The fate of the carboxyl oxygens during D-proline reduction by clostridial proline reductase.

Abstract:

:D-Proline is converted to 5-amino valeric acid by D-proline reductase. This conversion involves the reductive cleavage of the alpha-carbon-nitrogen bond. We have examined the fate of the carboxyl oxygen atoms during conversion of D-proline to delta-NH2-valeric acid. 18O atoms from the carboxyl group of D-proline are not lost during conversion to product. In contrast, in the conversion of glycine to acetyl phosphate by glycine reductase a carboxyl oxygen atom is lost to solvent. An intermediate acyl-enzyme is found during the reduction of glycine. We conclude that the reduction of proline proceeds without the formation of an acyl enzyme intermediate.

journal_name

Arch Biochem Biophys

authors

Arkowitz RA,Dhe-Paganon S,Abeles RH

doi

10.1006/abbi.1994.1262

subject

Has Abstract

pub_date

1994-06-01 00:00:00

pages

457-9

issue

2

eissn

0003-9861

issn

1096-0384

pii

S0003986184712628

journal_volume

311

pub_type

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