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在添加还原剂受限或过量的条件下,特定硝基化合物对体外瘤胃发酵的影响。

Effects of select nitrocompounds on in vitro ruminal fermentation during conditions of limiting or excess added reductant.

作者信息

Anderson Robin C, Krueger Nathan A, Stanton Thaddeus B, Callaway Todd R, Edrington Thomas S, Harvey Roger B, Jung Yong Soo, Nisbet David J

机构信息

United States Department of Agriculture, Agricultural Research Service, College Station, TX 77845, USA.

出版信息

Bioresour Technol. 2008 Dec;99(18):8655-61. doi: 10.1016/j.biortech.2008.04.064. Epub 2008 Jun 5.

DOI:10.1016/j.biortech.2008.04.064
PMID:18538564
Abstract

Ruminal methane (CH(4)) production results in the loss of up to 12% of gross energy intake and contributes nearly 20% of the United States' annual emission of this greenhouse gas. We report the effects of select nitrocompounds on ruminal fermentation after 22 h in vitro incubation (39 degrees C) with or without additions of hydrogen (H(2)), formate or both. In incubations containing no added reductant, CH(4) production was inhibited 41% by 2-nitro-1-propanol (2NPOH) and >97% by 3-nitro-1-propionic acid (3NPA), nitroethane (NE) and 2-nitroethanol (2NEOH) compared to non-treated controls and H(2) did not accumulate. With formate as the sole added reductant, nitro-treatment reduced CH(4) production by >99% and caused 42% to complete inhibition of formate catabolism compared to controls, and the accumulation of H(2) increased slightly. Nitro-treatment decreased CH(4) production 57-98% from that of controls when supplied H(2) or formate plus H(2). Formate catabolism was decreased 42-84% from that in controls by all nitro-treatments except 3NPA with both formate and H(2). Greater than 97% of the added H(2) was catabolized within controls; >84% was catabolized in nitro-treated incubations. Acetate, propionate and butyrate accumulations were unaffected by nitro-treatment irregardless of reductant; however, effects on ammonia and branched chain fatty acid accumulations varied. These results suggest that nitro-treatment inhibited formate dehydrogenase/formate hydrogen lyase and hydrogenase activity.

摘要

瘤胃甲烷(CH₄)的产生导致高达12%的总能摄入量损失,并且占美国该温室气体年排放量的近20%。我们报告了在39℃体外培养22小时后,添加或不添加氢气(H₂)、甲酸盐或两者时,特定硝基化合物对瘤胃发酵的影响。在未添加还原剂的培养中,与未处理的对照相比,2-硝基-1-丙醇(2NPOH)使CH₄产量降低41%,3-硝基-1-丙酸(3NPA)、硝基乙烷(NE)和2-硝基乙醇(2NEOH)使CH₄产量降低>97%,且H₂没有积累。以甲酸盐作为唯一添加的还原剂时,与对照相比,硝基处理使CH₄产量降低>99%,并导致甲酸盐分解代谢完全抑制42%,且H₂的积累略有增加。当供应H₂或甲酸盐加H₂时,硝基处理使CH₄产量比对照降低57 - 98%。除了同时添加甲酸盐和H₂的3NPA外,所有硝基处理均使甲酸盐分解代谢比对照降低42 - 84%。在对照中,超过97%添加的H₂被分解代谢;在硝基处理的培养中,>84%被分解代谢。无论还原剂如何,乙酸盐、丙酸盐和丁酸盐的积累不受硝基处理的影响;然而,对氨和支链脂肪酸积累的影响各不相同。这些结果表明,硝基处理抑制了甲酸盐脱氢酶/甲酸盐氢裂解酶和氢化酶的活性。

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