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一种计算大肠杆菌K-12在琥珀酸上生长热的替代方法。

An alternate method of calculating the heat of growth of Escherichia coli K-12 on succinic acid.

作者信息

Battley E H

机构信息

Department of Ecology and Evolution, State University of New York at Stony Brook, Stony Brook, New York 11794-5345, USA.

出版信息

Biotechnol Bioeng. 1991 Aug 20;38(5):480-92. doi: 10.1002/bit.260380506.

Abstract

The DeltaH(f)(0) unit weight of a complex substance such as a biological macromolecule is almost always obtained by means of combustion analysis. In theory, this can also be done by summing the DeltaH(f)(0) values for the monomers comprising the macromolecule plus the enthalpic energies involved in their polymerization. The enthalpy of formation of one unit-carbon formula weight of dried Escherichia coli K-12 cells was determined by summing the values of the enthalpies of formation of the quantities of monomers in the major classes of macromolecules substances comprising the cellular biomass and the enthalpic energies involved in their polymerizations. To this value was added the enthalpy of formation of the cellular ions in their aqueous standard states, per unit-carbon formula weight of cellular substance and the enthalpy change with respect to the ionization of the protein amino acid side chains. If it is assumed that the cellular fabric is insoluble and that the ions are soluble, the sum of the enthalpies of formation of all the cellular components should closely approximate the enthalpy of formation of one unit-carbon formula weight equivalent of living cells. Using this value, a calculation of the enthalpy change accompanying anabolism shows this latter to be effectively zero, indicating that the heat of growth (anabolism plus catabolism) is equal to that calculated for catabolism alone. This conclusion is in accord with those of several investigators who have used manometry or direct calorimetry.

摘要

诸如生物大分子这样的复杂物质的标准生成焓(ΔH(f)(0))单位重量几乎总是通过燃烧分析来获得。理论上,这也可以通过将构成大分子的单体的标准生成焓(ΔH(f)(0))值与它们聚合过程中涉及的焓能相加来完成。通过将构成细胞生物质的主要大分子物质类别中单体数量的生成焓值与它们聚合过程中涉及的焓能相加,确定了每单位碳分子式重量的干燥大肠杆菌K - 12细胞的生成焓。对于每单位碳分子式重量的细胞物质,向该值中加入细胞离子在其水标准状态下的生成焓以及蛋白质氨基酸侧链电离的焓变。如果假设细胞结构是不溶性的且离子是可溶性的,那么所有细胞成分的生成焓之和应非常接近相当于一个单位碳分子式重量活细胞的生成焓。使用该值,对合成代谢伴随的焓变进行计算表明,后者实际上为零,这表明生长热(合成代谢加分解代谢)等于仅针对分解代谢计算出的热量。这一结论与几位使用测压法或直接量热法的研究者的结论一致。

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