نتایج جستجو برای: plasmid transformation

تعداد نتایج: 253370  

شمس شهرآبادی, محمود, قاضی , فریده , گرزین, علی‌اکبر , دبیرمنش , بهاره,

    Background & Aim: Human parechovirus is a genus of picornaviruses which includes a number of important viruses of clinical significance. Recent sequence analysis suggests that human parechovirus type 1(HPEV-1) is distinct from other picornaviruses and lacks the motives believed to be involved in the protease function of 2A. The aim of this study was to analyse proteolytic activity of 3C pro...

2002
CHARLENE CHU CHRISTINA HAN HIROMI SHIMIZU

This study investigated the effects of the size of chromosomal DNA fragments on transformation efficacy of a plasmid. In our experiment, each of three chromosomal fragment sizes were co-transformed with varying amounts of plasmid DNA and results show that the conditions, plasmid alone, plasmid with 10kb, and plasmid with 20kb fragments gave no significant differences. On the other hand, plasmid...

Journal: :Journal of bacteriology 1981
W L Albritton J W Bendler J K Setlow

Purified 34-megadalton-plasmid deoxyribonucleic acid from antibiotic-resistant strains of Haemophilus influenzae transforms competent strains of H. influenzae more efficiently if the recipient strains contain certain other 30-megadalton plasmids.

Journal: :Journal of general microbiology 1993
Y Wang K P Roos D E Taylor

Most strains of Helicobacter pylori are naturally competent for uptake of chromosomal DNA. Transformation frequencies for streptomycin resistance or rifampicin resistance markers ranged from 1 x 10(-4) to 1 x 10(-3) per viable cell using a plate transformation procedure. Transformation of a metronidazole resistance marker (MtrR) was demonstrated when either a laboratory-derived mutant or a MtrR...

Journal: :Analytical chemistry 2005
Kuniaki Nagamine Shiho Onodera Yu-Suke Torisawa Tomoyuki Yasukawa Hitoshi Shiku Tomokazu Matsue

On-chip transformation of Escherichia coli cells was accomplished for the first time using a microbial array chip. The continuous E. coli transformation procedures were performed on a chip in which the microcompartment was composed of PDMS microfluidic channels and a silicon substrate predeposited with different plasmid DNAs. The PDMS microfluidic device enabled the parallel transformation of E...

2011
Chenghua Gao Yanfen Xue Yanhe Ma

Among the diverse alkaliphilic Bacillus strains, only a little have been reported to be genetically transformed. In this study, an efficient protoplast transformation procedure was developed for recalcitrant alkaliphilic Bacillus sp. N16-5. The procedure involved polyethylene glycol-induced DNA uptake by the protoplasts and subsequent protoplast regeneration with a developed hard agar regenerat...

Journal: :Bioscience, biotechnology, and biochemistry 2005
Yuko Sato Noriyuki Kumazawa Kenichi Yoshikawa Yasurou Kurusu

Transformation system for Escherichia coli based upon introduction of plasmid DNA by natural phospholipids has been developed. Transformants are easily obtained by treatment with natural phospholipids such as phosphatidylethanolamine, phosphatidylcoline, and phosphatidylserine, where the presence of MgCl2 or CaCl2 is essential. This method of transformation is applicable not only for small plas...

2011
Rika Etchuuya Miki Ito Seiko Kitano Fukiko Shigi Rina Sobue Sumio Maeda

Escherichia coli is not assumed to be naturally transformable. However, several recent reports have shown that E. coli can express modest genetic competence in certain conditions that may arise in its environment. We have shown previously that spontaneous lateral transfer of non-conjugative plasmids occurs in a colony biofilm of mixed E. coli strains (a set of a donor strain harbouring a plasmi...

Journal: :Applied and environmental microbiology 1996
M J Laine H Nakhei J Dreier K Lehtilä D Meletzus R Eichenlaub M C Metzler

In this paper we describe transformation of Clavibacter michiganensis subsp. sepedonicus, the potato ring rot bacterium, with plasmid vectors. Three of the plasmids used, pDM100, pDM302, and pDM306, contain the origin of replication from pCM1, a native plasmid of C. michiganensis subsp. michiganensis. We constructed two new cloning vectors, pHN205 and pHN216, by using the origin of replication ...

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