Mechanism steroid biosynthesis

The mechanism by which TBT causes these effects has been extensively stiidied. The androgenic effects of TBT appear to be caused by interference with steroid biosynthesis rather than by mimicking the action of testosterone at the androgen receptor. Exposure of female molluscs to TBT leads to an elevation in testosterone in the haemolymph. " Much of the experimental evidence... 

Enzymes involved in steroid biosynthesis have proved to be good targets, both for therapeutic intervention and for mechanism-based inactivators (2). Aromatase, for example, catalyzes the final, rate-limiting step in estrogen biosynthesis (Equation 17.55). Aromatase has proved susceptible to mechanism-based inhibitors such as formestane and ex-emestane. These are now both used in the treatment of breast cancer (210). 

Comprehensive Biological Catalysis—a Mechanistic Reference Volume has recently been published. The fiiU contents list (approximate number of references in parentheses) is as follows S-adenosylmethionine-dependent methyltransferases (110) prenyl transfer and the enzymes of terpenoid and steroid biosynthesis (330) glycosyl transfer (800) mechanism of folate-requiring enzymes in one-carbon metabohsm (260) hydride and alkyl group shifts in the reactions of aldehydes and ketones (150) phosphoenolpyruvate as an electrophile carboxyvinyl transfer reactions (140) physical organic chemistry of acyl transfer reactions (220) catalytic mechanisms of the aspartic proteinases (90) the serine proteinases (135) cysteine proteinases (350) zinc proteinases (200) esterases and lipases (160) reactions of carbon at the carbon dioxide level of oxidation (390) transfer of the POj group (230) phosphate diesterases and triesterases (160) ribozymes (70) catalysis of tRNA aminoacylation by class I and class II aminoacyl-tRNA synthetases (220) thio-disulfide exchange of divalent sulfirr (150) and sulfotransferases (50). 

The factors leading to isoracemisation can lead to misinterpretation of isotope-ex-change experiments. The lack of exchange of the proton with solvent protons is classical evidence for hydride transfer in the Cannizzaro reaction and Meerwein-Pondorff-Verley reduction and in the rearrangements involved in steroid biosynthesis. For some time the lack of deuterium exchange in the glyoxalase reaction was attributed to a hydride-transfer mechanism (Eqn. 64). 

Originally only compounds with 10 carbon atoms (monoterpenes) were considered as T, and the oxygen-containing T. were classified as camphors. According to the mechanism of biosynthesis, however, all compounds derived from active isoprene are now classified as T. or isoprenes, including steroids, carotenoids, etc. 

Mosbach and colleagues have contributed extensively to a better understanding of the mechanism of biosynthesis of cholestanol. After intracardial administration of mevalonate- C to guinea pigs, radioactive cholestanol was isolated from liver, intestinal wall, and adrenals (117). With rat liver homogenates the incorporation of C-mevalonate or C-cholesteroI into C-cholestanol of the order of 0.05% in 4 hr (118).t The 5a-reductase of rat liver and adrenal localized (119) in the microsomal fraction, was shown to require NADPH, exhibited product inhibition, and was more active in preparations from female than male rats. The enzyme was considered distinct from the Cjg- and C2i-5a reductases, since it was inhibited by Cjg-3-keto-/I steroids. 

We turn now to the biosynthesis of lipid structures. We begin with a discussion of the biosynthesis of fatty acids, stressing the basic pathways, additional means of elongation, mechanisms for the introduction of double bonds, and regulation of fatty acid synthesis. Sections then follow on the biosynthesis of glyc-erophospholipids, sphingolipids, eicosanoids, and cholesterol. The transport of lipids through the body in lipoprotein complexes is described, and the chapter closes with discussions of the biosynthesis of bile salts and steroid hormones. 

In addition, it will be our intention to present a deeper insight into the biosynthesis of steroid hormones, which will allow definition of new targets and approaches for the treatment of endocrine-responsive cancer. Enzymes involved in mechanisms of steroid hormone biosynthesis might be novel targets for endocrine therapy. Moreover, further therapeutic indications for modulators of steroid hormone receptors will be discussed. In summary, many promising new opportunities for endocrine therapy of breast and prostate cancer are now arising. 

The concentration of dolichyl phosphate in eukaryotic tissues is very low and is probably rate-limiting for the glycosylation processes. Variation of the concentration in the endoplasmic-reticulum membranes is a possible way of controlling the rate of glycosylation. It is important to point out that the early steps in the dolichol biosynthesis are common to such other prenyl derivatives in plants as steroids, essential oils, hormones, phytol, and carotenes (see Scheme 1), and parameters affecting those reactions that may control the dolichol to dolichyl phosphate step could be another mechanism for regulation of the level of dolichyl phosphate. 

This chapter examines the biosynthesis of three important components of biological membranes—phospholipids, sphingolipids, and cholesterol (Chapter 12). Triacylglycerols also are considered here because the pathway for their synthesis overlaps that of phospholipids. Cholesterol is of interest both as a membrane component and as a precursor of many signal molecules, including the steroid hormones progesterone, testosterone, estrogen, and cortisol. The biosynthesis of cholesterol exemplifies a fundamental mechanism for the assembly of extended carbon skeletons from five-carbon units. 

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