Kim Y J, Liu R H, Bond D R, Russell J B
Departments of Food Science, Cornell University, Ithaca, New York 14853, USA.
Appl Environ Microbiol. 2000 Dec;66(12):5226-30. doi: 10.1128/AEM.66.12.5226-5230.2000.
Butyrivibrio fibrisolvens A38 inocula were inhibited by as little as 15 microM linoleic acid (LA), but growing cultures tolerated 10-fold more LA before growth was inhibited. Growing cultures did not produce significant amounts of cis-9, trans-11 conjugated linoleic acid (CLA) until the LA concentration was high enough to inhibit biohydrogenation, growth was inhibited, and lysis was enhanced. Washed-cell suspensions that were incubated anaerobically with 350 microM LA converted most of the LA to hydrogenated products, and little CLA was detected. When the washed-cell suspensions were incubated aerobically, biohydrogenation was inhibited, CLA production was at least twofold greater, and CLA persisted. The LA isomerase reaction was very rapid, but the LA isomerase did not recycle like a normal enzyme to catalyze more substrate. Cells that were preincubated with CLA lost their ability to produce more CLA from LA, and the CLA accumulation was directly proportional (r(2) = 0.98) to the initial cell density. Growing cells were as sensitive to CLA as LA, the LA isomerase and reductases of biohydrogenation were linked, and free CLA was not released. Because growing cultures of B. fibrisolvens A38 did not produce significant amounts of CLA until the LA concentration was high, biohydrogenation was arrested, and the cell density had declined, the flow of CLA from the rumen may be due to LA-dependent bacterial inactivation, death, or lysis.
溶纤维丁酸弧菌A38接种物在低至15微摩尔的亚油酸(LA)作用下就会受到抑制,但正在生长的培养物在生长受到抑制之前能够耐受10倍以上的LA。直到LA浓度高到足以抑制生物氢化作用、生长受到抑制且细胞裂解增强时,正在生长的培养物才会产生大量的顺式-9,反式-11共轭亚油酸(CLA)。用350微摩尔LA进行厌氧培养的洗涤细胞悬液将大部分LA转化为氢化产物,检测到的CLA很少。当洗涤细胞悬液进行需氧培养时,生物氢化作用受到抑制,CLA产量至少增加两倍,且CLA持续存在。LA异构酶反应非常迅速,但LA异构酶不像正常酶那样循环以催化更多底物。预先用CLA孵育的细胞失去了从LA产生更多CLA的能力,CLA积累与初始细胞密度直接成正比(r² = 0.98)。正在生长的细胞对CLA和LA一样敏感,生物氢化作用的LA异构酶和还原酶相互关联,且游离CLA不会释放。由于溶纤维丁酸弧菌A38正在生长的培养物直到LA浓度升高、生物氢化作用停止且细胞密度下降时才会产生大量CLA,瘤胃中CLA的产生可能是由于LA依赖的细菌失活、死亡或裂解。