Evidence map›Paper›PMID 34205848›Full record

ArticleMolecules (Basel, Switzerland)2021

Lipozyme 435-Mediated Synthesis of Xylose Oleate in Methyl Ethyl Ketone.

Maria Carolina Pereira Gonçalves, Jéssica Cristina Amaral, Roberto Fernandez-Lafuente, Ruy de Sousa Junior, Paulo Waldir Tardioli

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Enzyme Immobilization.Molecules (Basel, Switzerland) · 2023
    Article
  3. Enzymatic Transesterification of Atlantic Salmon (Materials (Basel, Switzerland) · 2023
    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

5 authors at 2 institutions in 3 countries.

Maria Carolina Pereira GonçalvesPostgraduate Program in Chemical Engineering, Laboratory of Enzyme Technologies (LabEnz), Department of Chemical Engineering, Federal University of São Carlos (UFSCar), Rodovia Washington Luís, km 235, São Carlos 13565-905, SP, Brazil.ORCID 0000-0003-4510-1393
Jéssica Cristina AmaralPostgraduate Program in Chemistry, Laboratory of Natural Products, Department of Chemistry, Federal University of São Carlos (UFSCar), Rodovia Washington Luís, km 235, São Carlos 13565-905, SP, Brazil.ORCID 0000-0002-4509-259X
Roberto Fernandez-LafuenteDepartamento de Biocatálisis, ICP-CSIC, Campus UAM-CSIC, 28049 Madrid, Spain.ORCID 0000-0003-4976-7096
Ruy de Sousa JuniorPostgraduate Program in Chemical Engineering, Laboratory for Development and Automation of Bioprocesses (LaDABio), Department of Chemical Engineering, Federal University of São Carlos (UFSCar), Rodovia Washington Luís, km 235, São Carlos 13565-905, SP, Brazil.ORCID 0000-0003-4916-173X
Paulo Waldir TardioliPostgraduate Program in Chemical Engineering, Laboratory of Enzyme Technologies (LabEnz), Department of Chemical Engineering, Federal University of São Carlos (UFSCar), Rodovia Washington Luís, km 235, São Carlos 13565-905, SP, Brazil.ORCID 0000-0002-5011-9881
Universidade Federal de São Carlos · BRConsejo Superior de Investigaciones Científicas · ES

Funding

Consejo Superior de Investigaciones Científicas AEP045Conselho Nacional de Desenvolvimento Científico e Tecnológico 315092/2020-3Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 001Fundação de Amparo à Pesquisa do Estado de São Paulo 2016/10636-8 and 2019/23908-4Ministerio de Ciencia e Innovación CTQ2017-86170-R
6 · The paper itself

Abstract

In this paper, we have performed the Lipozyme 435-catalyzed synthesis of xylose oleate in methyl ethyl ketone (MEK) from xylose and oleic acid. The effects of substrates' molar ratios, reaction temperature, reaction time on esterification rates, and Lipozyme 435 reuse were studied. Results showed that an excess of oleic acid (xylose: oleic acid molar ratio of 1:5) significantly favored the reaction, yielding 98% of xylose conversion and 31% oleic acid conversion after 24 h-reaction (mainly to xylose mono- and dioleate, as confirmed by mass spectrometry). The highest Lipozyme 435 activities occurred between 55 and 70 °C. The predicted Ping Pong Bi Bi kinetic model fitted very well to the experimental data and there was no evidence of inhibitions in the range assessed. The reaction product was purified and presented an emulsion capacity close to that of a commercial sugar ester detergent. Finally, the repeated use of Lipozyme 435 showed a reduction in the reaction yields (by 48 and 19% in the xylose and oleic acid conversions, respectively), after ten 12 h-cycles.

Indexed as

BiocatalysisButanonesEsterificationHot TemperatureLipaseOleic AcidXyloseButanonesLipaseLipozymemethylethyl ketoneOleic AcidXyloseLipozyme 435methyl ethyl ketoneoleic acidsugar fatty acid estersxylose

Identifiers

PMID34205848
PMCPMC8197991
OpenAlexW3170815569

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.