Dijkerman R, Ledeboer J, Prins RA
Department of Microbiology and Evolutionary Biology, Faculty of Science, University of Nijmegen, Toernooiveld 1, NL-6525 ED Nijmegen, The Netherlands
Curr Microbiol. 1997 Feb;34(2):91-6. doi: 10.1007/s002849900150.
The anaerobic fungus Neocallimastix sp. strain L2,isolated from the feces of a llama, was tested for growth on a range ofsoluble and insoluble carbohydrate substrates. The fungus was able to fermentglucose, cellobiose, fructose, lactose, maltose, sucrose, soluble starch,inulin, filter paper cellulose, and Avicel. No growth was observed onarabinose, galactose, mannose, ribose, xylose, sorbitol, pectin, xylan,glycerol, citrate, soya, and wheat bran. The fermentation products aftergrowth were hydrogen, formate, acetate, ethanol, and lactate. Thefermentation pattern was dependent on the carbon source. In general, higherhydrogen production resulted in decreased formation of lactate and ethanol.Recovery of the fermented carbon in products at the end of growth ranged from50% to 80%. (Hemi)cellulolytic enzyme activities were affectedby the carbon source. Highest activities were found in filtrates fromcultures grown on cellulose. Growing the fungus on inulin and lactose yieldedthe lowest cellulolytic activities. Highest specific activities foravicelase, endoglucanase, beta-glucosidase, and xylanase were obtained withAvicel as the substrate for growth (0.29, 5.9, 0.57, and 13IU · mg-1 protein, respectively). Endoglucanase activitybanding patterns after SDS-PAGE were very similar for all substrates. Minordifferences indicated that enzyme activities may in part be the result ofsecretion of different sets of isoenzymes.
从美洲驼粪便中分离出的厌氧真菌新丽鞭毛菌属(Neocallimastix sp.)菌株L2,针对一系列可溶性和不溶性碳水化合物底物进行了生长测试。该真菌能够发酵葡萄糖、纤维二糖、果糖、乳糖、麦芽糖、蔗糖、可溶性淀粉、菊粉、滤纸纤维素和微晶纤维素。在阿拉伯糖、半乳糖、甘露糖、核糖、木糖、山梨醇、果胶、木聚糖、甘油、柠檬酸盐、大豆和麦麸上未观察到生长。生长后的发酵产物为氢气、甲酸、乙酸、乙醇和乳酸。发酵模式取决于碳源。一般来说,氢气产量增加会导致乳酸和乙醇生成量减少。生长结束时产物中发酵碳的回收率在50%至80%之间。(半)纤维素酶活性受碳源影响。在以纤维素为底物生长的培养物滤液中发现最高活性。在菊粉和乳糖上培养该真菌产生的纤维素酶活性最低。以微晶纤维素作为生长底物时,获得了最高的微晶纤维素酶、内切葡聚糖酶、β-葡萄糖苷酶和木聚糖酶比活性(分别为0.29、5.9、0.57和13IU·mg-1蛋白质)。SDS-PAGE后内切葡聚糖酶活性条带模式在所有底物上非常相似。微小差异表明酶活性可能部分是不同同工酶分泌的结果。