Evidence map›Paper›PMID 31938970›Full record

ArticleAMB Express2020

A novel trehalosamine isolated from Bacillus amyloliquefaciens and its antibacterial activities.

Ying Wang, Bo Zhao, Yaping Liu, Linjing Mao, Xuanming Zhang, Wu Meng, Kechun Liu, Jie Chu

Abstract read
In one paragraph

Article in AMB Express, 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
–field-weighted citation impact
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.

  1. Article
  2. 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

8 authors.

Ying WangBiology Institute, Qilu University of Technology (Shandong Academy of Sciences), 28789 East Jingshi Road Ji'nan, Shandong, 250103, China.
Bo ZhaoBiology Institute, Qilu University of Technology (Shandong Academy of Sciences), 28789 East Jingshi Road Ji'nan, Shandong, 250103, China.
Yaping LiuSchool of Medical Instrument and Food Engineering, University of Shanghai for Science and Technology, Shanghai, 200093, China.
Linjing MaoCollege of Animal Science and Technology, Shandong Agricultural University, Tai'an,, 271018, Shandong, China.
Xuanming ZhangBiology Institute, Qilu University of Technology (Shandong Academy of Sciences), 28789 East Jingshi Road Ji'nan, Shandong, 250103, China.
Wu MengState Key Laboratory of Biobased Material and Green Papermaking (LBMP), Qilu University of Technology (Shandong Academy of Sciences), Jinan, Shandong, 250353, China.
Kechun LiuBiology Institute, Qilu University of Technology (Shandong Academy of Sciences), 28789 East Jingshi Road Ji'nan, Shandong, 250103, China.
Jie ChuBiology Institute, Qilu University of Technology (Shandong Academy of Sciences), 28789 East Jingshi Road Ji'nan, Shandong, 250103, China. chujie6532@163.com.ORCID http://orcid.org/0000-0002-4037-5558

Funding

Cooperative Fund for Young Doctors of Qilu University(Shandong Academy of Sciences) 2018BSHZ0030National Key Research and Development Plan of China 2016YFE0111600National Science and Technology Cooperation Program of Shandong Academy of Science 2019GHPY14Shandong Academy of Science Fund for Distinguished Young Schlolars LKYZ2018-60
6 · The paper itself

Abstract

Bacillus amyloliquefaciens has been widely used as a probiotic in the field of biological control,and its antibacterial compounds plays an important role in the prevention and control of plant, livestock and poultry diseases. It has the advantages of green, safe and efficiency. This study aims to separate and purify active ingredient from Bacillus amyloliquefaciens GN59 and study its antibacterial activity. A novel compound was isolated from GN59 by column chromatography on silica gel and HPLC purification. The chemical structure was identified as α-D-glucopyranosyl-(1 → 1')-3'-amino-3'-deoxy-β-D-glucopyranoside (a,β-3-trehalosamine) on the basis of spectroscopic analysis. This is the first report about a,β-3-trehalosamine isolated from biological resources on an antibiotic activity against pathogenic bacterium. The 3'-neotrehalosamine displayed antibacterial activity across a broad spectrum of microorganisms, including different gram-positive and gram-negative bacteria, with minimal inhibitory concentration (MIC) values ranging from 0.5 to 0.7 mg/mL. The results indicated that the 3'-neotrehalosamine from GN59 might be a potential candidate for bactericide.

Indexed as

Antibacterial activityBacillus amyloliquefaciensEnvironmental friendlyIdentification

Identifiers

PMID31938970
PMCPMC6960277

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.