See how sequential organic solvent, surfactant, and alkali treatments transform mycelium into l
A toxin-antitoxin RNA selection scheme removes antibiotics from plasmid production, improving purity, safety, yield, and transfection efficiency.
Engineered dehydrogenases boost activity with nicotinamide-based unnatural cofactors, improving redox cofactor recycling in biotransformations.
A single-domain antibody CAR targets CLL1+ AML cells to improve tumor killing while reducing the bone marrow toxicity that limits AML CAR-T therapy.
Metabolic edits block competing pathways and relieve phosphoenolpyruvate carboxylase feedback to raise sugar-to-aspartic acid yield.
Replacing Pol I origins with a Pol III-dependent origin boosts nanoplasmid yield while avoiding promiscuous replication and antibiotic marker transfer.
A163T substitution in an NMN transporter boosts energy flux in Corynebacterium, increasing L-glutamic acid yield with targeted protein tuning.
Using lignin and biosurfactants, this drilling fluid improves filtrate control and rheology while resisting sulfate reducing bacteria.
A yeast-cellulose nutrient blend restores fermentation support after clarification while limiting oxidation, aroma loss, and browning.
Modified and homologous α1,3-fucosyltransferases raise 3-fucosyllactose productivity by improving enzyme activity in microbial production.
Targeted ketoreductase mutations boost activity and stereoselectivity for making diastereomerically pure 1,3-indane diols used in belzutifan synthesis.
Controlled β-mannanase hydrolysis lowers guar gum viscosity while preserving prebiotic activity and high solubility for food use.
An Aspergillus niger fructosyltransferase converts sucrose in liquid foods into FOS while limiting hydrolysis, turbidity, and viscosity.
A PtlpA-based promoter cassette boosts protein expression in Lactobacillus and supports plasmid retention across generations.
Targeted IolT2 amino acid substitution boosts L-glutamic acid productivity in Corynebacterium without broad pathway redesign.
A P247C isopropylmalate synthase mutant reduces L-leucine feedback inhibition and raises enzyme activity for higher-yield production.
Specific amino acid changes in an MFS transporter raise XMP and GMP output in Corynebacterium without changing the overall fermentation process.
Introducing an anaerobic plsA gene into aerobic bacteria enables plasmalogen biosynthesis without laborious anaerobic culturing.
Weakening SEQ ID NO: 1 protein activity in Corynebacterium boosts citrulline and other glutamate-based amino acid yields for fermentation.
A P247 isopropylmalate synthase mutation reduces L-leucine feedback inhibition while preserving catalysis for higher production yield.
Boosting SarA activity in actinomycetes unlocks biosynthetic pathways, raising metabolite output and revealing 49 new compounds.
Targeted amino acid substitutions in isopropylmalate synthase overcome L-leucine feedback inhibition and raise fermentation yield.
A recombinant E. coli enzyme cascade converts benzaldehyde and pyruvic acid into L-homophenylalanine with high yield and lower cost.
An enzymatic sucrose-to-amylose route raises beta-cyclodextrin yield and purity while reducing starch supply risk and byproduct waste.
By blocking acetoin and 2,3-butanediol pathways, this engineered strain redirects α-acetolactate flux to raise L-valine yield and purity.
A thermostable GH16B β-agarase liquefies agarose above its gelling temperature to raise NA4 and NA6 purity and yield.
A dual α-2,3/α-2,6 sialyltransferase enables one engineered cell to produce 3′SL and 6′SL with lower metabolic burden and stable yield.