Aguilar P S, Lopez P, de Mendoza D
Instituto de Biología Molecular y Celular de Rosario (IBR) and Departamento de Microbiología, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, 2000-Rosario, Argentina.
J Bacteriol. 1999 Nov;181(22):7028-33. doi: 10.1128/JB.181.22.7028-7033.1999.
The Bacillus subtilis des gene encodes the cold-inducible Delta5 lipid desaturase involved in the formation of unsaturated fatty acids from saturated phospholipid precursors. Here, we describe the expression pattern of the des gene in response to a temperature downshift from 37 to 20 degrees C. We found that the synthesis of des mRNA is undetectable at 37 degrees C but dramatically induced upon the temperature downshift. Decay characteristics of the des transcript as well as the in vivo decay of B. subtilis bulk mRNA were investigated. The results showed that the stability of the des transcript as well as of bulk mRNA lasted substantially longer at 20 degrees C than at 37 degrees C. Functional expression of des at 37 degrees C was achieved by exchanging its promoter with the non-cold shock spac promoter. These data provide the first direct evidence that temperature-mediated control of transcription is the major mechanism regulating the mRNA levels of the B. subtilis desaturase. The present results also demonstrate that the only component of the desaturation system regulated by temperature is the desaturase enzyme.
枯草芽孢杆菌des基因编码参与从饱和磷脂前体形成不饱和脂肪酸的冷诱导Δ5脂质去饱和酶。在此,我们描述了des基因在温度从37℃降至20℃时的表达模式。我们发现,在37℃时检测不到des mRNA的合成,但在温度下降时会显著诱导。研究了des转录本的衰变特征以及枯草芽孢杆菌总mRNA的体内衰变。结果表明,des转录本以及总mRNA的稳定性在20℃时比在37℃时持续长得多。通过将其启动子与非冷休克spac启动子交换,实现了des在37℃时的功能性表达。这些数据提供了首个直接证据,即温度介导的转录调控是调节枯草芽孢杆菌去饱和酶mRNA水平的主要机制。目前的结果还表明,去饱和系统中受温度调节的唯一成分是去饱和酶。