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Inhibitory Interaction and Pharmacological Analyses of Berries Phenolics Against Listeria monocytogenes Virulent Protein Internalin B
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作者 Abhishek Kumar Archana Vimal Awanish Kumar 《World Journal of Traditional Chinese Medicine》 CAS CSCD 2023年第1期71-80,共10页
Background: Traditional plants, their parts, and phytochemicals obtained from them are beneficial for human beings. They are used as potent antimicrobials, but very little research is conducted on the use of tradition... Background: Traditional plants, their parts, and phytochemicals obtained from them are beneficial for human beings. They are used as potent antimicrobials, but very little research is conducted on the use of traditional medicine against food-borne infection. Different berry plants are rich in phenolic compounds and conventionally known to have many properties such as antioxidants, anti-carcinogenic, anti-inflammatory, anti-bacterial, and anti-diabetics. However, only limited polyphenols are known for their antilisterial effect. The present study aimed to explore the antimicrobial efficacy of phenolic compounds of berries for the treatment of food-borne infection caused by the bacteria Listeria monocytogenes. Materials and Methods: Molecular docking studies employing the Swiss DOCK server were performed to evaluate the antimicrobial activity of phenolic compounds obtained from different varieties of berries. Internalin B(Inl B), a virulence protein of L. monocytogenes was selected as a target. The absorption, distribution, metabolism, excretion, and toxicity profiling of each test ligand was done through the Swiss ADME tool. Results: Among all the test ligands, p-coumaric acid, epicatechins, chlorogenic acid, and quercetin showed better binding efficiency with the target protein Inl B. The binding energy obtained for quercetin, p-coumaric acid, chlorogenic acid, and epicatechins was-8.93,-8.23,-8.18,-7.58, kcal/mol, respectively. Quercetin and p-coumaric acid were forming 4 H-bonds, whereas chlorogenic acid and epicatechins were forming 3-H bonds inside the binding pocket. Conclusion: In a nutshell, analyses indicated that identified ligands have the potential to block the virulent protein Inl B of L. monocytogenes and help combat Listeria infection. These phenolic compounds could be a substitute for synthetic antimicrobials and can be used in food preservation and combat food-borne diseases. However, future in-depth in vitro and in vivo analysis is needed to get more information on these four phenolic ligands of berries. 展开更多
关键词 berry plant internalin b Listeria monocytogenes pharmacological analyses phenolics potent inhibitor traditional medicine
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不同来源单核细胞增多性李氏杆菌inlB和actA基因的克隆测序分析及基因缺失株的毒力试验 被引量:1
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作者 赵新斐 尚文婧 +1 位作者 王静梅 剡根强 《中国动物传染病学报》 CAS 2012年第5期32-38,共7页
根据GeneBank上发表的单核细胞增多性李氏杆菌(Listeria monocytogenes,LM)的内化素B(internalin B,inlB)和肌动蛋白A(actin A,actA)基因设计特异性引物,对5株不同来源的健康绵羊单核细胞增多性李氏杆菌和一株临床分离的单核细胞增多性... 根据GeneBank上发表的单核细胞增多性李氏杆菌(Listeria monocytogenes,LM)的内化素B(internalin B,inlB)和肌动蛋白A(actin A,actA)基因设计特异性引物,对5株不同来源的健康绵羊单核细胞增多性李氏杆菌和一株临床分离的单核细胞增多性李氏杆菌的inlB及actA基因进行PCR扩增,克隆测序分析其序列,并对2株部分基因缺失的单增李氏杆菌进行小鼠攻毒试验。结果表明:5株健康绵羊分离株单增李氏杆菌与临床分离株有较高的同源性,并且发现2株部分基因缺失的单增李氏杆菌;小鼠攻毒试验表明缺失株毒力有降低,但是不明显。 展开更多
关键词 单核细胞增多性李氏杆菌 内化素b 肌动蛋白A 克隆测序
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单核细胞增生性李斯特菌inlA和inlB基因缺失菌株的构建 被引量:2
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作者 刘武康 李森 +5 位作者 陈国薇 罗勤 吴嫚 丁承超 谢曼曼 刘箐 《微生物学杂志》 CAS CSCD 2017年第1期64-69,共6页
单核细胞增生性李斯特菌(Listeria monocytogenes,LM)是人畜共患的食源性致病菌,其对恶劣环境有较强的抵抗力,广泛存在于各种食品加工环境,容易引起严重的食品安全问题。LM是一种胞内寄生菌,其毒力因子内化素A(internalin A,InlA)和内化... 单核细胞增生性李斯特菌(Listeria monocytogenes,LM)是人畜共患的食源性致病菌,其对恶劣环境有较强的抵抗力,广泛存在于各种食品加工环境,容易引起严重的食品安全问题。LM是一种胞内寄生菌,其毒力因子内化素A(internalin A,InlA)和内化素B(internalin B,InlB)被认为在LM穿透宿主屏障、入侵宿主细胞以及胞间传播等过程中起到重要作用。本文利用同源重组法将LM野生菌株EGDe的inlA和inlB基因的敲除,对inlA和inlB基因缺失菌株的基本生物学特性进行研究,并运用RealTime-PCR监测LM的毒力基因表达。实验结果表明,基因的缺失对突变菌株的生长以及对环境中的氯化钠(NaCl)和乙醇(EtOH)的耐受能力没有影响,但多个毒力基因的表达量明显下降。该缺失菌株的构建为进一步研究InlA和InlB在LM入侵宿主细胞过程中的具体功能提供了重要材料。 展开更多
关键词 单核细胞增生性李斯特菌 内化素A 内化素b 基因敲除 RealTime-PCR
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单增李斯特菌InlB的原核表达与多克隆抗体制备 被引量:1
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作者 方小伟 施鹏 +2 位作者 彭鼎 杨玉莹 方春 《黑龙江畜牧兽医》 CAS 北大核心 2020年第10期51-54,61,149,150,共7页
为了进一步研究单增李斯特菌分泌的细菌侵袭相关蛋白内化素B(InlB)的功能,试验通过原核表达载体pET-28a分别表达InlB的N36~321和C392~630,并通过Ni^2+亲和层析柱对重组蛋白进行纯化,纯化的蛋白免疫Balb/c小鼠,制备多克隆抗体,通过Wester... 为了进一步研究单增李斯特菌分泌的细菌侵袭相关蛋白内化素B(InlB)的功能,试验通过原核表达载体pET-28a分别表达InlB的N36~321和C392~630,并通过Ni^2+亲和层析柱对重组蛋白进行纯化,纯化的蛋白免疫Balb/c小鼠,制备多克隆抗体,通过Western-blot检测单增李斯特菌InlB的表达情况。结果表明:成功构建重组表达质粒及诱导表达重组蛋白,制备的针对InlB N端和C端的多克隆抗体均能特异性检测单增李斯特菌中的InlB,但不能通过免疫荧光检测该菌表面的InlB。说明本研究制备的多克隆抗体可进一步用于研究单增李斯特菌InlB的功能。 展开更多
关键词 单增李斯特菌 表面蛋白 内化素b 原核表达 纯化 多克隆抗体
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