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Essential biosynthesis

Normal liver cells are known to perform only functionally essential biosynthesis. The rate of mitoses of these cells is 0.8%. After partial hepatectomy (resection of 2/3 of liver) a sharp intensification of biosynthesis with accelerating cell division takes place. [Pg.90]

The first "statin" was discovered by Endo and coworkers at Sankyo in Tokyo in 1976. After testing over 8,000 microbial extracts, they found a compound, named mevastatin (ML-236B) (Figure 9), from Penicillium citrinum which showed specific inhibition of HMG CoA reductase and functioned in vivo, lowering serum cholesterol levels. Further development of mevastatin was curtailed because inhibition of cholesterol biosynthesis was not restricted to the liver. The compound enters the lens and adrenals, where it blocks the essential biosynthesis of cholesterol. The same compound was also isolated by a team at the Beecham Research Laboratories in Brockham Park, Surrey. Whilst screening for antifungal activity, they isolated the compound, which they named compactin, from Pencillium brevicompactum, but apparently failed to recognise it as a potent inhibitor of HMG CoA reductase. [Pg.81]

Deoxy-2 -fluoromethylene nucleosides are potential inhibitors of ribonucleoside diphosphate reductase (RDPR), which catalyzes the essential biosynthesis path of deoxyri-bonucleoside in the DNA synthesis system. Initial hydrogen abstraction at the C-3 position by tyrosyl radical has been proposed for the RDPR catalysis system (see from 71 to 73 in... [Pg.217]

Prostaglandins arise from unsaturated C20 carboxylic acids such as arachidonic acid (see Table 26 1) Mammals cannot biosynthesize arachidonic acid directly They obtain Imoleic acid (Table 26 1) from vegetable oils m their diet and extend the car bon chain of Imoleic acid from 18 to 20 carbons while introducing two more double bonds Lmoleic acid is said to be an essential fatty acid, forming part of the dietary requirement of mammals Animals fed on diets that are deficient m Imoleic acid grow poorly and suffer a number of other disorders some of which are reversed on feed mg them vegetable oils rich m Imoleic acid and other polyunsaturated fatty acids One function of these substances is to provide the raw materials for prostaglandin biosynthesis... [Pg.1080]

Isotope incorporation experiments have demonstrated the essential correctness of the scheme presented m this and preceding sections for terpene biosynthesis Considerable effort has been expended toward its detailed elaboration because of the common biosyn thetic origin of terpenes and another class of acetate derived natural products the steroids... [Pg.1093]

L Glutamic acid is not an essential ammo acid It need not be present m the diet because animals can biosynthesize it from sources of a ketoglutaric acid It is however a key intermediate m the biosynthesis of other ammo acids by a process known as transamination L Alanine for example is formed from pyruvic acid by transamination from L glutamic acid... [Pg.1124]

The biosynthesis process, which consists essentially of radical coupling reactions, sometimes followed by the addition of water, of primary, secondary, and phenohc hydroxyl groups to quinonemethide intermediates, leads to the formation of a three-dimensional polymer which lacks the regular and ordered repeating units found in other natural polymers such as cellulose and proteins. [Pg.137]

All these polyesters are produced by bacteria in some stressed conditions in which they are deprived of some essential component for thek normal metabohc processes. Under normal conditions of balanced growth the bacteria utilizes any substrate for energy and growth, whereas under stressed conditions bacteria utilize any suitable substrate to produce polyesters as reserve material. When the bacteria can no longer subsist on the organic substrate as a result of depletion, they consume the reserve for energy and food for survival or upon removal of the stress, the reserve is consumed and normal activities resumed. This cycle is utilized to produce the polymers which are harvested at maximum cell yield. This process has been treated in more detail in a paper (71) on the mechanism of biosynthesis of poly(hydroxyaIkanoate)s. [Pg.478]

Biosynthesis of coen2yme A (CoA) ia mammalian cells incorporates pantothenic acid. Coen2yme A, an acyl group carrier, is a cofactor for various en2ymatic reactions and serves as either a hydrogen donor or an acceptor. Pantothenic acid is also a stmctural component of acyl carrier protein (AGP). AGP is an essential component of the fatty acid synthetase complex, and is therefore requited for fatty acid synthesis. Free pantothenic acid is isolated from hver, and is a pale yeUow, viscous, and hygroscopic oil. [Pg.56]

