Enzymes sterol ester hydrolase

The luminal requirements for bile salts are general, and do not adequately describe the known specifity for cholate and its conjugates which has been demonstrated in several species including man. This specifity appears to be a function, at least in part, of a cholic acid - dependent enzyme, sterol ester hydrolase (cholesterol esterase). 

Fig. 8. A schematic diagram showing cellular processes known to require SCP2. The reactions in cholesterol biosynthesis and esterification have been shown for liver. The reactions involving cholesterol transport from cytoplasmic lipid inclusion droplets to mitochondria have been demonstrated in endocrine tissues. Choi and C. cholesterol ACAT, acyl-CoA cholesterol acyl transferase C.E., cholesterol ester SEH, sterol ester hydrolase (hormone-dependent) P-450s,, cytochrome P-450 cholesterol side-chain cleavage enzyme PREG, pregnenolone.

Finally it is clear that, unlike long-chain fatty acids which can appear in portal blood in limited amounts[32], cholesterol is absorbed exclusively into the lymphatic circulation[32,33]. A small amount of unesterified cholesterol can appear in lymph and is largely associated with chylomicron and lipoprotein "coat , or limiting membrane. However, this coat has a limited capability for significant transport, and the mass transport cholesterol (like that of triglycerides) requires esterification and incorporation into the lipoprotein core. Thus, the transfer of significant amounts of cholesterol from intestinal lumen to l3onph is associated with extensive esterification (70-90%) with fatty acids, and this occurs in the mucosal epithelial cells[11]. There are two intestinal enzymes potentially important in the esterification of unesterified cholesterol cholesterol esterase, or sterol ester hydrolase (EC. 

Of the two potentially esterifying enzymes associated with intestinal mucosa, sterol ester hydrolase, also referred to as cholesterol esterase (CE ase) has been extensively investigated in... 

The overall metabolism of vitamin A in the body is regulated by esterases. Dietary retinyl esters are hydrolyzed enzymatically in the intestinal lumen, and free retinol enters the enterocyte, where it is re-esterified. The resulting esters are then packed into chylomicrons delivered via the lymphatic system to the liver, where they are again hydrolyzed and re-esterified for storage. Prior to mobilization from the liver, the retinyl esters are hydrolyzed, and free retinol is complexed with the retinol-binding protein for secretion from the liver [101]. Different esterases are involved in this sequence. Hydrolysis of dietary retinyl esters in the lumen is catalyzed by pancreatic sterol esterase (steryl-ester acylhydrolase, cholesterol esterase, EC 3.1.1.13) [102], A bile salt independent retinyl-palmitate esterase (EC 3.1.1.21) located in the liver cell plasma hydrolyzes retinyl esters delivered to the liver by chylomicrons. Another neutral retinyl ester hydrolase has been found in the nuclear and cytosolic fractions of liver homogenates. This enzyme is stimulated by bile salts and has properties nearly identical to those observed for... 

Cholesteryl esters that are internalized via the LDL receptor are hydrolyzed to produce cholesterol and an acyl chain. Cholesterol, in (urn, activates the enzyme acyl-CoA cholesterol acyl-transferase (ACAT) which re-esterifies cholesterol. In an apparently futile cycle, the cholesteryl esters are hydrolyzed by cholesteryl ester hydrolase. The cholesterol moiety has several fates it may leave the cell and bind to an acceptor such as high-density lipoprotein (HDL), it may be converted to steroid hormones, or it may be reesterified by ACAT. When the cellular cholesterol concentration falls, the activity of HMG-CoA reductase is increased, as is the number of LDL receptors, which results in an increase of cellular cholesterol, due both to de novo synthesis and to the uptake of cholesterol-rich lipoproteins in the circulation. An increase in cellular cholesterol results in the rapid decline in the mRNA levels for both HMG-CoA reductase and the LDL receptor. This coordinated regulation is brought about by the presence of an eight nucleotide sequence on the genes which code for both proteins this is termed the sterol regulatory element-1. 

Methods have been published that allow the classification of two types of esterases, the carboxylic ester hydrolases (CEHs) and the phosphoric triester hydrolases (PTEHs) (Anspaugh and Roe, 2004). The CEHs contain the B-esterases, which are inhibited by organophosphates. B-esierases include many other esterases, such as CarbE, acetylcholinesterase (AChE), cholinesterases (ChE), aryleslerases, sterol esterases, insect juvenile hormone esterases, aixl others. The determination of A-esterases uses a protocol for the detection of PTEHs. The PTEH assay allows for the identification of two subclasses of esterases, the A-esterase (known as aiyldialkylphos-phatase) and ditsopropyl fluorophosphatase. Both these enzymes metabolize OP compounds. 

A carboxylesterase (EC 3.1.1.1) from T. fusca [8, 86] and a steryl esterase (EC 3.1.1.13) from Melanocarpus albomyces [59] have also shown activity with PET oligomers and fabrics. The enzyme from M. albomyces with high specificity for fatty acid esters of sterols increased the hydrophilicity of PET fabrics. The highly hydrophobic serine hydrolase from T. fusca with a catalytic triad composed of serine, glutamic acid, and histidine hydrolyzed CTR and PET nanoparticles. The esterase showed high specificity towards short and middle chain-length fatty acyl esters of p-nitrophenol. In addition, p-nitrobenzyl esterases from Bacillus subtilis and B. licheniformis that hydrolyzed short chain dialkylphthalates and PET nanoparticles have been reported [74, 87]. 

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