Muscle enzymes lactate dehydrogenase

Quantitative Assay for Lactate Dehydrogenase The muscle enzyme lactate dehydrogenase catalyzes the reaction... 

Figure 8.10 The quaternary structure of proteins. The enzyme lactate dehydrogenase (EC 1.1.1.27) has a relative molecular mass of approximately 140 000 and occurs as a tetramer produced by the association of two different globular proteins (A and B), a characteristic that results in five different hybrid forms of the active enzyme. The A and B peptides are enzymically inactive and are often indicated by M (muscle) and H (heart). The A4 tetramer predominates in skeletal muscle while the B4 form predominates in heart muscle but all tissues show most types in varying amounts.

For example, when a heart attack occurs, a lack of blood supplied to the heart muscle causes some of the heart muscle cells to die. These cells release their contents, including their enzymes, into the bloodstream. Simple tests can be done to measure the amounts of certain enzymes in the blood. Such tests, called enzyme assays, are very precise and specific because they are based on the specificity of the enzyme-substrate complex. If you wish to test for the enzyme lactate dehydrogenase (LDH), you need only to add the appropriate substrate, in this case pyruvate and NADH. The reaction that occurs is the oxidation of NADH to NAD+ and the reduction of pyruvate to lactate. To measure the rate of the chemical reaction, one can measure the disappearance of the substrate or the accumulation of one of the products. In the case of LDH, spectrophotometric methods (based on the light-absorbing properties of a substrate or product) are available to measure the rate of production of NAD+. The choice of substrate determines what enz)rme activity is to be measured. 

Similarly, if one compares the form of the enzyme lactate dehydrogenase found in heart muscle to the type found in skeletal muscle, one can see small differences in amino acid composition. These differences in turn affect the reaction catalyzed by this enzyme, the conversion of pyruvate to lactate. The heart type has a high Kf, or a low afiinity for pyruvate, and the muscle type has a low K, or a high afiinily for pyruvate. This means that the pyruvate win be preferentially converted to lactate in the muscle but will be preferentially used for aerobic metabolism in the heart, rather than being converted to lactate. These conclusions are consistent with the known biology and metabolism of these two tissues. 

How does the conversion of pyruvate to lactate take place in muscle There are two fates for pyruvate in anaerobic metabolism. The common outcome is reduction to lactate, catalyzed by the enzyme lactate dehydrogenase. NAD+ is recycled in the process. 

Lactic acid bacteria and muscle tissue also catabolize glucose by the BMP pathway but regenerate NAD- by reducing pyruvic acid to lactic acid using the enzyme lactate dehydrogenase ... 

The answer b 2 ff VA 2 c (2) (e)). Muscle necrosis irxluced by ionophore toxicosb causes the moiferateto massive release of creatine kinase, a musde enzyme. Levek of the other enzymes [lactate dehydrogenase (LDH) and alkaline phosphatase (AP)) may be moderately or mildly efevated. caldum and... 

Another interesting example of a redox neutral cascade has been proposed for the multienzymatic synthesis of (JJ)-3-fluorolactic acid together with the resolution of racemic 3-fluoroalanine (Scheme 11.5b) [13]. Optically enriched (S)-3-fluoroalanine (88% ee) was recovered unreacted after the enantioselective oxidative deamination of the racemic substrate catalyzed by the L-alanine dehydrogenase (i-AlaDH) from Bacillus subtilis. This oxidative reaction, which is thermodynamically unfavorable, was driven by the coupled reduction reaction of the intermediate 3-fluoropyruvate catalyzed by rabbit muscle i-lactate dehydrogenase (L-LDH). Since both enzymes are NADH dependent, this coupled... 

Figure 2. Purification of rabbit muscle L-lactate dehydrogenase (LDH) on TSK GSOOOPW-Procion Blue MX-R. HPAC column, TSK GSOOOPW-Ptocioo blue MX-R (13 /ond/g dry gfft. 5.0 cm x 0.45 cm sample applied, 1 ml, 100 units LX>H, 12.3 rag protein flow-rate, I ml/niin startii solvent, 0.05 M sodium phosphate buffer (pH 7.0) eluant, linear gradient of NaQ (10 ml 0—4 M) in buffer. CoUect 2 mlfractioiis. f — ) enzyme activity, (0-0) protein -42go, (—) NaCI gradient.

