To assess the applicability of latex cell coatings as an ?off-the-shelf? biocatalyst, the effect of osmoprotectants, temperature, humidity and O<
sub>
2<
/sub>
on preservation of H<
sub>
2<
/sub>
production in Rhodopseudomonas palustris coatings was evaluated. Immediately following latex coating coalescence (24 h) and for up to 2 weeks of dry storage, rehydrated coatings containing different osmoprotectants displayed similar rates of H<
sub>
2<
/sub>
production. Beyond 2 weeks of storage, sorbitol-treated coatings lost all H<
sub>
2<
/sub>
production activity, whereas considerable H<
sub>
2<
/sub>
production was still detected in sucrose- and trehalose-stabilized coatings. We stored the coatings at a relative humidity level which significantly impacts the recovery and subsequent rates of H<
sub>
2<
/sub>
production. After 4 weeks storage under air at 60% humidity, coatings produced only trace amounts of H<
sub>
2<
/sub>
(0?0.1% headspace accumulation), whereas those stored at <
5% humidity retained 27?53% of their H<
sub>
2<
/sub>
production activity after 8 weeks of storage. Furthermore, when stored in argon at <
5% humidity and room temperature, R. palustris coatings retained full H<
sub>
2<
/sub>
production activity for 3 months, implicating oxidative damage as a key factor limiting coating storage. Ultimately, the results demonstrate that biocatalytic latex coatings are an attractive cell immobilization platform for preservation of bioactivity in the dry state.