|
HS Code |
773595 |
| Product Name | Dorea formicigenerans (Holdeman and Moore 1974) |
| Type | Bacterial strain |
| Taxonomy | Bacteria; Firmicutes; Clostridia; Clostridiales; Lachnospiraceae; Dorea |
| Atcc Number | ATCC 27755 |
| Dsm Number | DSM 3992 |
| Isolation Source | Human feces |
| Gram Stain | Gram-positive |
| Cell Shape | Rod-shaped |
| Oxygen Requirement | Anaerobic |
| Motility | Non-motile |
| Spore Formation | Non-spore-forming |
| Temperature Range | Mesophilic (typically 37°C optimal) |
| Biosafety Level | BSL-1 |
| Metabolism | Formic acid production from carbohydrate fermentation |
| Genome Status | Genome sequenced |
As an accredited Dorea Formicigenerans (Holdeman And Moore 19 .. factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for **Dorea formicigenerans** (Holdeman and Moore 1974) contains 500 mg freeze-dried culture in a sterile, sealed vial. |
| Shipping | Dorea formicigenerans (Holdeman and Moore 1974) is shipped as a lyophilized culture or in a sealed ampoule containing viable cells on a transport medium. The shipment is typically packed at ambient temperature, but may require cold packs depending on destination and regulations. All handling follows international guidelines for biological materials. |
| Storage | **Storage of Dorea formicigenerans (Holdeman and Moore 1974):** Dorea formicigenerans should be stored as a freeze-dried (lyophilized) culture or as a glycerol stock at -80°C for long-term preservation. For short-term use, it can be maintained on appropriate anaerobic agar or broth under strict anaerobic conditions at 4°C. Protect the culture from oxygen exposure to ensure viability and purity. |
| Purity 99%: Dorea Formicigenerans (Holdeman And Moore 19 .. Purity 99% is used in gut microbiome research, where high purity ensures reproducible experimental results. Cell concentration 1x10^9 CFU/mL: Dorea Formicigenerans (Holdeman And Moore 19 .. Cell concentration 1x10^9 CFU/mL is used in probiotic formulation studies, where high viable cell counts promote efficient colonization. Lyophilized form: Dorea Formicigenerans (Holdeman And Moore 19 .. Lyophilized form is used in long-term microbial storage, where enhanced stability extends shelf life. Stability at 4°C: Dorea Formicigenerans (Holdeman And Moore 19 .. Stability at 4°C is used in clinical sample storage, where low-temperature stability maintains organism viability. Strain specificity: Dorea Formicigenerans (Holdeman And Moore 19 .. Strain specificity is used in taxonomy characterization, where genetic accuracy supports precise identification. Antibiotic susceptibility profile: Dorea Formicigenerans (Holdeman And Moore 19 .. Antibiotic susceptibility profile is used in antibiotic impact assays, where defined response profiles facilitate therapeutic research. Anaerobic cultivation requirements: Dorea Formicigenerans (Holdeman And Moore 19 .. Anaerobic cultivation requirements are used in controlled fermentation studies, where strict anaerobiosis optimizes biomass yield. Genomic DNA availability: Dorea Formicigenerans (Holdeman And Moore 19 .. Genomic DNA availability is used in molecular diagnostics, where high-quality DNA enables accurate PCR analysis. Cryoprotectant inclusion: Dorea Formicigenerans (Holdeman And Moore 19 .. Cryoprotectant inclusion is used in freezing protocols, where improved survival rates ensure post-thaw culture viability. Batch consistency: Dorea Formicigenerans (Holdeman And Moore 19 .. Batch consistency is used in industrial microbiome product manufacturing, where uniformity supports regulatory compliance. |
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Crafting pure, stable strains has always demanded a keen eye and a careful hand. Over the years in our own fermentation rooms and analytical labs, Dorea formicigenerans has stood out for its unique behavior and performance compared to other commonly handled gut flora and anaerobic isolates. This strain, first described by Holdeman and Moore, owes much of its stability and coverage in lab studies to its precise handling, consistent input substrate, and strict environmental controls during its entire development.
By nurturing this strain on-site from single-colony origins, we’re able to guarantee recovery and purity benchmarks that meet advanced research and diagnostics, particularly in the study of gut microbial communities. Dorea formicigenerans has drawn more research attention as a notable member of the Lachnospiraceae family, not just because of its taxonomic profile, but also because of its reliable production of formic acid—a functional marker and metabolic output with wide implications in industrial microbiology and clinical work alike.
