The use of gas-phase substrates to study enzyme catalysis at low hydration
- PMID: 15306385
- PMCID: PMC1693412
- DOI: 10.1098/rstb.2004.1494
The use of gas-phase substrates to study enzyme catalysis at low hydration
Abstract
Although there are varying estimates as to the degree of enzyme hydration required for activity, a threshold value of ca. 0.2 g of water per gram of protein has been widely accepted. The evidence upon which this is based is reviewed here. In particular, results from the use of gas-phase substrates are discussed. Results using solid-phase enzyme-substrate mixtures are not altogether in accord with those obtained using gas-phase substrates. The use of gaseous substrates and products provides an experimental system in which the hydration of the enzyme can be easily controlled, but which is not limited by diffusion. All the results show that increasing hydration enhances activity. The results using gas-phase substrates do not support the existence of a critical hydration value below which enzymatic activity is absent, and suggest that enzyme activity is possible at much lower hydrations than previously thought; they do not support the notion that significant hydration of the surface polar groups is required for activity. However, the marked improvement of activity as hydration is increased suggests that water does play a role, perhaps in optimizing the structure or facilitating the flexibility required for maximal activity.
Similar articles
-
Lipase hydration state in the gas phase: sorption isotherm measurements and inverse gas chromatography.Biotechnol J. 2010 Nov;5(11):1216-25. doi: 10.1002/biot.201000272. Biotechnol J. 2010. PMID: 21058322
-
Enzymatic oxidation of ethanol in the gaseous phase.Biotechnol Bioeng. 1989 Nov;34(9):1178-85. doi: 10.1002/bit.260340908. Biotechnol Bioeng. 1989. PMID: 18588215
-
Enzymatic dehalogenation of gas phase substrates with haloalkane dehalogenase.Biotechnol Bioeng. 2000 Aug 5;69(3):235-41. Biotechnol Bioeng. 2000. PMID: 10861403
-
Gold catalysts for pure hydrogen production in the water-gas shift reaction: activity, structure and reaction mechanism.Phys Chem Chem Phys. 2006 Dec 21;8(47):5483-500. doi: 10.1039/b607837k. Epub 2006 Oct 2. Phys Chem Chem Phys. 2006. PMID: 17136264 Review.
-
Characteristics of nearly dry enzymes in organic solvents: implications for biocatalysis in the absence of water.Philos Trans R Soc Lond B Biol Sci. 2004 Aug 29;359(1448):1299-307; discussion 1307, 1323-8. doi: 10.1098/rstb.2004.1506. Philos Trans R Soc Lond B Biol Sci. 2004. PMID: 15306384 Free PMC article. Review.
Cited by
-
Enzyme activity and flexibility at very low hydration.Biophys J. 2005 Aug;89(2):1282-7. doi: 10.1529/biophysj.104.058677. Epub 2005 May 13. Biophys J. 2005. PMID: 15894640 Free PMC article.
-
Lone pair ... pi interactions between water oxygens and aromatic residues: quantum chemical studies based on high-resolution protein structures and model compounds.Protein Sci. 2009 Mar;18(3):595-605. doi: 10.1002/pro.67. Protein Sci. 2009. PMID: 19241386 Free PMC article.
-
What can we learn by studying enzymes in non-aqueous media?Philos Trans R Soc Lond B Biol Sci. 2004 Aug 29;359(1448):1287-96; discussion 1296-7, 1323-8. doi: 10.1098/rstb.2004.1505. Philos Trans R Soc Lond B Biol Sci. 2004. PMID: 15306383 Free PMC article. Review.
-
The role of water mobility on water-responsive actuation of silk.Nat Commun. 2024 Sep 27;15(1):8287. doi: 10.1038/s41467-024-52715-6. Nat Commun. 2024. PMID: 39333569 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources