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DedA 蛋白与海洋海绵大环生物碱卤环胺 A 的作用机制有关,卤环胺 A 是一种抗休眠分枝杆菌物质。

DedA protein relates to action-mechanism of halicyclamine A, a marine spongean macrocyclic alkaloid, as an anti-dormant mycobacterial substance.

机构信息

Graduate School of Pharmaceutical Sciences, Osaka University, Yamada-oka 1-6, Suita, Osaka 565-0871, Japan.

Department of Chemistry, Faculty of Science, Lampung University, Jl. Prof. Dr. Sumantri Brodjonegoro No. 1, Bandar Lampung 35145, Indonesia.

出版信息

Mar Drugs. 2011;9(6):984-993. doi: 10.3390/md9060984. Epub 2011 Jun 8.

Abstract

A macrocyclic alkaloid, halicyclamine A, was re-discovered from an Indonesian marine sponge of Haliclona sp. 05A08 as an anti-dormant mycobacterial substance. To clarify action-mechanism of halicyclamine A, halicyclamine A-resistant strains were screened from the transformants of Mycobacterium smegmatis with the genomic DNA library of M. bovis BCG, which were constructed in the multi-copy shuttle cosmid pYUB145. Sequencing analysis of the cosmids isolated from the halicyclamine A-resistant transformants revealed that the responsible gene was involved in the genome region between 2920.549 kb and 2933.210 kb. Further experiments using the transformants over-expressing individual gene contained in the responsible region were executed, and the transformant, which over-expressed BCG2664 gene assigned as dedA gene, was found to become halicyclamine A-resistant. This evidence strongly suggested that DedA protein correlates with the action-mechanism of halicyclamine A as an anti-dormant mycobacterial substance.

摘要

一种大环生物碱——卤环胺 A,从印度尼西亚海绵 Haliclona sp. 05A08 中重新被发现,是一种抗休眠分枝杆菌物质。为了阐明卤环胺 A 的作用机制,从含有牛分枝杆菌基因组 DNA 文库的 M. smegmatis 转化子中筛选出卤环胺 A 抗性株。该文库构建在多拷贝穿梭质粒细胞 pYUB145 中。从卤环胺 A 抗性转化子中分离出的质粒细胞的测序分析表明,负责的基因参与了基因组区域在 2920.549 kb 和 2933.210 kb 之间。使用负责区域中包含的单个基因的过表达转化子进一步进行实验,发现过表达分配为 dedA 基因的 BCG2664 基因的转化子对卤环胺 A 具有抗性。这一证据强烈表明 DedA 蛋白与卤环胺 A 作为抗休眠分枝杆菌物质的作用机制相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/3131556/bc4570fdfbaa/marinedrugs-09-00984f1.jpg

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