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Antibacterial activity of Cyt1Aa from Bacillus thuringiensis subsp. israelensis

机译:甲硝酸芽孢杆菌患者的Cyt1AA抗菌活性。以色列人

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Cyt1Aa is a δ-endotoxin protein that is produced by Bacillus thuringiensis subsp. israelensis. It is a membrane pore-forming toxin that is lethal to insect larvae and is broadly cytolytic to vertebrate as well as invertebrate cells. Cyt1Aa is produced as a protoxin of 27?kDa. Proteolytic activation results in a reduction of the molecular mass to approximately 23–24?kDa and a threefold increase in activity. In this research, Cyt1Aa crystals were purified from B. thuringiensis IPS78/11 harbouring the expression vector pHT-cyAp20. The activity of the activated form of Cyt1Aa (23–24?kDa) was examined on a pathogenic strain of the Gram-negative Escherichia coli and the Gram-positive species Staphylococcus aureus. The Cyt1Aa minimal inhibitory concentration for E. coli and S. aureus was 1.25 and 5?μg?ml?1, respectively. Cyt1Aa was found to be bactericidal for E. coli, whereas it was bacteriostatic for S. aureus. Furthermore, Cyt1Aa increased the lethal effect when acting in combination with antibiotics. The association of Cyt1Aa with cells of these two bacteria was demonstrated by Western blot analysis using antibodies against the whole δ-endotoxin crystal. Scanning electron microscopy displayed damage to Cyt1Aa-treated cells. Ion imbalance due to damage of the cell walls and membranes was confirmed by X-ray microanalysis. These experiments show that Cyt1Aa has an antibacterial effect on pathogenic species and demonstrate, apparently for the first time, that exogenous Cyt1Aa has a bactericidal effect upon Gram-negative bacteria.
机译:Cyt1aa是由芽孢杆菌胚子产生的δ-内毒素蛋白。以色列人。它是一种膜孔隙成形毒素,对昆虫幼虫致死,并且广泛细胞分解对脊椎动物以及无脊椎动物细胞。 Cyt1aa作为27μlkda的原生毒素制备。蛋白水解活化导致分子量的降低至约23-24 kda和活性的三倍。在该研究中,从含表达载体pHT-Cyap20的B. thuringiensis IPS78 / 11纯化Cyt1AA晶体。在革兰氏阴性大肠杆菌和革兰氏阳性物种金黄色葡萄球菌的致病菌菌株上检查活化形式的Cyt1AA(23-24 kda)的活性。大肠杆菌和金黄色葡萄球菌的Cyt1aa最小抑制浓度分别为1.25和5?μg≤1。发现Cyt1AA是大肠杆菌的杀菌剂,而它是金黄色葡萄球菌的抑菌。此外,Cyt1AA在与抗生素组合起作用时增加了致命作用。通过使用针对全部δ-内臭素晶体的抗体进行蛋白质印迹分析,通过Western印迹分析证明了Cyt1Aa与这两个细菌的细胞。扫描电子显微镜显示对Cyt1AA处理细胞的损伤。通过X射线微基分析证实了由于细胞壁和膜的损坏引起的离子不平衡。这些实验表明,Cyt1AA对致病物种具有抗菌作用,并且显然是首次证明外源性Cyt1AA对革兰氏阴性细菌具有杀菌作用。

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