Evidence map›Paper›PMID 33225887›Full record

ArticleBMC genomics2020

The expression of the acarbose biosynthesis gene cluster in Actinoplanes sp. SE50/110 is dependent on the growth phase.

Julian Droste, Vera Ortseifen, Lena Schaffert, Marcus Persicke, Susanne Schneiker-Bekel, Alfred Pühler, Jörn Kalinowski

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2020. 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
0.8field-weighted citation impact, top 27% 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

12 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Enhancement of Acarbose Production inJournal of agricultural and food chemistry · 2025
    Article
  6. Article
  7. Sigma Factor Engineering inMicroorganisms · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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

7 authors at 1 institution in 1 country.

Julian DrosteMicrobial Genomics and Biotechnology, Center for Biotechnology, Bielefeld University, Sequenz 1, Bielefeld, 33615, Germany.
Vera OrtseifenSenior Research Group in Genome Research of Industrial Microorganisms, Center for Biotechnology, Bielefeld University, Sequenz 1, 33615, Bielefeld, Germany.
Lena SchaffertMicrobial Genomics and Biotechnology, Center for Biotechnology, Bielefeld University, Sequenz 1, Bielefeld, 33615, Germany.
Marcus PersickeMicrobial Genomics and Biotechnology, Center for Biotechnology, Bielefeld University, Sequenz 1, Bielefeld, 33615, Germany.
Susanne Schneiker-BekelSenior Research Group in Genome Research of Industrial Microorganisms, Center for Biotechnology, Bielefeld University, Sequenz 1, 33615, Bielefeld, Germany.
Alfred PühlerSenior Research Group in Genome Research of Industrial Microorganisms, Center for Biotechnology, Bielefeld University, Sequenz 1, 33615, Bielefeld, Germany.
Jörn KalinowskiMicrobial Genomics and Biotechnology, Center for Biotechnology, Bielefeld University, Sequenz 1, Bielefeld, 33615, Germany. Joern.Kalinowski@CeBiTec.Uni-Bielefeld.DE.ORCID http://orcid.org/0000-0002-9052-1998
Bielefeld University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundActinoplanes sp. SE50/110 is the natural producer of the diabetes mellitus drug acarbose, which is highly produced during the growth phase and ceases during the stationary phase. In previous works, the growth-dependency of acarbose formation was assumed to be caused by a decreasing transcription of the acarbose biosynthesis genes during transition and stationary growth phase.

resultsIn this study, transcriptomic data using RNA-seq and state-of-the-art proteomic data from seven time points of controlled bioreactor cultivations were used to analyze expression dynamics during growth of Actinoplanes sp. SE50/110. A hierarchical cluster analysis revealed co-regulated genes, which display similar transcription dynamics over the cultivation time. Aside from an expected metabolic switch from primary to secondary metabolism during transition phase, we observed a continuously decreasing transcript abundance of all acarbose biosynthetic genes from the early growth phase until stationary phase, with the strongest decrease for the monocistronically transcribed genes acbA, acbB, acbD and acbE. Our data confirm a similar trend for acb gene transcription and acarbose formation rate. Surprisingly, the proteome dynamics does not follow the respective transcription for all acb genes. This suggests different protein stabilities or post-transcriptional regulation of the Acb proteins, which in turn could indicate bottlenecks in the acarbose biosynthesis. Furthermore, several genes are co-expressed with the acb gene cluster over the course of the cultivation, including eleven transcriptional regulators (e.g. ACSP50_0424), two sigma factors (ACSP50_0644, ACSP50_6006) and further genes, which have not previously been in focus of acarbose research in Actinoplanes sp. SE50/110.

conclusionIn conclusion, we have demonstrated, that a genome wide transcriptome and proteome analysis in a high temporal resolution is well suited to study the acarbose biosynthesis and the transcriptional and post-transcriptional regulation thereof.

Indexed as

AcarboseActinoplanesMultigene FamilyProteomeProteomicsAcarboseProteomeAcarboseActinoplanesCo-regulationExpression dynamicsProteomicTranscriptomic

Identifiers

PMID33225887
PMCPMC7682106
OpenAlexW3108445597

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LicenceCC BY
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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.