» Articles » PMID: 2168380

Soluble Cytochromes from the Marine Methanotroph Methylomonas Sp. Strain A4

Overview
Journal J Bacteriol
Specialty Microbiology
Date 1990 Sep 1
PMID 2168380
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Soluble c-type cytochromes are central to metabolism of C1 compounds in methylotrophic bacteria. In order to characterize the role of c-type cytochromes in methane-utilizing bacteria (methanotrophs), we have purified four different cytochromes, cytochromes c-554, c-553, c-552, and c-551, from the marine methanotroph Methylomonas sp. strain A4. The two major species, cytochromes c-554 and c-552, were monoheme cytochromes and accounted for 57 and 26%, respectively, of the soluble c-heme. The approximate molecular masses were 8,500 daltons (Da) (cytochrome c-554) and 14,000 Da (cytochrome c-552), and the isoelectric points were pH 6.4 and 4.7, respectively. Two possible diheme c-type cytochromes were also isolated in lesser amounts from Methylomonas sp. strain A4, cytochromes c-551 and c-553. These were 16,500 and 34,000 Da, respectively, and had isoelectric points at pH 4.75 and 4.8, respectively. Cytochrome c-551 accounted for 9% of the soluble c-heme, and cytochrome c-553 accounted for 8%. All four cytochromes differed in their oxidized versus reduced absorption maxima and their extinction coefficients. In addition, cytochromes c-554, c-552, and c-551 were shown to have different electron paramagnetic spectra and N-terminal amino acid sequences. None of the cytochromes showed significant activity with purified methanol dehydrogenase in vitro, but our data suggested that cytochrome c-552 is probably the in vivo electron acceptor for the methanol dehydrogenase.

Citing Articles

Oxygen Generation via Water Splitting by a Novel Biogenic Metal Ion-Binding Compound.

Dershwitz P, Bandow N, Yang J, Semrau J, McEllistrem M, Heinze R Appl Environ Microbiol. 2021; 87(14):e0028621.

PMID: 33962982 PMC: 8231713. DOI: 10.1128/AEM.00286-21.


High-molecular-mass multi-c-heme cytochromes from Methylococcus capsulatus bath.

Bergmann D, Zahn J, Dispirito A J Bacteriol. 1999; 181(3):991-7.

PMID: 9922265 PMC: 93468. DOI: 10.1128/JB.181.3.991-997.1999.


Methanol oxidation genes in the marine methanotroph Methylomonas sp. strain A4.

Dispirito A, Chistoserdova L, Lidstrom M J Bacteriol. 1993; 175(12):3767-75.

PMID: 7685335 PMC: 204793. DOI: 10.1128/jb.175.12.3767-3775.1993.


Localization of cytochromes to the outer membrane of anaerobically grown Shewanella putrefaciens MR-1.

Myers C, Myers J J Bacteriol. 1992; 174(11):3429-38.

PMID: 1592800 PMC: 206023. DOI: 10.1128/jb.174.11.3429-3438.1992.

References
1.
Lidstrom M . Isolation and characterization of marine methanotrophs. Antonie Van Leeuwenhoek. 1988; 54(3):189-99. DOI: 10.1007/BF00443577. View

2.
Nunn D, Anthony C . The nucleotide sequence and deduced amino acid sequence of the genes for cytochrome cL and a hypothetical second subunit of the methanol dehydrogenase of Methylobacterium AM1. Nucleic Acids Res. 1988; 16(15):7722. PMC: 338444. DOI: 10.1093/nar/16.15.7722. View

3.
Day D, Nunn D, Anthony C . Characterization of a novel soluble c-type cytochrome in a moxD mutant of Methylobacterium extorquens AM1. J Gen Microbiol. 1990; 136(1):181-8. DOI: 10.1099/00221287-136-1-181. View

4.
LOWRY O, ROSEBROUGH N, FARR A, RANDALL R . Protein measurement with the Folin phenol reagent. J Biol Chem. 1951; 193(1):265-75. View

5.
Laemmli U . Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970; 227(5259):680-5. DOI: 10.1038/227680a0. View