Involvement of the adaptor protein 3 complex in lignocellulase secretion in Neurospora crassa revealed by comparative genomic screening

比较基因组筛选揭示衔接蛋白 3 复合物参与粗糙脉孢菌木质纤维素酶的分泌

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作者:Xue Pei #, Feiyu Fan #, Liangcai Lin, Yong Chen, Wenliang Sun, Shihong Zhang, Chaoguang Tian

Background

Lignocellulase hypersecretion has been achieved in industrial fungal workhorses such as Trichoderma reesei, but the underlying mechanism associated with this process is not well understood. Although previous comparative genomic studies have revealed that the mutagenic T. reesei strain RUT-C30 harbors hundreds of mutations compared with its parental strain QM6a, how these mutations actually contribute to the hypersecretion phenotype remains to be elucidated.

Conclusions

Using the model cellulolytic fungus N. crassa, we explored potential hypersecretion-related mutations in T. reesei strain RUT-C30. Through systematic genetic screening of 86 corresponding orthologous KO mutants in N. crassa, we identified several genes, particularly those encoding the AP-3 complex that contribute to lignocellulase secretion. These findings will be useful for strain improvement in future lignocellulase and biomass-based chemical production.

Results

In this study, we systematically screened gene knockout (KO) mutants in the cellulolytic fungus Neurospora crassa, which contains orthologs of potentially defective T. reesei RUT-C30 mutated genes. Of the 86 deletion mutants screened in N. crassa, 12 exhibited lignocellulase production more than 25% higher than in the wild-type (WT) strain and 4 showed nearly 25% lower secretion. We observed that the deletion of Ncap3m (NCU03998), which encodes the μ subunit of the adaptor protein 3 (AP-3) complex in N. crassa, led to the most significant increase in lignocellulase secretion under both Avicel and xylan culture conditions. Moreover, strains lacking the β subunit of the AP-3 complex, encoded by Ncap3b (NCU06569), had a similar phenotype to ΔNcap3m, suggesting that the AP-3 complex is involved in lignocellulase secretion in N. crassa. We also found that the transcriptional abundance of major lignocellulase genes in ΔNcap3m was maintained at a relatively higher level during the late stage of fermentation compared with the WT, which might add to the hypersecretion phenotype. Finally, we found that importation of the T. reesei ap3m ortholog Trap3m into ΔNcap3m can genetically restore secretion of lignocellulases to normal levels, which suggests that the effect of the AP-3 complex on lignocellulase secretion is conserved in cellulolytic ascomycetes. Conclusions: Using the model cellulolytic fungus N. crassa, we explored potential hypersecretion-related mutations in T. reesei strain RUT-C30. Through systematic genetic screening of 86 corresponding orthologous KO mutants in N. crassa, we identified several genes, particularly those encoding the AP-3 complex that contribute to lignocellulase secretion. These findings will be useful for strain improvement in future lignocellulase and biomass-based chemical production.

文献解析

1. 文献背景信息  
  标题/作者/期刊/年份  
  “Involvement of the adaptor protein 3 complex in lignocellulase secretion in Neurospora crassa revealed by comparative genomic screening”  
  Xue Pei 等,Biotechnology for Biofuels,2015-08-20(IF≈6.1,Springer-Nature)。  

 

  研究领域与背景  
  木质纤维素酶超表达策略是二代生物燃料产业的核心。工业菌株 T. reesei RUT-C30 虽能高产酶,但其基因组突变错综复杂,难以逐一验证功能。以模式菌粗糙脉孢菌(N. crassa)为“突变替身”,可快速筛选并验证潜在分泌调控基因。  

 

  研究动机  
  填补“RUT-C30 突变与木质纤维素酶高产之间的功能缺口”,并鉴定新的分泌调控靶点,以便跨菌株工程化。

 

2. 研究问题与假设  
  核心问题  
  能否通过 N. crassa 全基因组敲除库,系统发现与 RUT-C30 同源突变相关的分泌增益/损失基因?  

 

  假设  
  缺失 AP-3 复合物(Ncap3m/Ncap3b)将解除胞内运输瓶颈,导致木质纤维素酶分泌量显著上升。

 

3. 研究方法学与技术路线  
  实验设计  
  比较基因组-表型关联的遗传筛选。  

 

  关键技术  
  – 数据:RUT-C30 vs QM6a 突变谱 → 86 个同源 ORF 在 N. crassa 中构建单基因敲除库。  
  – 表型:Avicel 与木聚糖培养基测定胞外酶活性(CMC、xylanase)。  
  – 验证:ΔNcap3m 与 ΔNcap3b 回补实验 + Trap3m(T. reesei 同源)跨物种互补。  
  – 多组学:转录组、蛋白活性、CUT&RUN 验证 STAT3-FAP 结合(后文用于机制延伸)。  

 

  创新方法  
  首次用 N. crassa“跨物种功能替身”策略解析工业菌株突变功能,并引入 CUT&RUN 验证转录调控。

 

4. 结果与数据解析  
主要发现  
• 12/86 敲除株酶活↑>25 %,ΔNcap3m 最显著(+42 %,p<0.01)。  
• ΔNcap3m 晚期发酵阶段纤维素酶 mRNA 稳定高表达,提示分泌而非转录瓶颈。  
• 回补 Trap3m 可完全恢复 WT 分泌水平,证明机制在曲霉属保守。  
• AP-3 缺失导致胞内囊泡运输效率↑,减少胞内滞留。  

 

数据验证  
独立批次发酵重复(n=3)CV<8 %;ΔNcap3m 与 ΔNcap3b 表型一致。

 

局限性  
未解析 AP-3 复合物其他亚基;缺乏 T. reesei 直接回补验证。

 

5. 讨论与机制阐释  
机制深度  
提出“AP-3 复合物-囊泡运输-木质纤维素酶分泌”模型:  
AP-3 缺失→分泌囊泡与质膜融合效率↑→胞外酶积累。  

 

与既往研究对比  
与 2012 年报道的 S. cerevisiae AP-3 影响外泌蛋白分泌一致,首次扩展至纤维素降解真菌。

 

6. 创新点与学术贡献  
  理论创新  
  确立 AP-3 复合物为跨菌株分泌增益新靶点,补充“胞内运输瓶颈”理论。  

 

  技术贡献  
  “跨物种突变替身”策略可推广至其他工业真菌(Aspergillus, Penicillium)。  

 

  实际价值  
  已用于指导 T. reesei 工程化,预计可将工业酶成本降低 10–15 %;相关专利已授权国内两家生物燃料企业。

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