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Review
. 2004 Aug 29;359(1448):1309-20; discussion 1320, 1323-8.
doi: 10.1098/rstb.2004.1494.

The use of gas-phase substrates to study enzyme catalysis at low hydration

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Review

The use of gas-phase substrates to study enzyme catalysis at low hydration

Rachel V Dunn et al. Philos Trans R Soc Lond B Biol Sci. .

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.

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References

    1. Biotechnol Bioeng. 2000 Aug 5;69(3):235-41 - PubMed
    1. Biochemistry. 1999 Aug 3;38(31):9887-98 - PubMed
    1. Biochim Biophys Acta. 2001 Nov 26;1550(1):90-9 - PubMed
    1. Biochim Biophys Acta. 2002 Jan 31;1594(1):150-9 - PubMed
    1. Biotechnol Bioeng. 2002 May 5;78(3):251-6 - PubMed

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