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首页> 外文期刊>Comparative biochemistry and physiology, Part B. Biochemistry & molecular biology >Multiple antibacterial histone H2B proteins are expressed in tissues of American oyster
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Multiple antibacterial histone H2B proteins are expressed in tissues of American oyster

机译:多种抗菌组蛋白H2B蛋白质组织中表达美国的牡蛎

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摘要

We have previously identified a histone H2B isomer (cvH2B-1) from tissue extracts of the bivalve mollusk, the American oyster (Crassostrea virginica). In this paper, we isolate an additional three antibacterial proteins from acidified gill extract by preparative acid-urea-polyacrylamide gel electrophoresis and reversed-phase high performance liquid chromatography. Extraction of these proteins from tissue was best accomplished by briefly boiling the tissues in a weak acetic acid solution. Addition of protease inhibitors while boiling resulted in somewhat lower yields, with one protein being totally absent with this method. Via mass spectrometry, the masses of one of these purified proteins was 13607.0 Da (peak 2), which is consistent with the molecular weight of histone H2B. In addition, via western-blotting using anti-calf histone H2B antibody, all three proteins were positive and were thus named cvH2B-2, cvH2B-3 and cvH2B-4. The antibacterial activity of cvH2B-2 was similar to that of cvH2B-1, with activity against a Gram-positive bacterium (Lactococcus lactis subsp. lactis; minimum effective concentration [MEC] 52-57 μg/mL) but inactive against Staphylococcus aureus (MEC > 250 μg/mL). However, both proteins had relatively potent activity against the Gram-negative oyster pathogen Vibrio parahemolyticus (MEC 11.5-14 μg/mL) as well as the human pathogen Vibrio vulnificus (MEC 21.3-25.3 μg/mL). cvH2B-3 and cvH2B-4 also had similarly strong activity against. Vibrio vulnificus. These data provide further evidence for the antimicrobial function of histone H2B isomers in modulating bacterial populations in oyster tissues. The combined estimated concentrations of these histone H2B isomers were far above the inhibitory concentrations for the tested vibrios, including human pathogens. Our results indicate that the highly conserved histone proteins might be important components not only of immune defenses in oysters but have the potential to influence the abundance of a ubiquitous microbial resident of oyster tissues that is the major source of seafood-borne illness in humans.
机译:之前我们已经发现了一种组蛋白H2B异构体从组织中提取的双壳类(cvH2B-1)软体动物,美国牡蛎(Crassostreavirginica)。额外的三个抗菌蛋白通过制备酸化吉尔提取acid-urea-polyacrylamide凝胶电泳,反相高效液相色谱法。组织是最好通过简要地沸腾组织在疲软的乙酸溶液。添加蛋白酶抑制剂而沸腾导致产量稍低外,有一个蛋白质是完全没有使用这种方法。通过质谱、群众的其中之一纯化蛋白质13607.0 Da(2)峰值,的分子量是一致的吗组蛋白H2B。使用anti-calf组蛋白H2B抗体,所有三个蛋白质是积极的,因此命名cvH2B-2, cvH2B-3 cvH2B-4。活动cvH2B-2是相似的对革兰氏阳性cvH2B-1,活动细菌(Lactococcus lactis无性系种群。最低有效浓度(MEC) 52-57μg / mL),但对金黄色葡萄球菌活性(MEC > 250μg / mL)。对相对有效的活动革兰氏阴性牡蛎病原弧菌parahemolyticus (MEC 11.5 -14μg / mL)以及人类病原体创伤弧菌(MEC21.3 - -25.3μg / mL)。同样强烈的活动。本文描述。组蛋白H2B的抗菌功能同分异构体在调节细菌种群牡蛎组织。这些组蛋白浓度H2B同分异构体远高于的抑制浓度测试弧菌属,包括人类病原体。结果表明,高度保守的组蛋白蛋白质可能是重要组成部分但不仅是免疫防御的牡蛎潜在影响的丰富无处不在的微生物牡蛎的居民组织这是seafood-borne疾病的主要来源在人类身上。

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