Evidence map›Paper›PMID 31183516›Full record

ArticleCurrent microbiology2019

Cloning and Analysis of Genes Controlling Antibacterial Activities of Burkholderia pyrrocinia Strain Lyc2.

Xiaoqiang Wang, Dexin Chen, Jing Wang, Chao Feng, Wenjing Wang, Wei Zhang, Bin Li, Jiamin Yu, Bo Xia

Abstract read
PubMed Publisher
In one paragraph

Article in Current microbiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

9 authors at 4 institutions in 1 country.

Xiaoqiang WangTobacco Research Institute of Chinese Academy of Agricultural Sciences (CAAS), Qingdao, 266101, Shandong, People's Republic of China.
Dexin ChenTobacco Research Institute of Chinese Academy of Agricultural Sciences (CAAS), Qingdao, 266101, Shandong, People's Republic of China. chendexin@caas.cn.
Jing WangTobacco Research Institute of Chinese Academy of Agricultural Sciences (CAAS), Qingdao, 266101, Shandong, People's Republic of China.
Chao FengTobacco Research Institute of Chinese Academy of Agricultural Sciences (CAAS), Qingdao, 266101, Shandong, People's Republic of China.
Wenjing WangTobacco Research Institute of Chinese Academy of Agricultural Sciences (CAAS), Qingdao, 266101, Shandong, People's Republic of China.
Wei ZhangTobacco Research Institute of Chinese Academy of Agricultural Sciences (CAAS), Qingdao, 266101, Shandong, People's Republic of China.
Bin LiChina National Tobacco Corporation, Sichuan Company, Chengdu, 610017, People's Republic of China.
Jiamin YuChina National Tobacco Corporation, Sichuan Company, Chengdu, 610017, People's Republic of China.
Bo XiaDepartment of Plant Pathology, College of Plant Protection, Shenyang Agricultural University, Shenyang, 110866, People's Republic of China.
Chinese Academy of Agricultural Sciences · CNChina Tobacco · CNShenyang Agricultural University · CNTobacco Research Institute · CN

Funding

China National Tobacco Corporation Key Technology Project\ 110201601026(LS-06)China National Tobacco Corporation Key Technology Project\ SCYC201703Natural Science Foundation of Shandong Province ZR2018BC037Science Foundation for Young Scholars of Tobacco Research Institute of Chinese Academy of Agricultural Sciences 2017B03
6 · The paper itself

Abstract

The Burkholderia pyrrocinia Lyc2 strain isolated from healthy plant rhizosphere showed significant antimicrobial activities against a variety of plant pathogens. In this study, a random mutation library was constructed using an EZ-Tn5 transposome kit and Erwinia amylovora was used as an indicator to screen for mutants with defective antibacterial activity. The transposon gene was verified in the chromosome of the Lyc2 strain using polymerase chain reaction (PCR). The gene that was disrupted by transposon was amplified by rescue cloning for functional and bioinformatics analyses. Antibacterial analysis indicated that the mutant Lyc2-MT2918 was defective in antibacterial activity. Sequence alignment of the mutant suggested that the disrupted gene Glu-2918 was homologous to the glutathione (GSH) synthase gene Bamb-2918 of strain B. ambifaria AMMD. Genetic functional analysis and complementary assay of the disrupted gene, which was predicted to encode GSH synthase, indicated the essential role of the Glu-2918 gene in the antibacterial activity of strain Lyc2.

Indexed as

Cloning, MolecularSoil MicrobiologyAnti-Bacterial AgentsBacterial ProteinsBurkholderiaGene LibraryGlutathione SynthaseMutagenesis, InsertionalMutationPhylogenyRhizosphereAnti-Bacterial AgentsBacterial ProteinsGlutathione Synthase

Identifiers

PMID31183516
OpenAlexW2951652182

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.