Evidence map›Paper›PMID 31277643›Full record

ArticleMicrobial cell factories2019

Inducing perylenequinone production from a bambusicolous fungus Shiraia sp. S9 through co-culture with a fruiting body-associated bacterium Pseudomonas fulva SB1.

Yan Jun Ma, Li Ping Zheng, Jian Wen Wang

Open access · goldAbstract read
In one paragraph

Article in Microbial cell factories, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
6.3field-weighted citation impact, top 3% of its field
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

26 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
  2. Article
  3. Interplay betweenMycology · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Induced effect of NaWorld journal of microbiology & biotechnology · 2025
    Article
  8. Review
  9. Energy Metabolism Enhance Perylenequinone Biosynthesis inInternational journal of molecular sciences · 2024
    Article
  10. Article
  11. Volatiles ofSynthetic and systems biotechnology · 2023
    Article
  12. Article
  13. Article
  14. Article
  15. CRISPR/Cas9-Mediated Genome Editing forInternational journal of molecular sciences · 2022
    Article
  16. Review
  17. Article
  18. Fungal perylenequinones.Mycological progress · 2022
    Review
  19. Article
  20. Phylogenetic Position ofJournal of fungi (Basel, Switzerland) · 2021
    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

3 authors at 1 institution in 1 country.

Yan Jun MaCollege of Pharmaceutical Sciences, Soochow University, Suzhou, 215123, China.
Li Ping ZhengDepartment of Horticultural Sciences, Soochow University, Suzhou, 215123, China.
Jian Wen WangCollege of Pharmaceutical Sciences, Soochow University, Suzhou, 215123, China. jwwang@suda.edu.cn.ORCID http://orcid.org/0000-0002-3095-7394
Soochow University · CN

Funding

National Natural Science Foundation of China 81473183National Natural Science Foundation of China 81773696Priority Academic Program Development of the Jiangsu Higher Education Institutes PAPDthe Postgraduate Research & Practice Innovation Program of Jiangsu Province KYCX17_2042
6 · The paper itself

Abstract

backgroundFungal perylenequinonoid (PQ) pigments from Shiraia fruiting body have been well known as excellent photosensitizers for medical and agricultural uses. The fruiting bodies are colonized by a diverse bacterial community of unknown function. We screened the companion bacteria from the fruiting body of Shiraia sp. S9 and explored the bacterial elicitation on fungal PQ production.

resultsA bacterium Pseudomonas fulva SB1 isolated from the fruiting body was found to stimulate the production of fungal PQs including hypocrellins A, C (HA and HC), and elsinochromes A-C (EA, EB and EC). After 2 days of co-cultures, Shiraia mycelium cultures presented the highest production of HA (325.87 mg/L), about 3.20-fold of that in axenic culture. The co-culture resulted in the induction of fungal conidiation and the formation of more compact fungal pellets. Furthermore, the bacterial treatment up-regulated the expression of polyketide synthase gene (PKS), and activated transporter genes of ATP-binding cassette (ABC) and major facilitator superfamily transporter (MFS) for PQ exudation.

conclusionsWe have established a bacterial co-culture with a host Shiraia fungus to induce PQ biosynthesis. Our results provide a basis for understanding bacterial-fungal interaction in fruiting bodies and a practical co-culture process to enhance PQ production for photodynamic therapy medicine.

Indexed as

AscomycotaCoculture TechniquesFruiting Bodies, FungalFungal ProteinsMicrobial InteractionsPerylenePhenolPolyketide SynthasesPseudomonasQuinonesSpores, Fungalelsinochrome AFungal Proteinshypocrellin Ahypocrellin CPerylenePhenolPolyketide SynthasesQuinonesAssociated bacteriaCo-cultureFruiting bodyHypocrellin APerylenequinonesShiraia

Identifiers

PMID31277643
PMCPMC6612088
OpenAlexW2955278823

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.