Department of Microbiology and Institute of Ecology, University of Georgia, Athens, Georgia 30602.
Appl Environ Microbiol. 1984 May;47(5):998-1004. doi: 10.1128/aem.47.5.998-1004.1984.
Specifically radiolabeled [C-lignin]lignocelluloses and [C-polysaccharide]lignocelluloses were prepared from a variety of marine and freshwater wetland plants including a grass, a sedge, a rush, and a hardwood. These [C]lignocellulose preparations and synthetic [C]lignin were incubated anaerobically with anoxic sediments collected from a salt marsh, a freshwater marsh, and a mangrove swamp. During long-term incubations lasting up to 300 days, the lignin and polysaccharide components of the lignocelluloses were slowly degraded anaerobically to CO(2) and CH(4). Lignocelluloses derived from herbaceous plants were degraded more rapidly than lignocellulose derived from the hardwood. After 294 days, 16.9% of the lignin component and 30.0% of the polysaccharide component of lignocellulose derived from the grass used (Spartina alterniflora) were degraded to gaseous end products. In contrast, after 246 days, only 1.5% of the lignin component and 4.1% of the polysaccharide component of lignocellulose derived from the hardwood used (Rhizophora mangle) were degraded to gaseous end products. Synthetic [C]lignin was degraded anaerobically faster than the lignin component of the hardwood lignocellulose; after 276 days, 3.7% of the synthetic lignin was degraded to gaseous end products. Contrary to previous reports, these results demonstrate that lignin and lignified plant tissues are biodegradable in the absence of oxygen. Although lignocelluloses are recalcitrant to anaerobic biodegradation, rates of degradation measured in aquatic sediments are significant and have important implications for the biospheric cycling of carbon from these abundant biopolymers.
具体来说,[C-木质素]木质纤维素和 [C-多糖]木质纤维素是由各种海洋和淡水湿地植物制备的,包括草、莎草、灯心草和硬木。这些[C]木质纤维素制剂和合成[C]木质素与从盐沼、淡水沼泽和红树林沼泽收集的缺氧沉积物在无氧条件下孵育。在长达 300 天的长期孵育过程中,木质素和多糖成分的木质纤维素在无氧条件下缓慢降解为 CO(2)和 CH(4)。草类植物来源的木质纤维素比硬木来源的木质纤维素降解得更快。294 天后,用作草(互花米草)的木质纤维素中 16.9%的木质素成分和 30.0%的多糖成分被降解为气态终产物。相比之下,在 246 天后,用作硬木(红树)的木质纤维素中只有 1.5%的木质素成分和 4.1%的多糖成分被降解为气态终产物。合成[C]木质素比硬木木质纤维素的木质素成分在无氧条件下更快降解;276 天后,3.7%的合成木质素被降解为气态终产物。与之前的报告相反,这些结果表明,木质素和木质化植物组织在缺氧的情况下是可生物降解的。尽管木质纤维素对厌氧生物降解具有抗降解性,但在水生沉积物中测量的降解速率是显著的,对这些丰富的生物聚合物从生物圈循环中碳的生物循环具有重要意义。