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Antibacterial activity of naringin derivatives against pathogenic strains.

机译:柚皮苷衍生物对致病菌株的抗菌活性。

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Aims: To study the antimicrobial activity of naringin (NAR), a flavonoid extracted from citrus industry waste, and NAR derivatives (naringenin (NGE), prunin and alkyl prunin esters) against pathogenic bacteria such as L. monocytogenes, E. coli O157:H7 and S. aureus. The relationship between the structure of the chemical compounds and their antagonistic effect was also analysed. Methods and Results: The agar dilution technique and direct contact assaying were applied. NGE, prunin and NAR showed no antimicrobial activity at a concentration of 0 25 mmol l--1. Similarly, fatty acids with a chain length between C2 and C18 showed no antimicrobial activity at the same concentration. However, prunin-6''-O-acyl esters presented high antibacterial activity, mainly against Gram-positive strains. This activity increased with increasing chain length (up to 10-12 carbon atoms). Alkyl prunin esters with 10-12 carbon atoms diminished viability of L. monocytogenes by about 3 log orders and S. aureus by 6 log orders after 2 h of contact at 37 degrees C and at a concentration of 0 25 mmol l--1. The compounds examined were not effective against any of the Gram-negative strains assayed, even at the highest concentration. Conclusions: Addition of sugars to the aglycone did not enhance its antimicrobial activity. Attachment of a saturated aliphatic chain with 10-12 carbon atoms to the A ring of the flavonoid (or to sugars attached to this ring), seems to be the most promising modification. In conclusion, alkyl prunin esters with a chain length of C10-C12 have promising features as antimicrobial agents because of their high antilisterial and antistaphylococcal activity. Significance and Impact of the Study: This study shows that it is possible to obtain NAR derivatives with important antimicrobial activity, especially against Gram-positive pathogenic bacteria. It also provides guidelines on the structural modifications in similar molecules to enhance the antimicrobial activity
机译:目的:研究柚皮苷(NAR)(一种从柑桔工业废料中提取的黄酮类)和NAR衍生物(柚皮苷(NGE),李宁和烷基李宁酯)的抗微生物活性,它们对诸如L的致病菌具有抗菌作用。单核细胞增生, E。大肠杆菌O157:H7和 S。金黄色。还分析了化合物的结构与其拮抗作用之间的关系。方法和结果:采用琼脂稀释技术和直接接触分析法。 NGE,脯氨酸和NAR在0 25 mmol l -1 时均无抗菌活性。同样,链长在C2和C18之间的脂肪酸在相同浓度下也没有抗菌活性。然而,脯氨酸6′-O-酰基酯表现出高的抗菌活性,主要针对革兰氏阳性菌株。该活性随链长的增加(最多10-12个碳原子)而增加。具有10-12个碳原子的烷基脯氨酸酯降低了L的生存力。单核细胞增生病按3个对数顺序和 S。在37摄氏度和浓度为0 25 mmol l -1 的情况下接触2小时后,金黄色葡萄球菌按6个对数顺序变化。所检查的化合物即使在最高浓度下也不能有效对抗任何革兰氏阴性菌。结论:糖苷配基中添加糖并没有增强其抗菌活性。具有10-12个碳原子的饱和脂族链与类黄酮的A环(或与该环相连的糖)的连接似乎是最有希望的修饰。总之,链长为C10-C12的烷基李宁酯具有很高的抗李斯特菌和抗葡萄球菌活性,因此具有作为抗菌剂的广阔前景。研究的意义和影响:该研究表明,有可能获得具有重要抗菌活性的NAR衍生物,尤其是针对革兰氏阳性病原菌。它还提供了有关相似分子的结构修饰以增强抗菌活性的指南

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