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Partial inhibition of biohydrogenation of linoleic acid can increase the conjugated linoleic acid production of Butyrivibrio fibrisolvens A38

机译:亚油酸生物氢化的部分抑制作用可以增加纤维溶丁酸杆菌A38的共轭亚油酸产量

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Butyrivibrio, fibrisolvens A38, one of the most active rumen bacteria in conjugated linoleic acid (CLA) production, was characterized in vitro. Previous findings that some inhibitory levels of substrate for biohydrogenation (BH) by B. fibrisolvens A38 resulted in more CLA accumulation led to a prediction that partial inhibition of BH could increase ruminal CLA production. The inhibitory conditions for bacterial growth were less effective on the isomerization step than on the following reduction step. Linoleic acid (LA) was inhibitory not only to cell growth but also to LA hydrogenation, and this effect was greater at high concentrations. The reduction step, converting CLA to hydrogenated products (trans-C18:1 and C18:0), was significantly inhibited, and more CLA accumulated during aerobic incubation when LA was added along with a glycolytic inhibitor, iodoacetate (IAA), to cells that were pre-adapted to LA (1 g/OD at 600 nm/L, P < 0.05). Monensin was more inhibitory than IAA to cell growth but less effective for CLA accumulation. Rumen fluid in the culture medium appeared to activate BH even in an aerobic condition, resulting in a lower CLA level than the control group (P < 0.05). Because the isomerization and reduction steps are coupled reactions in BH of most hydrogenating bacteria including B. fibrisolvens A38 cells, both positive and negative modulations of the reduction steps could be key determinants for CLA accumulation in the rumen. [References: 18]
机译:在体外对Butyrivibrio纤溶蛋白A38(共轭亚油酸(CLA)生产中最活跃的瘤胃细菌之一)进行了表征。以前的发现,即纤维状芽孢杆菌A38对生物氢化(BH)的底物的某些抑制水平导致更多的CLA积累,导致了对BH的部分抑制可以增加瘤胃CLA产生的预测。细菌生长的抑制条件在异构化步骤上比在随后的还原步骤上更不起作用。亚油酸(LA)不仅抑制细胞生长,而且抑制LA氢化,在高浓度下这种作用更大。将LA与糖酵解抑制剂碘乙酸盐(IAA)一起添加时,在将CLA转化为氢化产物(trans-C18:1和C18:0)的还原步骤受到了显着抑制,并且在有氧培养过程中积累了更多的CLA。预先适应于LA(1 g / OD在600 nm / L,P <0.05)。莫能菌素对细胞生长的抑制作用大于IAA,但对CLA积累的抑制作用较小。即使在有氧条件下,培养基中的瘤胃液似乎也能激活BH,导致CLA水平低于对照组(P <0.05)。因为异构化和还原步骤是大多数氢化细菌(包括纤溶双歧杆菌A38细胞)在BH中的偶联反应,所以还原步骤的正向和负向调节都可能是瘤胃中CLA积累的关键决定因素。 [参考:18]

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