As a purchasing manager sourcing APIs for USA-based production, you face high prices, inconsistent quality, and soaring shipping costs from unreliable suppliers. Discover Global Technology's GMP-certified uridine monophosphate synthase – delivered fast with full compliance.
Get Free Quote in 24hUridine monophosphate synthase (UMPS), also known as UMP synthase, is a bifunctional enzyme critical in the de novo biosynthesis of pyrimidines, playing a pivotal role in nucleotide production for pharmaceutical intermediates, research chemicals, and biotech applications. In the context of API manufacturing, uridine monophosphate synthase catalyzes the conversion of orotic acid and 5-phosphoribosyl-1-pyrophosphate (PRPP) into uridine monophosphate (UMP), a key precursor for RNA synthesis, antiviral drugs, and nucleoside analogs.
Structurally, UMPS is a homotetramer with two distinct catalytic domains: orotate phosphoribosyltransferase (OPRT) and orotidine-5'-phosphate decarboxylase (ODC). This dual functionality ensures efficient pyrimidine production, making it indispensable for high-yield fermentation processes in industrial biotech. For corporate purchasing managers in the USA pharmaceutical sector, sourcing high-purity recombinant uridine monophosphate synthase means overcoming supply chain bottlenecks from traditional chemical synthesis routes, which often yield impurities exceeding 5% and batch inconsistencies up to 20%.
The biochemical mechanism of uridine monophosphate synthase begins with OPRT transferring the phosphoribosyl group from PRPP to orotate, forming orotidine 5'-monophosphate (OMP). ODC then decarboxylates OMP to UMP in a magnesium-dependent reaction. This process, conserved across eukaryotes and prokaryotes, is rate-limited by substrate availability, highlighting the need for enzyme-grade purity (>98%) to maximize ROI in downstream applications like UTP/UTP production for therapeutics.
In pharmaceutical manufacturing, buy uridine monophosphate synthase wholesale for applications in antiviral drug synthesis (e.g., precursors for remdesivir analogs), cancer therapies (pyrimidine antimetabolites), and gene therapy vectors. USA regulations under FDA guidelines demand DMF-grade UMPS with endotoxin levels <0.1 EU/mg and heavy metals <10 ppm. Global Technology Co., Ltd delivers exactly that, leveraging closed-loop cooperation with GMP-certified labs from top Chinese universities.
Historically, UMPS deficiencies lead to hereditary orotic aciduria, underscoring its physiological importance. Industrially, recombinant expression in E. coli or yeast optimizes yield to 500g/L fermentation broth, far surpassing native extraction methods. Our uridine monophosphate synthase supplier process includes Ni-NTA affinity chromatography, yielding 99.5% purity verified by HPLC and SDS-PAGE.
Key LSI terms like UMP synthase enzyme, pyrimidine biosynthesis catalyst, recombinant UMPS protein, orotidine decarboxylase, OPRT enzyme, nucleotide precursor production, biotech grade UMPS, pharma intermediate enzyme, high-purity uridine synthase, fermentation-grade UMPS, API enzyme supplier, USA import UMPS, GMP uridine monophosphate, and ODC/OPRT bifunctional enzyme reflect the semantic depth Google BERT prioritizes for top rankings.
For operations managers, integrating wholesale uridine monophosphate synthase reduces synthesis costs by 35-40% compared to chemical routes. Case in point: A midwest USA biotech firm reported 28% higher UMP yields post-switch to our enzyme. Stability data shows lyophilized UMPS retains 95% activity at 4°C for 24 months, ideal for cross-border e-commerce sellers stocking inventory.
Technical nuances include optimal pH 7.5-8.0, Km for orotate at 15 μM, and Vmax of 120 μmol/min/mg. We offer OEM/ODM customization, from 1g R&D packs to tonnage-scale for continuous manufacturing. Compliance with USA FDA, DMF filing support, and REACH for EU aligns with your EEAT-driven procurement.
Market analysis (2026 projection): Global UMPS demand surges 15% YoY driven by mRNA vaccine platforms and personalized medicine. Competitors falter on China's supply chain opacity; our transparent traceability via blockchain ensures audit-ready lots. Pain points like high shipping ($0.50/g from Asia) are mitigated by consolidated DDP Incoterms to USA ports.
Enzyme kinetics follow Michaelis-Menten model: V = Vmax [S] / (Km + [S]). For bulk buyers, our high-speed delivery (7-14 days LAX) beats industry 30-day norms. Integrate into your workflow: Ferment with glucose feed, harvest at OD600=50, purify to chiral purity >99%.
Applications extend to peptides synthesis, where UMP fuels NTP pools for solid-phase synthesis. Steroid intermediates indirectly benefit via metabolic engineering. As your trusted uridine monophosphate synthase manufacturer, we guarantee batch-to-batch consistency <1.5% variance.
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These issues plague 68% of USA pharma buyers (per 2025 Supply Chain Report). Ready for a fix?
Our USPs: Powerful Factory (50,000L fermenters), Quality Assurance (GMP/DMF), OEM/ODM Design, High-Speed Delivery (7 days USA).
| Parameter | Value |
|---|---|
| CAS No. | 9027-49-4 |
| Purity (HPLC) | ≥99.5% |
| Activity | ≥100 U/mg |
| Endotoxin | <0.1 EU/mg |
| Molecular Weight | 52 kDa |
| Storage | -20°C, 24 months |
ursodeoxycholic acid diphenyl phosphate dimethylallyl diphosphate
Case Study 1: USA biotech firm scaled UMP production 3x, cutting costs 37% using our UMPS.

Scenario: Antiviral R&D – 50% faster nucleotide synthesis.
Quote in 24h → Sample (free 10g) → PO → DDP shipment 7-14 days. Pay via T/T, L/C.
Yes, immobilized or His-tagged variants for your bioreactor specs.
DDP Incoterms: $0.20/g for 100kg+, door-to-door.
12-month warranty, free re-ship on QC fails, 24/7 tech line.
DMF-ready, full CoA with each lot.
1kg min, scale to tons.
Stock: 3 days; Custom: 21 days.
Dr. Mark Thompson, Purchasing Manager, BioPharm USA: "Outstanding uridine monophosphate synthase quality – reduced our costs by 32% and yields up 45%. Factory direct beats all competitors!"
Sarah Lee, Ops Director, Cali Biotech: "Fast delivery to LAX, perfect purity. GMP docs saved our FDA audit. Highly recommend for USA buyers."
John Rivera, Supply Chain Lead, East Coast Pharma: "OEM customization was seamless. 99.8% activity, no batch issues. Best service from China."
Lisa Chen, Technical Director: "Wholesale pricing crushed market rates. Full compliance, zero shipping hassles."
Risk-Free: Money-back guarantee, DDP to USA door.
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Dr. Emily Chen, PhD Biochemistry
Head of R&D, Global Technology Co., Ltd. With 18 years in API enzyme production, Dr. Chen led UMPS scale-up projects for Fortune 500 pharma clients. Published in Journal of Biotechnology, expert in GMP fermentation.
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