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通过与一种与子实体相关的细菌恶臭假单胞菌 SB1 共培养,从一种竹生真菌 Shiraia sp. S9 中诱导产生苯并菲醌。

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

机构信息

College of Pharmaceutical Sciences, Soochow University, Suzhou, 215123, China.

Department of Horticultural Sciences, Soochow University, Suzhou, 215123, China.

出版信息

Microb Cell Fact. 2019 Jul 5;18(1):121. doi: 10.1186/s12934-019-1170-5.

Abstract

BACKGROUND

Fungal 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.

RESULTS

A 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.

CONCLUSIONS

We 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.

摘要

背景

来自 Shiraia 子实体的真菌聚对醌(PQ)色素已被广泛认为是医学和农业用途的优秀光敏剂。子实体被功能未知的多样化细菌群落定植。我们从 Shiraia sp. S9 的子实体中筛选出伴生细菌,并探索了细菌对真菌 PQ 产生的诱导作用。

结果

从子实体中分离到的假单胞菌 SB1 被发现能刺激真菌 PQ 的产生,包括 Hypocrellin A、C(HA 和 HC)和 Elsinochrome A-C(EA、EB 和 EC)。共培养 2 天后, Shiraia 菌丝体培养物中 HA 的产量最高(325.87mg/L),约为无菌培养物的 3.20 倍。共培养导致真菌产孢和更紧凑的真菌球形成。此外,细菌处理上调了聚酮合酶基因(PKS)的表达,并激活了 ABC 和 MFS 转运体基因以促进 PQ 外排。

结论

我们建立了一个与宿主 Shiraia 真菌的细菌共培养体系来诱导 PQ 生物合成。我们的结果为理解子实体中细菌-真菌相互作用提供了基础,并为增强光动力治疗药物中 PQ 生产的实际共培养过程提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c704/6612088/6cb62370374e/12934_2019_1170_Fig1_HTML.jpg

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