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Prokaryotes biosynthetic pathway

Arginine is an essential molecule that is synthesized through different pathways and intermediates in eukaryotes and prokaryotes. Two key differences in the prokaryotic biosynthetic pathway (eight steps overall) are (1) the acetylation... [Pg.571]

Particularly important to the pathways of modular synthases is the incorporation of novel precursors, including nonproteinogenic amino acids in NRP systems [17] and unique CoA thioesters in PK and fatty acid synthases [18]. These building blocks expand the primary metabolism and offer practically unlimited variability applied to natural products. Noteworthy within this context is the contiguous placement of biosynthetic genes for novel precursors within the biosynthetic gene cluster in prokaryotes. Such placement has allowed relatively facile elucidation of biosynthetic pathways and rapid discovery of novel enzyme mechanisms to create such unique building blocks. These new pathways offer a continued expansion of the enzymatic toolbox available for chemical catalysis. [Pg.292]

Glycolysis is a set of reactions that take place in the cytoplasm of prokaryotes and eukaryotes. The roles of glycolysis are to produce energy (both directly and by supplying substrate for the citric acid cycle and oxidative phosphorylation) and to produce intermediates for biosynthetic pathways. [Pg.278]

Depict biosynthetic pathways for eukaryotic and prokaryotic tRNA and highlight the differences between the two systems. [Pg.160]

In general, plant biosynthetic pathways are understood poorly when compared with prokaryotic and fungal metabolic pathways. A major reason for this poor understanding is that genes that express complete plant pathways typically are not clustered together on the genome. Therefore, each plant enzyme often is isolated individually and cloned independently. However, several enzymes involved in plant alkaloid biosynthesis... [Pg.1]

The lack of a murein cell-wall sacculus and the discovery of different cell-envelope polymers and structures in some physiologically unusual prokaryotes, was one of the first biochemical and cytological evidences in favour of Carl Woese s archaebacteria concept [46,149,150]. Since then, increasingly more unique cell-envelope polymers and new types of biosynthetic pathways have become known. These findings corroborate the proposal that the archaea represent a third lineage of organisms [150] in addition to bacteria and eucarya, and that the common ancestor or ancestral population of the archaea did not evolve any cell-wall polymer before it radiated into the various sublineages known today [46,151]. [Pg.252]

Of the two existing isoprenoid biosynthetic pathways (Fig. 3), DXP is used by most prokaryotes for production of IPP and dimethylallyl diphosphate (DMAPP) [65,66]. With the available knowledge of the genes involved in the DXP pathway, several groups have studied the impact of changed expression levels of these genes on the production of reporter terpenoids. Farmer and liao reconstructed the isoprene biosynthetic pathway in Escherichia coli (E. colt) to produce lycopene, which was used as an indication... [Pg.16]

So far, the acceptor specificity of nearly 20 eu- and prokaryotic sialyltransferases has been elucidated and 15 different cDNA clones of these enzymes have been obtained (Table 14 and references therein). This list demonstrates the rapid progress in this field and also includes the first cloning of mammalian polysialyltransferase (polysialyltransferase-1 from hamster ovary cells) [620]. The same group has recently published the molecular analysis of the biosynthetic pathway of the a-2,8-polysialic acid capsule by Neisseria meningitidis serogroup B [658]. [Pg.320]

A second level of control of the tryptophan biosynthetic pathway was discovered by Charles Yanofsky when he characterized mutants in the trp operon that did not affect Trp repressor binding. Yanofsky and his colleagues characterized a novel form of transcriptional control they called attenuation, which depends on the unique linkage between transcription and translation in prokaryotes. As shown in Figure 28.11, the intracellular concentration of TRP-tRNATrp determines if the ribosome will pause at a set of codons in the trp mRNA that specify consecutive Trp residues. When tryptophan levels are high, and TRP-tRNATrp is available, then the transcriptional termination hairpin loop forms and RNA polymerase disengages from the DNA template just downstream of a polyuridine... [Pg.809]

Phosphopantothenoylcysteine decarboxylase (PPC-DC) is an essential flavoenzyme in the CoA biosynthetic pathway that catalyzes the decarboxylation of phosphopantothenoylcysteine (PPC). In many prokaryotes, PPC-DC is fused with PPC synthetase to form a bifunctional enzyme, while in most eukaryotes it is a... [Pg.90]

In plant seeds, glycerolipids can be synthesized in two similar pathways, which are known as prokaryotic and eukaryotic systems. These pathways are localized in different subcellular compartments and are characterized by a similar two-stage enzymatic conversion of 5 n-glycero-3-phosphate (G3P) into phosphatidic acid (PA), but different further conversions of PA into structural, storage, or signaling lipids [65]. Despite the closeness of these two biosynthetic pathways, enzymes that catalyze acylation reactions are unique to each system. [Pg.134]

Prokaryotic thiamin biosynthesis is well known [340], The thiamin biosynthetic pathways ofE coli [341-350] and , subtilis [344,351,352] are the two best studied examples. [Pg.499]

Enzyme repression blockage of the synthesis of enzymes of a biosynthetic pathway by the end product of the same pathway. This type of regulation is found in prokaryotes, in particular for operons of amino acid biosynthesis. If an amino acid is available in the growth medium, the synthesis of all the enzymes in the operon is turned off, but if it is in short supply, the operon is derepressed (see Derepression). See also Attenuation. [Pg.195]

The successful construction of an artificial plant flavonoid biosynthetic pathway in microbes, combined with the first report of functional activity of IFS in yeast microsomes by Akashi and coworkers in 1999, paved the way for high-level isoflavonoid production [69]. However, a significant barrier to prokaryotic... [Pg.1658]


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See also in sourсe #XX -- [ Pg.322 ]




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