPA所致。通过凝胶过滤测定,胺脱氢酶分子量约为38,500。

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