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Thermal decomposition of the amino acids glycine, cysteine, aspartic acid, asparagine, glutamic acid, glutamine, arginine and histidine

Ingrid M. Weiss, Christina Muth, Robert Drumm, Helmut O.K. Kirchner
doi: https://doi.org/10.1101/119123
Ingrid M. Weiss
INM-Leibniz Institute for New Materials, Campus D2 2, D-66123 Saarbruecken Germany
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Christina Muth
INM-Leibniz Institute for New Materials, Campus D2 2, D-66123 Saarbruecken Germany
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Robert Drumm
INM-Leibniz Institute for New Materials, Campus D2 2, D-66123 Saarbruecken Germany
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Helmut O.K. Kirchner
INM-Leibniz Institute for New Materials, Campus D2 2, D-66123 Saarbruecken Germany
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Abstract

Calorimetry, thermogravimetry and mass spectrometry were used to follow the thermal decomposition of the eight amino acids G, C, D, N, E, Q, R and H between 185°C and 280°C. Endothermic heats of decomposition between 72 and 151 kJ/mol are needed to form 12 to 70 % volatile products. This process is neither melting nor sublimation. With exception of cysteine they emit mainly H2O, some NH3 and no CO2. Cysteine produces CO2 and little else. The reactions are described by polynomials, AA ^ a (NH3) + b (H2O) + c (CO2) + d (H2S) + e (residue), with integer or half integer coefficients. The solid monomolecular residues are rich in peptide bonds.

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Posted March 22, 2017.
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Thermal decomposition of the amino acids glycine, cysteine, aspartic acid, asparagine, glutamic acid, glutamine, arginine and histidine
Ingrid M. Weiss, Christina Muth, Robert Drumm, Helmut O.K. Kirchner
bioRxiv 119123; doi: https://doi.org/10.1101/119123
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Thermal decomposition of the amino acids glycine, cysteine, aspartic acid, asparagine, glutamic acid, glutamine, arginine and histidine
Ingrid M. Weiss, Christina Muth, Robert Drumm, Helmut O.K. Kirchner
bioRxiv 119123; doi: https://doi.org/10.1101/119123

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