Evidence map›Paper›PMID 35610221›Full record

ArticleNature communications2022

An in vivo gene amplification system for high level expression in Saccharomyces cerevisiae.

Bingyin Peng, Lygie Esquirol, Zeyu Lu, Qianyi Shen, Li Chen Cheah, Christopher B Howard, Colin Scott, Matt Trau, Geoff Dumsday, Claudia E Vickers

Abstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Enhancing delta-tocotrienol production inSynthetic and systems biotechnology · 2026
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  4. CRISPR-based synthetic biology toolkit development inSynthetic and systems biotechnology · 2026
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  5. Review
  6. Transposon engineering ofEngineering in life sciences · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Cyanamide-inducible expression of homing nucleaseSynthetic and systems biotechnology · 2024
    Article
  11. High-level biosynthesis of enantiopure germacrene D in yeast.Applied microbiology and biotechnology · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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

10 authors.

Bingyin PengAustralian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane, QLD, 4072, Australia. bingyin.peng@qut.edu.au.ORCID 0000-0001-6918-6016
Lygie EsquirolAustralian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane, QLD, 4072, Australia.ORCID 0000-0002-4887-3260
Zeyu LuAustralian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane, QLD, 4072, Australia.
Qianyi ShenAustralian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane, QLD, 4072, Australia.
Li Chen CheahAustralian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane, QLD, 4072, Australia.ORCID 0000-0002-0072-2885
Christopher B HowardAustralian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane, QLD, 4072, Australia.
Colin ScottCSIRO Synthetic Biology Future Science Platform, Commonwealth Scientific and Industrial Research Organisation (CSIRO), Black Mountain, ACT, 2601, Australia.ORCID 0000-0001-6110-6982
Matt TrauAustralian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane, QLD, 4072, Australia.ORCID 0000-0001-5516-1280
Geoff DumsdayCSIRO Manufacturing, Clayton, VIC, 3169, Australia.
Claudia E VickersCSIRO Synthetic Biology Future Science Platform, Commonwealth Scientific and Industrial Research Organisation (CSIRO), Black Mountain, ACT, 2601, Australia. claudia.vickers@qut.edu.au.ORCID 0000-0002-0792-050X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bottlenecks in metabolic pathways due to insufficient gene expression levels remain a significant problem for industrial bioproduction using microbial cell factories. Increasing gene dosage can overcome these bottlenecks, but current approaches suffer from numerous drawbacks. Here, we describe HapAmp, a method that uses haploinsufficiency as evolutionary force to drive in vivo gene amplification. HapAmp enables efficient, titratable, and stable integration of heterologous gene copies, delivering up to 47 copies onto the yeast genome. The method is exemplified in metabolic engineering to significantly improve production of the sesquiterpene nerolidol, the monoterpene limonene, and the tetraterpene lycopene. Limonene titre is improved by 20-fold in a single engineering step, delivering ∼1 g L

Indexed as

Saccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsGene AmplificationLimoneneMetabolic EngineeringLimoneneSaccharomyces cerevisiae Proteins

Identifiers

PMID35610221
PMCPMC9130285

What OpenQuestion holds

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LicenceCC BY
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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.