Evidence map›Paper›PMID 29737437›Full record

ArticleJournal of industrial microbiology & biotechnology2018

Construction of a plasmid interspecific transfer system in Bacillus species with the counter-selectable marker mazF.

XingYa Zhao, JianYong Xu, Ming Tan, ZhenXiao Yu, ShiBin Yang, HongChen Zheng, Hui Song

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Journal of industrial microbiology & biotechnology, 2018. 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
0.1field-weighted citation impact, top 53% 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, 6 citations in OpenAlex.

  1. Article
  2. Microorganisms · 2023
    Review
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

7 authors at 3 institutions in 1 country.

XingYa ZhaoUniversity of Chinese Academy of Sciences, Beijing, 100049, China.
JianYong XuIndustrial Enzymes National Engineering Laboratory, Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, 300308, China.
Ming TanIndustrial Enzymes National Engineering Laboratory, Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, 300308, China.
ZhenXiao YuUniversity of Chinese Academy of Sciences, Beijing, 100049, China.
ShiBin YangUniversity of Chinese Academy of Sciences, Beijing, 100049, China.
HongChen ZhengIndustrial Enzymes National Engineering Laboratory, Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, 300308, China. zheng_hc@tib.cas.cn.
Hui SongUniversity of Chinese Academy of Sciences, Beijing, 100049, China. song_h@tib.cas.cn.ORCID http://orcid.org/0000-0003-2642-1850
Chinese Academy of Sciences · CNTianjin Institute of Industrial Biotechnology · CNUniversity of Chinese Academy of Sciences · CN

Funding

the Key Deployment Project in Chinese Academy of Sciences KFJ-STS-ZDTP-016-1the Key Deployment Project in Chinese Academy of Sciences KFZD-SW-211-2the National Natural Science Fund of China 31701534the Tianjin Science & Technology Planning Project 15YFYssy00040the Tianjin Science & Technology Planning Project 16YFXTSY00530the Tianjin Science & Technology Planning Project 16YFZCSY00790
6 · The paper itself

Abstract

Bacillus sp. strains as attractive hosts for the production of heterologous secretory proteins usually play important roles in bio-industry. However, low transformation efficiency of exogenous plasmids limited the application of Bacillus species. Here, a novel plasmid interspecific transfer system, with high transformation efficiency, high positive rate, and convenient manipulation, has been successfully constructed. A high electrotransformation efficiency strain Bacillus subtilis F-168 containing the counter-selectable marker mazF was used as the plasmid donor strain in this transfer method. A shuttled plasmid pBE980 and its recombinant plasmids pBE980::pulA and pBE980::HSPA were successfully transferred into the recipient Bacillus strains (Bacillus amyloliquefaciens 66, Bacillus licheniformis 124 and Bacillus megaterium 258) by this method. After co-culturing the donor cells (OD

Indexed as

Recombination, GeneticBacillus megateriumBacillus subtilisBacterial ProteinsCoculture TechniquesEndoribonucleasesGenetic MarkersIndustrial MicrobiologyPlasmidsTemperatureBacterial ProteinsEndoribonucleasesGenetic MarkersBacillus speciesB. subtilis 168Counter-selectable markermazF-cassettepBE980Plasmid interspecific transformation

Identifiers

PMID29737437
OpenAlexW2800977865

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.