» Articles » PMID: 35999640

Contrasting Regulation of Live Bacillus Cereus No.1 and Its Volatiles on Shiraia Perylenequinone Production

Overview
Publisher Biomed Central
Date 2022 Aug 23
PMID 35999640
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Fungal perylenequinones (PQs) are a class of photoactivated polyketide mycotoxins produced by plant-associated fungi. Hypocrellins, the effective anticancer photodynamic therapy (PDT) agents are main bioactive PQs isolated from a bambusicolous Shiraia fruiting bodies. We found previously that bacterial communities inhabiting fungal fruiting bodies are diverse, but with unknown functions. Bacillus is the most dominant genus inside Shiraia fruiting body. To understand the regulation role of the dominant Bacillus isolates on host fungus, we continued our work on co-culture of the dominant bacterium B. cereus No.1 with host fungus Shiraia sp. S9 to elucidate bacterial regulation on fungal hypocrellin production.

Results: Results from "donut" plate tests indicated that the bacterial culture could promote significantly fungal PQ production including hypocrellin A (HA), HC and elsinochrome A-C through bacterial volatiles. After analysis by gas chromatograph/mass spectrometer and confirmation with commercial pure compounds, the volatiles produced by the bacterium were characterized. The eliciting roles of bacterial volatile organic compounds (VOCs) on HA production via transcriptional regulation of host Shiraia fungus were confirmed. In the established submerged bacterial volatile co-culture, bacterial volatiles could not only promote HA production in the mycelium culture, but also facilitate the release of HA into the medium. The total production of HA was reached to 225.9 mg/L, about 1.87 times that of the fungal mono-culture. In contrast, the live bacterium suppressed markedly fungal PQ production in both confrontation plates and mycelium cultures by direct contact. The live bacterium not only down-regulated the transcript levels of HA biosynthetic genes, but also degraded extracellular HA quickly to its reductive product.

Conclusion: Our results indicated that bacterial volatile release could be a long-distance signal to elicit fungal PQ production. Biodegradation and inhibition by direct contact on fungal PQs were induced by the dominate Bacillus to protect themselves in the fruiting bodies. This is the first report on the regulation of Bacillus volatiles on fungal PQ production. These findings could be helpful for both understanding the intimate fungal-bacterial interactions in a fruiting body and establishing novel cultures for the enhanced production of bioactive PQs.

Citing Articles

Volatiles of fruiting body-associated No.24 stimulate fungal hypocrellin production.

Xu R, Huang Q, Shen W, Li X, Zheng L, Wang J Synth Syst Biotechnol. 2023; 8(3):427-436.

PMID: 37409170 PMC: 10319174. DOI: 10.1016/j.synbio.2023.06.004.

References
1.
Sun C, Ma Y, Wang J . Enhanced production of hypocrellin A by ultrasound stimulation in submerged cultures of Shiraia bambusicola. Ultrason Sonochem. 2017; 38:214-224. DOI: 10.1016/j.ultsonch.2017.03.020. View

2.
Lei X, Zhang M, Ma Y, Wang J . Transcriptomic responses involved in enhanced production of hypocrellin A by addition of Triton X-100 in submerged cultures of Shiraia bambusicola. J Ind Microbiol Biotechnol. 2017; 44(10):1415-1429. DOI: 10.1007/s10295-017-1965-5. View

3.
Ma Y, Zheng L, Wang J . Inducing perylenequinone production from a bambusicolous fungus Shiraia sp. S9 through co-culture with a fruiting body-associated bacterium Pseudomonas fulva SB1. Microb Cell Fact. 2019; 18(1):121. PMC: 6612088. DOI: 10.1186/s12934-019-1170-5. View

4.
Effmert U, Kalderas J, Warnke R, Piechulla B . Volatile mediated interactions between bacteria and fungi in the soil. J Chem Ecol. 2012; 38(6):665-703. DOI: 10.1007/s10886-012-0135-5. View

5.
Cawoy H, Mariutto M, Henry G, Fisher C, Vasilyeva N, Thonart P . Plant defense stimulation by natural isolates of bacillus depends on efficient surfactin production. Mol Plant Microbe Interact. 2013; 27(2):87-100. DOI: 10.1094/MPMI-09-13-0262-R. View