The Measurement of the CO2 Hb Binding Curve of Human Hemoglobin by 13C-NMR Spectrometry

Author(s):  
O. Burkhard ◽  
W. K. R. Barnikol

1979 ◽  
Vol 34 (12) ◽  
pp. 1112-1120
Author(s):  
O. Burkhard ◽  
W. K. R. Barnikol

The detailed structure of the CO2 Hb binding curve is of considerable physiological interest, because the carbamino derivates, which are formed by the reaction of CO2 with Hb, are respon­sible for the well known Haldane effect. Under physiological conditions CO2 binds to the four terminal NH2-groups of the protein chains of Hb and it is generally assumed, that there exists no cooperativity between these groups. To examine whether this assumption is correct or not, we have measured the CO2Hb binding curve over a wide PCO2-range (from 0 kPa to about 70 kPa) by using 13C-NMR spectrometry. Morrow and coworkers (1976) have shown that carbamino-Hb causes a specific NMR signal. The quantitative analysis of the NMR spectra were done according to the method of internal standard. By analyzing mixtures of known composition, we were able to show that this method is working. So we had to use the following equation: Z is the CO2 saturation of Hb, I is the intensity of the carbamino signal, and IHb is the intensity of the carbons of Hb, which are involved in the amide binding. (I/IHb)max is (I/IHb) at high PCO2, where Hb is completely saturated by CO2. For our experiments we used solutions of human desoxygenated Hb, which were equilibrated with a mixture of N2 and CO2. The CO2 contained 90% 13C-isotope. The pH was adjusted by titration to 7.2. The NMR measurements were mainly done with a Varian XL 100 NMR spec­trometer. The CO2 Hb binding curve, we have measured, is S-shaped and has an average Hill value (n̅) of 2.1. This result is quite striking with respect to the findings of other groups. A Hill value of 2.1 proves that CO2 like O2 binds to Hb in a cooperative manner. The discrepancy to the results of other groups may be explained by the fact that these authors measured the CO2 Hb binding curve only at comparatively low PCO2. In our opinion one can only get reliable n-values from the whole CO2 Hb binding curve.



Plants ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 1117
Author(s):  
Clémentine Baccati ◽  
Marc Gibernau ◽  
Mathieu Paoli ◽  
Patrick Ollitrault ◽  
Félix Tomi ◽  
...  

The Papeda Citrus subgenus includes several species belonging to two genetically distinct groups, containing mostly little-exploited wild forms of citrus. However, little is known about the potentially large and novel aromatic diversity contained in these wild citruses. In this study, we characterized and compared the essential oils obtained from peels and leaves from representatives of both Papeda groups, and three related hybrids. Using a combination of GC, GC-MS, and 13C-NMR spectrometry, we identified a total of 60 compounds in peel oils (PO), and 76 compounds in leaf oils (LO). Limonene was the major component in almost all citrus PO, except for C. micrantha and C. hystrix, where β-pinene dominated (around 35%). LO composition was more variable, with different major compounds among almost all samples, except for two citrus pairs: C. micrantha/C. hystrix and two accessions of C. ichangensis. In hybrid relatives, the profiles were largely consistent with their Citrus/Papeda parental lineage. This high chemical diversity, not only among the sections of the subgenus Papeda, but also between species and even at the intraspecific level, suggests that Papeda may be an important source of aroma diversity for future experimental crosses with field crop species.



1972 ◽  
Vol 13 (26) ◽  
pp. 2701-2704 ◽  
Author(s):  
Mikio Yamazaki ◽  
Fumio Katoh ◽  
Jun-ichi Ohnishi and Yasumasa Koyama
Keyword(s):  
13C Nmr ◽  


1986 ◽  
Vol 50 (8) ◽  
pp. 1951-1957 ◽  
Author(s):  
Fumitaka HAYASE ◽  
Seon Bong KIM ◽  
Hiromichi KATO


1992 ◽  
Vol 56 (4) ◽  
pp. 1753-1757 ◽  
Author(s):  
John I. Hedges ◽  
Patrick G. Hatcher ◽  
John R. Ertel ◽  
Kathleen J. Meyers-Schulte


2009 ◽  
Vol 75 (2) ◽  
pp. 404
Author(s):  
H.-J. Hawkins ◽  
J. McKenzie ◽  
J. Rohwer ◽  
M.D. Cramer


ChemInform ◽  
2010 ◽  
Vol 22 (1) ◽  
pp. no-no
Author(s):  
C. TSIAO ◽  
D. R. CORBIN ◽  
C. DYBOWSKI
Keyword(s):  
13C Nmr ◽  


Talanta ◽  
2006 ◽  
Vol 70 (2) ◽  
pp. 315-322 ◽  
Author(s):  
Robert Q. Thompson ◽  
Michael J. Pennino ◽  
Michael J. Brenner ◽  
Manish A. Mehta
Keyword(s):  
13C Nmr ◽  


1982 ◽  
Vol 35 (12) ◽  
pp. 1670-1674 ◽  
Author(s):  
KAZUMICHI UOTANI ◽  
HIROSHI NAGANAWA ◽  
TAKAAKI AOYAGI ◽  
HAMAO UMEZAWA


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