| Literature DB >> 226150 |
Abstract
The stereospecificity of hydrogen transfer in the synthesis of saccharopine from alpha-ketoglutarate and L-lysine catalyzed by saccharopine dehydrogenase (N5-(1,3-dicarboxypropyl)-L-lysine: NAD oxidoreductase (L-lysine-forming), EC 1.5.1.7) was examined by using [4A-3H]- and [4B-3H]NADH. The enzyme showed the A-stereospecificity. The NMR analysis of the saccharopine prepared with [4"A-2H]NADH revealed that the label was incorporated into the C-2 of the glutaryl moiety.Entities:
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Year: 1979 PMID: 226150 DOI: 10.1016/0005-2744(79)90215-8
Source DB: PubMed Journal: Biochim Biophys Acta ISSN: 0006-3002