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In vivo quantification of polyhydroxybutyrate (PHB) in the alphaproteobacterial methanotroph, Methylocystis sp. Rockwell.
Lazic, Marina; Gudneppanavar, Ravindra; Whiddon, Kyle; Sauvageau, Dominic; Stein, Lisa Y; Konopka, Michael.
Afiliación
  • Lazic M; Department of Biological Sciences, University of Alberta, CW 405 Bio Sci Bldg, Edmonton, AB, T6G 2E9, Canada.
  • Gudneppanavar R; Department of Chemistry, University of Akron, Akron, OH, USA.
  • Whiddon K; Department of Chemistry, University of Akron, Akron, OH, USA.
  • Sauvageau D; Department of Chemical and Materials Engineering, University of Alberta, 12th floor Donadeo ICE Building, Edmonton, AB, T6G 1H9, Canada. dominic.sauvageau@ualberta.ca.
  • Stein LY; Department of Biological Sciences, University of Alberta, CW 405 Bio Sci Bldg, Edmonton, AB, T6G 2E9, Canada. lisa.stein@ualberta.ca.
  • Konopka M; Department of Chemistry, University of Akron, Akron, OH, USA.
Appl Microbiol Biotechnol ; 106(2): 811-819, 2022 Jan.
Article en En | MEDLINE | ID: mdl-34921330
Methane is a common industrial by-product that can be used as feedstock for production of the biopolymer polyhydroxybutyrate (PHB) by alphaproteobacterial methanotrophs. In vivo assessment of PHB production would shed light on the biosynthesis process and guide design of improved production strategies, but it is currently difficult to perform efficiently. In this study, the alphaproteobacterial methanotroph Methylocystis sp. Rockwell was grown on methane with three different nitrogen sources (ammonium, nitrate, and atmospheric nitrogen), and biomass samples were harvested at defined time points during lag, exponential, and stationary growth phases. PHB cell content was analyzed at these sampling points via a standard gas chromatography-flame ionization detector method, which requires hydrolysis of PHB and esterification of the resulting monomer under acidic conditions, and a novel, rapid, cost-effective approach based on fixation and staining of bacterial cells via Nile Blue A fluorescent dye enabling differential staining of cell membranes and intracellular PHB granules for single-cell analysis through fluorescence microscopy. Overall, the two PHB quantification approaches were in agreement at all stages of growth and in all three growing conditions tested. The PHB cell content was greatest with atmospheric nitrogen as a nitrogen source, followed by ammonium and nitrate. Under atmospheric nitrogen and ammonium conditions, PHB cell content decreased with growth progression, while under nitrate conditions PHB cell content remained unchanged in all growth phases. In addition to presenting a rapid, efficient method enabling in vivo quantification of PHB production, the present study highlights the impact of nitrogen source on PHB production by Methylocystis sp. Rockwell. KEY POINTS: • A novel fluorescence microscopy method to quantify PHB in single cells was developed • The microscopy method was validated by the derivation/gas chromatography method • Methylocystis sp. Rockwell synthesizes PHB granules without nutrient stress.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Methylocystaceae Idioma: En Revista: Appl Microbiol Biotechnol Año: 2022 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Methylocystaceae Idioma: En Revista: Appl Microbiol Biotechnol Año: 2022 Tipo del documento: Article País de afiliación: Canadá
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