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通过快速微酸量滴定法从初代培养平板中筛查产青霉素酶淋病奈瑟菌的可行性。

Feasibility of screening for penicillinase-producing Neisseria gonorrhoeae from primary culture plates by using a rapid microacidometric test.

作者信息

Weissfeld A S, Sanner G D, Childress J R, Dyckman J D, Huber T W, Williams R P

出版信息

Antimicrob Agents Chemother. 1977 Dec;12(6):703-6. doi: 10.1128/AAC.12.6.703.

Abstract

We have shown that it is possible to screen for penicillinase-producing Neisseria gonorrhoeae directly from primary culture plates. Experiments involving the cocultivation of four genera of beta-lactamase-positive (beta-lac(+)) bacteria and a beta-lactamase-negative (beta-lac(-)) N. gonorrhoeae on modified Thayer-Martin medium indicated that suppressed or inhibited beta-lac(+) bacteria did not give false-positive results when isolated beta-lac(-) colonies of gonococci were tested. Colonies were assayed for beta-lac production by an adaptation of a microacidometric method in which bacteria could be tested before or after the addition of oxidase reagent.

摘要

我们已经证明,直接从原代培养平板上筛选产青霉素酶的淋病奈瑟菌是可行的。在改良的Thayer-Martin培养基上,将4属β-内酰胺酶阳性(β-lac(+))细菌与1株β-内酰胺酶阴性(β-lac(-))淋病奈瑟菌共培养的实验表明,当检测分离出的β-lac(-)淋球菌菌落时,受抑制的β-lac(+)细菌不会产生假阳性结果。通过一种微量酸度测定法的改良方法检测菌落的β-lac产生情况,该方法可以在添加氧化酶试剂之前或之后对细菌进行检测。

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Penicillinase-producing Gonococci in Liverpool.利物浦的产青霉素酶淋球菌
Lancet. 1976 Dec 25;2(8000):1379-82. doi: 10.1016/s0140-6736(76)91919-x.
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Penicillinase-producing Neisseria gonorrhoeae.产青霉素酶淋病奈瑟菌
Lancet. 1976 Sep 25;2(7987):657-8. doi: 10.1016/s0140-6736(76)92467-3.
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