scholarly journals High efficiency, Site-specific Transfection of Adherent Cells with siRNA Using Microelectrode Arrays (MEA)

10.3791/4415 ◽  
2012 ◽  
Author(s):  
Chetan Patel ◽  
Jit Muthuswamy
Keyword(s):  
High Efficiency ◽  
Microelectrode Arrays ◽  
Adherent Cells ◽  
Site Specific

scholarly journals Agrobacterium tumefaciens-Mediated Transformation of NHEJ Mutant Aspergillus nidulans Conidia: An Efficient Tool for Targeted Gene Recombination Using Selectable Nutritional Markers

2021 ◽  
Vol 7 (11) ◽  
pp. 961
Author(s):  
Virginia Casado-del Castillo ◽  
Andrew P. MacCabe ◽  
Margarita Orejas
Keyword(s):  
Agrobacterium Tumefaciens ◽  
Aspergillus Nidulans ◽  
High Efficiency ◽  
Recombinant Dna ◽  
Attractive Alternative ◽  
Nutritional Requirement ◽  
Position Effects ◽  
Site Specific ◽  
Enzyme Preparations ◽  
Site Specific Integration

Protoplast transformation for the introduction of recombinant DNA into Aspergillus nidulans is technically demanding and dependant on the availability and batch variability of commercial enzyme preparations. Given the success of Agrobacterium tumefaciens-mediated transformation (ATMT) in diverse pathogenic fungi, we have adapted this method to facilitate transformation of A. nidulans. Using suitably engineered binary vectors, gene-targeted ATMT of A. nidulans non-homologous end-joining (NHEJ) mutant conidia has been carried out for the first time by complementation of a nutritional requirement (uridine/uracil auxotrophy). Site-specific integration in the ΔnkuA host genome occurred at high efficiency. Unlike other transformation techniques, however, cross-feeding of certain nutritional requirements from the bacterium to the fungus was found to occur, thus limiting the choice of auxotrophies available for ATMT. In complementation tests and also for comparative purposes, integration of recombinant cassettes at a specific locus could provide a means to reduce the influence of position effects (chromatin structure) on transgene expression. In this regard, targeted disruption of the wA locus permitted visual identification of transformants carrying site-specific integration events by conidial colour (white), even when auxotrophy selection was compromised due to cross-feeding. The protocol described offers an attractive alternative to the protoplast procedure for obtaining locus-targeted A. nidulans transformants.

scholarly journals A Novel Site-Specific Integration System for Genetic Modification of Aspergillus flavus

2019 ◽  
Vol 10 (2) ◽  
pp. 605-611
Author(s):  
Fang Tao ◽  
Kai Zhao ◽  
Qianqian Zhao ◽  
Fangzhi Xiang ◽  
Guomin Han
Keyword(s):  
Aspergillus Flavus ◽  
High Efficiency ◽  
Genetic Manipulation ◽  
Fungal Growth ◽  
Egfp Expression ◽  
Regulation Mechanism ◽  
Site Specific ◽  
Site Specific Integration ◽  
Foreign Dna ◽  
Novel Strategy

Aspergillus flavus is a fungus that produces aflatoxin B1, one of the most carcinogenic secondary metabolites. Understanding the regulation mechanism of aflatoxin biosynthesis in this fungus requires precise methods for genomic integration of mutant alleles. To avoid the disadvantage of DNA integration into the genome by non-homologous or ectopic recombination, we developed a novel strategy for site-specific integration of foreign DNA by using a carboxin-resistant sdh2R allele (His 249 Leu). Our results demonstrated that the transformants were generated with a high efficiency (>96%) of correct integration into the sdh2-lcus of the genome of A. flavus NRRL 3357. The advantage of this method is that introduction of the eGFP expression cassette into the sdh2-locus had little effect on fungal growth and virulence while also being rapid and efficient. This system will be a valuable tool for genetic manipulation in A. flavus. To the best of our knowledge, this is the first report on the efficient site-specific integration at the sdh2-locus in the genome of Aspergillus.

Transgene Coplacement and High Efficiency Site-Specific Recombination With the Cre/loxP System in Drosophila

Genetics ◽  
1996 ◽  
Vol 144 (2) ◽  
pp. 715-726 ◽  
Author(s):  
Mark L Siegal ◽  
Daniel L Hartl
Keyword(s):  
Germ Cells ◽  
Maternal Effect ◽  
High Efficiency ◽  
Loxp Site ◽  
Position Effects ◽  
Site Specific ◽  
Site Specific Recombination ◽  
Bacteriophage P1 ◽  
Eye Color ◽  
F2 Generation

Abstract Studies of gene function and regulation in transgenic Drosophila are often compromised by the possibility of genomic position effects on gene expression. We have developed a method, called transgene coplacement, in which any two sequences can be positioned at exactly the same site and orientation in the genome. Transgene coplacement makes use of the bacteriophage P1 system of Cre/loxP site-specific recombination, which we have introduced into Drosophila. In the presence of a cre transgene driven by a dual hsp70-Mosl promoter, a white reporter gene flanked by loxP sites is excised with virtually 100% efficiency both in somatic cells and in germ cells. A strong maternal effect, resulting from Cre recombinase present in the oocyte, is observed as white or mosaic eye color in F1 progeny. Excision in germ cells of the F1 yields a strong grand-maternal effect, observed as a highly skewed ratio of eye-color phenotypes in the F2 generation. The excision reactions of Cre/loxP and the related FLP/FRT system are used to create Drosophila lines in which transgenes are at exactly allelic sites in homologous chromosomes.

