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Precursor and temperature modulation of fatty acid composition and growth of Listeria monocytogenes cold-sensitive mutants with transposon-interrupted branched-chain α-keto acid dehydrogenase

机译:脂肪酸组成的前体和温度调节及李斯特菌单核细胞增生的生长冷敏突变体具有转座子中断的支链α-酮酸脱氢酶的冷敏突变体

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Branched-chain fatty acids (BCFAs) typically constitute more than 90?% of the fatty acids of Listeria monocytogenes. The authors have previously described two Tn917-induced, cold-sensitive, BCFA-deficient (40?%) L. monocytogenes mutants (cld-1 and cld-2) with lowered membrane fluidity. Sequence analyses revealed that Tn917 was inserted into different genes of the branched-chain α-keto acid dehydrogenase cluster (bkd) in these two mutants. The cold-sensitivity and BCFA deficiency of cld-1, in which Tn917 was inserted into bkdB, were complemented in trans by cloned bkdB. The growth and corresponding BCFA content of the mutants at 37?°C were stimulated by fatty acid precursors bypassing Bkd, 2-methylbutyrate (precursor for odd-numbered anteiso-fatty acids), isobutyrate (precursor for even-numbered iso-fatty acids) and isovalerate (precursor for odd-numbered iso-fatty acids). In contrast, the corresponding Bkd substrates, α-ketomethylvalerate, α-ketoisovalerate and α-ketoisocaproate, exhibited much poorer activity. At 26?°C, 2-methylbutyrate and isovalerate stimulated the growth of the mutants, and at 10?°C, only 2-methylbutyrate stimulated growth. Pyruvate depressed the BCFA content of cld-2 from 33?% to 27?%, which may be close to the minimum BCFA requirement for L. monocytogenes. The transcription of bkd was enhanced by Bkd substrates, but not by low temperature. When provided with the BCFA precursors, cld-2 was able to increase its anteiso-C15?:?0 fatty acid content at 10?°C compared to 37?°C, which is the characteristic response of L. monocytogenes to low temperature. This implies that Bkd is not the major cold-regulation point of BCFA synthesis.
机译:分枝链脂肪酸(BCFA)通常构成李斯特菌单核细胞增生的脂肪酸的大于90℃。作者以前描述了两种TN917诱导的,冷敏感的BCFA缺陷(<40×%)L.单核细胞元突变体(CLD-1和CLD-2),具有降低的膜流动性。序列分析显示,在这两个突变体中插入支链α-酮酸脱氢酶簇(BKD)的不同基因中。 CLD-1的冷灵敏度和BCFA缺乏,其中将TN917插入BKDB中,通过克隆的BKDB互补。通过绕过BKD,2-甲基丁酸酯(前体为奇数甲基脂肪酸的前体),异丁酸酯(偶数异脂肪酸前体)刺激37Ω·℃的生长和相应的BCFA含量并异维(奇数异脂肪酸的前体)。相反,相应的BKD底物,α-酮甲基甲基戊烯,α-酮戊酸和α-酮异肽,表现出较差的活性。在26℃,2-甲基丁酸盐和异维刺激突变体的生长,并且在10?℃下,仅为2-甲基丁酯刺激生长。丙酮酸从33〜%至27℃的CLD-2的BCFA含量抑制了CLD-2的BCFA含量,这可能接近L.单核细胞增生的最小BCFA要求。 BKD基材增强BKD的转录,但不通过低温而增强。当随着BCFA前体提供时,CLD-2能够增加其Anteiso-C15?:0脂肪酸含量在10℃下,与37Ω℃相比,这是L.单核细胞生成低温的特征响应。这意味着BKD不是BCFA合成的主要冷凝点。

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