Identification of amino acids in the fast atom bombardment mass spectra of peptides

1988 ◽  
Vol 16 (1-12) ◽  
pp. 155-159 ◽  
Author(s):  
Wigger Heerma ◽  
Willem Kulik
1991 ◽  
Vol 37 (4) ◽  
pp. 276-280 ◽  
Author(s):  
Lolita O. Zamir ◽  
Kenneth A. Devor ◽  
Roy A. Jensen ◽  
Robert Tiberio ◽  
Françoise Sauriol ◽  
...  

The shikimate metabolites are key precursors to a large number of natural products, including aromatic amino acids. Chorismic acid is an important branch point in the biosynthetic pathway to aromatic amino acids. Chorismic acid is also unique among natural products since it is the only compound known to undergo an enzymatic Claisen rearrangement. A metabolite of chorismic acid, isochorismic acid, first observed in Aerobacter aerogenes differs in its chemical structure by the location of the hydroxyl group and the double bonds. Isochorismic acid is a precursor to a growing number of shikimate-derived metabolites. Isochorismic acid has also been postulated to be an intermediate of m-carboxyaromatic amino acids, implying another enzymatic Claisen rearrangement. In this publication, we have isolated isochorismate synthase and found that on lyophilization the enzyme is stable for at least 6 months at −20 °C. Incubation of chorismate with this preparation in water enriched with 18O led to incorporation of one atom of 18O as proven from the fast atom bombardment mass spectra of the HPLC purified derived isochorismate. Key words: chorismate, isochorismate, rearrangement, H218O, isochorismate synthetase.


1988 ◽  
Vol 23 (9) ◽  
pp. 674-676 ◽  
Author(s):  
Richard D. Bowen ◽  
Timothy N. Danks ◽  
David Mitchell ◽  
Susan E. Thomas

1992 ◽  
Vol 6 (4) ◽  
pp. 257-264 ◽  
Author(s):  
Bradley L. Ackermann ◽  
Robert J. Barbuch ◽  
John E. Coutant ◽  
John L. Krstenansky ◽  
Thomas J. Owen

1990 ◽  
Vol 38 (12) ◽  
pp. 3389-3394 ◽  
Author(s):  
Michiaki YONEDA ◽  
Kazuo TSUJIMOTO ◽  
Mamoru OHASHI ◽  
Masami SHIRATSUCHI ◽  
Yasushi OHKAWA ◽  
...  

1995 ◽  
Vol 30 (2) ◽  
pp. 282-289 ◽  
Author(s):  
Gary J. Kunkel ◽  
Kenneth L. Busch ◽  
Richard Dunphy ◽  
David J. Burinsky ◽  
Ruth Barak ◽  
...  

2009 ◽  
Vol 15 (4) ◽  
pp. 497-506 ◽  
Author(s):  
Tomasz Pospieszny ◽  
Elżbieta Wyrzykiewicz

Electron ionisation (EI) and fast atom bombardment (FAB) mass spectral fragmentations of nine 2,4-(and 2,1-) disubstituted o-( m- and p-)nitro-(chloro- and bromo-)-2-thiocytosinium halides are investigated. Fragmentation pathways, whose elucidation is assisted by accurate mass measurements and metastable transitions [EI-mass spectrometry (MS)], as well as FAB/collision-induced dissociation (CID) mass spectra measurements are discussed. The correlations between the abundances of the (C11H10N4SO2)+1–3; (C11H10N3SCl)+4–6 and (C11H10N3SBr)+7–9 ions and the selected fragment ions (EI-MS), as well as (C18H16N5SO4)+1–3; (C18H16N3SCl2)+4–6 and (C18H16N3SBr2) + 7–9 ions and the selected ions (C7H6NO2)+1–3; (C7H6Cl)+ 4–6; (C7H6Br)+ 7–9 (FAB-MS) are discussed. The data obtained can be used for distinguishing isomers.


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