Structure and function of eukaryotic fatty acid synthases

被引:106
作者
Maier, Timm [1 ]
Leibundgut, Marc [1 ]
Boehringer, Daniel [1 ]
Ban, Nenad [1 ]
机构
[1] Swiss Fed Inst Technol, Inst Mol Biol & Biophys, CH-8093 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
ACYL-CARRIER PROTEIN; CRYSTAL-STRUCTURE; MULTIENZYME COMPLEX; ELECTRON-MICROSCOPY; ACTIVE-SITE; 3-DIMENSIONAL RECONSTRUCTION; CONFORMATIONAL FLEXIBILITY; SYNTHETASE COMPLEX; POLYPEPTIDE-CHAIN; RADIATION-DAMAGE;
D O I
10.1017/S0033583510000156
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In all organisms, fatty acid synthesis is achieved in variations of a common cyclic reaction pathway by stepwise, iterative elongation of precursors with two-carbon extender units. In bacteria, all individual reaction steps are carried out by monofunctional dissociated enzymes, whereas in eukaryotes the fatty acid synthases (FASs) have evolved into large multifunctional enzymes that integrate the whole process of fatty acid synthesis. During the last few years, important advances in understanding the structural and functional organization of eukaryotic FASs have been made through a combination of biochemical, electron microscopic and X-ray crystallographic approaches. They have revealed the strikingly different architectures of the two distinct types of eukaryotic FASs, the fungal and the animal enzyme system. Fungal FAS is a 2.6 MDa alpha(6)beta(6) heterododecamer with a barrel shape enclosing two large chambers, each containing three sets of active sites separated by a central wheel-like structure. It represents a highly specialized micro-compartment strictly optimized for the production of saturated fatty acids. In contrast, the animal FAS is a 540 kDa X-shaped homodimer with two lateral reaction clefts characterized by a modular domain architecture and large extent of conformational flexibility that appears to contribute to catalytic efficiency.
引用
收藏
页码:373 / 422
页数:50
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