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在通常与尿路感染有关的大肠杆菌及其他肠杆菌科的原养型和营养缺陷型变体中β-D-葡萄糖醛酸酶活性。

Beta-D-Glucuronidase activity among prototrophic and auxotrophic variants of Escherichia coli and other Enterobacteriaceae commonly implicated in urinary tract infections.

作者信息

Tapsall J W, McIver C J

机构信息

Microbiology Department, Prince of Wales Hospital, Randwick NSW, Australia.

出版信息

Diagn Microbiol Infect Dis. 1995 Jul;22(3):261-6. doi: 10.1016/0732-8893(95)00097-t.

Abstract

Glucuronidase (GUD) activity of 102 prototrophic, 91 cysteine-requiring, and 19 thymidine-requiring strains of Escherichia coli was examined using growth from MacConkey, CLED, and enriched brain heart infusion (BHI) agars. After 24 h incubation, GUD activity was detected in 92%-96% of prototrophic strains and a similar proportion of thymidine-requiring strains with most reactions detectable in shorter incubation periods. GUD activity among strains requiring cysteine was significantly less than that found amongst prototrophic strains. The effects of different sources of inocula were evident in the shorter incubation periods. Other strains of the Enterobacteriaceae and oxidative strains frequently implicated in urinary tract infection were also tested. Here, positive reactions were detected among Citrobacter and Enterobacter spp. and a strain of Klebsiella oxytoca, but only after 24 h incubation. GUD activity was not detected among the oxidative strains tested under the same conditions. Although an incubation time of 24 h is necessary to detect activity in a small number of "slow hydrolyzing" E. coli, the increased sensitivity thus attained compromises the specificity of the test for this organism by simultaneously enhancing detection of the enzyme in other enterobacteria.

摘要

利用在麦康凯琼脂、CLED琼脂和强化脑心浸液(BHI)琼脂上的生长情况,检测了102株原养型、91株半胱氨酸需求型和19株胸苷需求型大肠杆菌的葡萄糖醛酸酶(GUD)活性。培养24小时后,在92%-96%的原养型菌株和相似比例的胸苷需求型菌株中检测到GUD活性,大多数反应在较短培养时间内即可检测到。半胱氨酸需求型菌株中的GUD活性显著低于原养型菌株。在较短培养时间内,不同接种源的影响很明显。还测试了其他经常与尿路感染有关的肠杆菌科菌株和氧化型菌株。在此,在柠檬酸杆菌属和肠杆菌属以及一株产酸克雷伯菌中检测到阳性反应,但仅在培养24小时后。在相同条件下测试的氧化型菌株中未检测到GUD活性。虽然检测少数“缓慢水解”大肠杆菌的活性需要24小时的培养时间,但由此获得的灵敏度提高同时增强了对其他肠杆菌中该酶的检测,从而损害了该检测针对这种微生物的特异性。

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