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Under the optimized conditions the twenty D. hansenii isolates showed increased lipase activity fluctuating between 6.00 and 7.44 U/mL.
According to Abramic et al. 10 mM of Ca2+ slightly increased lipase activity of Streptomyces rimosus while Cu2+ at this concentration slightly reduced its lipase activity.
Increased lipase activity in Mtb-infected macrophages was confirmed by high performance liquid chromatography and mass spectroscopy (HPLC/MS).
Increased lipase activity may be due to enhanced FGF21 signaling.
We therefore, hypothesized that increased lipase activity in MCD-fed ob/ob mice may be due to increased FGF21 signaling.
Enhanced FGF21 signaling and its influence on adipose depots may partly be responsible for increased lipase activity in adipose depots.
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MCD model of NASH increases lipase activity in WAT as a critical determinant of hepatic FA flux and lipotoxicity.
Immersion of lipases in t-butanol and other alcohols with a carbon number of more than three was claimed as a pretreatment method to increase lipase activity in synthesis of methyl esters [ 34, 35].
We have earlier shown that short-term MCD feeding or cancer-induced cachexia increases lipase activity and causes WAT loss in WT and HSL-KO mice and that ATGL-KO mice are partially protected from WAT loss [3,43].
Besides that, 0.01%% of Triton X-100 and 0.1%% of Tween 20 and Tween 80 increased lipase depolymerizing activity of lipase from M. javanicus while others inhibited its lipase activity.
When the incubation temperature was increased, lipase production, specific activity, and cell growth also increased up to 27.5°C.
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