Ruminococcus flavefaciens FD-1: Difference between revisions
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== Culturing Conditions == | == Culturing Conditions == | ||
''R. flavefaciens'' FD-1 grown well in [[M2GSC]] and [[M10 Medium|M10]] medium at 37°C. Plating efficiency of ''R. falvefaciens'' FD-1 on M10 agar is close to 72%. | ''R. flavefaciens'' FD-1 grown well in [[M2GSC Medium|M2GSC]] and [[M10 Medium|M10]] medium at 37°C. Plating efficiency of ''R. falvefaciens'' FD-1 on M10 agar is close to 72%. | ||
== Antimicrobial MIC Tests == | == Antimicrobial MIC Tests == | ||
Revision as of 22:14, 29 October 2026
Introduction
Ruminococcus flavefaciens FD-1
Ruminococcus flavefaciens FD-1 is a strictly anaerobic bacterium isolated from the bovine rumen by Marvin P. Bryant in 1953. This bacterium is known to deconstruct lignocellulose efficiently using cellulosomes, which are highly modular enzymatic complexes [1]. The efficient degradation of lignocellulose by strain FD-1 results in the production of volatile fatty acids that are absorbed across the rumen epithelium, directly supporting the metabolic and energetic requirements of the ruminant host. Furthermore, the hydrogen evolved during its fermentation process is utilized by syntrophic methanogens, linking the robust fibrolytic activity of FD-1 to ruminal methanogenesis. The extensive genetic and structural mapping of R. flavefaciens FD-1 has established it as a critical benchmark strain for understanding the molecular assembly of bacterial cellulosomes and exploring biotechnological applications in lignocellulose bioconversion.
LPSN: Ruminococcus flavefaciens Sijpesteijn 1948
NCBI: Ruminococcus flavefaciens FD-1
GTDB: Ruminococcus flavefaciens
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 |
| GA(6mA)GG | 99.08 |
| TGAA(6mA)T | 80.83 |
| GC(6mA)YNNNNNTCG | 95.53 |
| (6mA)CGNNNNNNTCAA | 96.06 |
| CGCC(6mA)G | 89.77 |
| CCN(6mA)CC | 93.94 |
| TTG(6mA)NNNNNNCGT | 98.13 |
| GTA(6mA)NNNNNGRTA | 97.72 |
| CG(6mA)NNNNNRTGC | 98.68 |
| T(6mA)YCNNNNNTTAC | 92.71 |
| CACA(6mA)TW | 77.18 |
| SAG(5mC)TS | 81.6 |
| GGN(5mC)C | 47.52 |
Methylating E. coli
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Culturing Conditions
R. flavefaciens FD-1 grown well in M2GSC and M10 medium at 37°C. Plating efficiency of R. falvefaciens FD-1 on M10 agar is close to 72%.
Antimicrobial MIC Tests
Note: Antimicrobial MIC was assessed using M2GSC liquid medium.
| Antibiotic | Concentration (µg/ml) |
|---|---|
| Ampicilin | 0.13 |
| Chlorhamphenicol | 1.8 |
| Erythromycin | 1.7 |
| Gentamycin | 0.5 |
| Kanamycin | Resistance (>200) |
| Streptomycin | 0.1 |
| Tetracycline | 0.1 |
Protocols
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Transformation Results
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External Links
[1] Israeli-Ruimy V, Bule P, Jindou S, Dassa B, Moraïs S, Borovok I, Barak Y, Slutzki M, Hamberg Y, Cardoso V, Alves VD, Najmudin S, White BA, Flint HJ, Gilbert HJ, Lamed R, Fontes CMGA, Bayer EA. 2017. Complexity of the Ruminococcus flavefaciens FD-1 cellulosome reflects an expansion of family-related protein-protein interactions. Sci Rep 7:42355.
