End-to-end microbiome R&D for Clostridium butyricum—from anaerobic isolation and strain analytics to formulation, bioprocess optimization, and functional readouts—so research teams can rapidly de-risk candidates and generate publication-ready evidence with Creative Biolabs.
Selected by biotech, nutrition, and microbiome ventures seeking rigorous, strain-level data packages and dependable execution.
Clostridium butyricum is a spore-forming, butyrate-producing gut symbiont with decades of research use. Its metabolites, especially butyrate, are central to epithelial barrier support and immune crosstalk, making well-characterized strains valuable tools across host–microbe studies.
Yet this organism is technically demanding: strict anaerobiosis, strain-specific carbohydrate use, spore biology, and formulation stability all influence performance. Creative Biolabs combines anaerobe-first infrastructure with standardized assays to help you compare strains, quantify function, and scale the best candidates with confidence.
We enrich spores and vegetative cells under strict anaerobiosis, isolate colonies on selective media, and deploy high-throughput pre-screens (butyrate production, gas profiles, bile/acid tolerance). Parallel phenotyping identifies robust, fast-growing isolates with desirable spore yields and functional readouts suited to your downstream models.
Strain identity and safety markers are resolved with 16S rRNA sequencing plus whole-genome sequencing (WGS). We annotate carbohydrate-active enzymes (CAZymes), predict metabolic routes to butyrate, assess plasmids, and screen for known virulence or AMR determinants to support risk assessment in research contexts.
Because C. butyricum is a spore former, we quantify heat-resistant spore counts, engineer stress-protection matrices (e.g., trehalose, skim milk, proteins), and test survival across acid, bile, moisture, oxygen, and temperature excursions. Stability reports include accelerated and real-time studies aligned to your storage conditions and logistics.
We formulate spores or mixed populations for oral or experimental delivery, evaluating microencapsulation (alginate, HPMC), granulation, and excipient compatibility. GI-simulation assays track release kinetics and viability; we also examine co-formulation with carbohydrates that favor butyrate flux from lactate/acetate where relevant.
We map carbon utilization and flux to SCFAs (GC/LC-MS for butyrate, acetate, lactate). Multi-substrate panels and transcript-level insights clarify how CAZyme repertoires drive fermentation across fiber classes—data you can use to tune media, diet components, or synbiotic designs.
Under CLSI-aligned anaerobic conditions, we determine MICs for antibiotics of interest and evaluate probiotic–antibiotic co-exposure viability. These studies quantify compatibility and resilience—important for model design when antibiotics are part of your experimental system.
From bench to pilot, we optimize media, pH and redox control, gas transfer, and fed-batch regimes to maximize spore yield and metabolic outputs. Harvest, washing, drying (including lyophilization), and in-process QC are integrated to deliver scalable, reproducible lots ready for extended research studies.
Creative Biolabs develops engineered C. butyricum for research, using CRISPR editing and pathway modulation to boost butyrate output, substrate range, and spore resilience. Modular promoters and markerless constructs improve stability. Deliverables include annotated genomes, benchmarks, and scale-up guidance for consortia and formulations.
Define hypotheses, matrices (strain, media, substrate), functional endpoints, and success criteria with our scientific leads.
Source or receive material, isolate colonies/spores, and pre-screen traits under anaerobic SOPs.
Perform WGS, CAZyme and AMR screening, SCFA quantification, and carbohydrate flux mapping.
Build spore-centric formulations, run GI-simulation, and conduct accelerated/real-time stability.
Scale fermentation and downstream operations to deliver consistent, research-ready material.
Execute host-microbe assays (barrier, immune, colonization resistance) and deliver a cohesive data package.
From hypothesis framing to strain analytics, formulation, and functional readouts, Creative Biolabs streamlines the entire program so teams get coherent, decision-ready data packages.
Anaerobe-capable labs, standardized SOPs, and fit-for-purpose QC workflows reduce variability and enhance reproducibility across isolation, bioprocess, and assay stages.
