In a brief 30-minute reaction, the top performing enzyme achieved a 63% conversion to the desired chiral alcohol and delivered perfect stereoselectivity, meeting the stringent purity requirements for pharmaceutical ingredients.
In a brief 30-minute reaction, the top performing enzyme achieved a 63% conversion to the desired chiral alcohol and delivered perfect stereoselectivity, meeting the stringent purity requirements for pharmaceutical ingredients.
The introduction of “Feasibility Assessments” —a rapid, preliminary study designed to predict a project’s chances of success before any major investment— led to our overall project success rate soaring from 53% to 85%, providing a level of transparency and risk mitigation previously unheard of in the industry.
The entire discovery-to-validation cycle was completed in a fraction of the time required for traditional approaches, dramatically de-risking the R&D process, lowering costs, and accelerating the timeline for bringing new products to market.
After five intensive rounds of directed evolution, a leading biotech company had achieved an 8x increase in enzyme activity and a 12x increase in enzyme specificity. However, they had reached a plateau.
By screening a small number of mutant enzymes, the team discovered two individual single distant mutations —located more than 11 Å from the active site— that significantly improved the enzyme’s properties.
In only one month, we went from a highly specific bacterial peroxygenase to a versatile enzyme capable of hydroxylating both indole and thioanisole, two substrates it previously could not act on.
Create new products and processes, adapt existing ones or develop completely new biochemistry. Zymvol is here to guide you in any stage of your journey.
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