Evidence map›Paper›PMID 39014484›Full record

ArticleBiotechnology for biofuels and bioproducts2024

Deciphering the genetic landscape of enhanced poly-3-hydroxybutyrate production in Synechocystis sp. B12.

Anna Santin, Flavio Collura, Garima Singh, Maria Silvia Morlino, Edoardo Bizzotto, Alessandra Bellan, Ameya Pankaj Gupte, Lorenzo Favaro, Stefano Campanaro, Laura Treu and 1 more

Abstract read
In one paragraph

Article in Biotechnology for biofuels and bioproducts, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. 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

11 authors.

Anna SantinDepartment of Biology, University of Padova, 35131, Padua, Italy. anna.santin@unipd.it.
Flavio ColluraDepartment of Biology, University of Padova, 35131, Padua, Italy.
Garima SinghDepartment of Biology, University of Padova, 35131, Padua, Italy.
Maria Silvia MorlinoDepartment of Biology, University of Padova, 35131, Padua, Italy.
Edoardo BizzottoDepartment of Biology, University of Padova, 35131, Padua, Italy.
Alessandra BellanDepartment of Biology, University of Padova, 35131, Padua, Italy.
Ameya Pankaj GupteWaste to Bioproducts Lab, Department of Agronomy Food Natural Resources Animals and Environment, University of Padova - Agripolis, 35020, Legnaro, PD, Italy.
Lorenzo FavaroWaste to Bioproducts Lab, Department of Agronomy Food Natural Resources Animals and Environment, University of Padova - Agripolis, 35020, Legnaro, PD, Italy.
Stefano CampanaroDepartment of Biology, University of Padova, 35131, Padua, Italy.
Laura TreuDepartment of Biology, University of Padova, 35131, Padua, Italy.
Tomas MorosinottoDepartment of Biology, University of Padova, 35131, Padua, Italy.

Funding

Horizon 2020 Framework Programme 691712Ministero dell'Istruzione, dell'Università e della Ricerca 327331
6 · The paper itself

Abstract

backgroundMicrobial biopolymers such as poly-3-hydroxybutyrate (PHB) are emerging as promising alternatives for sustainable production of biodegradable bioplastics. Their promise is heightened by the potential utilisation of photosynthetic organisms, thus exploiting sunlight and carbon dioxide as source of energy and carbon, respectively. The cyanobacterium Synechocystis sp. B12 is an attractive candidate for its superior ability to accumulate high amounts of PHB as well as for its high-light tolerance, which makes it extremely suitable for large-scale cultivation. Beyond its practical applications, B12 serves as an intriguing model for unravelling the molecular mechanisms behind PHB accumulation.

resultsThrough a multifaceted approach, integrating physiological, genomic and transcriptomic analyses, this work identified genes involved in the upregulation of chlorophyll biosynthesis and phycobilisome degradation as the possible candidates providing Synechocystis sp. B12 an advantage in growth under high-light conditions. Gene expression differences in pentose phosphate pathway and acetyl-CoA metabolism were instead recognised as mainly responsible for the increased Synechocystis sp. B12 PHB production during nitrogen starvation. In both response to strong illumination and PHB accumulation, Synechocystis sp. B12 showed a metabolic modulation similar but more pronounced than the reference strain, yielding in better performances.

conclusionsOur findings shed light on the molecular mechanisms of PHB biosynthesis, providing valuable insights for optimising the use of Synechocystis in economically viable and sustainable PHB production. In addition, this work supplies crucial knowledge about the metabolic processes involved in production and accumulation of these molecules, which can be seminal for the application to other microorganisms as well.

Indexed as

CyanobacteriaLightPoly-3-hydroxybutyrateStarvationTranscriptomics

Identifiers

PMID39014484
PMCPMC11253406

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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.