Identification and structural characterization of a new pro-apoptotic cyclic octapeptide cyclosaplin from somatic seedlings of Santalum album L.

Peptides ◽  
2014 ◽  
Vol 54 ◽  
pp. 148-158 ◽  
Author(s):  
Abheepsa Mishra ◽  
Samiran S. Gauri ◽  
Sourav K. Mukhopadhyay ◽  
Soumya Chatterjee ◽  
Shibendu S. Das ◽  
...  
2021 ◽  
Vol 183 ◽  
pp. 112610
Author(s):  
Xinhua Zhang ◽  
Jaime A. Teixeira da Silva ◽  
Meiyun Niu ◽  
Ting Zhang ◽  
Huanfang Liu ◽  
...  

1996 ◽  
Vol 32 (3) ◽  
pp. 123-128 ◽  
Author(s):  
K. Sankara Rao ◽  
N. K. Chrungoo ◽  
Amares Sinha

2017 ◽  
Vol 17 (2) ◽  
pp. 1-8
Author(s):  
Siuli Batabyal ◽  
Priyanka Mukhopadhyay ◽  
Soumendranath Chatterjee ◽  
Jagatpati Tah ◽  
Nimai Saha

1974 ◽  
Vol 141 (1) ◽  
pp. 147-153 ◽  
Author(s):  
Uliyar V. Mani ◽  
Amurtur N. Radhakrishnan

1. A hydroxyproline-containing protein was isolated from the soluble fraction of sandal leaves (Santalum album L.) and the purified protein was homogeneous by disc electrophoresis. 2. It is a glycoprotein containing 16% carbohydrate, the components of which were mainly arabinose, with only small amounts (about 5%) of galactose. The principal amino acids were glutamic acid, aspartic acid, glycine, alanine, arginine, lysine, proline and hydroxyproline, which together comprised 60% of the total. The number of acidic amino acids exceeds the number of basic amino acids. By Sephadex gel filtration, the approximate molecular weight was found to be about 63000. The ratio of residues of hydroxyproline to those of arabinose was 1:2. 3. The native protein is resistant to the action of several proteolytic enzymes. After partial hydrolysis with 0.1m-HCl, the protein became susceptible to attack by Pronase but remained resistant to collagenase.


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.


2011 ◽  
Vol 44 (06) ◽  
Author(s):  
A Bracher ◽  
C Kozany ◽  
AK Thost ◽  
F Hausch

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