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首页> 外文期刊>Journal of bacteriology >Glucose transport in Streptococcus agalactiae and its inhibition by lactoperoxidase-thiocyanate-hydrogen peroxide.
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Glucose transport in Streptococcus agalactiae and its inhibition by lactoperoxidase-thiocyanate-hydrogen peroxide.

机译:无乳链球菌中的葡萄糖运输及其受乳过氧化物酶-硫氰酸酯-过氧化氢的抑制。

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摘要

Transport of 2-deoxyglucose or glucose in Streptococcus agalactiae was strongly inhibited if the cells were first exposed to a combination of lactoperoxidase-thiocyanate-hydrogen peroxide (LP-complex). The inhibition was completely reversible with dithiothreitol. N-ethylmaleimide and p-chloromercuribenzoate inhibited sugar transport, and the inhibition was also reversible with dithiothreitol. Sodium fluoride also inhibited sugar transport. Glucolysis was completely inhibited, and dithiothreitol completely reversed the inhibition. Phosphoenolpyruvate-dependent phosphotransferase activity in S. agalactiae was not strongly inhibited by the LP-complex. Interference of the entry of glucose into cells of S. agalactiae by the LP-complex could well account for its growth inhibitory properties with this organism. The inhibition of glucose transport by the LP-complex and its reversibility with dithiothreitol suggest the modification of functional sulfhydryl groups in the cell membrane as a cause of transport inhibition.
机译:如果首先将细胞暴露于乳过氧化物酶-硫氰酸盐-过氧化氢(LP-复合物)的组合,则无乳链球菌中的2-脱氧葡萄糖或葡萄糖的运输受到强烈抑制。二硫苏糖醇的抑制作用是完全可逆的。 N-乙基马来酰亚胺和对氯巯基苯甲酸抑制糖的转运,并且该抑制作用也可与二硫苏糖醇逆转。氟化钠也抑制糖的运输。糖酵解被完全抑制,二硫苏糖醇完全逆转了抑制作用。 LP-复合物未强烈抑制无乳链球菌中磷酸烯醇丙酮酸依赖性磷酸转移酶的活性。 LP复合物对葡萄糖进入无乳链球菌细胞的干扰可以很好地解释其对这种生物的生长抑制特性。 LP-复合物对葡萄糖转运的抑制及其与二硫苏糖醇的可逆性表明,细胞膜中功能性巯基的修饰是转运抑制的原因。

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