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Ka-Yiu San

Researcher at Rice University

Publications -  225
Citations -  10003

Ka-Yiu San is an academic researcher from Rice University. The author has contributed to research in topics: Escherichia coli & Catharanthus roseus. The author has an hindex of 58, co-authored 225 publications receiving 9482 citations. Previous affiliations of Ka-Yiu San include Konkuk University & California Institute of Technology.

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Novel pathway engineering design of the anaerobic central metabolic pathway in Escherichia coli to increase succinate yield and productivity

TL;DR: Experimental results indicated that these combined pathways gave the most efficient conversion of glucose to succinate with the highest yield using only 1.25 moles of NADH per mole of succinate in contrast to the sole fermentative pathway, which uses 2 moles in comparison to the maximum theoretical succinate yield.
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Metabolic Engineering of Escherichia coli: Increase of NADH Availability by Overexpressing an NAD+-Dependent Formate Dehydrogenase

TL;DR: A genetic means of manipulating the availability of intracellular NADH in vivo by regenerating NADH through the heterologous expression of an NAD(+)-dependent formate dehydrogenase is investigated.
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Metabolic engineering through cofactor manipulation and its effects on metabolic flux redistribution in Escherichia coli.

TL;DR: It is demonstrated that manipulation of cofactors can be achieved by external and genetic means and these manipulations have the potential to be used as an additional tool to achieve desired metabolic goals.
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Studies on on-line bioreactor identification. I. Theory.

TL;DR: The method does not require any model for the growth kinetics and is very successful in accurately estimating the above variables in the presence of intense noise and under both steady‐state and transient conditions.
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Metabolic engineering of aerobic succinate production systems in Escherichia coli to improve process productivity and achieve the maximum theoretical succinate yield

TL;DR: The two-route production system with ptsG inactivation and pepc overexpression demonstrated substantially higher succinate productivity than the previous system, a level unsurpassed for aerobic succinate production.