Nuclease for reducing DNA/RNA-driven viscosity in bacterial, yeast, and microbial lysates, improving clarification, filtration, and downstream process control.
Request pricingMicrobial disruption releases the target material — and a large burden of host DNA and RNA. In bacterial, yeast, and other microbial lysates, those nucleic acids can create high viscosity, stringiness, poor solids separation, slow filtration, and inconsistent transfer behavior.
Strandfall Nuclease is used after biomass disruption to degrade DNA and RNA into smaller fragments, helping convert a difficult lysate into a more controllable process stream.
After cell breakage, long DNA and RNA molecules can bind water, entangle cell debris, and increase apparent viscosity. The result is not just a thicker fluid — it is a lysate that can resist mixing, trap fines, blind filters, and behave differently from batch to batch.
A nuclease step cuts those nucleic acids into shorter fragments. When applied under compatible process conditions, this can reduce viscosity, improve process clarity, and make the lysate easier to clarify before downstream purification.
Nuclease treatment helps reduce DNA/RNA-driven thickness, enabling smoother agitation, transfer, and feed behavior.
Shorter nucleic acid fragments reduce entanglement with host debris, supporting more predictable centrifugation, settling, and primary clarification.
By decreasing stringiness and particulate drag, nuclease can help protect depth filters, membranes, and other clarification media from premature fouling.
A cleaner, less viscous lysate can support more stable operation before chromatography, precipitation, extraction, ultrafiltration, or other downstream steps.
For B2B production, the value is not only degradation of DNA and RNA. The value is repeatable lysate behavior across fermentation campaigns, scales, and equipment trains.
Typical use points include:
Strandfall can help position the nuclease step around your actual constraints: lysis method, biomass concentration, target product, process temperature, salt level, pH range, cofactor strategy, hold time, and downstream removal expectations.
The nuclease should be introduced where the lysate can be mixed uniformly. Poor contact can create uneven viscosity reduction and make scale-up difficult.
Temperature, pH, salt, detergents, chaotropes, reducing agents, and metal cofactors can influence process fit. Strandfall discusses compatibility in practical operating terms without exposing trader-confidential assay methods.
Depending on the product and process, teams may define nuclease removal, clearance, inactivation, or acceptable carry-through. The best approach depends on product class, purification train, regulatory expectations, and risk profile.
Procurement teams need more than a technical answer. Strandfall supports ordering decisions with lot documentation, packaging options, clear quotation terms, and scale-aware supply planning.
When requesting pricing, include as much of the following as possible:
Share your lysate conditions and sourcing requirements. Strandfall will respond with pricing, packaging options, lead time, and technical alignment for your microbial fermentation workflow.



Tell us your application and volume — we reply with pricing and lead time.