AUTHOR=Dzofou Ngoumelah Daniel , Harnisch Falk , Sulheim Snorre , Heggeset Tonje Marita Bjerkan , Aune Ingvild Haugnes , Wentzel Alexander , Kretzschmar Jörg 

TITLE=A unified and simple medium for growing model methanogens

JOURNAL=Frontiers in Microbiology

VOLUME=Volume 13 - 2022

YEAR=2023

URL=https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2022.1046260

DOI=10.3389/fmicb.2022.1046260

ISSN=1664-302X

ABSTRACT=<p>Apart from their archetypic use in anaerobic digestion (AD) methanogenic archaea are targeted for a wide range of applications. Using different methanogenic archaea for one specific application requires the optimization of culture media to enable the growth of different strains under identical environmental conditions, e.g., in microbial electrochemical technologies (MET) for (bio)electromethanation. Here we present a new culture medium (BFS01) adapted from the DSM-120 medium by omitting resazurin, yeast extract, casitone, and using a low salt concentration, that was optimized for <italic>Methanosarcina barkeri</italic>, <italic>Methanobacterium formicicum,</italic> and <italic>Methanothrix soehngenii</italic>. The aim was to provide a medium for follow-up co-culture studies using specific methanogens and <italic>Geobacter</italic> spp. dominated biofilm anodes. All three methanogens showed growth and activity in the BFS01 medium. This was demonstrated by estimating the specific growth rates (<inline-formula><mml:math id="M1" xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mi>μ</mml:mi></mml:math></inline-formula>) and doubling times (<inline-formula><mml:math id="M2" xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mrow><mml:msub><mml:mi>t</mml:mi><mml:mi>d</mml:mi></mml:msub></mml:mrow></mml:math></inline-formula>) of each methanogen. The <inline-formula><mml:math id="M3" xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mi>μ</mml:mi></mml:math></inline-formula> and <inline-formula><mml:math id="M4" xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mrow><mml:msub><mml:mi>t</mml:mi><mml:mi>d</mml:mi></mml:msub></mml:mrow></mml:math></inline-formula> based on methane accumulation in the headspace showed values consistent with literature values for <italic>M. barkeri</italic> and <italic>M. soehngenii</italic>. However, <inline-formula><mml:math id="M5" xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mi>μ</mml:mi></mml:math></inline-formula> and <inline-formula><mml:math id="M6" xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mrow><mml:msub><mml:mi>t</mml:mi><mml:mi>d</mml:mi></mml:msub></mml:mrow></mml:math></inline-formula> based on methane accumulation in the headspace differed from literature data for <italic>M. formicicum</italic> but still allowed sufficient growth. The lowered salt concentration and the omission of chemically complex organic components in the medium may have led to the observed deviation from <inline-formula><mml:math id="M7" xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mi>μ</mml:mi></mml:math></inline-formula> and <inline-formula><mml:math id="M8" xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mrow><mml:msub><mml:mi>t</mml:mi><mml:mi>d</mml:mi></mml:msub></mml:mrow></mml:math></inline-formula> for <italic>M. formicicum</italic> as well as the changed morphology. 16S rRNA gene-based amplicon sequencing and whole genome nanopore sequencing further confirmed purity and species identity.</p>