%0 Journal Article
%T Extraction of lipase from Burkholderia cepacia by PEG/Phosphate ATPS and its biochemical characterization
%A Padilha
%A Giovana da Silva
%A Santana
%A Jos¨¦ Carlos Curvelo
%A Alegre
%A Ranulfo Monte
%A Tambourgi
%A Elias Basile
%J Brazilian Archives of Biology and Technology
%D 2012
%I Tecpar
%R 10.1590/S1516-89132012000100002
%X this work aimed to study the partitioning of a lipase produced by burkholderia cepacia in peg/phosphate aqueous two phase system (atps) and its characterization. lipase was produced by b. cepacia strains in a fermenter. enzyme partitioning occurred at ph 6.0 and 8.0, using peg 1500 and 6000 on two tie lines. metal ions, ph and temperature effects on enzyme activity were evaluated. five milliliter of 7.5% olive oil emulsion with 2.5% gumarabic in 0.1m sodium phosphate buffer at ph 8.0 and 37oc were used for the activity determinations. results showed that crude stratum from b. cepacia was partitioned by peg1500/phosphate atps at ph 6.0 or 8.0 for, which the partitioning coefficients were 108-and 209-folds. lipase presented optimal activity conditions at 37oc and ph 8.0; it showed ph-stability for 4 h of incubation at different ph values at 37oc. metal ions such as mn2+ , co2+, i-and ca2+ sustained enzymatic activities; however, it was inhibited by the presence of fe2+, hg2+ and al3+ . km and vmax values were 0.258 u/mg and 43.90 g/l, respectively. a molecular weight of 33 kda and an isoelectric point at ph 5.0 were determined by sds-page and ifs electrophoresis, respectively.
%K lipase
%K burkholderia cepacia
%K aqueous two phase system
%K partitioning
%K characterization.
%U http://www.scielo.br/scielo.php?script=sci_abstract&pid=S1516-89132012000100002&lng=en&nrm=iso&tlng=en