Or-Rashid Mamun M, AlZahal Ousama, McBride Brian W
Department of Animal and Poultry Science, University of Guelph, Guelph, ON, N1G 2W1, Canada.
Appl Microbiol Biotechnol. 2008 Dec;81(3):533-41. doi: 10.1007/s00253-008-1690-0. Epub 2008 Sep 17.
The present study was designed to investigate the capability of mixed rumen protozoa to synthesize conjugated linoleic acid (CLA) from linoleic (LA) and vaccenic acids (VA). Rumen contents were collected from fistulated cows. The protozoal fraction was separated and washed several times with MB9 buffer and then resuspended in autoclaved rumen fluid. The suspensions were anaerobically incubated up to 18 h at 38.5 degrees C with substrates in the presence (P-AB) or the absence of antibacterial-agents (P-No-AB). Neither P-AB nor P-No-AB suspensions were capable of producing CLA from VA (11t-18:1). Linoleic acid was catabolized by P-No-AB to a greater extent than P-AB. Different isomers of CLA were synthesized by P-AB from LA. The 9c11t-CLA was predominant. Thirty seven percent of the maximum accumulated 9c11t-CLA was found in the P-AB suspension as early as 0.1 h into the incubation period. Accumulation of 10t12c-CLA in P-AB suspension was approximately 10.0 times lower than that of 9c11t-CLA. There were no significant productions of VA, 10t-18:1, and 18:0 in P-AB compared with the control, indicating that rumen protozoa have no ability to biohydrogenate CLA isomers. On the other hand, the concentrations of 10t-18:1, VA, and 18:0 in P-No-AB were greater (P < 0.05) compared with those in P-AB, indicating the role of symbiotic bacteria associated with P-No-AB in biohydrogenating CLA isomers. We concluded that mixed rumen protozoa are capable of synthesizing CLA from LA through isomerization reactions. However, they are incapable of metabolizing CLA further. They are also incapable of vaccenic acid biohydrogenation and/or desaturation.
本研究旨在调查混合瘤胃原虫从亚油酸(LA)和反油酸(VA)合成共轭亚油酸(CLA)的能力。从装有瘤胃瘘管的奶牛收集瘤胃内容物。分离出原虫部分,并用MB9缓冲液洗涤数次,然后重悬于高压灭菌的瘤胃液中。将悬浮液在38.5℃下与底物进行厌氧培养长达18小时,分别添加抗菌剂(P-AB)或不添加抗菌剂(P-No-AB)。P-AB和P-No-AB悬浮液均不能从VA(11t-18:1)产生CLA。亚油酸在P-No-AB中的分解代谢程度比P-AB更大。P-AB从LA合成了不同的CLA异构体。9c11t-CLA占主导地位。早在培养期开始0.1小时,P-AB悬浮液中就发现了最大积累量的9c11t-CLA的37%。P-AB悬浮液中10t12c-CLA的积累量比9c11t-CLA低约10.0倍。与对照组相比,P-AB中VA、10t-18:1和18:0的产生量无显著差异,表明瘤胃原虫没有将CLA异构体进行生物氢化的能力。另一方面,与P-AB相比,P-No-AB中10t-18:1、VA和18:0的浓度更高(P<0.05),表明与P-No-AB相关的共生细菌在CLA异构体生物氢化中的作用。我们得出结论,混合瘤胃原虫能够通过异构化反应从LA合成CLA。然而,它们无法进一步代谢CLA。它们也无法进行反油酸的生物氢化和/或去饱和作用。