Microbiologists, bioinformaticians, process engineers, and immunology specialists collaborate to design studies that actually answer the research question—efficiently and defensibly.
Modular work packages, transparent milestones, and scalable capacity let you start small, iterate quickly, and expand when signals are strong.
Traceable methods, version-controlled analytics, and publication-ready reports provide the auditability sponsors need for internal reviews and external communications.
Proactive communication, single-threaded ownership, and predictable timelines help teams de-risk execution and keep complex, multi-assay projects on track.
Link dietary fibers and carbohydrate classes to fermentation routes, quantify butyrate and lactate–acetate cross-feeding, and identify substrate preferences informing synbiotic design and media optimization for C. butyricum in controlled research systems.
Interrogate epithelial barrier function, mucus engagement, and tight junction signaling using co-culture platforms; measure TEER, junctional transcripts, and metabolite responses to characterize how C. butyricum influences host barrier biology across conditions.
Evaluate spore and vegetative viability under antibiotic co-exposure, simulate gastrointestinal environments, and align MIC data with functional outputs to design regimens quantifying resilience and compatibility of C. butyricum with antimicrobials.
Model microbiome-mediated resistance to Clostridioides difficile overgrowth, mapping C. butyricum-driven shifts in metabolites and community structure, and quantifying barrier and immune readouts that contextualize colonization dynamics in preclinical systems robustly.
Use epithelial and immune co-culture models to profile how C. butyricum modulates cytokine patterns, mucus biology, and barrier integrity within inflammation-focused programs relevant to inflammatory bowel disease research hypotheses testing.
Inform rational consortia design by pairing C. butyricum with complementary microbes or substrates, quantifying cross-feeding, coexistence stability, and functional robustness to support evidence-based selection of strains in multi-organism research platforms.
Below is a curated catalog that aligns with the service—organized for quick selection and side-by-side comparison.
Product Name | Catalog No. | Target | Product Overview | Size | Price |
---|---|---|---|---|---|
Clostridium butyricum; 19398 | LBST-061FG | Clostridium | Clostridium butyricum is a strictly anaerobic, endospore-forming, Gram-positive, butyric acid–producing bacillus. | 200 µg | $1,560.00 |
Clostridium butyricum; 1.2756 | LBST-062FG | Clostridium | Clostridium butyricum was isolated from activated sludge; strictly anaerobic, endospore-forming, Gram-positive, butyric acid–producing bacillus. | — | |
Clostridium butyricum; 185375 | LBST-063FG | Clostridium | Clostridium butyricum is a strictly anaerobic, endospore-forming, Gram-positive, butyric acid–producing bacillus. | 200 µg | $1,560.00 |
Clostridium butyricum DNA Standard | LBGF-0125-GF82 | Clostridium DNA Standard | Quantitative genomic DNA standard for research, assay development/verification/validation, and lab quality control. | — | |
Clostridium tyrobutyricum DNA Standard | LBGF-0125-GF83 | Clostridium DNA Standard | Quantitative genomic DNA standard for research, assay development/verification/validation, and lab quality control. | — |
C. butyricum is a Gram-positive, spore-forming anaerobic bacterium that produces butyric acid. This acid is vital for the health of intestinal cells and supports the growth of beneficial gut bacteria such as Bifidobacteria and Lactobacilli. It's recognized for its ability to enhance intestinal health and support the immune system.
C. butyricum has a long history of safe use in various therapeutic applications. It is non-toxigenic and has been effectively used to manage conditions such as Clostridium difficile infections by outcompeting harmful bacteria and restoring gut flora balance.
The discovery of C. butyricum strains involves advanced genomic and phenotypic methods, such as metagenomics, metatranscriptomics, and microbial identification techniques, ensuring the selection of strains with optimal therapeutic potential.
The service offers comprehensive scale-up support, from lab-scale production to GMP-compliant manufacturing, ensuring that probiotic products meet stringent quality standards necessary for clinical and therapeutic applications.
For Research Use Only. Not intended for use in food manufacturing or medical procedures (diagnostics or therapeutics). Do Not Use in Humans.
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