References
- Hochman A, Shemesh A. 1987. Purification and characterization of a catalase-peroxidase from the photosynthetic bacterium Rhodopseudomonas capsulata. J Biol Chem 262. 6871-6876
- Levy E, Eyal Z, Hochman A. 1992. Purification and characterization of a catalase-peroxidase from the fungus Septoria tritici. Arch Biochem Biophys 296 : 321-327 https://doi.org/10.1016/0003-9861(92)90579-L
- Loewen PC, Switala J, Triggs-Raine BL. 1985. Catalases HPI and HPII in Escherichia coli are induced independently. Arch Biochem Biphys 243 : 144-149 https://doi.org/10.1016/0003-9861(85)90782-9
- Loewen PC, Triggs BL, George CS, et al. 1985. Genetic mapping of katG, a locus that affects synthesis of the bifunctional catalase‒eroxidase hydro‒peroxidase I in Escherichia coli. J Bacteriol 162 : 661-667
- Triggs-Raine BL, Loewen PC. 1987. Physical characterization of Kat G encoding catalase HPI of Escherichia coli. Gene 52 : 121-128 https://doi.org/10.1016/0378-1119(87)90038-2
- Triggs-Raine BL, Doble BW, Mulvey MR, et al. 1988. Nucleotide sequence of KatG, encoding catalase HPI of Escherichia coli. J Bacteriol 170 : 4415-4419 https://doi.org/10.1128/jb.170.9.4415-4419.1988
- Christman MF, Storz G, Ames BN. 1989. Oxy R, a positive regulator of hydrogen peroxide-inducible genes in Escherichia coli and Salmonella typhi‒murium, is homologous to a family of bacterial regulatory proteins. Proc Natl Acad Sci USA 86 : 3484-3488
- Von Ossowski I, Mulvey MR, Leco PA, et al. 1991. Nucleotide sequence of Escherichia coli katE, which encodes catalase HPII. J Bacteriol 173 : 514‒520
- Jenkins DE, Chaissons SA, Matin, A. 1990. Starvation-induced cross-protection against osmotic challenge in Escherichia coli. J Bacteriol 172 : 2779‒2781
- Wakabayashi S, Matsubara H, Webster DA. 1986. Primary sequence of a dimeric bacterial hemoglobin from Vitreoscilla. Nature 322 : 481-483 https://doi.org/10.1038/322481a0
- Orii Y, Webster DA. 1977. Oxygenated cytochrome o(Vitreoscilla) formed by treating oxidized cytochrome with superoxide anion. Plant Cell Physiol 18 : 521-526
- Abrams JJ, Webster DA. 1990. Purification, partial characterization, and possible role of catalase in the bacterium Vitreoscilla. Arch Biochem Biophys 279 : 54‒59
-
Park C, Moon JY, Cokic P, et al. 1996.
$Na^+$ ‒translocting cytochrome bo terminal oxidase from Vitreoscilla: Some parameters of its$Na^+$ pumping and orientation in synthetic vesicles. Biochemistry 35 : 19895-11900 - Lowry OH, Rosebrough NJ, Farr AL, Randall R. 1951. Protein measurement with the Folin phenol reagent. J Biol Chem 193 : 265-275
- Decker LA. 1988. Worthington enzyme manual. Worthington Biochemical Corporation. USA : 254-260
- Aebi H. 1974. Catalase. In : Methods of Enzymatic Analysis, Vol. 2. Academic Press. New York : 673-684
- Laemmli UK. 1970. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227 : 680-685 https://doi.org/10.1038/227680a0
- Wayne LG, Diaz GA. 1986. A double staining method for differentiating between two classes of mycobac‒terial catalase in polyacrylamide electrophoresis gels. Anal Biochem 157 : 89‒92
- Keston AS, Brandt R. 1965. The fluorometric analysis of ultramicro quantities of hydrogen peroxide. Anal Biochem 11 : 1-5 https://doi.org/10.1016/0003-2697(65)90034-5
-
Mongkolsuk S, Loprasert S, Vatta‒naviboon P, et al. 1996. Heterologous growth phase- and temperature-deficient expression and
$H_2O_2$ toxicity protection of a superoxide-inducible monofunctional catalase gene from Xanthomonas oryzae pv. oryzae. J Bacteriol 178 : 3578‒3584 - Heather RP, Mark RO. 2004. KatG is the primary detoxifier of hydrogen peroxide produced by aerobic metabolism in Bradyrhizobium japonicum. J Bacteriol 186 : 7874-7880 https://doi.org/10.1128/JB.186.23.7874-7880.2004
- Boerman SJ, Webster DA. 1982. Control of heme content in Vitreoscilla by oxygen. J Gen Appl Microbial 28 : 35-43 https://doi.org/10.2323/jgam.28.35
- Jakob W, Webster DA, Peter MHK. 1992. NADH-dependent methemoglobin reductase from the obligate aerobe Vitreoscilla: Improved method of purification and reexamination of prosthetic groups. Arch Biochem Biophys 292 : 29-33 https://doi.org/10.1016/0003-9861(92)90046-Y
- Dunford HB, Stillman JS. 1976. On the function and mechanism of action of peroxidase. Coord Chem Rev 19 : 187‒251
- Lange R, Hengge-Aronis R. 1991. Identification of a central regulator of stationary-phase gene expression in Escherichia coli. Mol Microbiol 5 : 49-59 https://doi.org/10.1111/j.1365-2958.1991.tb01825.x