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ABSTRACT Agrobacterium tumefaciens-mediated transformation with plasmids carrying the hygromycin B resistance gene hph frequently is being used for inserting genes into fungal spores and mycelial cells and for conducting insertional mutagenesis to identify genes connected to a particular phenotype. In this article, we report that stable hygromycin B resistance can develop spontaneously in germinating conidia from Monilinia fructicola and that the mutants exhibit altered phenotypes. One spontaneously developing hygromycin B-resistant colony developed per 2.5 x 10(5) germinating conidia. Mutants grew significantly slower on potato dextrose agar, were 2.4- to 3.1-fold more sensitive to demethylation inhibitor fungicides, lacked melanization, and did not produce spores. The mode of action of hygromycin B resistance in the mutants seemed to be different from the hph transgene-mediated hygromycin B resistance based on different phenotypic characters. The ability of M. fructicola and possibly other fungi to spontaneously develop hygromycin B resistance associated with an altered phenotype may interfere with the selection of true transformants if hygromycin B is used as selective agent. This is particularly confounding if the hph gene is used as selectable marker in insertional mutagenesis experiments conducted for the identification of genes involved in melanization, sporulation, or fungicide resistance.
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http://dx.doi.org/10.1094/PHYTO.2003.93.11.1354 | DOI Listing |
GM Crops Food
December 2025
National Institute for Biotechnology and Genetic Engineering (NIBGE), Faisalabad, Pakistan.
Physiologically, salinity causes osmotic stress due to high solute concentration in soil and disturbs the metabolic and photosynthetic activity of the cells by increasing the toxicity of Na in the cytoplasm. Plant adaptation to salt stress is characterized by cellular ion homeostasis and vacuolar sequestration of toxic ions from cytosol mediated by H-pyrophosphatase (). The gene was cloned under the control of the promoter for yeast transformation and the promoter for tobacco transformation.
View Article and Find Full Text PDFBMC Plant Biol
August 2025
College of Horticulture, Sichuan Agricultural University, Huimin Road 211#, Chengdu, 611130, China.
Background: CRISPR/Cas9 technology has garnered increasing attention for its simplicity and precision in genome editing, making it an indispensable tool for gene function research and crop genetic improvement. However, the inefficiency and time-consuming nature of genetic transformation continue to pose substantial challenges to its widespread application in woody plants.
Results: In this study, we developed a rapid and efficient Agrobacterium-mediated transformation system using petioles as explants for kiwifruit.
Bioresour Technol
December 2025
Department of Food Science, Purdue University, West Lafayette, IN 47907, USA; Whistler Center for Carbohydrate Research, Purdue University, West Lafayette, IN 47907, USA. Electronic address:
Efficient bioconversion of acetate-rich lignocellulosic biomass into value-added chemicals remains a major challenge due to the toxicity of acetic acid. In this study, we developed an acid-tolerant Issatchenkia orientalis strain (IoDY01H) capable of producing 3-hydroxypropionic acid (3-HP), a key bioplastic precursor, from glucose, xylose, and acetate. Using a Cas9-based genome editing system with a hygromycin B resistance marker, we introduced heterologous genes encoding xylose utilization and β-alanine-based 3-HP biosynthetic pathways into the I.
View Article and Find Full Text PDFSci Rep
July 2025
Malopolska Centre of Biotechnology, Jagiellonian University, Krakow, Poland.
Genetic transformation of plants is pivotal for advancing biotechnology, with success depending largely on effective selection methods. Marchantia polymorpha has emerged as a model plant due to its evolutionary importance, ease of manipulation, and simple genetic structure. However, inconsistent antibiotic performance and limited studies on optimal selection agent concentrations have posed challenges.
View Article and Find Full Text PDFFront Genome Ed
July 2025
Department of Microbiology, University of Innsbruck, Innsbruck, Austria.
is a well-known mycoparasitic fungus widely used for the biological control of fungal plant pathogens. However, genetic manipulation in this organism remains challenging due to the limited availability of versatile and efficient molecular tools. Here, we present a CRISPR/Cas9-based method for targeted gene manipulation using ribonucleoprotein (RNP) complexes combined with a transiently stable telomere vector.
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