Evidence map›Paper›PMID 35705566›Full record

ArticleNature communications2022

Complete biosynthetic pathway to the antidiabetic drug acarbose.

Takeshi Tsunoda, Arash Samadi, Sachin Burade, Taifo Mahmud

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.0field-weighted citation impact, top 3% 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

23 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. NonglycosidicSynthetic and systems biotechnology · 2025
    Article
  8. Article
  9. Enhancement of Acarbose Production inJournal of agricultural and food chemistry · 2025
    Article
  10. Article
  11. Article
  12. Sigma Factor Engineering inMicroorganisms · 2024
    Article
  13. Review
  14. A comprehensiveFrontiers in pharmacology · 2024
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Advances in Zebrafish for Diabetes Mellitus with Wound Model.Bioengineering (Basel, Switzerland) · 2023
    Review
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

4 authors at 1 institution in 1 country.

Takeshi TsunodaDepartment of Pharmaceutical Sciences, Oregon State University, Corvallis, OR, 97331-3507, USA.ORCID 0000-0002-4374-7863
Arash SamadiDepartment of Pharmaceutical Sciences, Oregon State University, Corvallis, OR, 97331-3507, USA.ORCID 0000-0003-4367-6409
Sachin BuradeDepartment of Pharmaceutical Sciences, Oregon State University, Corvallis, OR, 97331-3507, USA.
Taifo MahmudDepartment of Pharmaceutical Sciences, Oregon State University, Corvallis, OR, 97331-3507, USA. Taifo.Mahmud@oregonstate.edu.ORCID 0000-0001-9639-526X
Oregon State University · US

Funding

Biochemical and Mechanistic Studies of PseudoglycosyltransferasesR15GM112068 · NIGMS · OREGON STATE UNIVERSITY · PI MAHMUD, TAIFO · 2014 to 2014
$312k
NIGMS NIH HHS R15 GM112068
6 · The paper itself

Abstract

Acarbose is a bacterial-derived α-glucosidase inhibitor clinically used to treat patients with type 2 diabetes. As type 2 diabetes is on the rise worldwide, the market demand for acarbose has also increased. Despite its significant therapeutic importance, how it is made in nature is not completely understood. Here, we report the complete biosynthetic pathway to acarbose and its structural components, GDP-valienol and O-4-amino-(4,6-dideoxy-α-D-glucopyranosyl)-(1→4)-O-α-D-glucopyranosyl-(1→4)-D-glucopyranose. GDP-valienol is derived from valienol 7-phosphate, catalyzed by three cyclitol modifying enzymes, whereas O-4-amino-(4,6-dideoxy-α-D-glucopyranosyl)-(1→4)-O-α-D-glucopyranosyl-(1→4)-D-glucopyranose is produced from dTDP-4-amino-4,6-dideoxy-D-glucose and maltose by the glycosyltransferase AcbI. The final assembly process is catalyzed by a pseudoglycosyltransferase enzyme, AcbS, which is a homologue of AcbI but catalyzes the formation of a non-glycosidic C-N bond. This study clarifies all previously unknown steps in acarbose biosynthesis and establishes a complete pathway to this high value pharmaceutical.

Indexed as

AcarboseDiabetes Mellitus, Type 2Biosynthetic PathwaysGlycoside Hydrolase InhibitorsHumansHypoglycemic AgentsAcarboseGlycoside Hydrolase InhibitorsHypoglycemic Agents

Identifiers

PMID35705566
PMCPMC9200736
OpenAlexW4282930101

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.