Our facility runs continuous environmental logging, maintaining oxygen-free chambers and meticulously monitored nutrient feeds. Even temperature drift by a fraction of a degree can tilt the output. We don’t outsource any essential step, from sub-culturing to transfer and downstream concentration, so every vial or ampoule represents the same high bar set across our batches. That transparency builds trust with downstream users, whose experiment validity often hangs on strain integrity and supply reliability.
On our floors, we combine legacy anaerobic techniques with automation for bottling and lyophilization. That means shorter lead times and more predictable supply windows. We take critical pride in the fact that researchers and biotech processors see fewer anomalies or contaminants in our lots, keeping trial repeatability sharp and analytical signals clean.
Dorea formicigenerans from our lines exhibits short, rod-shaped cells when stained and assessed under direct microscopy. We don’t just rely on shape—our QA teams frequently pull random sampling for full gene sequencing checks, confirming strain identity and absence of contaminant DNA signatures or rogue cell populations. The model strain, historically labeled after Holdeman and Moore’s protocols, maintains robust, consistent growth in reinforced clostridial medium under strict anaerobic conditions.
Our standard catalog supplies come in both glycerol suspensions and lyophilized pellets to match a variety of workflows—be that high-throughput sequencing units or culture-dependent functional analysis. Quantitative recovery sits above laboratory minimums thanks to rigor in inoculum density at dispensation and validated cold-chain shipping protocols. No guesswork comes into play over colony-forming units or expected morphology, sidestepping problems we’ve seen in outsourced or loosely handled stocks from secondary suppliers.
Dorea formicigenerans supports a wide spread of scientific studies. In host-microbe interaction models, our customers often rely on it to understand shifts in gut fermentation products, such as formate and acetate, particularly as the global field races to link microbiome balance with chronic disease risk and gut-brain signaling. Bioprocessors have leveraged its robust metabolic profile for formate production studies, sitting alongside more conventional clostridia but offering specific strain fidelity that some broader consortia lack.
Analytical microbiology clients praise the strain’s reliable readouts in both 16S rRNA gene sequencing and shotgun metagenomic workflows. Because Dorea formicigenerans delivers unambiguous signals against common reagent, polymerase, and environmental backgrounds, users spend less time troubleshooting contamination or misattribution between similarly named genera and more time focusing on hypothesis-driven results.
Educators, too, source it for hands-on training, since it behaves predictably with students learning the rigors of anaerobic culture and streak isolation. Even subtle features like growth kinetics or trace metabolite formation give learners exposure to core microbiology skills seldom picked up using freeze-dried, multi-strain mixes from generalist suppliers.
While at surface level the genus Dorea occupies a similar ecological niche as other Lachnospiraceae, our work has shown that Dorea formicigenerans brings pronounced formate production, as opposed to only minor levels in most Bacteroides- or Clostridium-centric samples. We’ve tracked this with in-house mass spectrometry—showing predictable metabolite patterns that run consistently batch after batch.
Other isolates, be they Roseburia, Coprococcus, or even close cousin Dorea longicatena, link more strongly to butyrate outputs or display volatile carbohydrate breakdown profiles. Our product, by contrast, delivers metabolic ‘signatures’ with far less drift. This consistency makes it easier for researchers looking to compare host outcomes or to revalidate findings from earlier literature using models tightly matched in strain origin.
We’ve found subtle differences in antimicrobial resistance gene carriage—or more accurately, the low baseline presence of such markers in our in-house Dorea formicigenerans lines compared to control stock sent for external testing. Lower risk of vector mobility matters in translational research or in any models destined to underpin clinical-grade therapeutics.
Microbial manufacturing never stops posing new hurdles. Anaerobe recoveries can fail due to oxygen ingress—a problem minimized here with fully nitrogen-purged glove boxes and pre-tested gas-tight seals. Reproducible output also relies on the water source, so our filtration, UV sterilization, and frequent conductivity checks stop waterborne contaminants before they reach growth chambers.
Freeze-drying brings its own set of stressors: cell membranes may rupture under improper pressure/time cycles. Through patient small-batch trials, we optimized the lyophilization process to preserve viability, based on both short-term cfu recovery and long-term stability on rehydration. We rarely need to reprocess, a difference our repeat customers will clearly recognize from their own experiences with competitor strains.
