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用奈斯勒试剂识别革兰氏阴性发酵菌对赖氨酸、鸟氨酸和精氨酸的分解作用(作者译)

[Use of Nessler's reagent for recognition of lysine, ornithine, and arginine decomposition by gramnegative fermentative bacteria (author's transl)].

作者信息

Hahn H, Bockemühl J, Döll W

出版信息

Zentralbl Bakteriol Orig A. 1976 Oct;236(1):120-6.

PMID:998031
Abstract

The reactions of lysine, ornithine and arginine decomposition are often difficult to read in Falkow's medium because either the decolorization of the indicator or the lack of sharp colour differences between positive and negative reactions. In such cases Nessler's reagent may be a useful aid. A volume of about 0.2 ml is added to the cultures after 4 days incubation through the mineral oil layer by means of a pipette. A positive reaction is indicated by an immediate white precipitation in case of lysine and ornithine decarboxylation, and a white or brownish precipitate which indicates arginine decomposition. A delayed opacity should be regarded as a negative reaction. Only unequivocal reactions should be considered. The specificity of the reactions was tested with pure substances of compounds which are formed by the decomposition of lysine, ornithine and arginine. Further studies of bacterial cultures in Falkow's medium and in a synthetic, amino acid containing medium without peptone gave identical results and showed that peptone derivates do not cause a false positive reaction with Nessler's reagent (Table 1). Comparative studies on 605 strains of Enterobacteriaceae and Vibrio in Falkow's medium with and without added Nessler's reagent gave corresponding results except some strains of Escherichia coli and Citrobacter freundii with different arginine reactions (Table 2). Strains of these species mostly decolorized the indicator thereby hindering the recognition of either a true positive or a true negative reaction. In these cases, however, the results obtained after addition of Nessler's reagent corresponded closely to the percentage of positive reactions cited in the literature.

摘要

在福尔科夫培养基中,赖氨酸、鸟氨酸和精氨酸分解反应的结果往往难以判读,因为要么指示剂会褪色,要么阳性和阴性反应之间缺乏明显的颜色差异。在这种情况下,奈斯勒试剂可能会有所帮助。培养4天后,通过移液管经矿物油层向培养物中加入约0.2毫升奈斯勒试剂。赖氨酸和鸟氨酸脱羧反应呈阳性时,会立即产生白色沉淀;精氨酸分解则会产生白色或褐色沉淀。延迟出现的浑浊应视为阴性反应。只应考虑明确的反应。用赖氨酸、鸟氨酸和精氨酸分解形成的化合物的纯物质对反应的特异性进行了测试。在福尔科夫培养基和不含蛋白胨的合成氨基酸培养基中对细菌培养物进行的进一步研究得出了相同的结果,表明蛋白胨衍生物不会与奈斯勒试剂产生假阳性反应(表1)。在添加和不添加奈斯勒试剂的福尔科夫培养基中对605株肠杆菌科细菌和弧菌进行的比较研究得出了相应的结果,但一些大肠杆菌和弗氏柠檬酸杆菌菌株的精氨酸反应不同(表2)。这些菌种的菌株大多会使指示剂褪色,从而妨碍对真阳性或真阴性反应的识别。然而,在这些情况下,添加奈斯勒试剂后获得的结果与文献中引用的阳性反应百分比非常接近。

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