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大风子油酸抑制分枝杆菌繁殖的机制。

Mechanism by which hydnocarpic acid inhibits mycobacterial multiplication.

作者信息

Jacobsen P L, Levy L

出版信息

Antimicrob Agents Chemother. 1973 Mar;3(3):373-9. doi: 10.1128/AAC.3.3.373.

Abstract

Recent work in this laboratory has shown that hydnocarpic acid (HA), a principal constituent of chaulmoogra oil, inhibits multiplication in vitro of a number of mycobacterial species. This activity of HA was not shared by several straight-chain fatty acids and by dihydrochaulmoogric acid. A study of the interaction of HA with biotin has been undertaken, based on a structural analogy between biotin and the cyclopentenyl fatty acid. The multiplication of a strain of Mycobacterium intracellulare susceptible to 2 mug of HA/ml was measured turbidimetrically in Dubos medium, in the presence and absence of biotin and several other compounds. Biotin and, to a lesser extent, adenine plus guanine, palmitic acid, and linoleic acid antagonized growth inhibition by HA. Desthiobiotin, thioctic acid, and succinic acid did not block inhibition of bacterial multiplication by HA. HA may act by blocking the coenzymatic activity of biotin, or it may inhibit microbial biotin synthesis. Resumption of multiplication of M. intracellulare after a period of inhibition by HA in broth culture was found to be accompanied by reduction of the effective concentration of the drug; this could have resulted from metabolism of HA or production of an antagonist to HA by the organisms. Also, those organisms that multiplied in the presence of HA were found to represent HA-resistant mutants of M. intracellulare.

摘要

本实验室最近的研究表明,大风子油酸(HA)是大风子油的主要成分,能抑制多种分枝杆菌在体外的繁殖。几种直链脂肪酸和二氢大风子油酸没有这种HA活性。基于生物素与环戊烯基脂肪酸之间的结构相似性,对HA与生物素的相互作用进行了研究。在有无生物素及其他几种化合物存在的情况下,于杜博斯培养基中通过比浊法测定了对2μg/ml HA敏感的胞内分枝杆菌菌株的繁殖情况。生物素,以及程度稍轻的腺嘌呤加鸟嘌呤、棕榈酸和亚油酸可拮抗HA对生长的抑制作用。脱硫生物素、硫辛酸和琥珀酸不会阻止HA对细菌繁殖的抑制作用。HA可能通过阻断生物素的辅酶活性起作用,或者它可能抑制微生物生物素的合成。发现在肉汤培养中经HA抑制一段时间后胞内分枝杆菌恢复繁殖伴随着药物有效浓度的降低;这可能是由于HA的代谢或生物体产生了HA的拮抗剂所致。此外,发现在HA存在下繁殖的那些生物体代表了胞内分枝杆菌的HA抗性突变体。

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本文引用的文献

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BIOCHEMISTRY OF BIOTIN.生物素的生物化学
Vitam Horm. 1964;22:1-55. doi: 10.1016/s0083-6729(08)60335-0.

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