Antibacterial activity of naringin derivatives against pathogenic strains

被引:114
|
作者
Celiz, G. [1 ]
Daz, M. [1 ]
Audisio, M. C. [1 ]
机构
[1] Univ Nacl Salta, Inst Invest Ind Quim INIQUI CONICET, Salta, Argentina
关键词
antibacterial activity; flavonoid esters; Listeria monocytogenes; Naringin; Staphylococcus aureus ATCC29213; RESISTANT STAPHYLOCOCCUS-AUREUS; CHAIN FATTY-ACIDS; ANTIMICROBIAL ACTIVITY; BIOCATALYTIC PREPARATION; LISTERIA-MONOCYTOGENES; ANTIBIOTIC-RESISTANCE; FLAVANONE GLUCOSIDE; PHENOLIC-COMPOUNDS; ORAL BACTERIA; FLAVONOIDS;
D O I
10.1111/j.1365-2672.2011.05070.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
引用
收藏
页码:731 / 738
页数:8
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