The most important oxirane, from an anthropocentric viewpoint, is probably squalene oxide (72), a precursor of lanosterol (73) and thus of the maligned but essential cholesterol (74 Scheme 87) 78MI50501). The cyclization of (72) to (73) represents nucleophilic tr-attack on oxirane carbon cf. Section 5.05.3.4.3(t)()), and the process has also been extensively investigated in vitro (68ACR1). Oxiranes are even more ubiquitous in steroid biosynthesis than had been thought, for a cholesterol epoxide has been shown to be a product of mammalian steroid biosynthesis <81JA6974). [Pg.119]

The 4-phosphopantetheine group of CoA is also utilized (for essentially the same purposes) in acyl carrier proteins (ACPs) involved in fatty acid biosynthesis (see Chapter 25). In acyl carrier proteins, the 4-phosphopantetheine is covalently linked to a serine hydroxyl group. Pantothenic acid is an essential factor for the metabolism of fat, protein, and carbohydrates in the tricarboxylic acid cycle and other pathways. In view of its universal importance in metabolism, it is surprising that pantothenic acid deficiencies are not a more serious problem in humans, but this vitamin is abundant in almost all foods, so that deficiencies are rarely observed. [Pg.593]

Vnother pathway of glucose catabolism, the pentose phosphate pathway, is the primary source of N/ E)PH, the reduced coenzyme essential to most reductive biosynthetic processes. For example, N/VDPH is crucial to the biosynthesis of... [Pg.742]

Rittenberg and Bloch showed in the late 1940s that acetate units are the building blocks of fatty acids. Their work, together with the discovery by Salih Wakil that bicarbonate is required for fatty acid biosynthesis, eventually made clear that this pathway involves synthesis of malonyl-CoA. The carboxylation of acetyl-CoA to form malonyl-CoA is essentially irreversible and is the committed step in the synthesis of fatty acids (Figure 25.2). The reaction is catalyzed by acetyl-CoA carboxylase, which contains a biotin prosthetic group. This carboxylase is the only enzyme of fatty acid synthesis in animals that is not part of the multienzyme complex called fatty acid synthase. [Pg.805]

Biological examples of pericyclic reactions are relatively rare, although one much-studied example occurs during biosynthesis in bacteria of the essential amino acid phenylalanine. Phenylalanine arises from the precursor chorismate,... [Pg.1194]

Since amino adds are used as essential components of the microbial cells and their biosynthesis is regulated to maintain an optimal level, they are normally synthesised in feedback limited amounts and are subjed to negative feedback control. The main problem using control strains is, therefore, the production of minor amounts of amino adds at an early... [Pg.240]

An example for proteases are the (3-lactamases that hydrolyse a peptide bond in the essential (3-lactam ring of penicillins, cephalosporins, carbapenems and monobac-tams and, thereby, iireversibly inactivate the diug. 13-lactamases share this mechanism with the penicillin binding proteins (PBPs), which are essential enzymes catalyzing the biosynthesis of the bacterial cell wall. In contrast to the PBPs which irreversibly bind (3-lactams to the active site serine, the analogous complex of the diug with (3-lactamases is rapidly hydrolyzed regenerating the enzyme for inactivation of additional (3-lactam molecules. [Pg.103]


See other pages where Essential biosynthesis is mentioned: [Pg.240]    [Pg.240]    [Pg.267]    [Pg.50]    [Pg.107]    [Pg.112]    [Pg.427]    [Pg.295]    [Pg.87]    [Pg.304]    [Pg.466]    [Pg.467]    [Pg.68]    [Pg.78]    [Pg.29]    [Pg.127]    [Pg.287]    [Pg.100]    [Pg.813]    [Pg.1014]    [Pg.1080]    [Pg.10]    [Pg.25]    [Pg.335]    [Pg.39]    [Pg.863]    [Pg.1286]    [Pg.285]    [Pg.579]    [Pg.494]    [Pg.228]    [Pg.139]   
See also in sourсe #XX -- [ Pg.169 ]




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Biosynthesis of the essential amino acids

Biosynthesis of the non-essential amino acids

Essential fatty acids and the biosynthesis of eicosanoids

Essential monosaccharide biosynthesis

Essential oils biosynthesis

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