Chorismate synthetase

A 1,4-conjugate elimination of phosphoric acid then transforms 5-enolpyruvylshikimate-3-phosphate (8) into chorismate (9) (Fig. 7.1). The 6-pro-R hydrogen atom is labile in the chorismate synthetase reaction hence, the reaction occurs with overall trans-g ometry. 

The reactions of the shikimate pathway pose a number of interesting questions of both a mechanistic and stereochemical nature. Detailed studies have been made of the DAHP synthetase, 3-dehydroquinate dehydratase, 5-enolpyruvylshikimate-3-phosphate synthetase and chorismate synthetase reactions which have added further important knowledge to this area of molecular biology. Whilst these investigations have done nothing to detract from the important dictum that cells obey the laws of chemistry , they have nevertheless revealed some of the distinctive facets of enzyme chemistry and have highlighted some of the important differences between enzyme and relat chemically catalysed reactions. 

Of the enzymes associated with aromatic amino acid biosynthesis, there is good evidence that unique isozymes of DAHP (Rubin and Jensen, 1985), chorismate synthetase (d Amato et al 1984), and anthranilate synthase (Brotherton et ai, 1986) are differentially localized within chloroplasts and in the cytoplasm. The regulatory properties of the plastid isozymes are consistent with their involvement in amino acid synthesis. Many of the remaining pathway enzymes have also been detected in plastids, including all those required for the synthesis of EPSP [(1) to (6)] (Mousdale and Coggins, 1985). These results, combined with those obtained during measurements of the biosynthetic capabilities of isolated chloroplasts (Bickel and Schultz, 1979 Buchholz and Schultz, 1980 Schulze-Siebert et ai, 1984), leave little doubt that these organelles are a primary site of aromatic amino acid biosynthesis. 

BUTYRYLCHOLINE ESTERASE CHOLINE SULFATASE CHOLINE SULFOTRANSFERASE CHOLOYL-OoA SYNTHETASE OHONDROITIN 4-SULFOTRANSFERASE OHONDROSULFATASES CHORISMATE MUTASE CHORISMATE SYNTHASE Chromatin self-assembly,... 

Chloramphenicol.—A synthetase which converts chorismic acid into p-amino-phenylalanine (an intermediate in chloramphenicol biosynthesis) has been partly characterized it requires an aminotransferase and pyridoxal phosphate for activity.58... 

The quinone ring is derived from isochorismic acid, formed by isomerization of chorismic acid, an intermediate in the shikirnic acid pathway for synthesis of the aromatic amino acids. The first intermediate unique to menaquinone formation is o-succinyl benzoate, which is formed by a thiamin pyrophosphate-dependent condensation between 2-oxoglutarate and chorismic acid. The reaction catalyzed by o-succinylbenzoate synthetase is a complex one, involving initially the formation of the succinic semialdehyde-thiamin diphosphate complex by decarboxylation of 2-oxoglutarate, then addition of the succinyl moiety to isochorismate, followed by removal of the pyruvoyl side chain and the hydroxyl group of isochorismate. 

Several studies of the biosynthesis of chloramphenicol have led to the conclusion that it is formed via the shikimic acid pathway, specifically from chorismic acid. An arylamine synthetase promotes formation of p-amino-L-phenyl alanine (1 ) 50>51. This product is converted to chloramphenicol (15) by oxidation of the amine function to a nitro group, by hy-droxylation of the benzylic methylene group, reduction of the carboxyl... 

In B. subtilis, the pathway from chorismate to tryptophan is feedback-inhibited by tryptophan, which suppresses anthranilate synthase activity. Mutant B. subtilis that lacks tryptophan synthetase can grow on minimal medium only when supplemented with exogenous tryptophan. Under these conditions, none of the intermediates in the tryptophan biosynthetic pathway from anthranilate to indole 3-glycerol phosphate are produced. However, when the bacteria have depleted the medium of tryptophan, the levels of those intermediates increase, even though there is no net production of tryptophan. Why ... 

