Abstract

BackgroundCellulase synthesized by fungi can environment-friendly and sustainably degrades cellulose to fermentable sugars for producing cellulosic biofuels, biobased medicine and fine chemicals. Great efforts have been made to study the regulation mechanism of cellulase biosynthesis in fungi with the focus on the carbon sources, while little attention has been paid to the impact and regulation mechanism of nitrogen sources on cellulase production.ResultsGlutamine displayed the strongest inhibition effect on cellulase biosynthesis in Trichoderma reesei, followed by yeast extract, urea, tryptone, ammonium sulfate and l-glutamate. Cellulase production, cell growth and sporulation in T. reesei RUT-C30 grown on cellulose were all inhibited with the addition of glutamine (a preferred nitrogen source) with no change for mycelium morphology. This inhibition effect was attributed to both l-glutamine itself and the nitrogen excess induced by its presence. In agreement with the reduced cellulase production, the mRNA levels of 44 genes related to the cellulase production were decreased severely in the presence of glutamine. The transcriptional levels of genes involved in other nitrogen transport, ribosomal biogenesis and glutamine biosynthesis were decreased notably by glutamine, while the expression of genes relevant to glutamate biosynthesis, amino acid catabolism, and glutamine catabolism were increased noticeably. Moreover, the transcriptional level of cellulose signaling related proteins ooc1 and ooc2, and the cellular receptor of rapamycin trFKBP12 was increased remarkably, whose deletion exacerbated the cellulase depression influence of glutamine.ConclusionGlutamine may well be the metabolite effector in nitrogen repression of cellulase synthesis, like the role of glucose plays in carbon catabolite repression. Glutamine under excess nitrogen condition repressed cellulase biosynthesis significantly as well as cell growth and sporulation in T. reesei RUT-C30. More importantly, the presence of glutamine notably impacted the transport and metabolism of nitrogen. Genes ooc1, ooc2, and trFKBP12 are associated with the cellulase repression impact of glutamine. These findings advance our understanding of nitrogen regulation of cellulase production in filamentous fungi, which would aid in the rational design of strains and fermentation strategies for cellulase production in industry.

Highlights

  • Cellulase synthesized by fungi can environment-friendly and sustainably degrades cellulose to fer‐mentable sugars for producing cellulosic biofuels, biobased medicine and fine chemicals

  • The inhibition effect on cellulase biosynthesis was found for all the tested types of nitrogen sources, indicating that the addition of more nitrogen into Trichoderma minimal media (TMM) caused nitrogen excess that compromised the cellulase production

  • Using T. reesei as an example, we first studied the effect of glutamine on cellulase-producing fungi under cellulose condition, including cellulase production, cell growth, sporulation, mycelium morphology and transcriptome

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Summary

Introduction

Cellulase synthesized by fungi can environment-friendly and sustainably degrades cellulose to fer‐mentable sugars for producing cellulosic biofuels, biobased medicine and fine chemicals. Great efforts have been made to study the regulation mechanism of cellulase biosynthesis in fungi with the focus on the carbon sources, while little attention has been paid to the impact and regulation mechanism of nitrogen sources on cellulase production. (2021) 14:199 preferential use of primary nitrogen sources (ammonium and glutamine) and confers the ability to use many different secondary nitrogen sources (i.e., nitrate) when appropriate [2,3,4,5,6], which is similar to carbon catabolite repression (CCR). The standard model of NCR is that AreA mediates de-repression of genes for utilization of secondary nitrogen sources in the absence of ammonium or glutamine. Study has been making progress on the effect and regulation mechanism of nitrogen sources on cellulase production

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