Literature DB >> 16207923

Effect of methanobactin on the activity and electron paramagnetic resonance spectra of the membrane-associated methane monooxygenase in Methylococcus capsulatus Bath.

Dong W Choi1, William E Antholine, Young S Do, Jeremy D Semrau, Clint J Kisting, Ryan C Kunz, Damon Campbell, Vinay Rao, Scott C Hartsel, Alan A DiSpirito.   

Abstract

Improvements in the purification of methanobactin (mb) from either Methylosinus trichosporium OB3b(T) or Methylococcus capsulatus Bath resulted in preparations that stimulated methane-oxidation activity in both whole-cell and cell-free fractions of Methylococcus capsulatus Bath expressing the membrane-associated methane monooxygenase (pMMO). By using washed membrane factions with pMMO activities in the 290 nmol propylene oxidized min(-1) (mg protein)(-1) range, activities approaching 400 nmol propylene oxidized min(-1) (mg protein)(-1) were commonly observed following addition of copper-containing mb (Cu-mb), which represented 50-75 % of the total whole-cell activity. The stimulation of methane-oxidation activity by Cu-mb was similar to or greater than that observed with equimolar concentrations of Cu(II), without the inhibitory effects observed with high copper concentrations. Stimulation of pMMO activity was not observed with copper-free mb, nor was it observed when the copper-to-mb ratio was <0.5 Cu atoms per mb. The electron paramagnetic resonance (EPR) spectra of mb differed depending on the copper-to-mb ratio. At copper-to-mb ratios of <0.4 Cu(II) per mb, Cu(II) addition to mb showed an initial coordination by both sulfur and nitrogen, followed by reduction to Cu(I) in <2 min. At Cu(II)-to-mb ratios between 0.4 and 0.9 Cu(II) per mb, the intensity of the Cu(II) signal in EPR spectra was more representative of the Cu(II) added and indicated more nitrogen coordination. The EPR spectral properties of mb and pMMO were also examined in the washed membrane fraction following the addition of Cu(II), mb and Cu-mb in the presence or absence of reductants (NADH or duroquinol) and substrates (CH4 and/or O2). The results indicated that Cu-mb increased electron flow to the pMMO, increased the free radical formed following the addition of O2 and decreased the residual free radical following the addition of O2 plus CH4. The increase in pMMO activity and EPR spectral changes to the pMMO following Cu-mb addition represent the first positive evidence of interactions between the pMMO and Cu-mb.

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Year:  2005        PMID: 16207923     DOI: 10.1099/mic.0.28169-0

Source DB:  PubMed          Journal:  Microbiology        ISSN: 1350-0872            Impact factor:   2.777


  18 in total

Review 1.  Chemistry and biology of the copper chelator methanobactin.

Authors:  Grace E Kenney; Amy C Rosenzweig
Journal:  ACS Chem Biol       Date:  2011-12-12       Impact factor: 5.100

Review 2.  Copper active sites in biology.

Authors:  Edward I Solomon; David E Heppner; Esther M Johnston; Jake W Ginsbach; Jordi Cirera; Munzarin Qayyum; Matthew T Kieber-Emmons; Christian H Kjaergaard; Ryan G Hadt; Li Tian
Journal:  Chem Rev       Date:  2014-03-03       Impact factor: 60.622

Review 3.  Chalkophores.

Authors:  Grace E Kenney; Amy C Rosenzweig
Journal:  Annu Rev Biochem       Date:  2018-04-18       Impact factor: 23.643

4.  Particulate methane monooxygenase contains only mononuclear copper centers.

Authors:  Matthew O Ross; Fraser MacMillan; Jingzhou Wang; Alex Nisthal; Thomas J Lawton; Barry D Olafson; Stephen L Mayo; Amy C Rosenzweig; Brian M Hoffman
Journal:  Science       Date:  2019-05-10       Impact factor: 47.728

5.  A comparison of methanobactins from Methylosinus trichosporium OB3b and Methylocystis strain Sb2 predicts methanobactins are synthesized from diverse peptide precursors modified to create a common core for binding and reducing copper ions.

Authors:  Benjamin D Krentz; Heidi J Mulheron; Jeremy D Semrau; Alan A Dispirito; Nathan L Bandow; Daniel H Haft; Stéphane Vuilleumier; J Colin Murrell; Marcus T McEllistrem; Scott C Hartsel; Warren H Gallagher
Journal:  Biochemistry       Date:  2010-11-04       Impact factor: 3.162

6.  Binding Selectivity of Methanobactin from Methylosinus trichosporium OB3b for Copper(I), Silver(I), Zinc(II), Nickel(II), Cobalt(II), Manganese(II), Lead(II), and Iron(II).

Authors:  Jacob W McCabe; Rajpal Vangala; Laurence A Angel
Journal:  J Am Soc Mass Spectrom       Date:  2017-08-30       Impact factor: 3.109

7.  Methane monooxygenase gene expression mediated by methanobactin in the presence of mineral copper sources.

Authors:  Charles W Knapp; David A Fowle; Ezra Kulczycki; Jennifer A Roberts; David W Graham
Journal:  Proc Natl Acad Sci U S A       Date:  2007-07-05       Impact factor: 11.205

Review 8.  Copper methanobactin: a molecule whose time has come.

Authors:  Ramakrishnan Balasubramanian; Amy C Rosenzweig
Journal:  Curr Opin Chem Biol       Date:  2008-03-17       Impact factor: 8.822

9.  NMR, mass spectrometry and chemical evidence reveal a different chemical structure for methanobactin that contains oxazolone rings.

Authors:  Lee A Behling; Scott C Hartsel; David E Lewis; Alan A DiSpirito; Dong W Choi; Larry R Masterson; Gianluigi Veglia; Warren H Gallagher
Journal:  J Am Chem Soc       Date:  2008-08-27       Impact factor: 15.419

10.  Variations in methanobactin structure influences copper utilization by methane-oxidizing bacteria.

Authors:  Abdelnasser El Ghazouani; Arnaud Baslé; Joe Gray; David W Graham; Susan J Firbank; Christopher Dennison
Journal:  Proc Natl Acad Sci U S A       Date:  2012-05-10       Impact factor: 11.205

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