In Figure 5.41 are depicted the early steps of the lAA biosynthesis in Ara-bidopsis leading to Trp (Figure 5.41). Chorismate (CHO) is converted into anthranilate (ANA) through the catalysis of the a and p subunits of ANA synthetase. Phosphoribosylanthranilate transferase (PAT) and phosphoribo-sylanthranilate isomerase (PAI) control the two successive steps, producing... 

Figure 5.41 Early steps of the proposed indole acetic acid biosynthesis pathways for Ara-bidopsis. CHO, chorismate ANA, anthranilate PANA, 5-phosphoribosylanthranilate CADP, l-(o-carboxyphenylamino)-l-deoxyribulose-5-phosphate IGP, indole-3-glycerol phosphate TRP, tryptophan. Enzymes ASA, anthranilate synthetase, suhunit a ASB, anthranilate synthetase, suhunit P PAT, phosphorihosylanthranUate transferase PAI, phosphoiibosylanthrani-late isomerase IGS, indole-3-glycerol-phosphate synthase TSA, tryptophan synthase, subunit a and TSB, tryptophan synthase, suhunit p.

The synthesis of tryptophan in microorganisms is affected at several levels by end-product inhibition. Thus, end-product feedback inhibition partly regulates the synthesis of chorismic acid which is the final product of the common aromatic pathway and serves as a substrate for the first reaction in the tryptophan-synthesizing branch pathway (see Fig. 2). Regulation of the common aromatic pathway was recently reviewed by Doy [72]. The first enzyme of the common aromatic pathway, 3-deoxy-D-flrah/>jo-heptulosonate 7-phosphate synthetase (DAHPS), has been reported to exist as at least three isoenzymes, each specifically susceptible to inhibition by one of the aromatic amino acid end products (tyrosine, phenylalanine, and tryptophan), in E. coli (see reference [3]). It should be noted that many reports have indicated that in E. coli the DAHPS (trp), the isoenzyme whose synthesis is repressed specifically by tryptophan, was not sensitive to end-product inhibition by tryptophan. Recently, however, tryptophan inhibition of DAHPS (trp) activity has been demonstrated in E. coli [3,73,74]. The E. coli pattern, therefore, represents an example of enzyme multiplicity inhibition based on the inhibition specificity of isoenzymes. It is interesting to note the report by Wallace and Pittard [75] that even in the presence of an excess of all three aromatic amino acids enough chorismate is synthesized to provide for the synthesis of the aromatic vitamins whose individual pathways branch from this last common aromatic intermediate. In S. typhimurium, thus far, only two DAHPS isoenzymes, DAHPS (tyr) and DAHPS (phe) have been identified as sensitive to tyrosine and phenylalanine, respectively [76]. 

End-product inhibition of AS activity by tryptophan appears to be a rather common control mechanism among microorganisms. Nester and Jensen [71] described tryptophan inhibition of B. subtilis AS activity as the first step in sequential feedback control. Excess tryptophan would result in inhibition of the conversion of chorismate to anthrani-late. The consequent accumulation of chorismic acid would then serve as a feedback inhibitor of the DAMPS, the first enzyme in the pathway leading to chorismate synthesis. Bacillus alvei has an anthranilate synthetase which is extremely sensitive to inhibition by tryptophan [98]. In contrast to the mode of AS feedback inhibition in E. coli and S. typhimurium, the B. alvei AS is inhibited by tryptophan noncom-petitively with respect to chorismate and uncompetitively with respect to glutamine. It is the only Bacillus species, among 21 studied, which did not exhibit a sequential feedback control pattern [79]. 

Anthranilate synthetase the enzyme which catalyses the formation of anthranilate (34) from chorismate (14) and L-glutamine (Figure 1.14) has been isolated and characterised from a number of microorganisms. Two main types have been identified in bacteria. Type I has been obtained uncontaminated with other enzymes of the... 

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