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食品中梭状芽孢杆菌检测与计数所涉及的原理。

Principles involved in the detection and enumeration of clostridia in foods.

作者信息

Mead G C

机构信息

Department of Animal Health, Royal Veterinary College, Potters Bar, England, UK.

出版信息

Int J Food Microbiol. 1992 Oct;17(2):135-43. doi: 10.1016/0168-1605(92)90111-f.

DOI:10.1016/0168-1605(92)90111-f
PMID:1486022
Abstract

The clostridia are a group of anaerobic bacteria that vary considerably in their biochemical and physiological properties. Not surprisingly, attempts to develop a single isolation medium for all species that occur in foods have not been entirely successful, and the problem is compounded by the need to recover both vegetative cells and spores, some of the latter being unable to germinate without heat activation. Most available isolation media, except some of those used in the dairy industry, include sulphite and an appropriate iron salt, so that blackening due to sulphite reduction can serve as a differential test for clostridia. The limitations of this test in solid agar media are discussed and some advantages described in relation to its use in liquid media for Most Probable Number determinations. A medium favoured for the purpose is the Differential Reinforced Clostridial Medium of Gibbs and Freame (1965). An unresolved issue is whether or not special precautions are needed to exclude oxygen during food sample preparation and dilution, preparation of media, and in conditions used for anaerobic incubation. Although such stringency may be required for maximum recovery of sub-lethally damaged cells or spores, practical constraints in food control laboratories necessitate use of relatively simple procedures for detecting clostridia routinely.

摘要

梭菌是一类厌氧细菌,其生化和生理特性差异很大。不出所料,试图开发一种适用于食品中所有梭菌种类的单一分离培养基并不完全成功,而且由于需要同时回收营养细胞和孢子,问题变得更加复杂,其中一些孢子如果没有热激活就无法萌发。除了乳制品行业使用的一些培养基外,大多数现有的分离培养基都含有亚硫酸盐和适当的铁盐,因此亚硫酸盐还原导致的变黑可作为梭菌的鉴别试验。本文讨论了该试验在固体琼脂培养基中的局限性,并描述了其在液体培养基中用于最可能数测定的一些优点。为此目的,一种受青睐的培养基是吉布斯和弗雷姆(1965年)的鉴别强化梭菌培养基。一个尚未解决的问题是,在食品样品制备和稀释、培养基制备以及厌氧培养条件下,是否需要采取特殊预防措施来排除氧气。尽管为了最大限度地回收亚致死损伤的细胞或孢子可能需要如此严格的条件,但食品控制实验室的实际限制使得有必要使用相对简单的程序来常规检测梭菌。

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