Weiss S L, Lee E A, Diamond J
Physiology Department, University of California Medical School, Los Angeles, CA 90095-1751, USA.
Proc Natl Acad Sci U S A. 1998 Mar 3;95(5):2117-21. doi: 10.1073/pnas.95.5.2117.
Safety factors of enzymes and transporters are defined as the ratio of Vmax (maximal reaction rates at high substrate concentrations) to the reaction rate under actual physiological conditions. Although corresponding safety factors have been measured for macroscopic biological structures and for human-engineered structures, safety factors have been little studied at the molecular level. Some evolutionary considerations suggest that safety factors should be modestly in excess of 1.0 ("enough but not too much") and should tend to be similar for the various steps of a pathway consisting of two or more elements arranged in series. Hence we used a preparation of intact mouse small intestine to measure Vmax values (capacities) of brush-border sucrase (yielding glucose plus fructose) and of the brush-border glucose transporter, for comparison with each other and with dietary sucrose loads. Load was manipulated by varying dietary sucrose level or by studying lactating mice with increased energy requirements. Capacities both of sucrase and the glucose transporter increased with sucrose load (i.e., both proteins are inducible) and remained approximately matched to each other except on a carbohydrate-free diet. Their safety factors decreased from ca. 2.7 at low load to 1.0 at high load. Thus, neither sucrase nor the glucose transporter is the rate-limiting step for sucrose digestion; both steps are equally limiting. The modest safety factors and matched capacities must be genetically programmed through natural selection, with benefits of excess capacities being balanced against costs of biosynthetic energy and limited membrane space.
酶和转运蛋白的安全系数定义为Vmax(高底物浓度下的最大反应速率)与实际生理条件下反应速率的比值。尽管已经针对宏观生物结构和人工构建结构测量了相应的安全系数,但在分子水平上对安全系数的研究却很少。一些进化方面的考虑表明,安全系数应略高于1.0(“足够但不过多”),并且对于由两个或更多个串联排列的元件组成的途径的各个步骤而言,安全系数应趋于相似。因此,我们使用完整的小鼠小肠制剂来测量刷状缘蔗糖酶(产生葡萄糖加果糖)和刷状缘葡萄糖转运蛋白的Vmax值(容量),以便相互比较并与膳食蔗糖负荷进行比较。通过改变膳食蔗糖水平或研究能量需求增加的哺乳期小鼠来控制负荷。蔗糖酶和葡萄糖转运蛋白的容量均随蔗糖负荷增加(即两种蛋白质都是可诱导的),并且除了无碳水化合物饮食外,它们大致保持相互匹配。它们的安全系数从低负荷时的约2.7降至高负荷时的1.0。因此,蔗糖酶和葡萄糖转运蛋白都不是蔗糖消化的限速步骤;两个步骤的限制程度相同。适度的安全系数和匹配的容量必须通过自然选择进行基因编程,过量容量的益处与生物合成能量成本和有限膜空间成本相平衡。