打破障碍:黑曲霉几丁质合成酶复合物的综合功能分析。

Q1 Agricultural and Biological Sciences Fungal Biology and Biotechnology Pub Date : 2024-03-11 DOI:10.1186/s40694-024-00172-7
Lars Barthel, Timothy Cairns, Sven Duda, Henri Müller, Birgit Dobbert, Sascha Jung, Heiko Briesen, Vera Meyer
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引用次数: 0

摘要

背景:真菌王国的成员都是异养真核生物,细胞壁中含有几丁质。这种聚合物对细胞壁的硬度以及最终的细胞形状至关重要。大多数真菌基因组都包含许多假定的几丁质合成酶编码基因。然而,对特定物种的全部几丁质合成酶目录进行系统的功能分析却很少见。这极大地限制了对整个真菌王国几丁质合成的基本理解和潜在应用:在这项研究中,我们对多功能细胞工厂黑曲霉进行了硅分析,随后删除了所有预测的几丁质合成酶编码基因。系统进化分析表明,九种几丁质合成酶进化为三个不同的组。转录剖析和共表达网络的构建显示了明显的独立表达,有力地支持了各自几丁质合成酶的特定作用。缺失突变体证实,所有基因对萌发都是不可或缺的,但却会影响菌落孢子滴度、头层隔膜的几丁质含量以及沉水真菌颗粒的内部结构。我们还能确定单个几丁质合成酶的特定作用,包括影响菌落径向生长速率(ChsE、ChsF)、侧细胞壁几丁质含量(CsmA)、与分泌型抗真菌蛋白的化学基因相互作用(CsmA、CsmB、ChsE、ChsF)、对治疗药物的抗性(ChsE),以及调节液体培养中菌团直径的合成酶(ChsA、ChsB)。从应用的角度来看,我们发现与对照菌株相比,chsF 基因缺失会使培养上清液中的总蛋白增加三倍以上,这表明丝状真菌几丁质含量工程学是菌株优化的一个优先级很高但尚未得到充分开发的策略:本研究对黑僵菌的全部几丁质合成酶编码基因进行了广泛分析。我们首次揭示了几丁质合成酶在该真菌中的冗余和非冗余功能作用。我们的数据揭示了几丁质在真菌生长、形态、生存和分泌过程中复杂、多面和动态的作用,从而提高了对真菌的基本认识,并为真菌的生物技术应用开辟了新途径。
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Breaking down barriers: comprehensive functional analysis of the Aspergillus niger chitin synthase repertoire.

Background: Members of the fungal kingdom are heterotrophic eukaryotes encased in a chitin containing cell wall. This polymer is vital for cell wall stiffness and, ultimately, cell shape. Most fungal genomes contain numerous putative chitin synthase encoding genes. However, systematic functional analysis of the full chitin synthase catalogue in a given species is rare. This greatly limits fundamental understanding and potential applications of manipulating chitin synthesis across the fungal kingdom.

Results: In this study, we conducted in silico profiling and subsequently deleted all predicted chitin synthase encoding genes in the multipurpose cell factory Aspergillus niger. Phylogenetic analysis suggested nine chitin synthases evolved as three distinct groups. Transcript profiling and co-expression network construction revealed remarkably independent expression, strongly supporting specific role(s) for the respective chitin synthases. Deletion mutants confirmed all genes were dispensable for germination, yet impacted colony spore titres, chitin content at hyphal septa, and internal architecture of submerged fungal pellets. We were also able to assign specific roles to individual chitin synthases, including those impacting colony radial growth rates (ChsE, ChsF), lateral cell wall chitin content (CsmA), chemical genetic interactions with a secreted antifungal protein (CsmA, CsmB, ChsE, ChsF), resistance to therapeutics (ChsE), and those that modulated pellet diameter in liquid culture (ChsA, ChsB). From an applied perspective, we show chsF deletion increases total protein in culture supernatant over threefold compared to the control strain, indicating engineering filamentous fungal chitin content is a high priority yet underexplored strategy for strain optimization.

Conclusion: This study has conducted extensive analysis for the full chitin synthase encoding gene repertoire of A. niger. For the first time we reveal both redundant and non-redundant functional roles of chitin synthases in this fungus. Our data shed light on the complex, multifaceted, and dynamic role of chitin in fungal growth, morphology, survival, and secretion, thus improving fundamental understanding and opening new avenues for biotechnological applications in fungi.

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来源期刊
Fungal Biology and Biotechnology
Fungal Biology and Biotechnology Agricultural and Biological Sciences-Ecology, Evolution, Behavior and Systematics
CiteScore
10.20
自引率
0.00%
发文量
17
审稿时长
9 weeks
期刊最新文献
CRISPR-Cas9-mediated enhancement of Beauveria bassiana virulence with overproduction of oosporein. Quantification of fungal biomass in mycelium composites made from diverse biogenic side streams. Filamentous fungi as emerging cell factories for the production of aromatic compounds. Enhancement of antioxidant activity and total phenolic content of Fomitopsis pinicola mycelium extract. Development of a whole-cell SELEX process to select species-specific aptamers against Aspergillus niger.
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