Purification and Characterization of a Thermostable Lipase from Geobacillus thermodenitrificans IBRL-nra

Abstract EN

Thermostable lipase from Geobacillus thermodenitrificans IBRL-nra was purified and characterized.

The production of thermostable lipase from Geobacillus thermodenitrificans IBRL-nra was carried out in a shake-flask system at 65°C in cultivation medium containing; glucose 1.0% (w/v); yeast extract 1.25% (w/v); NaCl 0.45% (w/v) olive oil 0.1% (v/v) with agitation of 200 rpm for 24 hours.

The extracted extracellular crude thermostable lipase was purified to homogeneity by using ultrafiltration, Heparin-affinity chromatography, and Sephadex G-100 gel-filtration chromatography by 34 times with a final yield of 9%.

The molecular weight of the purified enzyme was estimated to be 30 kDa after SDS-PAGE analysis.

The optimal temperature for thermostable lipase was 65°C and it retained its initial activity for 3 hours.

Thermostable lipase activity was highest at pH 7.0 and stable for 16 hours at this pH at 65°C.

Thermostable lipase showed elevated activity when pretreated with BaCl2, CaCl2, and KCl with 112%, 108%, and 106%, respectively.

Lipase hydrolyzed tripalmitin (C16) and olive oil with optimal activity (100%) compared to other substrates.