The reaction of cytochrome omicron in Escherichia coli with oxygen. Low-temperature kinetic and spectral studies
- PMID: 393255
- PMCID: PMC1161773
- DOI: 10.1042/bj1840379
The reaction of cytochrome omicron in Escherichia coli with oxygen. Low-temperature kinetic and spectral studies
Abstract
1. The reactions of cytochrome omicron in intact cells of aerobically grown Escherichia coli with O2 and CO have been studied at low temperature. 2. Flash photolysis of CO-liganded cells in the presence of O2 and at temperatures between -79 and -102 degrees C results in the oxidation of kinetically heterogeneous beta-type cytochromes (including cytochrome omicron), but not of cytochrome d. 3. The reaction of reduced cytochrome omicron with O2 involves O2 binding to give intermediate(s) with spectral characteristics similar to that of the reduced oxidase-CO complex. Observation in the alpha-region suggests that unexplained ligand dissociation accompanies the initial O2 binding. 4. At temperatures below -98 degrees C, an 'end point' in the reaction is reached; further reaction and oxidation of cytochrome omicron occurs on raising the temperature. 5. There is a linear relationship between the rate of formation of the oxygen compound and the O2 concentration up to 0.5 mM. The second-order constant for its formation (k+1) is 0.91 M-1.S-1 at -101 degrees C. The reaction is not readily reversible, the value of k-1 being 1.4 X 10(-5) S-1 and the kd 1.5 X 10(-5) M. 6. The energy of activation for this reaction at low temperatures is 29.9kJ (7.1 kcal)/mol. 7. The reaction with O2 is distinguished from that with CO by the markedly lower velocity and high photolytic reversibility of the latter. 8. Comparisons are drawn between the intermediate(s) in the O2 reaction of cytochrome omicron in E. coli and those identified in other bacteria and in the reaction of cytochrome aa3 with O2.
Similar articles
-
The reaction of cytochrome o in Escherichia coli K12 with oxygen. Evidence for a spectrally and kinetically distinct cytochrome o in cells from oxygen-limited cultures.J Gen Microbiol. 1981 Oct;126(2):277-87. doi: 10.1099/00221287-126-2-277. J Gen Microbiol. 1981. PMID: 7040597
-
Low-temperature spectral and kinetic properties of cytochromes in Escherichia coli K-12 grown at lowered oxygen tension.Biochim Biophys Acta. 1980 Jul 8;591(2):471-82. doi: 10.1016/0005-2728(80)90177-2. Biochim Biophys Acta. 1980. PMID: 6994809
-
The room temperature reaction of carbon monoxide and oxygen with the cytochrome bd quinol oxidase from Escherichia coli.Biochemistry. 1994 Dec 20;33(50):15110-5. doi: 10.1021/bi00254a021. Biochemistry. 1994. PMID: 7999770
-
The light-reversible binding of carbon monoxide to cytochrome a1 in Escherichia coli K12.J Gen Microbiol. 1981 Aug;125(2):431-8. doi: 10.1099/00221287-125-2-431. J Gen Microbiol. 1981. PMID: 7033471
-
The high-spin cytochrome o' component of the cytochrome bo-type quinol oxidase in membranes from Escherichia coli: formation of the primary oxygenated species at low temperatures is characterized by a slow 'on' rate and low dissociation constant.Microbiology (Reading). 1994 May;140 ( Pt 5):1027-34. doi: 10.1099/13500872-140-5-1027. Microbiology (Reading). 1994. PMID: 8025668
Cited by
-
Oxygen reactions with bacterial oxidases and globins: binding, reduction and regulation.Antonie Van Leeuwenhoek. 1994;65(4):289-310. doi: 10.1007/BF00872215. Antonie Van Leeuwenhoek. 1994. PMID: 7832588 Review.
-
Identification of b, c, and d cytochromes in the membrane of Vitreoscilla.Arch Microbiol. 1987 Oct;148(4):328-33. doi: 10.1007/BF00456712. Arch Microbiol. 1987. PMID: 2825616
-
Redox analysis of the cytochrome o-type quinol oxidase complex of Escherichia coli reveals three redox components.Biochem J. 1991 Mar 15;274 ( Pt 3)(Pt 3):723-30. doi: 10.1042/bj2740723. Biochem J. 1991. PMID: 1849404 Free PMC article.
-
The orientation of iron-sulphur clusters in membrane multilayers prepared from aerobically-grown Escherichia coli K12 and a cytochrome-deficient mutant.Biochem J. 1980 Aug 15;190(2):385-93. doi: 10.1042/bj1900385. Biochem J. 1980. PMID: 6258566 Free PMC article.
-
Carbon monoxide- and oxygen-reacting haemoproteins in the mitochondrial fraction from the soil amoeba Acanthamoeba castellanii. Studies at subzero temperatures.Biochem J. 1981 Nov 15;200(2):337-42. doi: 10.1042/bj2000337. Biochem J. 1981. PMID: 7340835 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources