Evidence map›Paper›PMID 37836827›Full record

ArticleMolecules (Basel, Switzerland)2023

A Simple Screening and Optimization Bioprocess for Long-Chain Peptide Catalysts Applied to Asymmetric Aldol Reaction.

Shulin Wang, Haidong Teng, Lan Wang, Pengcheng Li, Xinghao Yuan, Xi Sang, Jianping Wu, Lirong Yang, Gang Xu

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 70% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 1 institution in 1 country.

Shulin WangCollege of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310058, China.ORCID 0000-0003-0210-8181
Haidong TengCollege of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310058, China.
Lan WangCollege of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310058, China.
Pengcheng LiCollege of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310058, China.
Xinghao YuanCollege of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310058, China.
Xi SangCollege of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310058, China.
Jianping WuCollege of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310058, China.
Lirong YangCollege of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310058, China.
Gang XuCollege of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310058, China.ORCID 0000-0001-8516-8731
Zhejiang University · CN

Funding

the National Key R&D Program of China 2019YFA09005000the National Natural Science Foundation of China 21878264
6 · The paper itself

Abstract

Peptides have demonstrated their efficacy as catalysts in asymmetric aldol reactions. But the constraints inherent in chemical synthesis have imposed limitations on the viability of long-chain peptide catalysts. A noticeable dearth of tools has impeded the swift and effective screening of peptide catalysts using biological methods. To address this, we introduce a straightforward bioprocess for the screening of peptide catalysts for asymmetric aldol reactions. We synthesized several peptides through this method and obtained a 15-amino acid peptide. This peptide exhibited asymmetric aldol catalytic activity, achieving 77% ee in DMSO solvent and 63% ee with over an 80.8% yield in DMSO mixed with a pH 9.0 buffer solution. The successful application of our innovative approach not only represents an advancement but also paves the way for currently unexplored research avenues.

Indexed as

Dimethyl SulfoxidePeptidesAldehydesCatalysisSolventsStereoisomerism3-hydroxybutanalAldehydesDimethyl SulfoxidePeptidesSolventsasymmetric aldol reactionfusion proteinpeptide catalysissimple bioprocess

Identifiers

PMID37836827
PMCPMC10574572
OpenAlexW4387459213

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.