Evidence map›Paper›PMID 31016583›Full record

ArticleJournal of industrial microbiology & biotechnology2019

Characterization and engineering of the Lrp/AsnC family regulator SACE_5717 for erythromycin overproduction in Saccharopolyspora erythraea.

Jing Liu, Yunfu Chen, Long Li, Endong Yang, Yansheng Wang, Hang Wu, Lixin Zhang, Weiyun Wang, Buchang Zhang

Abstract read
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In one paragraph

Article in Journal of industrial microbiology & biotechnology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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  12. Synthetic biology enabling access to designer polyketides.Current opinion in chemical biology · 2020
    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

9 authors.

Jing LiuSchool of Life Sciences, Anhui Agricultural University, Hefei, 230036, China.
Yunfu ChenInstitute of Physical Science and Information Technology, School of Life Sciences, Anhui University, Hefei, 230601, China.
Long LiSchool of Life Sciences, Anhui Agricultural University, Hefei, 230036, China.
Endong YangSchool of Life Sciences, Anhui Agricultural University, Hefei, 230036, China.
Yansheng WangInstitute of Physical Science and Information Technology, School of Life Sciences, Anhui University, Hefei, 230601, China.
Hang WuInstitute of Physical Science and Information Technology, School of Life Sciences, Anhui University, Hefei, 230601, China.
Lixin ZhangInstitute of Physical Science and Information Technology, School of Life Sciences, Anhui University, Hefei, 230601, China.
Weiyun WangSchool of Life Sciences, Anhui Agricultural University, Hefei, 230036, China. weiyunw@126.com.
Buchang ZhangInstitute of Physical Science and Information Technology, School of Life Sciences, Anhui University, Hefei, 230601, China. zhbc@ahu.edu.cn.

Funding

Initial Foundation of Scientific Research in Anhui Agricultural University yj2018-08National Natural Science Foundation of China 31300081National Natural Science Foundation of China 31570074National Natural Science Foundation of China 31600064National Natural Science Foundation of China 31800057National Program on Key Basic Research Project 2013CB734000
6 · The paper itself

Abstract

In this work, we found that the Lrp/AsnC family protein SACE_5717 negatively regulated erythromycin biosynthesis in S. erythraea. Disruption of SACE_5717 led to a 27% improvement in the yield of erythromycin in S. erythraea A226. SACE_5717 directly repressed its own gene expression, as well as that of the adjacent gene SACE_5716 by binding to the target sequence 5'-GAACGTTCGCCGTCACGCC-3'. The predicted LysE superfamily protein SACE_5716 directly influenced the export of lysine, histidine, threonine and glycine in S. erythraea. Arginine, tyrosine and tryptophan were characterized as the effectors of SACE_5717 by weakening the binding affinity of SACE_5717. In the industrial S. erythraea WB strain, deletion of SACE_5717 (WBΔSACE_5717) increased erythromycin yield by 20%, and by 36% when SACE_5716 was overexpressed in WBΔSACE_5717 (WBΔSACE_5717/5716). In large-scale 5-L fermentation experiment, erythromycin yield in the engineered strain WBΔSACE_5717/5716 reached 4686 mg/L, a 41% enhancement over 3323 mg/L of the parent WB strain.

Indexed as

ErythromycinProtein EngineeringSaccharopolysporaErythromycinEngineeringErythromycinLrp/AsnC family regulatorSaccharopolyspora erythraeaSACE_5717

Identifiers

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Registered trials

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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.