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Coenzyme coenzyme A

Coenzymes Coenzyme A Benzoyl-coenzyme A reductase, acetyl-coenzyme A carboxylase, 3 -methylcrotonyl-coenzyme-A carboxylase... [Pg.332]

The refers to the binding of the 2-carbon compound with a special coenzyme. Coenzyme A. The 1-carbon product is carbon dioxide. Pymvate can also be metabolized anaerobically, in which case it receives electrons that were initially removed during glycolysis ... [Pg.121]

In the cell the thioester of dihydrolipoic acid is not stored but is coupled to another sulfur containing coenzyme coenzyme A, CoA-SH, the universal acyl-transfer agent. [Pg.418]

Four decades elapsed before Lipmann (and, independently, Nachmansohn and Berman) discovered that a coenzyme is required for acetylation reactions. From the contributions of many workers we now know that the 2-carbon fragment is an acetylated derivative of this coenzyme, Coenzyme A. [Pg.278]

Coenzymes effecting transfer of groups. Examples of this class are adenosine triphosphate (ATP), biotin, coenzyme A and pyridoxal phosphate. [Pg.105]

Figure C2.5.5. Native stmcture of acyl-coenzyme A binding protein (first NMR stmcture out of 29 deposited to PDB). The figure was created using RasMol 2.6 [8],... Figure C2.5.5. Native stmcture of acyl-coenzyme A binding protein (first NMR stmcture out of 29 deposited to PDB). The figure was created using RasMol 2.6 [8],...
Figure 10.3-19. Representation of the reaction shown fn Figure 10.3-16, indicating all the atoms and bonds of the chemical structures as well as the reaction center. For the sake of clarity, the coenzyme A has been abbreviated. Figure 10.3-19. Representation of the reaction shown fn Figure 10.3-16, indicating all the atoms and bonds of the chemical structures as well as the reaction center. For the sake of clarity, the coenzyme A has been abbreviated.
Although a variety of oxidizing agents are available for this transformation it occurs so readily that thiols are slowly converted to disulfides by the oxygen m the air Dithiols give cyclic disulfides by intramolecular sulfur-sulfur bond formation An example of a cyclic disulfide is the coenzyme a lipoic acid The last step m the laboratory synthesis of a lipoic acid IS an iron(III) catalyzed oxidation of the dithiol shown... [Pg.650]

The form in which acetate is used in most of its important biochemical reactions is acetyl coenzyme A (Figure 26 la) Acetyl coenzyme A is a thwester (Section 20 13) Its for matron from pyruvate involves several steps and is summarized m the overall equation... [Pg.1070]

Coenzyme A was isolated and identified by Fritz Lipmann an American bio chemist Lipmann shared the 1953 Nobel Prize in physiol ogy or medicine for this work... [Pg.1070]

All the individual steps are catalyzed by enzymes NAD" (Section 15 11) is required as an oxidizing agent and coenzyme A (Figure 26 16) is the acetyl group acceptor Coen zyme A is a thiol its chain terminates m a sulfhydryl (—SH) group Acetylation of the sulfhydryl group of coenzyme A gives acetyl coenzyme A... [Pg.1070]

As we saw m Chapter 20 thioesters are more reactive than ordinary esters toward nucleophilic acyl substitution They also contain a greater proportion of enol at equilib rmm Both properties are apparent m the properties of acetyl coenzyme A In some reactions it is the carbonyl group of acetyl coenzyme A that reacts m others it is the a carbon atom... [Pg.1070]

Fatty acids are biosynthesized by way of acetyl coenzyme A The following sec tion outlines the mechanism of fatty acid biosynthesis... [Pg.1074]

We can descnbe the major elements of fatty acid biosynthesis by considering the for mation of butanoic acid from two molecules of acetyl coenzyme A The machinery responsible for accomplishing this conversion is a complex of enzymes known as fatty acid synthetase Certain portions of this complex referred to as acyl carrier protein (ACP), bear a side chain that is structurally similar to coenzyme A An important early step m fatty acid biosynthesis is the transfer of the acetyl group from a molecule of acetyl coenzyme A to the sulfhydryl group of acyl carrier protein... [Pg.1075]

Using HSCoA and HS—ACP as abbreviations for coenzyme A and acyl carrier protein respectively write a structural formula for the tetrahedral... [Pg.1075]

A second molecule of acetyl coenzyme A reacts with carbon dioxide (actually bicarbonate ion at biological pH) to give malonyl coenzyme A... [Pg.1075]

Formation of malonyl coenzyme A is followed by a nucleophilic acyl substitution which transfers the malonyl group to the acyl carrier protein as a thioester... [Pg.1075]

The four carbon atoms of the butanoyl group originate m two molecules of acetyl coenzyme A Carbon dioxide assists the reaction but is not incorporated into the prod uct The same carbon dioxide that is used to convert one molecule of acetyl coenzyme A to malonyl coenzyme A is regenerated m the decarboxylation step that accompanies carbon-carbon bond formation... [Pg.1075]

Two acyl coenzyme A molecules (R and R may be the same or they may be different)... [Pg.1077]

Hydrolysis of the phosphate ester function of the phosphatidic acid gives a diacylglycerol which then reacts with a third acyl coenzyme A molecule to produce a triacylglycerol... [Pg.1078]

The introduction to Section 26 8 pointed out that mevalonic acid is the biosynthetic pre cursor of isopentenyl pyrophosphate The early steps m the biosynthesis of mevalonate from three molecules of acetic acid are analogous to those m fatty acid biosynthesis (Sec tion 26 3) except that they do not involve acyl earner protein Thus the reaction of acetyl coenzyme A with malonyl coenzyme A yields a molecule of acetoacetyl coenzyme A... [Pg.1091]


See other pages where Coenzyme coenzyme A is mentioned: [Pg.212]    [Pg.27]    [Pg.12]    [Pg.12]    [Pg.29]    [Pg.101]    [Pg.105]    [Pg.105]    [Pg.105]    [Pg.193]    [Pg.194]    [Pg.248]    [Pg.296]    [Pg.394]    [Pg.556]    [Pg.63]    [Pg.1070]    [Pg.1070]    [Pg.1070]    [Pg.1070]    [Pg.1070]    [Pg.1070]    [Pg.1071]    [Pg.1071]    [Pg.1071]    [Pg.1071]    [Pg.1075]    [Pg.1075]    [Pg.1075]    [Pg.1075]    [Pg.1075]    [Pg.1075]    [Pg.1077]    [Pg.1077]    [Pg.1091]    [Pg.1091]   
See also in sourсe #XX -- [ Pg.18 ]




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Coenzyme A

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