Evidence map›Paper›PMID 41108018›Full record

ArticleBiotechnology for biofuels and bioproducts2025

The link of carbon catabolite repression elements, small RNAs CrcY and CrcZ and polyhydroxyalkanoate metabolism in Pseudomonas putida KT2440.

Yixin Che, Dominic Harris-Jukes, Elizabeth Sitko, Moya Brady, William Casey, Michael P Shaver, Kevin O'Connor, Tanja Narancic

Abstract read
In one paragraph

Article in Biotechnology for biofuels and bioproducts, 2025. 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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2 · The registry

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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

8 authors.

Yixin CheUCD Earth Institute and School of Biomolecular and Biomedical Science, University College Dublin, Belfield, Dublin 4, Ireland.
Dominic Harris-JukesSustainable Materials Innovation Hub, Department of Materials, University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
Elizabeth SitkoUCD Earth Institute and School of Biomolecular and Biomedical Science, University College Dublin, Belfield, Dublin 4, Ireland.
Moya BradyUCD Earth Institute and School of Biomolecular and Biomedical Science, University College Dublin, Belfield, Dublin 4, Ireland.
William CaseyUCD Earth Institute and School of Biomolecular and Biomedical Science, University College Dublin, Belfield, Dublin 4, Ireland.
Michael P ShaverSustainable Materials Innovation Hub, Department of Materials, University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
Kevin O'ConnorUCD Earth Institute and School of Biomolecular and Biomedical Science, University College Dublin, Belfield, Dublin 4, Ireland.
Tanja NarancicUCD Earth Institute and School of Biomolecular and Biomedical Science, University College Dublin, Belfield, Dublin 4, Ireland. tanja.narancic@ucd.ie.

Funding

China Scholarship Council (CSC) 202108110071SFI Research Centre for Energy, Climate and Marine 21/RC/1037_P2
6 · The paper itself

Abstract

backgroundPolyhydroxyalkanoates (PHAs), biodegradable polymers, can be synthesised and degraded by a number of bacteria. With a range of monomer composition and molecular weight, these polymers can be used for packaging to medical applications. However, the production cost, inadequate mechanical properties, and challenging melt processing properties are major impediments. Understanding and harnessing the regulatory networks underpinning PHA production in a model organism Pseudomonas putida KT2440 is an invaluable tool to increase PHA production and alter polymer properties for specific applications.

resultsThe small RNAs CrcY and CrcZ, key components of the carbon catabolite repression (CCR) system, are implicated in PHA metabolism in P. putida KT2440. Their in trans overexpression in P. putida KT2440 shows a 1.3- to 3.5-fold increase in PHA titre (g/L), using glucose or octanoate as feedstocks. This is accompanied by a decrease in the Mw of the synthesised polymer. Among the proteins showing differential expression in response to CrcY and CrcZ overexpression, glutaryl-CoA dehydrogenase GcdH, involved in the catabolism of lysine, hydroxylysine, and tryptophan, and gamma-glutamyl transpeptidase GGT, involved in glutathione metabolism, showed a consistent increase in abundance across different conditions. It also appears that CrcY and CrcZ can compensate for each other, as only when both sRNAs are removed is a 2.5-fold decrease in PHA observed. We also show that these sRNAs require other CCR elements, Hfq and Crc, for their role in PHA metabolism.

conclusionsOne strategy to overcome poor mechanical properties of PHAs is to blend them with a second polymer. Medium chain length (mcl)-PHA acts as a plasticiser when blended with poly-3-hydroxybutyrate (PHB), the most widespread used PHA resin. Here we show a clear effect of the overexpression of CCR elements CrcY and CrcZ in P. putida KT2440 on the amount of the accumulated mcl-PHA and its Mw, making this tool valuable to produce mcl-PHA-based additives. These findings highlight the complementary regulatory roles of CrcY and CrcZ in modulating CCR to optimise PHA production. This study provides insights into leveraging CCR elements to enhance the efficiency of PHA biosynthesis, contributing to the development of sustainable bioplastic production.

Identifiers

PMID41108018
PMCPMC12533007

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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.