BMC Microbiology | |
Development of a transformation system for Aspergillus sojae based on the Agrobacterium tumefaciens-mediated approach | |
Marcelo Fernandez-Lahore2  Amira M Rizk2  Judith Zimmermann1  Rodrigo Mora-Lugo2  | |
[1] Max Planck Institute for Marine Microbiology, Celsiusstrasse 1, Bremen, 28359, Germany;Jacobs University Bremen gGmbH, Campus Ring 1, Bremen, 28759, Germany | |
关键词: Western blot; Transfer DNA (T-DNA); Filamentous fungus; Enhanced green fluorescent protein (EGFP); Ble gene; | |
Others : 1170529 DOI : 10.1186/s12866-014-0247-x |
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received in 2014-06-04, accepted in 2014-09-15, 发布年份 2014 | |
【 摘 要 】
Background
Aspergillus sojae has been an important filamentous fungus in Biotechnology due to its use in diverse fermentative processes for the production of various food products. Furthermore, this fungus is a common expression system for the production of enzymes and other metabolites. The availability of molecular genetic tools to explore its biology is thus of big interest. In this study, an Agrobacterium tumefaciens-mediated transformation (ATMT) system for A. sojae was developed and its applicability evaluated.
Results
The donor plasmid named pRM-eGFP was constructed for ATMT of A. sojae. This plasmid contains the ble and egfp genes in its transfer DNA element (T-DNA) to confer phleomycin resistance and express the enhanced green fluorescent protein (EGFP) in A. sojae, respectively. Agrobacterium tumefaciens (LBA4404) harboring the donor plasmid and A. sojae (ATCC 20235) were co-cultured under diverse conditions to achieve ATMT. The maximum number of transformed fungi was obtained after three days of co-culturing at 28°C, and selection with 50 ?g/ml phleomycin. Polymerase chain reaction (PCR), fluorescence microscopy and Western Blot analysis for EGFP expression confirmed successful genomic integration of the T-DNA element in A. sojae. The T-DNA was mitotically stable in approximately 40% of the fungal transformants after four generations of sub-culturing under phleomycin pressure.
Conclusion
We successfully established a new ATMT protocol for A. sojae. This transformation system should enable further protein expression studies on this filamentous fungus.
【 授权许可】
2014 Mora-Lugo et al.; licensee BioMed Central Ltd.
【 预 览 】
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20150417020624631.pdf | 1863KB | download | |
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【 参考文献 】
- [1]Ushijima S, Nakadai T, Uchida K: Breeding of New Koji-Molds through Interspecific Hybridization between Aspergillus-Oryzae and Aspergillus-Sojae by Protoplast Fusion. Agr Biol Chem Tokyo 1990, 54(7):1667-1676.
- [2]Heerikhuisen M, van den Hondel C, Punt P: Protein production in Aspergillus sojae. Protein Science Encyclopedia 2008, 191-214.
- [3]Heerd D, Yegin S, Tari C, Fernandez-Lahore M: Pectinase enzyme-complex production by Aspergillus spp. in solid-state fermentation: A comparative study. Food Bioprod Process 2012, 90(C2):102-110.
- [4]Ozturk B, Cekmecelioglu D, Ogel ZB: Optimal conditions for enhanced beta-mannanase production by recombinant Aspergillus sojae. J Mol Catal B-Enzym 2010, 64(3¿4):135-139.
- [5]Ito K, Koyama Y, Hanya Y: Identification of the Glutaminase Genes of Aspergillus sojae Involved in Glutamate Production during Soy Sauce Fermentation. Biosci Biotech Bioch 2013, 77(9):1832-1840.
- [6]Matsushima K, Yashiro K, Hanya Y, Abe K, Yabe K, Hamasaki T: Absence of aflatoxin biosynthesis in koji mold (Aspergillus sojae). Appl Microbiol Biot 2001, 55(6):771-776.
- [7]Frandsen RJN: A guide to binary vectors and strategies for targeted genome modification in fungi using Agrobacterium tumefaciens-mediated transformation. J Microbiol Meth 2011, 87(3):247-262.
- [8]de Groot MJ, Bundock P, Hooykaas PJ, Beijersbergen AG: Agrobacterium tumefaciens-mediated transformation of filamentous fungi. Nat Biotechnol 1998, 16(9):839-842.
- [9]Wang D, He D, Li G, Gao S, Lv H, Shan Q, Wang L: An efficient tool for random insertional mutagenesis: Agrobacterium tumefaciens-mediated transformation of the filamentous fungus Aspergillus terreus. J Microbiol Methods 2014, 22:114-118.
- [10]Crespo-Sempere A, Lopez-Perez M, Martinez-Culebras PV, Gonzalez-Candelas L: Development of a green fluorescent tagged strain of Aspergillus carbonarius to monitor fungal colonization in grapes. Int J Food Microbiol 2011, 148(2):135-140.
- [11]Meyer V, Wu B, Ram AFJ: Aspergillus as a multi-purpose cell factory: current status and perspectives. Biotechnol Lett 2011, 33(3):469-476.
- [12]Shi L, Fang X, Li M, Mu D, Ren A, Tan Q, Zhao M: Development of a simple and efficient transformation system for the basidiomycetous medicinal fungus Ganoderma lucidum. World J Microbiol Biotechnol 2012, 28(1):283-291.
- [13]Melo SCO, Pungartnik C, Cascardo JCM, Brendel M: Rapid and efficient protocol for DNA extraction and molecular identification of the basidiomycete Crinipellis perniciosa. Genet Mol Res 2006, 5(4):851-855.
- [14]Sambrook JF, Russell DW: Molecular cloning: a laboratory manual, volume 1, 2, 3. Press, Cold Spring Harbour, New York; 2001.
- [15]Ruiz-Diez B: Strategies for the transformation of filamentous fungi. J Appl Microbiol 2002, 92(2):189-195.
- [16]John MA, Peberdy JF: Transformation of Aspergillus-Nidulans Using the Argb Gene. Enzyme Microb Tech 1984, 6(9):386-389.
- [17]Hahm YT, Batt CA: Genetic-transformation of an argb mutant of Aspergillus-Oryzae. Appl Environ Microb 1988, 54(6):1610-1611.
- [18]Ji YW, Xu Y, Li YP, Tu Z, Huang ZB, Liu X, Lei D: Application of Membrane filtration method to isolate uninuclei conidium in Aspergillus oryzae transformation system based on the pyrg marker. Food Sci Biotechnol 2013, 22(1):93-97.