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从不动杆菌 BJ-L 中分离得到琥珀酰亚胺二羧酸的结构确定及抗菌活性

Isolation, structure determination and antibacterial activities of succinamide conjugate diacid from Acinetobacter sp. BJ-L.

机构信息

College of Life Sciences, Beijing Normal University, China.

出版信息

Microbiol Res. 2011 Mar 20;166(3):155-60. doi: 10.1016/j.micres.2010.04.003. Epub 2010 Jul 13.

Abstract

Strain BJ-L was isolated from the a water sample taken from Xiao Yue River in Beijing and identified as Acinetobacter sp. BJ-L based on the study of its morphology, physiology, biochemistry and 16S rRNA gene sequence. A new antimicrobial substance was produced after the strain was incubated in potato extract medium at 15°C for 72 h. The antimicrobial substance was sequentially purified by reduced pressure condensation, EtOAc extract, and silica gel column chromatography. The structure of the antimicrobial substance was elucidated as succinamide conjugate diacid (SCD) by spectroscopic data interpretation. Structure analysis indicated that SCD is a novel compound and that it could inhibit the growth of some tested bacterial strains with the MIC of 2mg/ml, such as Staphylococcus aureus, Bacillus subtilis, Enterobacter aerogenes and Escherichia coli. Moreover, no obvious toxicity has been found on cultured HUVEC cells with different concentrations of SCD at 5, 10, 15, and 20mg/ml.

摘要

菌株 BJ-L 是从北京小月河的水样中分离出来的,根据其形态、生理、生化和 16S rRNA 基因序列的研究,被鉴定为鲍曼不动杆菌 BJ-L。该菌株在 15°C 的土豆提取物培养基中培养 72 小时后,会产生一种新的抗菌物质。抗菌物质通过减压浓缩、乙酸乙酯提取和硅胶柱层析进行顺序纯化。通过光谱数据分析,阐明了抗菌物质的结构为琥珀酰胺缩二酸(SCD)。结构分析表明,SCD 是一种新型化合物,能够抑制一些测试菌的生长,其 MIC 为 2mg/ml,如金黄色葡萄球菌、枯草芽孢杆菌、产气肠杆菌和大肠杆菌。此外,在浓度为 5、10、15 和 20mg/ml 的不同 SCD 作用于培养的 HUVEC 细胞时,没有发现明显的毒性。

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