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脂肪酰基辅酶A的物理性质。临界胶束浓度以及胶束的大小和形状。

Physical properties of fatty acyl-CoA. Critical micelle concentrations and micellar size and shape.

作者信息

Constantinides P P, Steim J M

出版信息

J Biol Chem. 1985 Jun 25;260(12):7573-80.

PMID:3997889
Abstract

Critical micelle concentrations (CMCs) of palmitoyl-CoA were determined by surface tension, conductivity, and fluorimetric measurements in a variety of buffers at several pH values and ionic strengths. They ranged from 7 to 250 microM and were frequently an order of magnitude higher than most reported values. The CMCs of stearoyl-CoA and oleoyl-CoA, determined fluorimetrically, were also high and consistent with the expected effects of chain length and unsaturation. The effects of ionic strength and temperature were analyzed to obtain the extent of counterion binding and the thermodynamic parameters of micellization. The values of delta H0, delta G0, and delta S0 obtained in 0.011 M Tris, pH 8.3, are -6 K X J X mol-1, -64 K X J X mol-1, and +193 J X mol-1 X K-1, and the average number of univalent ions bound per molecule in the micelles is 1.4. These values are within the range of those obtained for other univalent and polyvalent detergents. Analyzed by sedimentation and diffusion, the micelles are approximately spherical with an anhydrous mass of 50,000 daltons but with dimensions inconsistent with fully extended molecules. Correlation of the information obtained from the present physical studies with kinetic studies using long-chain fatty acyl-CoAs as enzyme substrates may be helpful for understanding the enzymology of these compounds, and some previously published kinetic studies of membrane-bound and soluble enzymes may bear reinterpretation.

摘要

在多种不同pH值和离子强度的缓冲液中,通过表面张力、电导率和荧光测量法测定了棕榈酰辅酶A的临界胶束浓度(CMC)。其范围为7至250微摩尔,且通常比大多数报道值高一个数量级。通过荧光法测定的硬脂酰辅酶A和油酰辅酶A的CMC也很高,与链长和不饱和度的预期影响一致。分析了离子强度和温度的影响,以获得反离子结合程度和胶束化的热力学参数。在0.011 M Tris(pH 8.3)中获得的ΔH0、ΔG0和ΔS0值分别为-6 K·J·mol-1、-64 K·J·mol-1和+193 J·mol-1·K-1,每个胶束分子结合的单价离子平均数量为1.4。这些值在其他单价和多价洗涤剂所获得的值的范围内。通过沉降和扩散分析,胶束近似球形,无水质量为50,000道尔顿,但尺寸与完全伸展的分子不一致。将目前物理研究获得的信息与使用长链脂肪酰辅酶A作为酶底物的动力学研究相关联,可能有助于理解这些化合物的酶学,并且一些先前发表的关于膜结合酶和可溶性酶的动力学研究可能需要重新解释。

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