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Differential carbohydrate media and anaerobic replica plating techniques in delineating carbohydrate-utilizing subgroups in rumen bacterial populations.

机译:差异碳水化合物培养基和厌氧复制平板技术用于确定瘤胃细菌群体中利用碳水化合物的亚组。

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摘要

A basal (BC) medium devoid of added carbohydrates, a complete (CC) medium containing nine carbohydrates were developed for enumerating rumen bacteria. The colony counts on the BC medium were 85 to 100% of those obtained on the CC medium. These colonies were pinpoint size (less than or equal to mm in diameter) but increased in size (2 to 5 mm in diameter) when carbohydrates were subsequently added. With the CC medium or other media tested, the colony counts were 20 to 50% higher on plates than on roll tubes and were about 35% of the direct cell counts. The lower colony counts on roll tubes were shown to result primarily from the loss of viability due to heat stress. The DC media were found by plating techniques to be suitable for differentiating mixed rumen bacterial populations into subgroups based upon carbohydrate utilization as shown by differences in subgroup profiles found within solid and liquid fractions of rumen contents, within rumen contents from animals fed high-forage and high-grain diets, and by correct colony formations by pure cultures of rumen bacteria on appropriate DC media. With simple modifications and use of an anaerobic glove box, replica plating methods and the CC and DC media were found to be a suitable means of rapidly determining the range of utilizable carbohydrate energy sources of rumen bacteria.
机译:一种基本(BC)培养基,不含添加的碳水化合物,已开发出一种包含九种碳水化合物的完整(CC)培养基,用于枚举瘤胃细菌。 BC培养基上的菌落数是CC培养基上的菌落数的85%至100%。这些菌落是精确的大小(直径小于或等于毫米),但随后添加碳水化合物时大小增加(直径为2至5毫米)。使用CC培养基或其他经过测试的培养基,平板上的菌落数比滚管上的菌落数高20至50%,约为直接细胞数的35%。滚动管上较低的菌落数表明主要是由于热应激导致的活力丧失。通过电镀技术发现DC培养基适合根据碳水化合物的利用将瘤胃中的混合瘤胃细菌分为不同的亚组,如瘤胃成分的固体和液体部分,饲喂高饲草的动物的瘤胃含量中的亚组分布差异所显示。高谷物饮食,并通过在适当的DC培养基上纯净瘤胃细菌的培养来纠正菌落的形成。通过简单的修改和使用厌氧手套箱,发现仿制电镀方法以及CC和DC介质是快速确定瘤胃细菌可利用的碳水化合物能源范围的合适方法。

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