Beauveria bassiana is an entomopathognic fungus, which is widely employed in the biological control of pests. Gene disruption is a common method for studying the functions of genes involved in fungal development or its interactions with hosts. However, generating gene deletion mutants was a time-consuming work. The transcriptional factor OpS3 has been identified as a positive regulator of a red secondary metabolite oosporein in B. bassiana. In this study, we have designed a new screening system by integrating a constitutive OpS3 expression cassette outside one of the homologous arms of target gene. Ectopic transformants predominantly exhibit a red colour with oosporein production, while knockout mutants appear as white colonies due to the loss of the OpS3 expression cassette caused by recombinant events. This screening strategy was used to obtain the deletion mutants of both tenS and NRPS genes. Correct mutants were obtained by screening fewer than 10 mutants with a positive efficiency ranging from 50% to 75%. This system significantly reduces the workload associated with DNA extraction and PCR amplification, thereby enhancing the efficiency of obtaining correct transformants in B. bassiana.
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http://dx.doi.org/10.1111/1751-7915.14512 | DOI Listing |
Plant Physiol
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Group of Biochemistry and Cell Signalling in Nitric Oxide, University Institute for Research in Olive Groves and Olive Oils, Department of Experimental Biology, Faculty of Experimental Sciences, Campus "Las Lagunillas" s/n, University of Jaén, E-23071, Jaén, Spain.
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Division of Molecular Psychiatry, Center of Mental Health, University of Hospital Würzburg, 97080 Würzburg, Germany.
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State Key Laboratory of Rice Biology and Breeding, China National Center for Rice Improvement, China National Rice Research Institute, Hangzhou 311400, China.
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The New Zealand Institute for Plant & Food Research Limited, 120 Mt Albert Road, Auckland 1025, New Zealand.
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View Article and Find Full Text PDFInt J Mol Sci
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Department of Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS 66160, USA.
We analyzed the transcriptome data of wildtype and estrogen receptor β knockout () rat ovaries during the early postnatal period and detected remarkable changes in epigenetic regulators and transcription factors. Compared with postnatal day (PD) 4.5 ovaries, PD 6.
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