Abstract:
:Cystine, selenocytsine, and several analogs were reduced by dithiothreitol (DTT), beta-mercaptoethanol (ME) and sodium borohydride (NaBH4). DTT was the most effective; DTT to cystine ratios from 10 to 80 were equally effective. With selenocysteine, however, absorption was considerably reduced at all ratios. Selenocysteine was identified as the reduction product by reaction with Gaitonde's reagent, comparison of absorption spectra, paper chromatograhy, utilization by cysteinyl-tRNA synthetase fro Paracoccus denitrificans and Vigna radiata, changes in solubility after DTT treatment, and comparison of infrared spectra. During the ATP-PPi exchange assay, DTT and ME convert cysteine and selenocysteine derivatives to cysteine and selenocysteine which serve as substrates for cysteinyl-tRNA synthetase.
journal_name
J Inorg Biochemjournal_title
Journal of inorganic biochemistryauthors
Burnell JN,Karle JA,Shrift Adoi
10.1016/s0162-0134(00)80275-5subject
Has Abstractpub_date
1980-07-01 00:00:00pages
343-51issue
4eissn
0162-0134issn
1873-3344pii
S0162-0134(00)80275-5journal_volume
12pub_type
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