Answers are grounded in this paper and cite their sources.
The stereochemistry of the hydrolysis of radioactive glyceryl trioleate and glyceryl diether-monoesters by lipase activity in post-heparin plasma from man, normal and hepatectomized rats, and rat liver perfusate was determined. The following substrates were chemically synthesized and employed in albumin-Triton X-100 emulsions: 1,2-dioleoyl-3-[9,10-3H]oleoyl-sn-glycerol; 1,3-dioleoyl-2-[1-14C]oleoyl-sn-glycerol; rac-1,2-octadecenyl-3-[9,10-3H]oleoyl-sn-glycerol; 2,3-octadecenyl-1-[9,10-3H]oleoyl-sn-glycerol; and 1,3-octadecenyl-2-[9,10-3H]oleoyl-sn-glycerol. The yields of free fatty acid and glycerol varied with different enzyme sources. Km values were determined. Lipases in post-heparin plasma of hepatic and extrahepatic origins attack preferentially positions 1 and 3 in sn-glycerides and do not appear to distinguish between them. The presence in plasma of monoglyceride hydrolase activity that is primarily derived from the liver was confirmed.
No takes yet. Share an insight, caveat, or question.
Assmann et al. (1973) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: