Evidence map›Paper›PMID 42045731›Full record

ArticleWorld journal of microbiology & biotechnology2026

Modulating 6 S RNA improves recombinant protein yield in Escherichia coli at lower temperatures.

Akram Valanik, Yaghoub Safdari, Faezeh Alinia, Mahdi Aalikhani, Zahra Bazi

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Article in World journal of microbiology & biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Akram ValanikDepartment of Medical Biotechnology, Faculty of Advanced Medical Technologies, Golestan University of Medical Sciences, Gorgan, Iran.
Yaghoub SafdariGolestan Research Center of Gastroenterology and Hepatology, Jorjani Clinical Sciences Research Institute, Golestan University of Medical Sciences, Gorgan, Iran.
Faezeh AliniaDepartment of Medical Biotechnology, Faculty of Advanced Medical Technologies, Golestan University of Medical Sciences, Gorgan, Iran.
Mahdi AalikhaniDepartment of Medical Biotechnology, School of Paramedicine, Bushehr University of Medical Sciences, Bushehr, Iran.
Zahra BaziDepartment of Medical Biotechnology, Faculty of Advanced Medical Technologies, Golestan University of Medical Sciences, Gorgan, Iran. zahrabazi1986@gmail.com.

Funding

Golestan University of Medical Sciences 111232
6 · The paper itself

Abstract

High-yield recombinant protein production in Escherichia coli requires balancing growth with proper folding at low temperatures. Here, we engineered 6 S RNA -a reversible σ⁷⁰ antagonist- as a modulator to enhance yields under cold stress (18 °C). Transcriptomic reanalysis of GSE74809 revealed growth phase-specific regulation: deletion of 6 S RNA upregulated amino acid biosynthesis during logarithmic growth but downregulated ribosomal and translation-related genes in the stationary phase. To test its functional impact, 6 S RNA and antisense constructs were cloned into pET‑24a(+), validated by RT‑qPCR, and evaluated at 18 °C and 37 °C. Both overexpression and knockdown impaired growth yet increased total protein levels (BCA, OD₆₀₀‑normalized). CFU enumeration confirmed reversible attenuation without toxicity, followed by asymmetric 18 h growth reduction: controls achieved 5.48‑fold expansion, whereas 6 S overexpression reached 2.39‑fold (44% of control) and anti‑6 S reached 2.95‑fold (67% of control). Critically, 6 S RNA overexpression at 18 °C boosted Cas9‑GFP mRNA fivefold and doubled functional GFP fluorescence.Overall, 6 S RNA enables tunable heterologous protein production by trading proliferation for enhanced folding capacity. Its targeted upregulation significantly improves recombinant protein yield under low‑temperature conditions, highlighting its potential for industrial bioprocessing.

Indexed as

Escherichia coliRecombinant ProteinsRNA, BacterialRNA, RibosomalCold TemperatureEscherichia coli ProteinsGene Expression Regulation, BacterialRNA, UntranslatedSigma Factor6S RNAEscherichia coli ProteinsRecombinant ProteinsRNA, BacterialRNA, RibosomalRNA, UntranslatedSigma Factor6S RNAEscherichia coliProtein yieldRecombinant protein expressionSigma 70

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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.