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Microbial Phospholipid Synthesis as a Marker for Microbial Protein Synthesis in the Rumen

机译:微生物磷脂合成作为瘤胃微生物蛋白质合成的标志

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摘要

Phosphate uptake into intracellular inorganic phosphorus and cellular phospholipids and the relationship between cell growth and phospholipid synthesis were studied with suspensions of washed ruminal bacteria in vitro with 33P-phosphorus. It was shown that ruminal bacteria accumulated inorganic phosphate at a low rate when incubated without substrate. Upon the addition of substrate, the rate of inorganic phosphorus uptake into the cells increased markedly, and phospholipid synthesis and cell growth commenced. There was a highly significant relationship (r = 0.98; P < 0.01) between phospholipid synthesis and cell growth. The specific activity of the intracellular inorganic phosphorus did not equilibrate with phosphorus medium. When ruminal contents from sheep fed a high or low protein diet were incubated in vitro, the rate of 33P incorporation into microbial phospholipids was higher for the high protein diet. Since there was a high relationship between phospholipid synthesis and growth, rumen contents were collected before and various times after feeding and incubated with 33P-phosphorus in vitro. The short-term, zero time approach was used to measure the rate of microbial phospholipid synthesis in whole rumen contents. In these studies the average specific activity of the intracellular inorganic phosphorus was used to represent the precursor pool specific activity. Microbial phospholipid synthesis was then related to protein (N × 6.25) synthesis with appropriate nitrogen-to-phospholipid phosphorus ratios. Daily true protein synthesis in a 4-liter rumen was 185 g. This represents a rate of 22 g of protein synthesized per 100 g of organic matter digested. These data were also corrected for ruminal turnover. On this basis the rate of true protein synthesis in a 4-liter rumen was 16.1 g of protein per 100 g of organic matter digested. This value represents a 30-g digestible protein-to-Mcal digestible energy ratio which is adequate for growing calves and lambs.
机译:用洗涤过的瘤胃细菌悬浮液中的 33 P-磷体外研究了细胞内无机磷和细胞磷脂的磷酸盐吸收以及细胞生长与磷脂合成的关系。结果表明,在没有底物的情况下,瘤胃细菌以较低的速率积累无机磷酸盐。加入底物后,无机磷摄入细胞的速率显着增加,并且磷脂合成和细胞开始生长。磷脂合成与细胞生长之间存在高度显着的关系(r = 0.98; P <0.01)。细胞内无机磷的比活性与磷培养基不平衡。将高蛋白饮食或低蛋白饮食的绵羊的瘤胃内容物进行体外培养时,高蛋白饮食的 33 P掺入微生物磷脂的比率更高。由于磷脂的合成与生长之间存在高度相关性,因此在进食前和进食后多次收集瘤胃内容物,并与 33 P-磷进行体外培养。短期零时间法用于测量整个瘤胃中微生物磷脂合成的速率。在这些研究中,细胞内无机磷的平均比活度用来代表前体池的比活度。然后,微生物磷脂的合成与蛋白质(N×6.25)的合成有关,氮与磷脂的磷比例合适。 4升瘤胃中的每日真实蛋白质合成量为185 g。这代表每100 g消化的有机物合成22 g蛋白质的速率。这些数据也针对瘤胃翻转进行了校正。在此基础上,每4克瘤胃内100克有机物质中的真实蛋白质合成率为16.1克蛋白质。该值代表30 g的可消化蛋白质与Mcal的可消化能量之比,足以满足犊牛和羔羊的生长。

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