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通过³²P标记的磷酸盐掺入量来体外测定瘤胃微生物的生长。

Determination of rumen microbial growth in vitro from 32P-labelled phosphate incorporation.

作者信息

van Nevel C J, Demeyer D I

出版信息

Br J Nutr. 1977 Jul;38(1):101-14. doi: 10.1079/bjn19770066.

Abstract
  1. The extracellular phosphate pool in incubations of rumen fluid or washed cell suspensions of mixed rumen bacteria (WCS) was labelled with 32P. From the constant extracellular phosphate pool specific activity and the amount of radioactivity incorporated during incubation, the amount of P incorporated in the microbial fraction was calculated. From the value for nitrogen: P determined in microbial matter, the amount of N incorporated was calculated as a measure of microbial growth. 2. Incorporation of soluble non-protein-N in incubations devoid of substrate protein was 50 and 80% of the values obtained using the isotope method for rumen fluid and WCS respectively. It is suggested that results obtained using the former method reflect 'net growth' of micro-organisms which is the result of simultaneous growth and degradation. The isotope method measures 'total growth', as isotope incorporation is not affected by degradation of non-growing cells. 3. Incorporation of 32P in P-containing microbial components (mainly nucleic acids) was compared with net synthesis of these components in incubations of WCS. The results showed different specific rates of synthesis and degradation for all components studied. It is concluded that the composition of microbial matter changed during growth. 4. When N incorporation, calculated from results obtained using the isotope method in incubations with rumen fluid, was compared with the amount of carbohydrate substrate fermented and the type of fermentation, values between 18-3 and 44-6 g N incorporated/kg of organic matter fermented were obtained. Low values were associated with large proportions of the substrate being fermented to lactate and the use of glucose instead of disaccharides as substrate. Part of the variation could also be attributed to differences in incubation period, reflected in different proportions of polysaccharide formed. 5. The use of isotopes for determination of rumen microbial growth in vitro is critically discussed.
摘要
  1. 瘤胃液或混合瘤胃细菌洗涤细胞悬液(WCS)培养物中的细胞外磷酸盐池用³²P进行标记。根据恒定的细胞外磷酸盐池比活性以及培养过程中掺入的放射性活度,计算出微生物部分中掺入的磷量。根据微生物物质中测定的氮磷比,计算出掺入的氮量,以此作为微生物生长的指标。2. 在没有底物蛋白的培养物中,可溶性非蛋白氮的掺入量分别为使用同位素法在瘤胃液和WCS中获得值的50%和80%。有人认为,使用前一种方法获得的结果反映了微生物的“净生长”,这是同时生长和降解的结果。同位素法测量的是“总生长”,因为同位素掺入不受非生长细胞降解的影响。3. 将³²P掺入含磷微生物成分(主要是核酸)的情况与WCS培养物中这些成分的净合成情况进行了比较。结果表明,所有研究成分的合成和降解比速率不同。得出的结论是,微生物物质的组成在生长过程中发生了变化。4. 当将根据瘤胃液培养物中使用同位素法获得的结果计算出的氮掺入量与发酵的碳水化合物底物量和发酵类型进行比较时,每千克发酵有机物中掺入的氮量在18.3至44.6克之间。低数值与大量底物发酵生成乳酸以及使用葡萄糖而非双糖作为底物有关。部分差异也可归因于培养期的不同,这反映在形成的多糖比例不同上。5. 对使用同位素测定体外瘤胃微生物生长的方法进行了批判性讨论。

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