COMPATIBLE SOLUTES OF HALOPHILIC EUBACTERIA - MOLECULAR PRINCIPLES, WATER-SOLUTE INTERACTION, STRESS PROTECTION

被引:241
作者
GALINSKI, EA
机构
[1] Institut für Mikrobiologie and Biotechnologie, Rheinische Friedrich-Wilhelms-Universität, Bonn 1, D-5300
来源
EXPERIENTIA | 1993年 / 49卷 / 6-7期
关键词
HALOPHILIC HALOTOLERANT BACTERIA; COMPATIBLE SOLUTE; OSMOLYTE; OSMOADAPTATION; ENZYME STABILIZATION; STRESS PROTECTION; WATER STRUCTURE FORMER; KOSMOTROPIC SOLUTE;
D O I
10.1007/BF01955150
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Compatible solutes are best described as organic osmolytes responsible for osmotic balance and at the same time compatible with the cells' metabolism. A comprehensive survey (using HPLC and NMR methods) on halophilic/halotolerant eubacteria has revealed the full diversity of compatible solutes employed in nature. Molecular principles derived from the spectrum of compounds found in the bacterial world may be summarized as follows. Compatible solutes are polar, highly soluble molecules and uncharged at physiological pH. With the exception of proline (a proteinogenic amino acid) they are characterized as amino acid derivatives of the following types: betaines, ectoines, N-acetylated diamino acids and N-derivatized carboxamides of glutamine. Using near-infrared spectroscopy we have also been able to demonstrate that compatible solutes are strong water-structure formers and as such probably excluded from the hydration shell of proteins. This ''preferential exclusion'' probably explains their function as effective stabilizers of the hydration shell of native proteins (protection against heating freezing and drying). Hence these typical products of halophilic eubacteria have a considerable potential as stabilizing/protecting agents on both molecular and whole-cell level. Thorough understanding of common structural principles and fundamental water-solute interactions will ultimately enable us to design novel highly efficient stress protectants and stabilizers of biomolecules.
引用
收藏
页码:487 / 496
页数:10
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