Evidence map›Paper›PMID 35953485›Full record

ArticleNature communications2022

Biocatalytic routes to stereo-divergent iridoids.

Néstor J Hernández Lozada, Benke Hong, Joshua C Wood, Lorenzo Caputi, Jérôme Basquin, Ling Chuang, Maritta Kunert, Carlos E Rodríguez López, Chloe Langley, Dongyan Zhao and 3 more

Erratum issuedOpen 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. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.6field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 3 countries.

Néstor J Hernández LozadaMax-Planck Institute for Chemical Ecology, Department of Natural Product Biosynthesis, Hans-Knoll Strasse 8, 07745, Jena, Germany.ORCID http://orcid.org/0000-0002-7347-988X
Benke HongMax-Planck Institute for Chemical Ecology, Department of Natural Product Biosynthesis, Hans-Knoll Strasse 8, 07745, Jena, Germany.
Joshua C WoodCenter for Applied Genetic Technologies, University of Georgia, Athens, GA, USA.
Lorenzo CaputiMax-Planck Institute for Chemical Ecology, Department of Natural Product Biosynthesis, Hans-Knoll Strasse 8, 07745, Jena, Germany.
Jérôme BasquinMax-Planck Institute for Biochemistry, Department of Structural Cell Biology, Am Klopferspitz 18, 82152, Martinsried, Germany.
Ling ChuangMax-Planck Institute for Chemical Ecology, Department of Natural Product Biosynthesis, Hans-Knoll Strasse 8, 07745, Jena, Germany.
Maritta KunertMax-Planck Institute for Chemical Ecology, Department of Natural Product Biosynthesis, Hans-Knoll Strasse 8, 07745, Jena, Germany.
Carlos E Rodríguez LópezMax-Planck Institute for Chemical Ecology, Department of Natural Product Biosynthesis, Hans-Knoll Strasse 8, 07745, Jena, Germany.
Chloe LangleyMax-Planck Institute for Chemical Ecology, Department of Natural Product Biosynthesis, Hans-Knoll Strasse 8, 07745, Jena, Germany.ORCID http://orcid.org/0000-0002-1943-7179
Dongyan ZhaoCenter for Applied Genetic Technologies, University of Georgia, Athens, GA, USA.ORCID http://orcid.org/0000-0002-2080-8416
C Robin BuellCenter for Applied Genetic Technologies, University of Georgia, Athens, GA, USA.
Benjamin R LichmanUniversity of York, Department of Biology, Centre for Agricultural Products, Wentworth Way, York, YO10 5DD, UK.ORCID http://orcid.org/0000-0002-0033-1120
Sarah E O'ConnorMax-Planck Institute for Chemical Ecology, Department of Natural Product Biosynthesis, Hans-Knoll Strasse 8, 07745, Jena, Germany. oconnor@ice.mpg.de.ORCID http://orcid.org/0000-0003-0356-6213
Max Planck Institute for Chemical Ecology · DEUniversity of Georgia · USMax Planck Institute of Biochemistry · DEUniversity of York · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thousands of natural products are derived from the fused cyclopentane-pyran molecular scaffold nepetalactol. These natural products are used in an enormous range of applications that span the agricultural and medical industries. For example, nepetalactone, the oxidized derivative of nepetalactol, is known for its cat attractant properties as well as potential as an insect repellent. Most of these naturally occurring nepetalactol-derived compounds arise from only two out of the eight possible stereoisomers, 7S-cis-trans and 7R-cis-cis nepetalactols. Here we use a combination of naturally occurring and engineered enzymes to produce seven of the eight possible nepetalactol or nepetalactone stereoisomers. These enzymes open the possibilities for biocatalytic production of a broader range of iridoids, providing a versatile system for the diversification of this important natural product scaffold.

Indexed as

Biological ProductsIridoidsBiocatalysisCyclopentanesStereoisomerismBiological ProductsCyclopentanesIridoids

Identifiers

PMID35953485
PMCPMC9372074
OpenAlexW4291173461

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.