Evidence map›Paper›PMID 39152436›Full record

ArticleMicrobial cell factories2024

Screening of broad-host expression promoters for shuttle expression vectors in non-conventional yeasts and bacteria.

Liyun Ji, Shuo Xu, Yue Zhang, Hairong Cheng

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Article in Microbial cell factories, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Metabolic Engineering for Gibberellic Acid Production inMolecules (Basel, Switzerland) · 2026
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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Liyun JiState Key Laboratory of Microbial Metabolism, and School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Shuo XuState Key Laboratory of Microbial Metabolism, and School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Yue ZhangState Key Laboratory of Microbial Metabolism, and School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Hairong ChengState Key Laboratory of Microbial Metabolism, and School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China. chrqrq@hotmail.com.

Funding

The National Key Research and Development Program of China 2021YFA0910503the Tianjin Synthetic Biotechnology Innovation Capacity Improvement Action TSBICIP-KJGG-012-02
6 · The paper itself

Abstract

backgroundNon-conventional yeasts and bacteria gain significance in synthetic biology for their unique metabolic capabilities in converting low-cost renewable feedstocks into valuable products. Improving metabolic pathways and increasing bioproduct yields remain dependent on the strategically use of various promoters in these microbes. The development of broad-spectrum promoter libraries with varying strengths for different hosts is attractive for biosynthetic engineers.

resultsIn this study, five Yarrowia lipolytica constitutive promoters (yl.hp4d, yl.FBA1in, yl.TEF1, yl.TDH1, yl.EXP1) and five Kluyveromyces marxianus constitutive promoters (km.PDC1, km.FBA1, km.TEF1, km.TDH3, km.ENO1) were selected to construct promoter-reporter vectors, utilizing α-amylase and red fluorescent protein (RFP) as reporter genes. The promoters' strengths were systematically characterized across Y. lipolytica, K. marxianus, Pichia pastoris, Escherichia coli, and Corynebacterium glutamicum. We discovered that five K. marxianus promoters can all express genes in Y. lipolytica and that five Y. lipolytica promoters can all express genes in K. marxianus with variable expression strengths. Significantly, the yl.TEF1 and km.TEF1 yeast promoters exhibited their adaptability in P. pastoris, E. coli, and C. glutamicum. In yeast P. pastoris, the yl.TEF1 promoter exhibited substantial expression of both amylase and RFP. In bacteria E. coli and C. glutamicum, the eukaryotic km.TEF1 promoter demonstrated robust expression of RFP. Significantly, in E. coli, The RFP expression strength of the km.TEF1 promoter reached ∼20% of the T7 promoter.

conclusionNon-conventional yeast promoters with diverse and cross-domain applicability have great potential for developing innovative and dynamic regulated systems that can effectively manage carbon flux and enhance target bioproduct synthesis across diverse microbial hosts.

Indexed as

Escherichia coliGenetic VectorsKluyveromycesPromoter Regions, GeneticYarrowiaalpha-AmylasesCorynebacterium glutamicumGenes, ReporterLuminescent ProteinsMetabolic EngineeringRed Fluorescent ProteinSaccharomycetalesalpha-AmylasesLuminescent ProteinsRed Fluorescent ProteinNon-conventional hostsPromoterShuttle expression

Identifiers

PMID39152436
PMCPMC11330142

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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.