Sargent M G
J Bacteriol. 1973 Oct;116(1):397-409. doi: 10.1128/jb.116.1.397-409.1973.
Synthesis of bacterial membranes has been investigated in Bacillus subtilis by examining incorporation of amino acids and glycerol into the protein and lipid of membranes of synchronous cultures. A simple reproducible fractionation scheme divides cellular proteins into three classes (i) truly cytoplasmic, (ii) loosely membrane bound, released by chelating agents, and (iii) tightly membrane bound. These comprise approximately 75, 10, and 15%, respectively, of cellular proteins in this organism. Incorporation of radioactivity into these fractions, using steady-state and pulse labeling has been followed during the cell cycle. Cytoplasmic proteins and the loosely membrane-bound proteins are labeled at an exponential rate throughout the cell cycle. The membrane fraction is labeled discontinuously in the cell cycle, with periods of rapid synthesis over the latter part of the cycle and a period with no net synthesis during the early part of the cycle. Pulse labeling indicates that synthesis of membrane occurs at a linear rate that doubles at a fixed time in each cycle, which coincides with the period of zero net synthesis. Rates of membrane synthesis measured by pulse labeling during the period of rapid membrane synthesis are significantly less than indicated by steady-state labeling. These discrepancies are consistent with the hypothesis that during the cell cycle certain proteins are added to the membrane from the cytoplasm and that during the period of zero net synthesis there is an efflux of proteins from the membrane. Evidence in favor of this has been presented. The activity of succinic dehydrogenase (a representative of class c) varies in a step-wise manner with periods of rapid increase, approximately coincident with bursts of membrane protein synthesis, alternating with periods without any increase in activity. The activities of malate dehydrogenase (class a) and reduced nicotinamide adenine dinucleotide dehydrogenase (class b) increased throughout the cell cycle. Phospholipid synthesis is continuous throughout the cell cycle.
通过检测同步培养物中氨基酸和甘油掺入细胞膜的蛋白质和脂质中,对枯草芽孢杆菌的细菌膜合成进行了研究。一种简单且可重复的分级分离方案将细胞蛋白质分为三类:(i)真正的细胞质蛋白,(ii)通过螯合剂释放的松散膜结合蛋白,以及(iii)紧密膜结合蛋白。在这种生物体中,这些蛋白分别约占细胞蛋白质的75%、10%和15%。在细胞周期中,利用稳态标记和脉冲标记追踪放射性掺入这些组分的情况。细胞质蛋白和松散膜结合蛋白在整个细胞周期中以指数速率被标记。膜组分在细胞周期中是间断标记的,在周期后期有快速合成期,而在周期早期有净合成零期。脉冲标记表明膜合成以线性速率进行,在每个周期的固定时间翻倍,这与净合成零期一致。在膜快速合成期通过脉冲标记测量的膜合成速率明显低于稳态标记所示的速率。这些差异与以下假设一致:在细胞周期中,某些蛋白质从细胞质添加到膜中,并且在净合成零期,有蛋白质从膜中流出。支持这一观点的证据已经给出。琥珀酸脱氢酶(c类的代表)的活性呈逐步变化,有快速增加期,大约与膜蛋白合成爆发同时发生,与无活性增加期交替出现。苹果酸脱氢酶(a类)和还原型烟酰胺腺嘌呤二核苷酸脱氢酶(b类)的活性在整个细胞周期中增加。磷脂合成在整个细胞周期中是连续的。