Recording electric potentials from single adherent cells with 3D microelectrode arrays after local electroporation

2010 ◽  
Vol 26 (4) ◽  
pp. 1731-1735 ◽  
Author(s):  
Philipp Julian Koester ◽  
Carsten Tautorat ◽  
Helmut Beikirch ◽  
Jan Gimsa ◽  
Werner Baumann
Keyword(s):  
Microelectrode Arrays ◽  
Adherent Cells ◽  
Electric Potentials

scholarly journals Improved variants of SrtA for site-specific conjugation on antibodies and proteins with high efficiency

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Long Chen ◽  
Justin Cohen ◽  
Xiaoda Song ◽  
Aishan Zhao ◽  
Zi Ye ◽  
...  
Keyword(s):  
High Efficiency ◽  
Site Specific

scholarly journals Genome Integration and Excision by a New Streptomyces Bacteriophage, ϕJoe

2016 ◽  
Vol 83 (5) ◽  
Author(s):  
Paul C. M. Fogg ◽  
Joshua A. Haley ◽  
W. Marshall Stark ◽  
Margaret C. M. Smith
Keyword(s):  
Synthetic Biology ◽  
High Efficiency ◽  
Dna Recombination ◽  
Streptomyces Venezuelae ◽  
Site Specific ◽  
Content Type ◽  
Wide Range ◽  
Serine Integrase

ABSTRACT Bacteriophages are the source of many valuable tools for molecular biology and genetic manipulation. In Streptomyces, most DNA cloning vectors are based on serine integrase site-specific DNA recombination systems derived from phage. Because of their efficiency and simplicity, serine integrases are also used for diverse synthetic biology applications. Here, we present the genome of a new Streptomyces phage, ϕJoe, and investigate the conditions for integration and excision of the ϕJoe genome. ϕJoe belongs to the largest Streptomyces phage cluster (R4-like) and encodes a serine integrase. The attB site from Streptomyces venezuelae was used efficiently by an integrating plasmid, pCMF92, constructed using the ϕJoe int-attP locus. The attB site for ϕJoe integrase was occupied in several Streptomyces genomes, including that of S. coelicolor, by a mobile element that varies in gene content and size between host species. Serine integrases require a phage-encoded recombination directionality factor (RDF) to activate the excision reaction. The ϕJoe RDF was identified, and its function was confirmed in vivo. Both the integrase and RDF were active in in vitro recombination assays. The ϕJoe site-specific recombination system is likely to be an important addition to the synthetic biology and genome engineering toolbox. IMPORTANCE Streptomyces spp. are prolific producers of secondary metabolites, including many clinically useful antibiotics. Bacteriophage-derived integrases are important tools for genetic engineering, as they enable integration of heterologous DNA into the Streptomyces chromosome with ease and high efficiency. Recently, researchers have been applying phage integrases for a variety of applications in synthetic biology, including rapid assembly of novel combinations of genes, biosensors, and biocomputing. An important requirement for optimal experimental design and predictability when using integrases, however, is the need for multiple enzymes with different specificities for their integration sites. In order to provide a broad platform of integrases, we identified and validated the integrase from a newly isolated Streptomyces phage, ϕJoe. ϕJoe integrase is active in vitro and in vivo. The specific recognition site for integration is present in a wide range of different actinobacteria, including Streptomyces venezuelae, an emerging model bacterium in Streptomyces research.

scholarly journals Development of strategy for competent cell preparation and high efficiency plasmid transformation using different methods

2011 ◽  
Vol 29 (1) ◽  
pp. 17 ◽  
Author(s):  
Anubhuti Sharma ◽  
Arushi Girdhar ◽  
Nidhi Srivastava
Keyword(s):  
High Efficiency ◽  
Transformation Efficiency ◽  
Great Influence ◽  
Competent Cell ◽  
Cell Preparation ◽  
Site Specific ◽  
E Coli ◽  
Cost Efficient ◽  
Normal Laboratory ◽  
Complete Genomic

Current cloning technologies based on site-specific recombination are efficient, simple to use, and flexible. With the recent availability of complete genomic sequences of many organisms and plants, high-throughput and cost-efficient systems for gene cloning and functional analysis are in great demand. This study compares two different methods of preparation of competent cells using two strains of E. coli DH5α and HB101. From results the most efficient strain was found DH5α for cloning as it supports blue white screening utilizing galactosidase activity. The concentration of calcium chloride is another important factor; various concentrations of CaCl2 were tried. Optimum concentration was found to be 75 mM. However PEG also has great influence on transformation efficiency, use of 40% PEG gave the best transformation efficiency. A convenient and rapid method for the genetic transformation of E. coli with appropriate plasmid is proposed which can be utilised for high efficiency transformation in normal laboratory conditions.

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