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Biosynthesis degradation products

The following chapters will be devoted to the production of j8-poly(L-malic acid) or its salt by fermentation, its Isolation, and physico-chemical characterization. The biosynthesis, degradation, and presumed physiological role will be also considered. [Pg.93]

The objectives of the soil persistence experiments were (1) to learn the effect of soil type and concentration on the TCDD degradation rate, (2) to isolate and characterize degradation products from DCDD and TCDD, and (3) to determine whether chlorodioxins could be formed from chlorophenol condensation in the soil environment. This last study was essential since quality control at the manufacturing level could reduce or eliminate the formed dioxin impurity. But the biosynthesis of chlorodioxins by chlorophenol condensation in the soil environment could not be controlled and would have connotations for all chlorophenol-de-rived pesticides if formation did occur. The same question needed to be answered for photochemical condensation reactions leading to chloro-... [Pg.107]

Since the chemistry of nucleic acids was last discussed in this Series,1 publications on the subject have appeared at an unprecedented rate. Degradation products have been further investigated and their structures are more firmly established. Moreover, studies of the properties of these materials have led to a fuller understanding of the behavior of polynucleotides. Emphasis will be laid on the organic chemistry of nucleic acids, and many physicochemical investigations will not be discussed. The period under review has seen the beginning of an understanding of the biosynthesis of nucleic acids, but space does not allow of a consideration of this aspect of the subject. [Pg.286]

FIGURE 2 Biosynthesis of ectocarpene in the higher plant S. isatideus (Aster-aceae). ro3 fatty acids and their degradation products (/3-oxidation) comprise the structural elements for the biosynthesis of ectocarpene in the higher plant S. isatideus. The structurally related trideca-3,6,9-trienoic acid is metabolized by analogy into the C 2 homoectocarpene. [Pg.103]

The other system controlling cholesterol biosynthesis involves both the cytosolic HMG-CoA synthase and the ER enzyme HMG-CoA reductase and is based on the cellular levels of respective mRNAs. Increasing free cholesterol decreases both enzyme activities by decreasing the levels of their mRNAs and increasing enzyme degradation processes. The half-life of HMG-CoA reductase may be as short as 1.7 h. Cellular uptake of LDL maintains cholesterol biosynthesis at a relatively low level, and this is achieved through an LDL degradation product-free cholesterol. Some authorities have maintained that hydroxylated... [Pg.525]

Although several properties of each of the three proteins have been investigated, most of our work has been done with the C form because (a) it has the highest affinity for crystalline cellulose (b) it is the predominant form in most, but not aU, T. viride cellulase preparations (c) it contains more carbohydrate than the A and B forms, suggesting that they may be degradation products from or intermediates in the biosynthesis of hydrocellulase C and (d) it forms a slightly more active hydrocellulase system when recombined with the enzymes of fraction I. [Pg.91]

Cox JE, Priestley ND. Nonactin biosynthesis the product of the resistance gene degrades nonactin stereospecifically to form homochiral nonactate diners. J. Am. Chem. Soc. 2005 127 7976-7977. [Pg.1548]

Degradation products of LOOHs are able to initiate the production of the ethylene, kinases and G-proteins required to induce an oxidative burst. These events are apparently followed by activation of the genes which encode the generation of jasmonic acid and of salicylic acid. These are in turn able to induce the production of enzymes of the phenylpropanoid pathway [149,150], and enzymes which initiate the biosynthesis of terpenes (e.g. 3-hydroxy-3-methylglutaryl coenzyme A reductase [145,151-153]) and lignins. [Pg.67]


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Biosynthesis products

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