Evidence map›Paper›PMID 23835156›Full record

ArticleJournal of biotechnology2013

Immobilized enzymes to convert N-sulfo, N-acetyl heparosan to a critical intermediate in the production of bioengineered heparin.

Jian Xiong, Ujjwal Bhaskar, Guoyun Li, Li Fu, Lingyun Li, Fuming Zhang, Jonathan S Dordick, Robert J Linhardt

Open access · greenAbstract read
In one paragraph

Article in Journal of biotechnology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 28 citations in OpenAlex.

  1. Synthetic biology for heparin biomanufacturing.Bioresources and bioprocessing · 2026
    Review
  2. Review
  3. Enzymatic Synthesis of Glycans and Glycoconjugates.Advances in biochemical engineering/biotechnology · 2021
    Review
  4. Article
  5. Review
  6. Engineered heparins as new anticoagulant drugs.Bioengineering & translational medicine · 2017
    Review
  7. Article
  8. Bioengineered heparins and heparan sulfates.Advanced drug delivery reviews · 2016
    Review
  9. Review
  10. Article
  11. Article
  12. Article
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

8 authors at 1 institution in 2 countries.

Jian XiongCollege of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou, Jiangsu Province 225002, China.
Ujjwal Bhaskar
Guoyun Li
Li Fu
Lingyun Li
Fuming Zhang
Jonathan S Dordick
Robert J Linhardt
Rensselaer Polytechnic Institute · US

Funding

In vitro synthesis of recombinant heparan sulfateR01HL094463 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LIU, JIAN, PAWLINSKI, RAFAL L · 2009 to 2021
$5.2M
Synthetic Heparan Sulfate: Probing Biosynthesis to Prepare Defined DrugsR01HL062244 · NHLBI · UNIVERSITY OF IOWA · PI DEANGELIS, PAUL L, LINHARDT, ROBERT J · 2001 to 2016
$4.1M
Development of a Bioengineered Heparin from a Non-Animal SourceR01HL096972 · NHLBI · RENSSELAER POLYTECHNIC INSTITUTE · PI DORDICK, JONATHAN S., LINHARDT, ROBERT J · 2009 to 2013
$3.9M
NHLBI NIH HHS HL094463NHLBI NIH HHS HL096972NHLBI NIH HHS HL62244NHLBI NIH HHS R01 HL062244NHLBI NIH HHS R01 HL094463NHLBI NIH HHS R01 HL096972
6 · The paper itself

Abstract

Heparin is a critically important anticoagulant drug that is prepared from pig intestine. In 2007-2008, there was a crisis in the heparin market when the raw material was adulterated with the toxic polysaccharide, oversulfated chondroitin sulfate, which was associated with 100 deaths in the U.S. alone. As the result of this crisis, our laboratory and others have been actively pursuing alternative sources for this critical drug, including synthetic heparins and bioengineered heparin. In assessing the bioengineering processing costs it has become clear that the use of both enzyme-catalyzed cofactor recycling and enzyme immobilization will be needed for commercialization. In the current study, we examine the use of immobilization of C₅-epimerase and 2-O-sulfotransferase involved in the first enzymatic step in the bioengineered heparin process, as well as arylsulfotransferase-IV involved in cofactor recycling in all three enzymatic steps. We report the successful immobilization of all three enzymes and their use in converting N-sulfo, N-acetyl heparosan into N-sulfo, N-acetyl 2-O-sulfo heparin.

Indexed as

BioengineeringBioreactorsCarbohydrate EpimerasesEnzymes, ImmobilizedEnzyme StabilityGlycosaminoglycansHeparinPhosphoadenosine PhosphosulfateSulfotransferasesCarbohydrate EpimerasesEnzymes, ImmobilizedGlycosaminoglycansHeparinN-acetylheparosanPhosphoadenosine PhosphosulfateSulfotransferases2OST2-O-sulfotransferase3′-phosphoadenosine-5′-phosphate3′-phosphoadenosine-5′-phosphosulfate4-nitrophenyl sulfatearylsulfotransferase IVAryl sulfotransferase IVAST-IVC(5)-epiC(5)-epimerasecGMPcurrent good manufacturing practiceselectrospray ionizationESIheparinHeparosanheteronuclear multiple-quantum coherenceHHCOSYHMQCHpImmobilized enzymesLC/MSliquid chromatography/mass spectrometryNACHpNMRnon-anticoagulant heparinNSNA2SHpNSNAHN-sulfo heparosan (NSH), N-sulfo, N-acetyl heparosanN-sulfo, N-acetyl, 2-O-sulfoheparinnuclear magnetic resonancePAPPAPSPNPSproton–proton correlation spectroscopy

Identifiers

PMID23835156
PMCPMC3780768
OpenAlexW2124679631

What OpenQuestion holds

Textmetadata
LicenceTDM
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.