首页> 外文期刊>Applied and Environmental Microbiology >Degradation of barley straw, ryegrass, and alfalfa cell walls by Clostridium longisporum and Ruminococcus albus.
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Degradation of barley straw, ryegrass, and alfalfa cell walls by Clostridium longisporum and Ruminococcus albus.

机译:长孢梭状芽胞杆菌和阿米诺氏球菌降解大麦秸秆,黑麦草和苜蓿细胞壁。

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The recently isolated ruminal sporeforming cellulolytic anaerobe Clostridium longisporum B6405 was examined for its ability to degrade barley straw, nonlignified cell walls (mesophyll and epidermis) and lignified cell walls (fiber) of ryegrass, and alfalfa cell walls in comparison with strains of Ruminococcus albus. R. albus strains degraded 20 to 28% of the dry matter in barley straw in 10 days, while the clostridium degraded less than 2%. A combined inoculum of R. albus SY3 and strain B6405 was no more efficient than SY3 alone, and the presence of Methanobacterium smithii PS did not increase the amount of dry matter degraded. In contrast, with alfalfa cell walls as the substrate, the clostridium was twice as active (28% weight loss) as R. albus SY3 (15%). The percentages of dry matter degraded from ryegrass cell walls of mesophyll, epidermis, and fiber for the clostridium were 50, 47, and 32%, respectively, and for R. albus SY3 they were 77, 73, and 63%, respectively. Analyses of the predominant neutral sugars (arabinose, xylose, and glucose) in the plant residues after bacterial attack were consistent with the values for dry matter weight loss. Measurements of the amount of carbon appearing in the fermentation products indicated that R. albus SY3 degraded ryegrass mesophyll cell walls most rapidly, with epidermis and fiber cell walls being degraded at similar rates. Strain B6405 attacked alfalfa cell walls at a rate greater than that of any of the ryegrass substrates. These results indicate an unexpected degree of substrate specificity in the ability of C. longisporum to degrade plant cell wall material.
机译:与新近分离的瘤胃Ruminococcus albus菌株相比,研究了最近分离出的瘤胃芽孢形成性纤维素分解厌氧菌长孢梭菌B6405的降解大麦秸秆,非木质化细胞壁(间叶和表皮)和木质化细胞壁(纤维)的黑麦草和苜蓿细胞壁的能力。在10天之内,白僵菌菌株在大麦秸秆中降解了20%至28%的干物质,而梭状芽胞杆菌的降解率不到2%。 R. albus SY3和菌株B6405的组合接种物没有比单独的SY3更有效,并且史密斯甲烷杆菌PS的存在不会增加降解的干物质的量。相反,以苜蓿细胞壁为底物,梭状芽胞杆菌的活性(重量损失28%)是R. albus SY3(15%)的两倍。从梭菌,叶肉和纤维的黑麦草细胞壁降解的干物质百分数为梭菌,分别为50%,47%和32%,而R. albus SY3分别为77%,73%和63%。细菌侵袭后植物残渣中主要的中性糖(阿拉伯糖,木糖和葡萄糖)的分析与干物质失重的值一致。对发酵产物中碳含量的测量表明,R。albus SY3降解黑麦草叶肉细胞壁的速度最快,表皮和纤维细胞壁的降解速度相似。菌株B6405攻击苜蓿细胞壁的速率比任何黑麦草底物都高。这些结果表明长孢梭菌降解植物细胞壁材料的能力中底物特异性的程度出乎意料。

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