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首页> 外文期刊>Natural product research >Dolastane diterpenes from Canistrocarpus cervicornis and their effects in modulation of drug resistance in Staphylococcus aureus
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Dolastane diterpenes from Canistrocarpus cervicornis and their effects in modulation of drug resistance in Staphylococcus aureus

机译:来自Canistrocarpus Cervicornis的Dolastane Diterpenes及其在金黄色葡萄球菌中耐药性的影响

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ABSTRACT: One new diterpene (4R,7R,14S)-4α,7α-diacetoxy-10-one-14α-hydroxydolasta-1(15),8-diene (1), and five known compounds (4R,7R,14S)-4α,7α-diacetoxy-14α-hydroxydolasta-1(15),8-diene (2), (4R,14S)-4α,14α-dihydroxydolasta-1(15),8-diene (3), (4S,9R,14S)-4α-acetoxy-9β,14α-dihydroxydolasta-1(15),7-diene (4), 4-acetoxy-14-hydroxydolasta-1(15),7,9-triene (5) and isolinearol (6), were isolated from Canistrocarpus cervicornis. In this study, dolastane diterpenes were isolated from the alga C. cervicornis and evaluated as modifiers of antibiotic activity in Staphylococcus aureus: SA-1199B, which overexpresses the norA gene RN-4220, which encodes for the protein efflux of macrolides (MRSA), and IS-58 which has the gene encoding the protein TetK. The minimum inhibitory concentrations (MICs) for norfloxacin, tetracycline and erythromycin were determined by the microdilution broth nutrient in the absence and presence of diterpenes at a sub-inhibitory concentration (MIC/4). The extracts of C. cervicornis and isolated diterpenes showed no antibacterial activity, but showed modulatory activity, decreasing the MIC of antibiotics by 4–256 fold. The results indicate that seaweed extracts and diterpenes are potential sources of antibiotic adjuvant, acting as potential inhibitors of efflux pump. ? 2018, ? 2018 Informa UK Limited, trading as Taylor & Francis Group.
机译:摘要:一种新的二萜(4R,7R,14s)-4α,7α-二乙氧基-10-14α-羟基醇-1(15),8-二烯(1)和五种已知的化合物(4R,7R,14s) -4α,7α-二乙酰氧基-14α-羟基醇-1(15),8-二烯(2),(4R,14s)-4α,14α-二氢吡咯烷-1(15),8-二烯(3),(4s, 9R,14s)-4α-乙酰氧基-9β,14α-二羟基醇-1(15),7-二烯(4),4-乙酰氧基-14-羟基醇-1(15),7,9-三烯(5)和ISOLINEALOL (6),从Canistrocarpus Cervicornis中分离出来。在该研究中,从藻类C. cervicornis中分离出偶联含量分离,并评估为金黄色葡萄球菌中的抗生素活性的改性剂:SA-1199b,其过表达Nora基因RN-4220,其编码MAROLIDES(MRSA)的蛋白质流出, IS-58具有编码蛋白质TETK的基因。通过在子抑制浓度(MIC / 4)的缺乏和存在下,通过微脱稀释肉碱菌丝测定用于NORFLOXACIN,四环素和红霉素的最小抑制浓度(MIC)。 C. cercicornis和分离的脱萜的提取物显示出抗菌活性,但显示出调节活性,将抗生素的MIC减少4-256倍。结果表明,海藻提取物和二萜是抗生素佐剂的潜在来源,作用为流出泵的潜在抑制剂。还2018年,? 2018年Informa UK Limited,贸易为泰勒&弗朗西斯集团。

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