Evidence map›Paper›PMID 25239890›Full record

ArticleApplied and environmental microbiology2014

Enzymatic Biosynthesis of Novel Resveratrol Glucoside and Glycoside Derivatives.

Ramesh Prasad Pandey, Prakash Parajuli, Ju Yong Shin, Jisun Lee, Seul Lee, Young-Soo Hong, Yong Il Park, Joong Su Kim, Jae Kyung Sohng

Open access · bronzeAbstract read
In one paragraph

Article in Applied and environmental microbiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
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  9. Exploring the NucleophilicJournal of microbiology and biotechnology · 2020
    Article
  10. OleD Loki as a Catalyst for Hydroxamate Glycosylation.Chembiochem : a European journal of chemical biology · 2020
    Article
  11. Review
  12. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Ramesh Prasad PandeyInstitute of Biomolecule Reconstruction, Department of Pharmaceutical Engineering, Sun Moon University, Tangjeonmyun, Asan-si, Chungnam, South Korea.
Prakash ParajuliInstitute of Biomolecule Reconstruction, Department of Pharmaceutical Engineering, Sun Moon University, Tangjeonmyun, Asan-si, Chungnam, South Korea.
Ju Yong ShinInstitute of Biomolecule Reconstruction, Department of Pharmaceutical Engineering, Sun Moon University, Tangjeonmyun, Asan-si, Chungnam, South Korea.
Jisun LeeDepartment of Biotechnology, Catholic University of Korea, Bucheon, Gyeonggi-do, South Korea.
Seul LeeDepartment of Biotechnology, Catholic University of Korea, Bucheon, Gyeonggi-do, South Korea.
Young-Soo HongChemical Biology Research Center, Korea Research Institute of Bioscience and Biotechnology, Ochang-eup, Chungbuk, South Korea.
Yong Il ParkDepartment of Biotechnology, Catholic University of Korea, Bucheon, Gyeonggi-do, South Korea.
Joong Su KimBioindustry Process Center, Jeonbuk Branch Institute, Korea Research Institute of Bioscience and Biotechnology, Jeonbuk, Jeong-Ub, South Korea.
Jae Kyung SohngInstitute of Biomolecule Reconstruction, Department of Pharmaceutical Engineering, Sun Moon University, Tangjeonmyun, Asan-si, Chungnam, South Korea sohng@sunmoon.ac.kr.
Sun Moon University · KRKorea Research Institute of Bioscience and Biotechnology · KRThe Catholic University of Korea Bucheon St. Mary's Hospital · KRCatholic University of Korea · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A UDP glucosyltransferase from Bacillus licheniformis was overexpressed, purified, and incubated with nucleotide diphosphate (NDP) d- and l-sugars to produce glucose, galactose, 2-deoxyglucose, viosamine, rhamnose, and fucose sugar-conjugated resveratrol glycosides. Significantly higher (90%) bioconversion of resveratrol was achieved with α-d-glucose as the sugar donor to produce four different glucosides of resveratrol: resveratrol 3-O-β-d-glucoside, resveratrol 4'-O-β-d-glucoside, resveratrol 3,5-O-β-d-diglucoside, and resveratrol 3,5,4'-O-β-d-triglucoside. The conversion rates and numbers of products formed were found to vary with the other NDP sugar donors. Resveratrol 3-O-β-d-2-deoxyglucoside and resveratrol 3,5-O-β-d-di-2-deoxyglucoside were found to be produced using TDP-2-deoxyglucose as a donor; however, the monoglycosides resveratrol 4'-O-β-d-galactoside, resveratrol 4'-O-β-d-viosaminoside, resveratrol 3-O-β-l-rhamnoside, and resveratrol 3-O-β-l-fucoside were produced from the respective sugar donors. Altogether, 10 diverse glycoside derivatives of the medically important resveratrol were generated, demonstrating the capacity of YjiC to produce structurally diverse resveratrol glycosides.

Indexed as

BacillusCarbohydratesCloning, MolecularCytosolGene ExpressionGlucuronosyltransferaseGlycosidesRecombinant ProteinsResveratrolStilbenesCarbohydratesGlucuronosyltransferaseGlycosidesRecombinant ProteinsResveratrolStilbenes

Identifiers

PMID25239890
PMCPMC4249177
OpenAlexW1992902358

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.