Biosynthesis of Proteins Nucleic Acids

The amount of amino acids in plant tissues are carefully used for biosynthesis of proteins, nucleic acids and other molecules needed to support the growtlr. 

A schematic block diagram of the metabolism of a typical aerobic heterotroph. The block labeled Catabolism represents pathways by which nutrients are converted to small-molecule starting materials for biosynthetic processes. Catabolism also supplies the energy (ATP) and reducing power (NADPH) needed for activities that occur in the second block these compounds shuttle between the two boxes. The block labeled Biosynthesis represents the synthesis of low- to medium-molecular-weight components of the cell as well as the synthesis of proteins, nucleic acids, lipids, and carbohydrates and the assembly of membranes, organelles, and the other structures of the cell. 

According to Ladonin and Spesivtsev (1974), maize tolerant to chloro-5-triazines stores the triazine taken up in the cytoplasm and in the sensitive pea it is stored in the nucleus, chloroplasts and mitochondria. They assume that the triazines are thus incorporated into proteins and nucleic acids as antimetabolites during the biosynthesis of internuclear nucleic acids. This may also be one of the explanations of the different sensitivity of plants to triazines. Black currant is also tolerant to 4 ppm simazine. According to Shone and Wood (1972) triazine translocated into the leaves of black currant cannot get from the tissue system into the mesophyll. The simazine taken up remains in the leaf veins and does not enter the chloroplasts. 

Cellular Protein Biosynthesis. The process of cellular protein biosynthesis is virtually the same in all organisms. The information which defines the amino acid sequence of a protein is encoded by its corresponding sequence of DNA (the gene). The DNA is composed of two strands of polynucleotides, each comprising some arrangement (sequence) of the four nucleotide building blocks of the nucleic acids adenine (A), thymine (T),... 

A rather limited collection of simple precursor molecules is sufficient to provide for the biosynthesis of virtually any cellular constituent, be it protein, nucleic acid, lipid, or polysaccharide. All of these substances are constructed from appropriate building blocks via the pathways of anabolism. In turn, the building blocks (amino acids, nucleotides, sugars, and fatty acids) can be generated from metabolites in the cell. For example, amino acids can be formed by amination of the corresponding a-keto acid carbon skeletons, and pyruvate can be converted to hexoses for polysaccharide biosynthesis. 

A wide variety of other biochemical effects has been reported to be associated with treatment of cells with vinblastine, vincristine, and related compounds (S). These effects include inhibition of the biosynthesis of proteins and nucleic acids and of aspects of lipid metabolism it is not clear whether such effects contribute to the therapeutic or toxic actions of vincristine and vinblastine. Vinblastine and vincristine inhibit protein kinase C, an enzyme system that modulates cell growth and differentiation (9). The pharmacological significance of such inhibition has not been established, however, and it must be emphasized that the concentrations of the drugs required to inhibit protein kinase C are several orders of magnitude higher than those required to alter tubulin polymerization phenomena (10). 

Of the four major classes of biochemicals (carbohydrates, proteins, nucleic acids and lipids), experiments have shown that the first three classes could have arisen through prebiotic chemistry. Although the biosynthesis of many natural products can be traced back to acetate (e.g. fatty acids, terpenes and polyketide biosynthesis) or amino acids (e.g. alkaloid biosynthesis), there are many whose biosynthetic origins are either obscure or result from a complex combination of pathways (Fig. 2). 

Berberine chloride was evaluated for antimalarial activity against Plasmodium falciparum in vitro (two clones of human malaria Plasmodium falciparum D-6 [Sierra Leone clone] and W-2 (Indochina clone) and Plasmodium berghei in vivo (mice). The alkaloid exhibited an antimalarial potency equivalent to that of quinine in vitro, but was inactive in vivo. The results were consistent with those of others who have found berberine to be a potent inhibitor in vitro of both nucleic acid and protein biosynthesis in P. falciparum, and have demonstrated a strong interaction of berberine with DNA. In addition, the lack of in vivo antimalarial activity in mice observed with berberine and other protoberberine alkaloids agrees with clinical reports that have claimed berberine to be inactive as an antimalarial drug [228]. 

The chapter concludes with a discussion of the nucleic acids, which are the genetic material of living systems and which direct the biosynthesis of proteins. These two types of biopolymers, nucleic acids and proteins, are the organic chemicals of life. 

This chapter revolves around proteins. The first third describes the building blocks of proteins, progressing through amino acids and peptides. The middle third deals with proteins themselves. The last third discusses nucleic acids and their role in the biosynthesis of proteins. 

Polymers are classified as either natural that resulted from natural biosynthesis, or synthetic. The natural (polysaccharides, proteins, nucleic acids, natural rubbers, cellulose, lignin, etc.) have been used for tens of thousands of years. In Egypt the musical string instruments, papyrus for writing, and styrene [in a tree balsam] for embalming were used 3,000 BC. For millennia shellac has been used in Indian turnery [Chattopadhyaya, 1986]. The natural rubber was used by Olmecs at least 3000 years ago [Stuart, 1993]. 

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