1990
DOI: 10.1016/0022-2364(90)90247-7
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Formation of carbamates of taurine and other amino acids during neutralization of tissue extracts with potassium carbonate/ bicarbonate

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Cited by 15 publications
(7 citation statements)
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“…Such adducts are unusual but not unprecedented; a similar N-terminal carbamate adduct is present in bacterial thymidylate synthase [52]. Such adducts form due to the nonenzymatic reaction of CO 2 with amines [5355] and although ubiquitous, only become significant in structures for which adduct formation significantly enhances stability. Nevertheless, carbamate adducts play critical roles in many protein systems, including CO 2 transport by hemoglobin [56] and CO 2 fixation by RUBISCO [57].…”
Section: Iv: the N-terminal Disulfide Switchmentioning
confidence: 99%
“…Such adducts are unusual but not unprecedented; a similar N-terminal carbamate adduct is present in bacterial thymidylate synthase [52]. Such adducts form due to the nonenzymatic reaction of CO 2 with amines [5355] and although ubiquitous, only become significant in structures for which adduct formation significantly enhances stability. Nevertheless, carbamate adducts play critical roles in many protein systems, including CO 2 transport by hemoglobin [56] and CO 2 fixation by RUBISCO [57].…”
Section: Iv: the N-terminal Disulfide Switchmentioning
confidence: 99%
“…Since proline is an imino acid, this adduct is more properly referred to as a carbimate, and is to the best of our knowledge, the first example of a carbimate adduct identified in a biological system. The in vitro CO 2 adducts of various amino acids including proline have previously been studied by NMR (Dettman et al, 1985; Morrow et al, 1974; Myers and Nelson, 1990; Sherry et al, 1990). …”
Section: Resultsmentioning
confidence: 99%
“…(a) The seminal plasma, after treatment with PCA, was neutralized with KOH instead of K 2 CO 3 . This preventive measure was according to Sherry et al 19 who had observed that taurine, a possible candidate for the X compound, was derivatized to its carbamate in extract solutions during neutralization with bicarbonate. (b) The lyophilizates were titrated to pH 7.…”
Section: Resultsmentioning
confidence: 99%
“…19 The carbon assignments followed from the subsequent C,H chemical shift correlation. The large one-bond C,H coupling of 145 Hz (Table 1) confirmed the assignment of the N-CH 2 carbon (compare 145 Hz for CH 3 + NH 3 and 138 Hz for CH 3 SR).…”
Section: Hypotaurinementioning
confidence: 99%