Nitrogen isotopic analyses by isotope-ratio-monitoring gas chromatography/mass spectrometry
Amino acids containing natural-abundance levels of 15N were derivatized and analyzed isotopically using a technique in which individual compounds are separated by gas chromatography, combusted on-line, and the product stream sent directly to an isotope-ratio mass spectrometer. For samples of N 2 gas...
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Published in: | Journal of the American Society for Mass Spectrometry Vol. 5; no. 5; pp. 387 - 397 |
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Abstract | Amino acids containing natural-abundance levels of
15N were derivatized and analyzed isotopically using a technique in which individual compounds are separated by gas chromatography, combusted on-line, and the product stream sent directly to an isotope-ratio mass spectrometer. For samples of N
2 gas, standard deviations of ratio measurement were better than 0.1%
0 (Units for δ are parts per thousand or per million (%
0).) for samples larger than 400 pmol and better than 0.5%
0 for samples larger than 25 pmol (0.1%
0
15N is equivalent to 0.00004 atom %
15N). Results duplicated those of conventional, batchwise analyses to within 0.05%
0. For combustion of organic compounds yielding CO
2/N
2 ratios between 14 and 28, in particular for N-acetyl
n-propyl derivatives of amino acids, δ values were within 0.25%
0 of results obtained using conventional techniques and standard deviations were better than 0.35%
0. Pooled data for measurements of all amino acids produced an accuracy and precision of 0.04 and 0.23%
0, respectively, when 2 nmol of each amino acid was injected on column and 20% of the stream of combustion products was delivered to the mass spectrometer. |
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AbstractList | Amino acids containing natural-abundance levels of 15N were derivatized and analyzed isotopically using a technique in which individual compounds are separated by gas chromatography, combusted on-line, and the product stream sent directly to an isotope-ratio mass spectrometer. For samples of N2 gas, standard deviations of ratio measurement were better than 0.1% (Units for delta are parts per thousand or per million (%).) for samples larger than 400 pmol and better than 0.5% for samples larger than 25 pmol (0.1% 15N is equivalent to 0.00004 atom % 15N). Results duplicated those of conventional, batchwise analyses to within 0.05%. For combustion of organic compounds yielding CO2/N2 ratios between 14 and 28, in particular for N-acetyl n-propyl derivatives of amino acids, delta values were within 0.25% of results obtained using conventional techniques and standard deviations were better than 0.35%. Pooled data for measurements of all amino acids produced an accuracy and precision of 0.04 and 0.23%, respectively, when 2 nmol of each amino acid was injected on column and 20% of the stream of combustion products was delivered to the mass spectrometer. Amino acids containing natural-abundance levels of 15N were derivatized and analyzed isotopically using a technique in which individual compounds are separated by gas chromatography, combusted on-line, and the product stream sent directly to an isotope-ratio mass spectrometer. For samples of N 2 gas, standard deviations of ratio measurement were better than 0.1% 0 (Units for δ are parts per thousand or per million (% 0).) for samples larger than 400 pmol and better than 0.5% 0 for samples larger than 25 pmol (0.1% 0 15N is equivalent to 0.00004 atom % 15N). Results duplicated those of conventional, batchwise analyses to within 0.05% 0. For combustion of organic compounds yielding CO 2/N 2 ratios between 14 and 28, in particular for N-acetyl n-propyl derivatives of amino acids, δ values were within 0.25% 0 of results obtained using conventional techniques and standard deviations were better than 0.35% 0. Pooled data for measurements of all amino acids produced an accuracy and precision of 0.04 and 0.23% 0, respectively, when 2 nmol of each amino acid was injected on column and 20% of the stream of combustion products was delivered to the mass spectrometer. |
