首页> 外文期刊>Journal of bacteriology >Energy Requirements for the Transport of Methylthio-β-d-Galactoside by Escherichia coli: Measurement by Microcalorimetry and by Rates of Oxygen Consumption and Carbon Dioxide Production
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Energy Requirements for the Transport of Methylthio-β-d-Galactoside by Escherichia coli: Measurement by Microcalorimetry and by Rates of Oxygen Consumption and Carbon Dioxide Production

机译:大肠杆菌运输甲硫基-β-d-半乳糖苷的能量需求:微量量热法以及耗氧量和二氧化碳产生速率的测量

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The energy cost for maintenance of gradients of methylthio-β-d-galactoside in Escherichia coli was evaluated. Information was also obtained concerning the energy flow associated with gradient establishment under some circumstances. Energy flow was evaluated from transport-induced changes in the rate of heat evolution, oxygen consumption, and carbon dioxide production in metabolically active cells. Heats were measured with an isothermal calorimeter. Energy expenditure behavior was characterized by a transition that depended on the level of accumulation. The data for steady-state maintenance could be rationalized in terms of the Mitchell hypothesis, two models for influx and efflux, and a transition between them. At low levels of uptake, steady-state proton-methylthio-β-d-galactoside (TMG) symport for influx and efflux occurred via a nonenergy-requiring exchange process. The only energy requirement was that necessary to pump back in any TMG exiting via a leakage pathway (model I). Above the transition, all influx occurred with proton symport, but all exit, leak and carrier mediated, occurred without proton symport (model II). The H+/TMG stoichiometric ratio computed for the region of model II applicability (carbon source present, high level of uptake) approached 1. This value agreed with that of other workers for downhill β-galactoside flow, suggesting that the energy cost for both downhill and uphill flow was approximately the same. For low levels of uptake, initial establishment of the gradient was followed by a burst of metabolism that was much larger than that expected on the basis of the chemiosmotic hypothesis. In the absence of carbon source, the stimulation in respiration was sufficient to produce 13 times more protons than are apparently necessary to establish the gradient. The results indicate also that the nature of the biochemical process stimulated by TMG depends on its level of uptake. Insight into several aspects of the nature of these processes was provided through analysis of the heat, oxygen, and CO2 data. The key factor controlling the transition in energy flow behavior is suggested to be rate of flux. The present data suggest that it occurs at a flux of ~120 nmol/min per mg of protein.
机译:评价了维持大肠杆菌中甲硫基-β-d-半乳糖苷梯度所需的能量成本。在某些情况下,还获得了有关与梯度建立相关的能量流的信息。通过运输诱导的代谢活跃细胞中放热,氧气消耗和二氧化碳生成速率的变化来评估能量流。用等温量热仪测量热量。能源消费行为的特征在于依赖于积累水平的转变。可以根据Mitchell假设,流入和流出的两个模型以及它们之间的过渡来合理化用于稳态维护的数据。在低吸收水平下,通过非能量交换过程发生了稳态质子-甲硫基-β-d-半乳糖苷(TMG)的流入和流出共聚。唯一的能源需求是必须抽回通过泄漏途径(模型I)流出的任何TMG。在过渡以上,所有的涌入都与质子同向发生,但是所有的出口,泄漏和载体介导的情况都没有质子同向发生(模型II)。针对II型适用性区域(存在碳源,高吸收水平)计算出的H + / TMG化学计量比接近1。该值与其他工人在下坡β-半乳糖苷流动时的值相同,这表明下坡和上坡流量的能源成本大致相同。对于低水平的摄取,梯度的最初建立是新陈代谢的爆发,其远大于基于化学渗透假说所预期的代谢。在没有碳源的情况下,呼吸刺激足以产生比建立梯度明显所需的质子多13倍的质子。结果还表明,TMG刺激的生化过程的性质取决于其摄取水平。通过对热量,氧气和CO 2 数据的分析,可以深入了解这些过程的本质。建议控制能流行为转变的关键因素是通量率。目前的数据表明,它的发生速度为每毫克蛋白质约120 nmol / min。

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