Environmental Engineering and Science, Department of Civil Engineering, Stanford University, Stanford, California 94305, and Department of Environmental Medicine and Department of Microbiology, New York University Medical Center, New York, New York 10016.
Appl Environ Microbiol. 1985 Feb;49(2):345-9. doi: 10.1128/aem.49.2.345-349.1985.
[C-lignin]lignocellulose was solubilized by alkaline heat treatment and separated into different molecular size fractions for use as the sole source of carbon in anaerobic enrichment cultures. This study is aimed at determining the fate of low-molecular-weight, polyaromatic lignin derivatives during anaerobic degradation. Gel permeation chromatography was used to preparatively separate the original C-lignin substrate into three component molecular size fractions, each of which was then fed to separate enrichment cultures. Biodegradability was assessed by monitoring total carbon dioxide and methane production, evolution of labeled gases, loss of C-activity from solution, and changes in gel permeation chromatographic elution patterns. Results indicated that the smaller the size of the molecular weight fraction, the more extensive the degradation to gaseous end products. In addition, up to 30% of the entire soluble lignin-derived carbon was anaerobically mineralized to carbon dioxide and methane.
[C-木质素]木质纤维素通过碱性热处理溶解,并分离成不同分子量的分数,用作厌氧富集培养中碳的唯一来源。本研究旨在确定低分子量、多芳烃木质素衍生物在厌氧降解过程中的命运。凝胶渗透色谱法用于将原始 C-木质素底物制备性地分离成三个组分的分子量分数,然后将每个分数分别进料到单独的富集培养物中。通过监测总二氧化碳和甲烷的产生、标记气体的演化、溶液中 C-活性的损失以及凝胶渗透色谱洗脱模式的变化来评估生物降解性。结果表明,分子量分数越小,降解为气态终产物的程度越大。此外,高达 30%的整个可溶性木质素衍生碳被厌氧矿化为二氧化碳和甲烷。