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The verification of Agrobacterium clones is a crucial step in molecular biology research, traditionally relying on bacterial culture endpoint PCR. However, this method is susceptible to contamination and false-negative/positive results. The existing methods focus on confirming DNA sequences and frequently overlook plasmid acceptance. This study presents an innovative and efficient approach that employs available commercial kits to isolate Agrobacterium tumefaciens (GV3101) plasmid DNA. This method includes slight modification of the standard kit protocol during the washing step, enhancing efficient plasmid retrieval. Despite lower yields, the recovered DNA allows PCR and enzymatic digestion, providing conclusive evidence of plasmid acceptance.
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http://dx.doi.org/10.1007/978-1-0716-4450-8_2 | DOI Listing |
Pestic Biochem Physiol
November 2025
Department of Agriculture, Forestry and Bioresources, College of Agriculture and Life Sciences, Seoul National University, Seoul 08826, Republic of Korea; Research Institute of Agriculture and Life Science, College of Agriculture and Life Sciences, Seoul National University, Seoul 08826, Republic of
In this study, we evaluated the antibacterial activities of plant essential oils (EOs) from the Lamiaceae family against Agrobacterium tumefaciens to find new eco-friendly antimicrobials. Thymus vulgaris L. (thyme white) EO demonstrated the most potent fumigant antibacterial activity among these.
View Article and Find Full Text PDFPlant Environ Interact
October 2025
Discipline of Plant Pathology, College of Agriculture, Engineering & Science; School of Agricultural, Earth and Environmental Sciences University of KwaZulu-Natal Pietermaritzburg Republic of South Africa.
Asian soybean rust (ASR) is caused by the biotrophic fungus Syd. & P. Syd.
View Article and Find Full Text PDFBMC Plant Biol
August 2025
College of Forestry, Shenyang Agricultural University, Shenyang, 110866, China.
The lack of an effective gene editing technology system for Fraxinus mandshurica makes it challenging to improve its traits through genetic engineering methods. In this study, an effective CRISPR/Cas9 gene editing system targeting plant growth points was established through the optimization of Agrobacterium tumefaciens concentration and infection duration. Furthermore, a tissue culture system for clustered buds was developed by supplementing the media with hormones at different concentrations.
View Article and Find Full Text PDFMethods Mol Biol
August 2025
Department of Plant Nutrition, Institute of Crop Science and Resource Conservation (INRES), University of Bonn, Bonn, Germany.
In recent years, there has been substantial progress in the development of methods to analyze inositol phosphates (InsPs) and inositol pyrophosphates (PP-InsPs). However, many of these techniques are labor- and cost-intensive and can usually only be carried out by laboratories specialized in InsPs/PP-InsPs analysis. In this chapter, we present a simple method that exploits the fact that phosphorylation and/or dephosphorylation of certain InsP/PP-InsP species induces the activation of promoters driving the expression of genes involved in phosphate starvation response (PSR).
View Article and Find Full Text PDFFEBS Open Bio
August 2025
The Second Hospital & Clinical Medical School, Lanzhou University, China.
Relatively little is known about the microbial variations within the human appendix niche. To overcome this knowledge gap, we employed endoscopic retrograde appendicitis treatment (ERAT) technology to collect microbial samples from the appendix lumen, followed by shotgun metagenomic sequencing on participants with acute appendicitis without antibiotic treatment. Compared to the cecum and terminal ileum, the appendix had a higher abundance at the genus level of Sphingobium, Leptotrichia and Oribacterium, as well as a significant increase in species-level abundance of oral bacteria, including Streptococcus sanguinis, Streptococcus australis, Streptococcus sp.
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