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The aim of this study was to determine the mobile genetic elements involved in the horizontal transfer of (T) in , and its transmission ability in heterologous hosts. A total of 159 erythromycin-resistant enterococci isolates were screened for the presence of macrolide resistance genes by PCR. Whole genome sequencing for (T)-carrying E165 was performed. The transmission ability in heterologous hosts was explored by conjugation, transformation, and fitness cost. The (T) gene was detected only in an isolate E165 (1/159), which was located on a 4,244-bp small plasmid, designed pE165. Using OG1RF as the recipient strain, pE165 is transferable. Natural transformation experiments using P1/7 and UA159 as the recipients indicated it is transmissible, which was also observed by electrotransformation using RN4220 as a recipient. The (T)-carrying pE165 can replicate in the heterologous host including OG1RF, P1/7, UA159, and RN4220 and conferred resistance to erythromycin and clindamycin to all hosts. Although there is no disadvantage of pE165 in the recipient strains in growth curve experiments, all the pE165-carrying recipients had a fitness cost compared to the corresponding original recipients in growth competition experiments. In brief, an (T)-carrying plasmid was for the first time described in and as transmissible to heterologous hosts.
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http://dx.doi.org/10.3389/fvets.2022.850466 | DOI Listing |
J Microbiol Biotechnol
September 2025
School of Life Sciences, BK21 FOUR KNU Creative BioResearch Group, Kyungpook National University, Daegu 41566, Republic of Korea.
Bacterial minicells are small and chromosome-free cells that result from aberrant cell division and represent a safe alternative to live microbial applications. However, most research on minicells has focused on , with few studies exploring their development in non-model, biocompatible hosts. In this study, we engineered a -deficient (formerly and ) strain capable of producing minicells and systematically evaluated its potential as a chassis for biotechnological applications.
View Article and Find Full Text PDFBiotechnol Adv
September 2025
BOKU University, Department of Biotechnology and Food Sciences (BTLW), Institute of Bioprocess Science and Engineering (IBSE), Muthgasse 18, 1190 Vienna, Austria. Electronic address:
Benzylisoquinoline alkaloids (BIAs) are a diverse group of plant secondary metabolites that play a key role as analgesics, anti-cancer, and anti-microbial medication. BIAs are currently exclusively produced through crop farming which adversely affects the supply chain resilience of BIA-based medication because availability is limited by low accumulation in plants and harvest seasons. Also, yields fluctuate due to annual weather changes and decrease overall due to global climate change impact on agriculture.
View Article and Find Full Text PDFPhilos Trans R Soc Lond B Biol Sci
September 2025
Laboratory of Molecular Microbiology, Global Health Institute, School of Life Sciences, Ecole Polytechnique Federale de Lausanne (EPFL), Lausanne, Switzerland.
the causative agent of cholera, has triggered seven pandemics, with the seventh pandemic emerging in 1961. The success of seventh pandemic El Tor (7PET) as a human pathogen is linked to its acquisition of mobile genetic elements (MGEs) like the CTXΦ prophage and pathogenicity island 1 (VPI-1). Additional MGEs, including VPI-2 and the seventh pandemic islands (VSP-I and VSP-II), are thought to have further enhanced the pathogen's virulence potential.
View Article and Find Full Text PDFFront Microbiol
August 2025
School of Bioengineering, Qilu University of Technology, Shandong Academy of Science, Jinan, China.
The nisin-controlled gene expression (NICE) system is an efficient and promising gene expression system for . To enhance the expression efficiency of the NICE system in ATCC19258, an inducible expression vector, pNZ8148-PnisA-gfp-PnisR-nisR-nisK, containing the regulatory element NisR/K and the promoter PnisR, was first constructed using the basic plasmid pNZ8148. Green fluorescent protein (GFP), as the reporter protein, was cloned downstream of PnisA in the vector pNZ8148 to detect protein expression.
View Article and Find Full Text PDFACS Synth Biol
September 2025
Department of Medicinal Chemistry, Center for Natural Products, Drug Discovery and Development (CNPD3), University of Florida, Gainesville, Florida 32610, United States.
Heterologous expression of biosynthetic gene clusters (BGCs) is a powerful strategy for natural product (NP) discovery, yet achieving consistent expression across microbial hosts remains challenging. Here, we developed cross-phyla vector systems enabling the expression of BGCs from cyanobacteria and other bacterial origins in Gram-negative , Gram-positive , and two model cyanobacterial strains including unicellular PCC 6803 and filamentous sp. PCC 7120.
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