Ruminococcus flavefaciens AE3010: Difference between revisions
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== Culturing Conditions == | == Culturing Conditions == | ||
''R. flavefaciens'' AE3010 grown well in [[M2GSC]] and [[M10 Medium|M10]] medium at 37°C. Plating efficiency of ''R. falvefaciens'' AE3010 on M10 agar is close to 66%. | ''R. flavefaciens'' AE3010 grown well in [[M2GSC Medium|M2GSC]] and [[M10 Medium|M10]] medium at 37°C. Plating efficiency of ''R. falvefaciens'' AE3010 on M10 agar is close to 66%. | ||
== Antimicrobial MIC Tests == | == Antimicrobial MIC Tests == | ||
Revision as of 22:13, 29 October 2026

Introduction
Ruminococcus flavefaciens AE3010
Ruminococcus flavefaciens AE3010 is an obligately anaerobic, fibrolytic bacterium isolated from the rumen of a cow in New Zealand and selected as a key reference genome for the global Hungate1000 project [1]. Exhibiting the core phenotypic traits of the species, AE3010 relies on the breakdown of complex structural polysaccharides for growth, utilizing an extensive array of highly conserved cohesin and dockerin modules to assemble its specialized cell-surface cellulosome [2].
Ruminococcus flavefaciens AE3010 (DSM 115568) was isolated from the plant-adherent fraction of bovine rumen contents in NZ [3, cow E]. AE3010 has not been phenotypically characterized but its genome encodes a broad range of carbohydrate active enzymes, many of which contain cohesion and dockerin domains. Like other rumen R. flavefaciens strains AE3010 is predicted to be cellulolytic and to produce a functional cellulosome [4].
The draft genome for AE3010 (3,705,946 bp) was generated through the Hungate1000 project with JGI [1].
NCBI: Ruminococcus flavefaciens.
GTDB: Ruminococcus flavefaciens_D. AE3010 belongs to a different species group than the type strain of R. flavefaciens (C94, ATCC 19208).
Risk group: 1.
Global Methane Hub Metadata
| Origin: | United States of America, Macike lab |
| Sequenced by: | Makoto Adachi |
| Assembled by: | William G. Alexander |
| Methylome called by: | William G. Alexander |
| Methyltransferases cloned by: | Roy Rodriguez Carrero |
| MIC and Culturing Conditions by: | Roy Rodriguez Carrero |
| Transformation by: |
Genome

DefenseFinder Results
Methylome
| Motif | Percent methylated |
| TGAA(6mA)T | 99.49 |
| CTTG(6mA)YG | 99.76 |
| CG(6mA)CC | 97.15 |
| CACA(6mA)T | 97.75 |
Methylating E. coli
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Culturing Conditions
R. flavefaciens AE3010 grown well in M2GSC and M10 medium at 37°C. Plating efficiency of R. falvefaciens AE3010 on M10 agar is close to 66%.
Antimicrobial MIC Tests
Note: Antimicrobial MIC was assessed using M2GSC liquid medium.
| Antibiotic | Concentration (µg/ml) |
|---|---|
| Ampicilin | 0.5 |
| Chlorhamphenicol | 0.3 |
| Erythromycin | 1.6 |
| Gentamycin | 0.5 |
| Kanamycin | 4.7 |
| Streptomycin | 0.5 |
| Tetracycline | 0.1 |
Protocols
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Transformation Results
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External Links
[1] Seshadri R, Leahy SC, Attwood GT, Teh KH, Lambie SC, Cookson AL, Eloe-Fadrosh EA, Pavlopoulos GA, Hadjithomas M, Varghese NJ, Paez-Espino D, Perry R, Henderson G, Creevey CJ, Terrapon N, Lapebie P, Drula E, Lombard V, Rubin E, Kyrpides NC, Henrissat B, Woyke T, Ivanova NN, Kelly WJ. 2018. Cultivation and sequencing of rumen microbiome members from the Hungate1000 Collection. Nat Biotechnol 36:359–367.
[2] Minor CM, Takayesu A, Ha SM, Salwinski L, Sawaya MR, Pellegrini M, Clubb RT. 2024. A genomic analysis reveals the diversity of cellulosome displaying bacteria. Front Microbiol 15:1473396.
[3] Noel S. 2013. Cultivation and community composition analysis of plant-adherent rumen bacteria. PhD dissertation. Massey University, Palmerston North, New Zealand. https://mro.massey.ac.nz/server/api/core/bitstreams/bcfbe4cb-19a9-40c0-b5e8-61f9ddb90ce0/content.
[4] Moraïs S, Winkler S, Zorea A, Levin L, Nagies FSP, Kapust N, Lamed E, Artan-Furman A, Bolam DN, Yadav MP, Bayer EA, Martin WF, Mizrahi I. 2024. Cryptic diversity of cellulose-degrading gut bacteria in industrialized humans. Science 383(6688): eadj9223. doi: 10.1126/science.adj9223.
