Streptococcus bovis JB1: Difference between revisions
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[[File:SEM_electron_micrograph_of_Streptococcus_bovis_JB1.jpg|thumb|300x300px|''S. azabuensis'' KH1P5 in liquid culture exhibiting its dense layer of EPS. Source: Dr. Roy Rodriguez Carrero]] | [[File:SEM_electron_micrograph_of_Streptococcus_bovis_JB1.jpg|thumb|300x300px|''S. azabuensis'' KH1P5 in liquid culture exhibiting its dense layer of EPS. Source: Dr. Roy Rodriguez Carrero]] | ||
[[File:S. bovis 1.jpg|alt=kk|thumb|kkk]] | |||
== Introduction == | == Introduction == | ||
Revision as of 23:15, 27 October 2026


Introduction
Streptococcus bovis JB1 was isolated from the rumen of alfalfa-fed cow. It is a major amylolytic bacterium that depolymerize starch to glucose, fermenting it to large amounts of lactic acid that can lead to lactic acidosis in ruminants.
Global Methane Hub Metadata
| Origin: | Illinois, Mackie Lab |
| Sequenced by: | Ahmed Hetta and Yuqi Li |
| Assembled by: | William G. Alexander |
| Methylome called by: | William G. Alexander |
| Methyltransferases cloned by: | No methylation motifs have been detected |
| MIC and Culturing Conditions by: | Ahmed Hetta and Yuqi Li |
| Transformation by: | Ahmed Hetta |
Genome

DefenseFinder Results
Methylome
No methylation motifs were detected in Streptococcus bovis JB1.
Methylating E. coli Strains
No E. coli methylation strain has been constructed for S. bovis JB1 strain
Culturing Conditions
Streptococcus bovis JB1 grows on both M2GSC and SDM (Semi Defined medium). Cells grow overnight at 37 °C in SDM or M2GSC culture medium with head space composed of 95% CO2 and 5% H2. Similarly, Streptococcus bovis JB1 grows overnight on SDM agar plates. Agar plates were placed in anaerobic Jar and incubated in anaerobic chamber under gas mixture that is composed of 95% CO2 and 5% H2.
Antibiotic MIC Tests

| antibiotic | concentration (ug/mL) |
|---|---|
| Ampicillin | 0.25 |
| Kanamycin | Resistant (>200 ug/mL) |
| Chloramphenicol | 0.50 |
| Tetracycline | 0.23 |
| Gentamicin | 1.0 |
| Streptomycin | Resistant (>200 ug/mL) |
| Erythromycin | 1 |
Protocols
- Preparation of SDM culture medium
- Preparation of M2GSC culture medium
Transformation Results
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; Hungate1000 project collaborators; 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. 2019. Cultivation and sequencing of rumen microbiome members from the Hungate1000 Collection. Nature Biotechnol 36: 359-367. doi: 10.1038/nbt.4110.
[2] Kumar S, Treloar BP, Teh KH, McKenzie CM, Henderson G, Attwood GT, Waters SM, Patchett ML, Janssen PH. 2018. Sharpea and Kandleria are lactic acid producing rumen bacteria that do not change their fermentation products when co-cultured with a methanogen. Anaerobe 54: 31-38. doi: 10.1016/j.anaerobe.2018.07.008.
[3] Kittelmann S, Pinares-Patiño CS, Seedorf H, Kirk MR, Ganesh S, McEwan JC, Janssen PH. 2014. Two different bacterial community types are linked with the low-methane emission trait in sheep. PLoS One 9: e103171. doi: 10.1371/journal.pone.0103171.
[4] Kamke J, Kittelmann S, Soni P, Li Y, Tavendale M, Ganesh S, Janssen PH, Shi W, Froula J, Rubin EM, Attwood GT. 2016. Rumen metagenome and metatranscriptome analyses of low methane yield sheep reveals a Sharpea-enriched microbiome characterised by lactic acid formation and utilisation. Microbiome 4: 56. doi: 10.1186/s40168-016-0201-2.
[5] Morita H, Shiratori C, Murakami M, Takami H, Toh H, Kato Y, Nakajima F, Takagi M, Akita H, Masaoka T, Hattori M. 2008. Sharpea azabuensis gen. nov., sp. nov., a Gram-positive, strictly anaerobic bacterium isolated from the faeces of thoroughbred horses. Int J Syst Evol Microbiol 58: 2682-2686 doi: 10.1099/ijs.0.65543-0.
