宝贵海蜇水华毛笔中溶菌酶的抗菌及抗膜特性研究

Muhammad Naveed , Anas Sajjad , Amjad Ali , Malik Wajid Hussain Chan , Fenghuan Wang
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引用次数: 0

摘要

为了展示巴基斯坦水母繁殖的有益方面,设计了这项研究。从佩氏毛笔中分离出溶菌酶,采用盐沉淀(硫酸铵)、透析、超滤等多步骤纯化。溶菌酶在浓度为70 % (NH4)2SO4时产率最高,为14.58 mg/mL,在浓度为20 % (NH4)2SO4时产率最低,为1.06 mg/mL。采用超滤法,得率为68% %,比酶活性为1952 U/mg。用超滤得到的溶菌酶对革兰氏阳性菌和革兰氏阴性菌的杀菌潜力进行了评价。抑菌区(ZOI)和最小抑菌浓度/最小杀菌浓度(MIC/MBC)等抑菌活性结果表明,溶菌酶对革兰氏阳性菌的抑菌潜力高于革兰氏阴性菌。抗菌指数(AMI)和百分比活性指数(PAI)结果表明,溶菌酶对金黄色葡萄球菌ATCC 25923具有最高的杀菌潜力。溶菌酶对金黄色葡萄球菌ATCC 25923的AMI值为1.30,PAI值为130。溶菌酶对革兰氏阳性菌的抗生物膜活性高于革兰氏阴性菌。经凝胶柱层析纯化,产率为15.07 %,比活性为1606 U/mg。通过聚丙烯酰胺凝胶电泳技术对所得溶菌酶进行进一步处理,得到的蛋白/溶菌酶酶活性为1732 U/mL。这表明溶菌酶在这一阶段仍保持其酶促潜能。纯化后的溶菌酶经SDS-PAGE(十二烷基硫酸钠聚丙烯酰胺凝胶电泳)技术进一步处理。结果表明,在70 % (NH4)2SO4浓度下得到的溶菌酶样品在20 kDa处有一个显著的蛋白带。采用扫描电镜(SEM)技术对2种革兰氏阳性菌(黄体革兰氏分枝杆菌和金黄色葡萄球菌)和2种革兰氏阴性菌(大肠杆菌和肺炎克雷伯菌)进行抑菌活性鉴定。用扫描电镜分析了溶菌酶的杀菌潜力。结果表明,经溶菌酶处理的细菌培养物对产膜细菌有明显的抑制作用。溶菌酶对这些细菌的抑菌活性分别为:黄体分枝杆菌ATCC 4698和金黄色葡萄球菌ATCC 25923的抑菌活性分别为31 mm ZOI和26 mm ZOI,大肠杆菌ATCC 25922和肺炎克雷默菌ATCC 13883的抑菌活性分别为18.5 mm ZOI和16 mm ZOI。本研究为从水母中分离纯化潜在溶菌酶提供了基础资料,为今后将水母华作为食品和医药食品工业的利用提供了基础资料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antibacterial and Antibiofilm Properties of Lysozyme Extracted from Catostylus perezi, an Invaluable Jellyfish Bloom
To show the beneficial aspect of jellyfish bloom in Pakistan, this study was designed. Lysozyme was isolated from Catostylus perezi and then purified by multistep methodological procedures such as salt precipitation (ammonium sulfate), dialysis and ultrafiltration. The lysozyme obtained at a 70 % concentration of (NH4)2SO4 had the highest yield of 14.58 mg/mL, while the lowest yield of 1.06 mg/mL was obtained at a 20 % concentration of (NH4)2SO4 solution. Using the ultrafiltration method, a yield of 68 % with a specific enzyme activity of 1952 U/mg was obtained. The lysozyme obtained by ultrafiltration was used for the evaluation of its bactericidal potential against various Gram-positive and Gram-negative species. The results of the antibacterial activity, e.g. the zones of inhibition (ZOI) and the minimum inhibitory concentration/minimum bactericidal concentration (MIC/MBC), showed that lysozyme has a higher bactericidal potential against Gram-positive than against Gram-negative bacterial strains. The results of antimicrobial index (AMI) and percent activity index (PAI) showed that lysozyme had the highest bactericidal potential against S. aureus ATCC 25923. The AMI value of Lysozyme against S. aureus ATCC 25923 was 1.30 and the PAI value was 130. Lysozyme had higher anti-biofilm activity against Gram-positive than Gram-negative species. The lysozyme was purified by gel column chromatography, resulting in a yield of 15.07 % with a specific activity of 1606 U/mg. The resulting lysozyme was further processed by native-PAGE (Polyacrylamide gel electrophoresis) technique and the protein/lysozyme obtained had an enzymatic activity of 1732 U/mL. This indicated that the lysozyme still retained its enzymatic potential at this stage. The purified lysozyme was also further processed by SDS-PAGE (Sodium-dodecyl sulfate polyacrylamide gel electrophoresis) technique. The results indicated, the lysozyme sample obtained by 70 % (NH4)2SO4 concentration had a prominent protein band at 20 kDa. The scanning electron microscopic (SEM) technique was used to confirm antibacterial activity for two Gram-positive (M. luteus and S. aureus) and two Gram-negative species (E. coli and K. pneumoniae). The bactericidal potential of lysozyme was analyzed by scanning electron microscopy (SEM). The results showed that the bacterial cultures treated with lysozyme exhibited a significant inhibition against biofilm producing bacteria. The antibacterial activity of lysozyme against these bacterial species was: 31 mm ZOI (zone of inhibition) for M. luteus ATCC 4698 and 26 mm ZOI for S. aureus ATCC 25923, while 18.5 mm ZOI for E. coli ATCC 25922 and 16 mm ZOI for K. pneumoniae ATCC 13883. It was concluded from this study that the isolation and purification of the potential lysozyme from the jellyfish provided fundamental information for the future use of jellyfish blooms as food and in the pharmaceutical and food industries.
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