Evidence map›Paper›PMID 31686390›Full record

ArticleJournal of microbiology (Seoul, Korea)2020

Identification and characterization of a novel light-induced promoter for recombinant protein production in Pleurotus ostreatus.

Chaomin Yin, Xiuzhi Fan, Kun Ma, Zheya Chen, Defang Shi, Fen Yao, Hong Gao, Aimin Ma

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of microbiology (Seoul, Korea), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 46% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. High-Throughput Analysis Reveals Stable Metabolome ofInternational journal of molecular sciences · 2026
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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 3 institutions in 1 country.

Chaomin YinInstitute of Agro-Products Processing and Nuclear-Agricultural Technology, Hubei Academy of Agricultural Sciences, Wuhan, 430064, P. R. China. yinchaomin@163.com.
Xiuzhi FanInstitute of Agro-Products Processing and Nuclear-Agricultural Technology, Hubei Academy of Agricultural Sciences, Wuhan, 430064, P. R. China.
Kun MaInstitute of Agro-Products Processing and Nuclear-Agricultural Technology, Hubei Academy of Agricultural Sciences, Wuhan, 430064, P. R. China.
Zheya ChenInstitute of Agro-Products Processing and Nuclear-Agricultural Technology, Hubei Academy of Agricultural Sciences, Wuhan, 430064, P. R. China.
Defang ShiInstitute of Agro-Products Processing and Nuclear-Agricultural Technology, Hubei Academy of Agricultural Sciences, Wuhan, 430064, P. R. China.
Fen YaoInstitute of Agro-Products Processing and Nuclear-Agricultural Technology, Hubei Academy of Agricultural Sciences, Wuhan, 430064, P. R. China.
Hong GaoInstitute of Agro-Products Processing and Nuclear-Agricultural Technology, Hubei Academy of Agricultural Sciences, Wuhan, 430064, P. R. China.
Aimin MaCollege of Food Science and Technology, Huazhong Agricultural University, Wuhan, 430070, P. R. China. aiminma@mail.hzau.edu.cn.
Hubei Academy of Agricultural Sciences · CNHuazhong Agricultural University · CNWuhan College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A lectin gene (plectin) with a high level of expression was previously identified by comparative transcriptome analysis of Pleurotus ostreatus. In this study, we cloned a 733-bp DNA fragment from the start codon of the plectin gene. Sequence analysis showed that the plectin promoter (Plp) region contained several eukaryotic transcription factor binding motifs, such as the TATA-box, four possible CAAT-box, light respon-siveness motifs and MeJA-responsiveness motifs. To deter-mine whether the Plp promoter was a light-regulated promoter, we constructed an expression vector with the fused egfp-hph fragment under the control of the Plp promoter and transformed P. ostreatus mycelia via Agrobacterium tunte-faciens. PCR and Southern blot analyses confirmed the Plp-egfp-hph fragment was integrated into the chromosomal DNA of transformants. qRT-PCR, egfp visualization, and intracellular egfp determination experiments showed the Plp promoter could be a light-induced promoter that may be suitable for P. ostreatus genetic engineering. This study lays the foundation for gene homologous expression in P. ostreatus.

Indexed as

Fungal ProteinsLectinsPleurotusRecombinant ProteinsAgrobacterium tumefaciensCloning, MolecularGene Expression Regulation, FungalGenetic EngineeringGreen Fluorescent ProteinsMyceliumPromoter Regions, GeneticFungal ProteinsGreen Fluorescent ProteinsLectinsRecombinant ProteinsAgrobacterium tumefacienslectinlight-inductionPleurotus ostreatuspromoter

Identifiers

PMID31686390
OpenAlexW2982981340

What OpenQuestion holds

Textmetadata
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.