Jervis used porous silica coated with chemisorbed polyacrylhydrazide for immobilization of adenosine monophosphate (AMP) [117]. After periodate oxidation of its ribose residue the ligand was coupled to the carrier and used for isolation of lactate dehydrogenase from rabbit muscle. The specific capacity was 2 mg of protein/g adsorbent with a ligand content of 10 pmol/g, whereas recovery of enzymatic activity after elution was 85%. Hipwell et al. [118] found that for effective binding of lactate dehydrogenases on AMP-o-aminoalkyl-Sepharose the spacer arm length required at least 4 methylene links. Apparently, a macromolecule of polyacrylhydrazide acts itself like an extended spacer arm and thus allow AMP to bind the enzyme. 

A key enzyme in the process of recycling lactate from muscle to liver is lactate dehydrogenase (LD) which catalyses the reversible interconversion of lactate and pyruvate. This important reaction is shown in Figure 7.10. 

Why is it desirable to have an enzyme in heart muscle which works efficiently to remove lactate, that is an isoenzyme of lactate dehydrogenase with a low Km for lactate ... 

One of the first enzymes found to have isozymes was lactate dehydrogenase (LDH) (p. 538), which, in vertebrate tissues, exists as at least five different isozymes separable by electrophoresis. All LDH isozymes contain four polypeptide chains (each of Mt 33,500), each type containing a different ratio of two lands of polypeptides. The M (for muscle) chain and the H (for heart) chain are encoded by two different genes. 

Reasons for the presence of enzymes in the plasma Enzymes can normally be found in the plasma either because they were specifically secreted to fulfill a function in the blood, or because they were released by dead or damaged cells. Many diseases that cause tissue damage result in an increased release of intracellular enzymes into the plasma. The activities of many of these enzymes (for example, creatine kinase, lactate dehydrogenase, and alanine aminotransferase) are routinely determined for diagnostic purposes in diseases of the heart, liver, skeletal muscle, and other tissues. 

Most NAD+- or NADP+- dependent dehydrogenases are dimers or trimers of 20- to 40-kDa subunits. Among them are some of the first enzymes for which complete structures were determined by X-ray diffraction methods. The structure of the 329-residue per subunit muscle (M4) isoenzyme of lactate dehydrogenases (see Chapter 11) from the dogfish was determined to 0.25 nm resolution by Rossmann and associates in 1971.2 1 More recently, structures have been determined for mammaliam muscle and heart type (H4) isoenzymes,5 for the testicular (C4) isoenzyme from the... 

The structure of an enzyme can also vary within a person, since different genes may encode enzymes that catalyse the same reaction. These enzymes are known as isozymes. Isozymes are often specific for different types of tissue. For example, lactate dehydrogenase (LDH) is produced in two forms, the M-type (muscle) and the H-type (heart). The M-type is predominates in tissue subject to anaerobic conditions, such as skeletal muscle and liver tissue, whereas the H-type predominates in tissue under aerobic conditions, such as the heart. Isozymes may be used as a diagnostic aid. For example, the presence of H-type LDH in the blood indicates a heart attack, since heart attacks cause the death of heart muscle with the subsequent release of H-type LDH into the circulatory system. 

An example of an enzyme which has different isoenzyme forms is lactate dehydrogenase (LDH) which catalyzes the reversible conversion of pyruvate into lactate in the presence of the coenzyme NADH (see above). LDH is a tetramer of two different types of subunits, called H and M, which have small differences in amino acid sequence. The two subunits can combine randomly with each other, forming five isoenzymes that have the compositions H4, H3M, H2M2, HM3 and M4. The five isoenzymes can be resolved electrophoretically (see Topic B8). M subunits predominate in skeletal muscle and liver, whereas H subunits predominate in the heart. H4 and H3M isoenzymes are found predominantly in the heart and red blood cells H2M2 is found predominantly in the brain and kidney while HM3 and M4 are found predominantly in the liver and skeletal muscle. Thus, the isoenzyme pattern is characteristic of a particular tissue, a factor which is of immense diagnostic importance in medicine. Myocardial infarction, infectious hepatitis and muscle diseases involve cell death of the affected tissue, with release of the cell contents into the blood. As LDH is a soluble, cytosolic protein it is readily released in these conditions. Under normal circumstances there is little LDH in the blood. Therefore the pattern of LDH isoenzymes in the blood is indicative of the tissue that released the isoenzymes and so can be used to diagnose a condition, such as a myocardial infarction, and to monitor the progress of treatment. 

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