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Fermentation of Isolated Pectin and Pectin from Intact Forages by Pure Cultures of Rumen Bacteria

机译:纯瘤胃细菌的纯培养物发酵分离的果胶和果胶

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摘要

Studies on the rate and extent of galacturonic acid and isolated pectin digestion were carried out with nine strains of rumen bacteria (Butyrivibrio fibrisolvens H10b and D16f, Bacteroides ruminicola 23 and D31d, Lachnospira multiparus D15d, Peptostreptococcus sp. D43e, B. succinogenes A3c, Ruminococcus flavefaciens B34b, and R. albus 7). Only three strains, 23, D16f, and D31d, utilized galacturonic acid as a sole energy source, whereas all strains except A3c and H10b degraded (solubilized) and utilized purified pectin. Nutrient composition of the basal medium and separate sterilization of the substrate affected the rate and extent of fermentation for both substrates. Pectin degradation and utilization were measured with two maturity stages each of intact bromegrass and alfalfa. For bromegrass I, all strains tested (B34b, 23, D16f, D31d, D15d, and D43e) degraded a considerable amount of pectin and, with the exception of B34b, utilized most of what was degraded. Similar, but lower, results were obtained with bromegrass II, except for the two strains of B. ruminicola, 23 and D31d, which were unable to degrade and utilize pectin from this forage. All strains were able to degrade and utilize pectin from both maturity stages of alfalfa; however, values were considerably lower for strains 23 and D31d. Synergism studies, in which a limited utilizing strain, B34b, was combined with the limited degrading strain, D31d, resulted in a slight increase in degradation and a very marked increase in utilization of the pectin in all four forages. Similar results were obtained on both alfalfa substrates with a combination of strains B34b and D16f; however, no increases were observed with this combination on bromegrass.
机译:用九种瘤胃细菌(纤维丁酸梭状芽胞杆菌H10b和D16f,Ruminicola ruminicola 23和D31d,Lachnospira multiparus D15d,Peptostreptococcuscus sp.D43e,A。succinica)对半乳糖醛酸和分离的果胶消化的速率和程度进行了研究。 flavefaciens B34b和R. albus 7)。只有三个菌株23,D16f和D31d使用半乳糖醛酸作为唯一能源,而除A3c和H10b以外的所有菌株均降解(溶解)并使用了纯果胶。基础培养基的营养成分和底物的单独灭菌影响了两种底物的发酵速率和程度。果胶的降解和利用是通过完整的肉眼草和苜蓿的两个成熟阶段进行的。对于婆罗门草I,所有测试菌株(B34b,23,D16f,D31d,D15d和D43e)降解了大量果胶,除B34b外,大部分降解果胶均得到利用。除草甘蓝B. ruminicola的两个菌株23和D31d无法降解和利用果胶以外,果蝇用草甘蓝II可获得相似但较低的结果。所有菌株都能够降解和利用苜蓿两个成熟阶段的果胶。但是,菌株23和D31d的值明显较低。协同研究,其中有限利用的菌株B34b与有限降解的菌株D31d结合在一起,导致所有四种草料的果胶利用率略有提高,并且果胶利用率显着提高。在苜蓿的两种底物上,菌株B34b和D16f的结合得到了相似的结果。但是,这种组合在草甘蓝上没有观察到增加。

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