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Effects of emulsified octadecanic acids on gas production and cellulolysis by the rumen anaerobic fungus, Piromyces communis M014

Authors
Kim, Chang-H.Lee, Shin J.Ha, Jong K.Kim, Wan Y.Lee, Sung S.
Issue Date
Feb-2008
Publisher
ELSEVIER SCI LTD
Keywords
rumen anaerobic fungus; octadecanic fatty acids; gas production; cellulolysis; Piromyces communis
Citation
ANAEROBE, v.14, no.1, pp 19 - 28
Pages
10
Indexed
SCIE
SCOPUS
Journal Title
ANAEROBE
Volume
14
Number
1
Start Page
19
End Page
28
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/27496
DOI
10.1016/j.anaerobe.2007.08.005
ISSN
1075-9964
1095-8274
Abstract
Responses of the rumen anaerobic fungus, Piromyces communis M014, to octadecanic long-chain fatty acids (LCFAs) were evaluated by measuring total and hydrogen gas productions, filter paper (FP) cellulose degradation and polysaccharidase enzyme activities. Octadecanic acids (stearic acid, C-18:0; oleic acid, C-18:1; linoleic acid, C-18:2 and linolenic acid, C-18:3) were emulsified by ultrasonication under anaerobic conditions, and added to the medium at the level of 0.00 1 %. When P. communis M014 was grown in culture with stearic and oleic acids, the cumulative gas production, FP cellulose digestion and enzyme activities were significantly (p < 0.05) increased in the early incubation times relative to those for the control. However, the addition of linolenic acid inhibited all of the investigated parameters, including cellulose degradation, enzyme activities and gas production, up to 168 h incubation. These results indicated that stearic and oleic acids tended to have stimulatory effects on fungal cellulolysis, whereas linolenic acid caused a significant (P<0.05) inhibitory effect on cellulolysis by the rumen fungus. The fungus, P. communis M014, can biohydrogenate C-18 unsaturated fatty acids to escape from their toxic effects. Therefore, in this study, the results indicated that the more highly the added C-18 LCFA to the fungal culture was unsaturated, the higher the inhibition of gas production and cellulase enzyme activity was. (C) 2007 Elsevier Ltd. All rights reserved.
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