McAllister T A, Bae H D, Yanke L J, Cheng K J, Muir A
Agriculture Canada Research Centre, Lethbridge, AB.
Can J Microbiol. 1994 Apr;40(4):298-305. doi: 10.1139/m94-048.
The ruminal fungi Neocallimastix frontalis RE1, Neocallimastix patriciarum 27, Piromyces communis 22, and Orpinomyces joyonii 19-2 were examined for their ability to digest filter paper in the presence of condensed tannins from birdsfoot trefoil (Lotus corniculatus L.). For all four fungi, inhibition of endoglucanases was evident at 100 micrograms condensed tannins.mL-1 with nearly complete inhibition at 300 micrograms condensed tannins.mL-1. At 100 and 200 micrograms condensed tannins.mL-1, the endoglucanase activity of N. frontalis RE1 was greater (P < 0.01) than that of the other three fungal species. Exposure to 100 micrograms condensed tannins.mL-1 did not affect the ability of N. frontalis RE1 or N. patriciarum 27 to digest filter paper, and although digestion was reduced, N. frontalis RE1 and P. communis 22 solubilized more than 20% of the filter paper at 500 micrograms condensed tannins.mL-1. In contrast, O. joyonii 19-2 was virtually unable to digest filter paper at 300 micrograms condensed tannins.L-1. Mycelia of fungi grown with condensed tannins were covered by filamentous material, which may have arisen from the formation of condensed tannin-protein complexes. Less than 86% of the condensed tannins (as measured by the H2SO4 method) were recovered after 120 h of incubation with N. frontalis RE1, P. communis 22, and N. patriciarum 27. The need for detailed studies to examine the ability of ruminal fungi to metabolize condensed tannins is evident.
对瘤胃真菌额叶新美鞭菌RE1、派氏新美鞭菌27、普通梨形鞭毛虫22和乔氏奥尔平鞭毛虫19 - 2在存在来自百脉根(Lotus corniculatus L.)的缩合单宁的情况下消化滤纸的能力进行了研究。对于所有这四种真菌,在缩合单宁浓度为100微克/毫升时内切葡聚糖酶受到明显抑制,在300微克/毫升时几乎完全抑制。在缩合单宁浓度为100和200微克/毫升时,额叶新美鞭菌RE1的内切葡聚糖酶活性高于其他三种真菌(P < 0.01)。暴露于100微克/毫升的缩合单宁中并不影响额叶新美鞭菌RE1或派氏新美鞭菌27消化滤纸的能力,并且尽管消化作用有所降低,但在缩合单宁浓度为500微克/毫升时,额叶新美鞭菌RE1和普通梨形鞭毛虫22仍能溶解超过20%的滤纸。相比之下,乔氏奥尔平鞭毛虫19 - 2在缩合单宁浓度为300微克/升时几乎无法消化滤纸。与缩合单宁一起生长的真菌菌丝体被丝状物质覆盖,这可能是由于缩合单宁 - 蛋白质复合物的形成所致。在用额叶新美鞭菌RE1、普通梨形鞭毛虫22和派氏新美鞭菌27培养120小时后,回收的缩合单宁(通过硫酸法测定)不到86%。显然需要进行详细研究以考察瘤胃真菌代谢缩合单宁的能力。