Structural characterization of the α-hemolysin monomer from Staphylococcus aureus

2008 ◽  
Vol 75 (1) ◽  
pp. 118-126 ◽  
Author(s):  
Christian Meesters ◽  
Antje Brack ◽  
Nadja Hellmann ◽  
Heinz Decker
2019 ◽  
Vol 61 (4) ◽  
pp. 274-285 ◽  
Author(s):  
Alejandro Favela-Candia ◽  
Alfredo Téllez-Valencia ◽  
Mara Campos-Almazán ◽  
Erick Sierra-Campos ◽  
Mónica Valdez-Solana ◽  
...  

PLoS ONE ◽  
2013 ◽  
Vol 8 (10) ◽  
pp. e76812 ◽  
Author(s):  
Michal Zdzalik ◽  
Magdalena Kalinska ◽  
Magdalena Wysocka ◽  
Justyna Stec-Niemczyk ◽  
Przemyslaw Cichon ◽  
...  

2006 ◽  
Vol 358 (1) ◽  
pp. 270-279 ◽  
Author(s):  
Grzegorz M. Popowicz ◽  
Grzegorz Dubin ◽  
Justyna Stec-Niemczyk ◽  
Anna Czarny ◽  
Adam Dubin ◽  
...  

Metallomics ◽  
2015 ◽  
Vol 7 (4) ◽  
pp. 613-621 ◽  
Author(s):  
H. Lebrette ◽  
E. Borezée-Durant ◽  
L. Martin ◽  
P. Richaud ◽  
E. Boeri Erba ◽  
...  

Staphylococcus aureuspossesses two canonical ABC-importers dedicated to nickel acquisition: the NikABCDE and the CntABCDF systems, active under different growth conditions.


PLoS ONE ◽  
2014 ◽  
Vol 9 (8) ◽  
pp. e102348 ◽  
Author(s):  
Parul Srivastava ◽  
Yogesh B. Khandokar ◽  
Crystall M. D. Swarbrick ◽  
Noelia Roman ◽  
Zainab Himiari ◽  
...  

Author(s):  
S. F. Hayes ◽  
M. D. Corwin ◽  
T. G. Schwan ◽  
D. W. Dorward ◽  
W. Burgdorfer

Characterization of Borrelia burgdorferi strains by means of negative staining EM has become an integral part of many studies related to the biology of the Lyme disease organism. However, relying solely upon negative staining to compare new isolates with prototype B31 or other borreliae is often unsatisfactory. To obtain more satisfactory results, we have relied upon a correlative approach encompassing a variety EM techniques, i.e., scanning for topographical features and cryotomy, negative staining and thin sectioning to provide a more complete structural characterization of B. burgdorferi.For characterization, isolates of B. burgdorferi were cultured in BSK II media from which they were removed by low speed centrifugation. The sedimented borrelia were carefully resuspended in stabilizing buffer so as to preserve their features for scanning and negative staining. Alternatively, others were prepared for conventional thin sectioning and for cryotomy using modified procedures. For thin sectioning, the fixative described by Ito, et al.


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