Audience | PUBLIC |
Author | Merritt, Dawn A. Hayes, J.M. |
Author_xml | – sequence: 1 givenname: Dawn A. surname: Merritt fullname: Merritt, Dawn A. – sequence: 2 givenname: J.M. surname: Hayes fullname: Hayes, J.M. |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/11539439$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Contributor | Hayes, J M |
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References | Bremner (BIB22) 1965 Merritt, D. A.; Freeman, K. H.; Ricci, M. P.; Studley, S. A.; Hayes, J. M. Submitted to Analytical Chemistry. Collister, Hayes (BIB19) 1991; 1973 Schurr (BIB10) 1989 DeNiro (BIB12) 1985; 317 Checkley, Miller (BIB16) 1990; 36 Ricci, Merritt, Freeman, Hayes (BIB36) 1994 Macko (BIB23) 1981 Junk, Svec (BIB37) 1958; 14 Gaebler, Vitti, Vukmirovich (BIB4) 1966; 44 Owens, Rees (BIB24) 1983; 108 Schoeninger, DeNiro (BIB7) 1984; 48 Owens (BIB15) 1987; 24 Foster, Schoenheimer, Rittenberg (BIB1) 1939; 127 Merritt, D. A.; Hayes, J. M. Submitted to Analytical Chemistry. Owens, Rees (BIB25) 1989; 114 Chace, Abramson (BIB28) 1989; 61 Merritt, Ricci, Studley, Hayes, Brand (BIB30) 1991 Chicarelli, Hayes, Popp, Eckhardt, Maxwell (BIB20) 1993; 57 Fry, Brand, Mersch, Tholke, Garritt (BIB26) 1992; 64 Gaebler, Choitz, Vitti, Vukmirovich (BIB3) 1963; 41 Ambrose (BIB21) 1991; 16 Engel, Hare (BIB34) 1985 Cammarata, Cohen (BIB2) 1950; 187 Tuross, Fogel, Hare (BIB9) 1988; 52 Matthews, Hayes (BIB29) 1978; 50 DeNiro (BIB11) 1987; 75 Brand, Tegtmeyer, Hilkert (BIB31) 1994 Macko, Fogel, Hare, Hoering (BIB6) 1987; 65 Vogel (BIB17) 1983; 14 Schoeninger, Moore, Murray, Kingston (BIB13) 1989; 4 Macko, Estep, Engel, Hare (BIB5) 1986; 50 Hare, Fogel, Stafford, Mitchell, Hoering (BIB8) 1991; 16 Merritt, Hayes (BIB35) 1994 Kreitler (BIB18) 1975; 83 Wada (BIB14) 1980 Chong, Houk (BIB27) 1987; 41 CR37/citCR37 Checkley D. M. (CR16/citCR16) 1990; 36 Cammarata P. S. (CR2/citCR2) 1950; 187 CR29/citCR29 CR34/citCR34 Collister J. W. (CR19/citCR19) 1991; 1973 CR33/citCR33 CR31/citCR31 CR4/citCR4 CR30/citCR30 CR3/citCR3 CR6/citCR6 Hare P. E. (CR8/citCR8) 1991; 16 Vogel J. C. (CR17/citCR17) 1983; 14 CR5/citCR5 CR32/citCR32 CR23/citCR23 CR7/citCR7 CR9/citCR9 CR22/citCR22 Owens N. J. P. (CR24/citCR24) 1983; 208 CR21/citCR21 CR13/citCR13 DeNiro M. J. (CR11/citCR11) 1987; 75 CR20/citCR20 CR12/citCR12 CR14/citCR14 CR10/citCR10 CR25/citCR25 CR26/citCR26 CR28/citCR28 Foster G. L. (CR1/citCR1) 1939; 127 CR35/citCR35 CR36/citCR36 Owens N. J. P. (CR15/citCR15) 1987; 24 CR27/citCR27 CR18/citCR18 |
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Snippet | Amino acids containing natural-abundance levels of
15N were derivatized and analyzed isotopically using a technique in which individual compounds are separated... Amino acids containing natural-abundance levels of 15N were derivatized and analyzed isotopically using a technique in which individual compounds are separated... |
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SubjectTerms | Amino Acids - analysis Carbon Dioxide - chemistry Chemistry Techniques, Analytical - instrumentation Chemistry Techniques, Analytical - methods Copper - chemistry Exobiology Gas Chromatography-Mass Spectrometry - instrumentation Gas Chromatography-Mass Spectrometry - methods Gases - analysis Nickel - chemistry Nitrogen - analysis Nitrogen Isotopes Space life sciences |
Title | Nitrogen isotopic analyses by isotope-ratio-monitoring gas chromatography/mass spectrometry |
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