Evidence map›Paper›PMID 42045357›Full record

ArticleScientific reports2026

Comparative study of phycoerythrobilin synthases for fine-tuning photosynthetic light-harvesting complexes, phycobilisomes.

Mizuho Sato, Mai Watanabe, Misaki Iwata, Kaisei Maeda, Kaori Nimura-Matsune, Masahiko Ikeuchi, Rei Narikawa, Satoru Watanabe

Abstract readComparative Study
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Mizuho SatoDepartment of Bioscience, Tokyo University of Agriculture, Tokyo, 156-8502, Japan.
Mai WatanabeDepartment of Biological Sciences, Graduate School of Science, Tokyo Metropolitan University, Tokyo, 192-0397, Japan.
Misaki IwataDepartment of Bioscience, Tokyo University of Agriculture, Tokyo, 156-8502, Japan.
Kaisei MaedaLaboratory for Chemistry and Life Science, Institute of Integrated Research, Institute of Science Tokyo, Yokohama, 226-8503, Japan.
Kaori Nimura-MatsuneDepartment of Bioscience, Tokyo University of Agriculture, Tokyo, 156-8502, Japan.
Masahiko IkeuchiGraduate School of Arts and Sciences, University of Tokyo, Tokyo, 153-0041, Japan.
Rei NarikawaDepartment of Biological Sciences, Graduate School of Science, Tokyo Metropolitan University, Tokyo, 192-0397, Japan.
Satoru WatanabeDepartment of Bioscience, Tokyo University of Agriculture, Tokyo, 156-8502, Japan. s3watana@nodai.ac.jp.ORCID https://orcid.org/0000-0001-7456-5053

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phycobilisomes serve as the major light-harvesting antenna complexes in cyanobacteria; they capture light and transfer excitation energy to the photosystems, and their spectral and functional properties are primarily determined by the types of bilin chromophores attached to phycobiliproteins. We previously revealed that the properties of phycobilisomes can be modulated by altering the biosynthesis of these bilin chromophores. In this study, we introduced two distinct phycoerythrobilin (PEB) biosynthetic enzymes, pcyX and pebS, into the cyanobacterium Synechococcus elongatus PCC 7942 and successfully enabled PEB incorporation into native phycobilisomes. PebS exhibited high PEB synthesis activity comparable to the canonical PebA-PebB pathway, whereas PcyX showed lower activity, enabling fine-tuning of PEB accumulation. Consistent with previous findings, moderate PEB supply enhanced growth under green light; notably, PcyX expression further promoted growth by providing a more balanced pigment supply. Transcriptome analysis confirmed comparable expression of pebA-pebB, pcyX, and pebS, and revealed that increased PEB accumulation triggered broad metabolic remodeling: genes for glucose metabolism, hydrogenase complexes, potassium transporters, and regulatory factors including sigma factors were upregulated, suggesting a shift toward dissipation of excess reducing power. Together, these findings demonstrate that engineering bilin biosynthesis modifies light-harvesting properties and influences cellular metabolic balance, illustrating the potential of pigment pathway manipulation for redesigning photosynthetic function.

Indexed as

Bacterial ProteinsLight-Harvesting Protein ComplexesPhotosynthesisPhycobilinsPhycobilisomesSynechococcusGreen LightPhycoerythrinBacterial ProteinsLight-Harvesting Protein ComplexesPhycobilinsPhycobilisomesPhycoerythrinphycoerythrobilinCyanobacteriaPhotosynthesisPhycobilisomePhycocyaninPhycoerythrin

Identifiers

PMID42045357
PMCPMC13197396

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