Methanocatella millerae SM9: Difference between revisions

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== Antimicrobial MIC Tests ==
== Antimicrobial MIC Tests ==
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[[File:Puromycin MIC determination in M. millerae SM9. Source- Dr. Nana Shao..jpg|thumb|246x246px|Puromycin MIC determination in ''M. millerae'' SM9. Source: Dr. Nana Shao]]
File:Puromycin MIC determination in M. millerae SM9. Source- Dr. Nana Shao..jpg|[[File:Puromycin MIC determination in M. millerae SM9. Source- Dr. Nana Shao..jpg|thumb|Puromycin MIC determination in ''M. millerae'' SM9. Source: Dr. Nana Shao.]]Puromycin MIC determination in ''M. millerae'' SM9. Source: Dr. Nana Shao
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== Protocols ==
== Protocols ==

Revision as of 17:05, 21 October 2026

Introduction

Methanocatella millerae SM9 (formerly Methanobrevibacter millerae) was isolated from the rumen of a sheep fed a fresh forage diet[1]. Although initially identified as Methanobrevibacter sp. or Methanobrevibacter smithii, SM9 shares 99% 16S rRNA gene sequence identity with the Methanocatella (Methanobrevibacter) millerae type strain ZA-10ᵀ (DSM 16643), supporting its assignment to this species[2]. Its robust growth and high plating efficiency make SM9 a strain of particular interest to the Global Methane Hub.

Global Methane Hub Metadata

Origin: Lucidome Bio, NZ
Sequenced by: Plasmidsaurus, ONT + Illumina
Assembled by: Nana Shao
Methylome called by: William G. Alexander
Methyltransferases cloned by: Roy Rodriguez Carrero
MIC and Culturing conditions by: Nana Shao
Transformation by:

Genome

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DefenseFinder Results

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Methylome

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Methylating E. coli

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Culturing Conditions

M. millerae SM9 is cultivated in Modified Methanobrevibacter smithii and Methanosphaera stadtmanae medium (MMSM) at 37°C. To ensure good gas transfer to the media, tubes are incubated on their sides (or at a shallow angle so that the media does not contact the stoppers) with gentle shaking at 50 rpm and 207 kPa of H2/CO2 (80:20, v/v) as an energy substrate for 2-4 days. This methanogen can also be cultivated on MMSM plates using 1.5% agar as a gelling agent with the same pressure of H2/CO2 as an energy substrate for 3-7 days.

Antimicrobial MIC Tests

Puromycin MIC determination in M. millerae SM9. Source: Dr. Nana Shao
Antibiotics Concentration
Liquid Solid
Puromycin
nourseothricin μM


Protocols

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Transformation Results

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  1. ↑ Joblin KN. (1999) Ruminal acetogens and their potential to lower ruminant methane emissions. Australian Journal of Agricultural Research 50, 1307–1314. https://doi.org/10.1071/AR99004
  2. ↑ Kelly WJ, Pacheco DM, Li D, Attwood GT, Altermann E, Leahy SC. The complete genome sequence of the rumen methanogen Methanobrevibacter millerae SM9. Stand Genomic Sci. 2016 Aug 17;11:49. doi: 10.1186/s40793-016-0171-9.