scispace - formally typeset
P

Prakash Parajuli

Researcher at Sun Moon University

Publications -  52
Citations -  946

Prakash Parajuli is an academic researcher from Sun Moon University. The author has contributed to research in topics: Chemistry & Engineering. The author has an hindex of 13, co-authored 44 publications receiving 741 citations.

Papers
More filters
Journal ArticleDOI

Probing 3-hydroxyflavone for in vitro glycorandomization of flavonols by YjiC.

TL;DR: In this article, 3-hydroxyflavone was selected as a probe for in vitro glycorandomization of all flavonols using diverse nucleotide diphosphate-d/l-sugars.
Journal ArticleDOI

Synthetic sugar cassettes for the efficient production of flavonol glycosides in Escherichia coli.

TL;DR: This multi-monocistronic synthetic vector in a microbial platform is customizable to defined task and would certainly be useful for applications in producing and modifying such therapeutically valued plant secondary metabolites.
Journal ArticleDOI

Enzymatic synthesis of epothilone A glycosides.

TL;DR: Epothilone A 7-O-β-D-glucoside was structurally elucidated by ultra-high performance liquid chromatography-photo diode array conjugated with high resolution quantitative time-of-flight-electrospray ionization mass spectroscopy (HR-QTOF ESI-MS/MS) supported by one-and two-dimensional nuclear magnetic resonance studies.
Journal ArticleDOI

Biosynthesis of flavone C -glucosides in engineered Escherichia coli

TL;DR: Two plant-originated C-glucosyltransferases from Glycine max and Gentiana triflora were accessed for glucosylation of selected flavones chrysin and luteolin, found to be more soluble and more stable to high temperature, different pH range, and β- glucosidase enzyme, than O-glUCosylated derivative of chrysIn.
Journal ArticleDOI

Combinatorial approach for improved cyanidin 3-O-glucoside production in Escherichia coli.

TL;DR: A synthetic vector system using different promoters has been developed and used for the synthesis of C3G in E. coli BL21 (DE3) by directing the metabolic flux towards the UDP-d-glucose.