发布: 2015年10月20日第5卷第20期 DOI: 10.21769/BioProtoc.1632 浏览次数: 7840
评审: Timo LehtiAnonymous reviewer(s)
相关实验方案
通过制备连续聚丙烯酰胺凝胶电泳和凝胶酶谱分析法纯化来自梭状龋齿螺旋体的天然Dentilisin复合物及其功能分析
Pachiyappan Kamarajan [...] Yvonne L. Kapila
2024年04月05日 1272 阅读
Abstract
Prominent accumulation of D-leucine, D-allo-isoleucine and D-valine was observed in the culture medium of the heterofermentative bacterial species, Lactobacillus otakiensis (L. otakiensis) JCM 15040. The racemase enzyme that resulted in this accumulation, isoleucine 2-epimerase, was purified from the bacterial cells. This is the first reported observation of such production of D-branched chain amino acids in lactic acid bacteria, and the first example of a racemase with isoleucine 2-epimerase activity in any organisms. In the described protocol, we introduce methods for purification of this protein from L. otakiensis JCM 15040. Because no specific ligand that has high affinity for this enzyme has been identified, the purification was performed using ammonium sulfate fraction, four types of column chromatography and preparative Native-PAGE, not using an affinity column chromatography. We hope that the protocol will provide useful information for purification of an enzyme that cannot easily be purified using an affinity column chromatography.
Keywords: Lactic acid bacteria (乳酸菌)Materials and Reagents
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文章信息
版权信息
© 2015 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Mutaguchi, Y. and Ohshima, T. (2015). Purification of a Protein Exhibiting Isoleucine 2-epimerase Activity from Lactobacillus otakiensis JCM 15040. Bio-protocol 5(20): e1632. DOI: 10.21769/BioProtoc.1632.
分类
微生物学 > 微生物生物化学 > 蛋白质
生物化学 > 蛋白质 > 分离和纯化
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