Contamination isn’t just about obvious invaders; cryptic cross-strain transfer in mixed facilities has ruined more than a few critical projects. We segregate lines, with strict tool markings and municipal air filtration. Every technician moves through sanitation checkpoints and follows batch-locked protocols to contain lineage purity.
Across the world, regulations increasingly call for traceability from strain ancestry to shelf. Since day one, we’ve kept digital and paper records for all working and master seed banks, batch generations, and process deviations—a practice that’s drawn positive reviews from both ISO auditors and client-side QA teams.
Instead of generic shipment, each output carries unique identifiers linked back to production documentation, sequence data, sterility observations, and the staff responsible for each stage. For pharmaceutical and clinical labs, this level of transparency means smoother submissions and easier source-verification as regulatory requirements evolve.
The bottom line: full traceability keeps everyone safer, and reduces duplicated work. In practice, these protocols cut down project delays that stem from missing records or ambiguous strain origin—a familiar roadblock in collaborative or regulatory-facing projects.
We’ve watched Dorea formicigenerans move from a microbe of interest in fecal 16S surveys to a measurable player in efforts to link diet, age, and health with gut chemistry. Studies increasingly point to differences in Dorea prevalence or activity after dietary fiber shifts, antibiotic courses, or probiotic interventions. The regularity and viability of our product means larger labs can expand cohort sizes, tracking not just who harbors Dorea, but how their versions behave and interact across populations.
Direct feedback from consortia running colorectal cancer and irritable bowel syndrome studies backs up what our own longitudinal batches have shown: Dorea formicigenerans, properly standardized and identified, contributes to signature patterns that help unlock structure-activity relationships in human health. Because our strain does not arrive as a composite mix, downstream analysis and functional assays show less baseline noise, and cross-study comparisons become more meaningful.
On the industrial side, some bioprocess engineers press Dorea formicigenerans into service as a metabolite platform, especially for small-molecule synthesis and preliminary toxin breakdown studies. The robust formate yield stands out in parallel fermentations, particularly where high throughput and product purity are top priorities.
Being in direct contact with large public health projects and startup biotech firms, we’ve tailored scale-up and custom batch options for partners seeking longitudinal access. This means overcoming traditional bottlenecks—such as limited batch size, unpredictable delivery time, or drift in phenotypic expression. Our approach always circles back to the basics: physical batch consistency, controlled hands-on handling, and clear lines of traceability.
Downstream clients have expressed appreciation for this ethos. We’ve seen it reflected in higher-yield sequencing runs, lower rejection rates in collaborative trials, and more publishable data sets. Diagnostic labs in particular cite our strain’s value in calibrating microbiome analysis, given its tight, well-documented phenotypic profiles in both aerobic and strict anaerobe panels.
Growing a microbe like Dorea formicigenerans in commercial volumes involves daily attention, technical improvement, and a bit of respect for the organism’s quirks. We draw from decades of collective experience with anaerobes, adapting best practices and integrating client feedback. Our batch data, sequencing resources, and handling protocols improve every year. Rather than chase only new strains, we see value in refining what we already excel at.
The early years sometimes meant stuck fermenters, delayed orders, or inconsistent viability. Careful investment in in-house QC and data tracking paid off—now, we routinely fill standing orders without interruption, and clients rarely encounter stock-outs or unanticipated phenotype shifts. This reliability builds confidence for critical projects, from exploratory research through to large-scale, high-impact clinical work.
As gut microbiota science grows, customer needs change. We keep our ears open for requests—be it higher-density formats for high-throughput screens, DNA-free confirmed stocks for omics applications, or co-culture packs that pair Dorea formicigenerans with other metabolically relevant strains. Innovation comes directly from these conversations and the practical challenges researchers bring to our doorstep.
Bigger batch sizes, advanced packaging, and evolving transportation methods all help logistics, but the essentials remain: trusted input, clean output, and honest data. Whether supplying small-volume trial users or national-scale projects, our goal stays focused on direct, effective delivery of Dorea formicigenerans with minimal risk and maximum research value.
Each improvement in strain handling—be it subtle updates to freeze-drying curves, more granular QA spot checks, or deployment of tighter environmental sensors—flows upstream to our partners. We’re not interested in flash-in-the-pan moves or shortcutting the science. Reliable Dorea formicigenerans supply is a cornerstone that helps labs build study depth and scientific confidence, one batch at a time.