首页> 美国卫生研究院文献>Biochemical Journal >The inhibition of streptococci by lactoperoxidase thiocyanate and hydrogen peroxide. The effect of the inhibitory system on susceptible and resistant strains of group N streptococci
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The inhibition of streptococci by lactoperoxidase thiocyanate and hydrogen peroxide. The effect of the inhibitory system on susceptible and resistant strains of group N streptococci

机译:乳过氧化物酶硫氰酸盐和过氧化氢对链球菌的抑制作用。抑制系统对N族链球菌敏感和耐药菌株的影响

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摘要

1. The growth of the lactoperoxidase-sensitive Streptococcus cremoris 972 in a synthetic medium was inhibited by lactoperoxidase and thiocyanate. The glycolysis and oxygen uptake of suspensions of Strep. cremoris 972 in glucose or lactose were also inhibited. The lactoperoxidase-resistant Strep. cremoris 803 was not inhibited under these conditions but was inhibited in the absence of a source of energy. 2. Lactoperoxidase (EC 1.11.1.7), thiocyanate and hydrogen peroxide completely inhibited the hexokinases of non-metabolizing suspensions of both strains. The inhibition was reversible, hexokinase and glycolytic activities of Strep. cremoris 972 being restored by washing the cells free from inhibitor. The aldolase and 6-phosphogluconate-dehydrogenase activities of Strep. cremoris 972 were partially inhibited but several other enzymes were unaffected. 3. The resistance of Strep. cremoris 803 to inhibition was not due to the lack of hydrogen peroxide formation, to the destruction of peroxide, to the inactivation of lactoperoxidase or to the operation of alternative pathways of carbohydrate metabolism. 4. A `reversal factor', which was partially purified from extracts of Strep. cremoris 803, reversed the inhibition of glycolysis of Strep. cremoris 972. The `reversal factor' also catalysed the oxidation of NADH2 in the presence of an intermediate oxidation product of thiocyanate and was therefore termed the NADH2-oxidizing enzyme. 5. The NADH2-oxidizing enzyme was present in lactoperoxidase-resistant streptococci but was absent from lactoperoxidase-sensitive streptococci.
机译:1.乳过氧化物酶和硫氰酸盐抑制了对乳过氧化物酶敏感的Cremoococcus cremoris 972在合成培养基中的生长。链球菌悬浮液的糖酵解和氧吸收。葡萄糖或乳糖中的cremoris 972也被抑制。耐乳过氧化物酶的链球菌。 cremoris 803在这些条件下不受抑制,但是在没有能源的情况下被抑制。 2.乳过氧化物酶(EC 1.11.1.7),硫氰酸盐和过氧化氢完全抑制两种菌株的非代谢悬浮液的己糖激酶。抑制是可逆的,己糖激酶和链球菌的糖酵解活性。通过清洗细胞中的抑制剂来恢复cremoris 972。链球菌的醛缩酶和6-磷酸葡糖酸脱氢酶活性。 creemoris 972被部分抑制,但其他几种酶未受影响。 3.链球菌的抵抗力。 cremoris 803的抑制作用并不是由于缺乏过氧化氢形成,过氧化物的破坏,乳过氧化物酶的失活或碳水化合物代谢的其他途径的操作。 4.一种“逆转因子”,其是从链球菌提取物中部分纯化的。 cremoris 803,逆转了链球菌糖酵解的抑制作用。 cremoris972。在存在硫氰酸盐的中间氧化产物的情况下,“逆转因子”还催化了NADH2的氧化,因此被称为NADH2氧化酶。 5. NADH2氧化酶存在于耐乳过氧化物酶的链球菌中,但不存在于对乳过氧化物酶敏感的链球菌中。

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