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Conversion of l-Leucine to Isovaleric Acid by Propionibacterium freudenreichii TL 34 and ITGP23

机译:费氏丙酸杆菌TL 34和ITGP23将L-亮氨酸转化为异戊酸

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摘要

Several branched-chain volatile compounds are involved in the flavor of Swiss cheese. These compounds are probably produced by enzymatic conversion of branched-chain amino acids, but the flora and the pathways involved remain hypothetical. Our aim was to determine the ability of Propionibacterium freudenreichii, which is one of the main components of the secondary flora of Swiss cheese, to produce flavor compounds during leucine catabolism. Cell extracts and resting cells of two strains were incubated in the presence of l-leucine, α-ketoglutaric acid, and cofactors, and the metabolites produced were determined by high-performance liquid chromatography and gas chromatography. The first step of leucine catabolism was a transamination that produced α-ketoisocaproic acid, which was enzymatically converted to isovaleric acid. Both reactions were faster at pH 8.0 than at acidic pHs. Cell extracts catalyzed only the transamination step under our experimental conditions. Small amounts of 3-methylbutanol were also produced by resting cells, but neither 3-methylbutanal norα-hydroxyisocaproic acid was detected. l-Isoleucine and l-valine were also converted to the corresponding acids and alcohols. Isovaleric acid was produced by both strains during growth in a complex medium, even under conditions simulating Swiss cheese conditions (2.1% NaCl, pH 5.4, 24°C). Our results show that P. frendenreichii could play a significant role in the formation of isovaleric acid during ripening.
机译:几种支链挥发性化合物与瑞士奶酪的风味有关。这些化合物可能是通过支链氨基酸的酶促转化产生的,但其菌群和涉及的途径仍然是假设的。我们的目标是确定弗氏丙酸杆菌(这是瑞士奶酪的次级菌群的主要成分之一)在亮氨酸分解代谢过程中产生风味化合物的能力。在1-亮氨酸,α-酮戊二酸和辅因子的存在下孵育两个菌株的细胞提取物和静息细胞,并通过高效液相色谱和气相色谱法测定产生的代谢产物。亮氨酸分解代谢的第一步是产生氨基α-酮异己酸的氨基转移反应,然后将其酶促转化为异戊酸。在pH 8.0时,两个反应都比在酸性pH时更快。在我们的实验条件下,细胞提取物仅催化转氨步骤。静止细胞也产生少量的3-甲基丁醇,但未检测到3-甲基丁醛或α-羟基异己酸。 1-异亮氨酸和1-缬氨酸也被转化为相应的酸和醇。即使在模拟瑞士干酪条件(2.1%NaCl,pH 5.4、24°C)的条件下,两种菌株在复杂培养基中生长期间也会产生异戊酸。我们的结果表明,P。frendenreichii可在成熟过程中在异戊酸的形成中发挥重要作用。

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