scholarly journals Metabolic engineering of the cellulolytic thermophilic fungus Myceliophthora thermophila to produce ethanol from cellobiose

2020 ◽  
Vol 13 (1) ◽  
Author(s):  
Jinyang Li ◽  
Yongli Zhang ◽  
Jingen Li ◽  
Tao Sun ◽  
Chaoguang Tian
2021 ◽  
Vol 12 ◽  
Author(s):  
Hanyu Wang ◽  
Tao Sun ◽  
Zhen Zhao ◽  
Shuying Gu ◽  
Qian Liu ◽  
...  

Efficient biological conversion of all sugars from lignocellulosic biomass is necessary for the cost-effective production of biofuels and commodity chemicals. Galactose is one of the most abundant sugar in many hemicelluloses, and it will be important to capture this carbon for an efficient bioconversion process of plant biomass. Thermophilic fungus Myceliophthora thermophila has been used as a cell factory to produce biochemicals directly from renewable polysaccharides. In this study, we draw out the two native galactose utilization pathways, including the Leloir pathway and oxido-reductive pathway, and identify the significance and contribution of them, through transcriptional profiling analysis of M. thermophila and its mutants on galactose. We find that galactokinase was necessary for galactose transporter expression, and disruption of galK resulted in decreased galactose utilization. Through metabolic engineering, both galactokinase deletion and galactose transporter overexpression can activate internal the oxido-reductive pathway and improve the consumption rate of galactose. Finally, the heterologous galactose-degradation pathway, De Ley–Doudoroff (DLD) pathway, was successfully integrated into M. thermophila, and the consumption rate of galactose in the engineered strain was increased by 57%. Our study focuses on metabolic engineering for accelerating galactose utilization in a thermophilic fungus that will be beneficial for the rational design of fungal strains to produce biofuels and biochemicals from a variety of feedstocks with abundant galactose.


Mycoscience ◽  
2016 ◽  
Vol 57 (6) ◽  
pp. 408-416 ◽  
Author(s):  
Santhaya Boonrung ◽  
Somporn Katekaew ◽  
Wiyada Mongkolthanaruk ◽  
Tadanori Aimi ◽  
Sophon Boonlue

2019 ◽  
Vol 12 (1) ◽  
Author(s):  
Qian Liu ◽  
Yongli Zhang ◽  
Fangya Li ◽  
Jingen Li ◽  
Wenliang Sun ◽  
...  

Abstract Background Thermophilic filamentous fungus Myceliophthora thermophila has great capacity for biomass degradation and is an attractive system for direct production of enzymes and chemicals from plant biomass. Its industrial importance inspired us to develop genome editing tools to speed up the genetic engineering of this fungus. First-generation CRISPR–Cas9 technology was developed in 2017 and, since then, some progress has been made in thermophilic fungi genetic engineering, but a number of limitations remain. They include the need for complex independent expression cassettes for targeting multiplex genomic loci and the limited number of available selectable marker genes. Results In this study, we developed an Acidaminococcus sp. Cas12a-based CRISPR system for efficient multiplex genome editing, using a single-array approach in M. thermophila. These CRISPR–Cas12a cassettes worked well for simultaneous multiple gene deletions/insertions. We also developed a new simple approach for marker recycling that relied on the novel cleavage activity of the CRISPR–Cas12a system to make DNA breaks in selected markers. We demonstrated its performance by targeting nine genes involved in the cellulase production pathway in M. thermophila via three transformation rounds, using two selectable markers neo and bar. We obtained the nonuple mutant M9 in which protein productivity and lignocellulase activity were 9.0- and 18.5-fold higher than in the wild type. We conducted a parallel investigation using our transient CRISPR–Cas9 system and found the two technologies were complementary. Together we called them CRISPR–Cas-assisted marker recycling technology (Camr technology). Conclusions Our study described new approaches (Camr technology) that allow easy and efficient marker recycling and iterative stacking of traits in the same thermophilic fungus strain either, using the newly established CRISPR–Cas12a system or the established CRISPR–Cas9 system. This Camr technology will be a versatile and efficient tool for engineering, theoretically, an unlimited number of genes in fungi. We expect this advance to accelerate biotechnology-oriented engineering processes in fungi.


1982 ◽  
Vol 28 (3) ◽  
pp. 271-277 ◽  
Author(s):  
Sribir Sen ◽  
T. K. Abraham ◽  
S. L. Chakrabarty

A thermophilic fungus, isolated from the city wastes and identified as Myceliophthora thermophila D-14, produces cellulase and β-glucosidase. The optimum pH, temperature, and incubation period for extracellular enzymes acting on different types of cellulosic substrates were determined. The apparent Km values of these enzymes were ascertained by using culture filtrates. Partial purification of the enzymes was carried out by (NH4)2SO4 precipitation and gel filtration. Electrophoresis of the fractions obtained from gel filtration revealed at least eight components in the enzymes. The involvement of all the components for degradation of native cellulosic wastes, especially cotton, was determined and synergestic effects were indicated.


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