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Fungal such as Aspergillus, Penicillium, Trichoderma, etc. are widely used as high-quality hosts for products such as proteins and secondary metabolites. CD BioGlyco provides professional GlycoChas™ Cells construction, Chassis Development, and Production services to clients relying on advanced technologies. Penicillium is widely found in air, soil, animal gut, plant tissues, and microorganisms. We provide highly efficient Penicillium engineering services by modulating the biosynthetic pathways and metabolic genetics of Penicillium. Moreover, we provide several chassis e.g. Plant Chassis, Microalgae Chassis, Insect Chassis, Bacteria Chassis, and Mammalian Chassis.
Improving Penicillium strain activity and yield is important in constructing fungal chassis. Microorganisms rely on genes to encode their activity information, and CD BioGlyco uses genetic manipulation to achieve optimization of strain activity. Moreover, we provide services for the optimization of strain culture conditions, taking care to analyze the influencing factors.
Most secondary metabolite-related genes are silent or poorly expressed in Penicillium, We use improved homologous recombination and clustered regularly interspaced short palindromic repeat sequences/CRISPR-associated nucleases 9 (CRISPR/Cas9) as a genome editing tool to enable specific gene expression or deletion.
Our lab uses promoters and terminators as building blocks and more complex regulatory devices to control gene expression. We significantly express enhanced genes by modulating transcription factors utilizing strong promoters. For designed strains (deleted or overexpressed genes), we offer polymerase chain reaction (PCR) validation services.
Fig.1 Schematic diagram of the regulatory targets of the designed engineered strains. (CD BioGlyco)
Technology: RNA-sequencing, Reverse transcription-quantitative PCR (RT-qPCR), Random mutagenesis, Genetic engineering
Journal: Microbial Cell Factories
Published: 2022
IF: 6.4
Results: This study confirmed that genetic engineering and random mutagenesis were effective in increasing raw starch-degrading enzyme (RSDE) production. The researchers isolated a total of 3,619 mutated P. oxalicum colonies using γ-ray mutagenesis with strain A2-13 as the parental strain. Among them, mutant TE4-10 was simultaneously deficient in transcriptional repressor gene PoxCxrC and activator gene PoxAmyR overexpression by gene regulation. The yield of the modified engineered strain increased by 15.6% relative to TE4-10.
Fig.2 Analysis of gene expression in engineered P. oxalicum strain relative to the parent strain. (Zhao, et al., 2022)
CD BioGlyco uses fungal strain to rapidly achieve the high-level production of a compound. Please feel free to
if you are interested in Penicillium engineering.References