نتایج جستجو برای: colicin

تعداد نتایج: 1137  

Journal: :Molecular microbiology 2009
Chuck R Smallwood Amparo Gala Marco Qiaobin Xiao Vy Trinh Salete M C Newton Phillip E Klebba

We studied the reactivity of 35 genetically engineered Cys sulphydryl groups at different locations in Escherichia coli FepA. Modification of surface loop residues by fluorescein maleimide (FM) was strongly temperature-dependent in vivo, whereas reactivity at other sites was much less affected. Control reactions with bovine serum albumin showed that the temperature dependence of loop residue re...

2015
Andreas Mader Benedikt von Bronk Benedikt Ewald Sara Kesel Karin Schnetz Erwin Frey Madeleine Opitz

The production of bacteriocins in response to worsening environmental conditions is one means of bacteria to outcompete other microorganisms. Colicins, one class of bacteriocins in Escherichia coli, are effective against closely related Enterobacteriaceae. Current research focuses on production, release and uptake of these toxins by bacteria. However, little is known about the quantitative aspe...

Journal: :Biochimie 2002
Raz Zarivach Efrat Ben-Zeev Nan Wu Tamar Auerbach Anat Bashan Karen Jakes Katherine Dickman Alexander Kosmidis Frank Schluenzen Ada Yonath Miriam Eisenstein Menachem Shoham

Colicin E3 is a protein that kills Escherichia coli cells by a process that involves binding to a surface receptor, entering the cell and inactivating its protein biosynthetic machinery. Colicin E3 kills cells by a catalytic mechanism of a specific ribonucleolytic cleavage in 16S rRNA at the ribosomal decoding A-site between A1493 and G1494 (E. coli numbering system). The breaking of this singl...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2005
Nicholas G Housden Steven R Loftus Geoffrey R Moore Richard James Colin Kleanthous

Binding of enzymatic E colicins to the vitamin B12 receptor, BtuB, is the first stage in a cascade of events that culminate in the translocation of the cytotoxic nuclease into the Escherichia coli cytoplasm and release of its tightly bound immunity protein. A dogma of colicin biology is that the toxin coiled-coil connecting its functional domains must unfold or unfurl to span the periplasm, wit...

Journal: :Biochimica et biophysica acta 2004
Stanislav D Zakharov Elena A Kotova Yuri N Antonenko William A Cramer

Insights into the protein-membrane interactions by which the C-terminal pore-forming domain of colicins inserts into membranes and forms voltage-gated channels, and the nature of the colicin channel, are provided by data on: (i) the flexible helix-elongated state of the colicin pore-forming domain in the fluid anionic membrane interfacial layer, the optimum anionic surface charge for channel fo...

Journal: :Journal of bacteriology 1960
L W PARR N N EL SHAWI M L ROBBINS

Journal: :Journal of bacteriology 1970
J Inselburg

The progeny cells of Escherichia coli strain P678-54, which normally do not contain deoxyribonucleic acid (DNA), were found to carry DNA when the parental cell carried colicin factor E1 (Col E1). The DNA found in the normally DNA-less segregants was shown to be Col E1 DNA, which is present primarily as a covalently closed circular molecule that can undergo more than one complete cycle of replic...

Journal: :Journal of bacteriology 2007
Denis Duché

Colicins reach their targets in susceptible Escherichia coli strains through two envelope protein systems: the Tol system is used by group A colicins and the TonB system by group B colicins. Colicin E2 (ColE2) is a cytotoxic protein that recognizes the outer membrane receptor BtuB. After gaining access to the cytoplasmic membrane of sensitive Escherichia coli cells, ColE2 enters the cytoplasm t...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید