Structural characterization and hypoglycemic activity of a polysaccharide isolated from the fruit of Physalis alkekengi L.

2008 ◽  
Vol 71 (2) ◽  
pp. 316-323 ◽  
Author(s):  
Haibin Tong ◽  
Zhongyan Liang ◽  
Guiyun Wang
2020 ◽  
Vol 11 (8) ◽  
pp. 7104-7114
Author(s):  
Kai Qian ◽  
Ting Tan ◽  
Hui Ouyang ◽  
Shi-Lin Yang ◽  
Wei-Feng Zhu ◽  
...  

A water-soluble neutral homopolysaccharide (PLP-1) was obtained from the roots of Pueraria lobata by DEAE cellulose and Sephadex G-200 gel chromatography purification.


LWT ◽  
2016 ◽  
Vol 70 ◽  
pp. 55-62 ◽  
Author(s):  
Tianle Chen ◽  
Min Zhang ◽  
Jinglei Li ◽  
Maheen Mahwish Surhio ◽  
Beibei Li ◽  
...  

2019 ◽  
Vol 209 ◽  
pp. 363-371 ◽  
Author(s):  
Wen-Na Zhang ◽  
Ri-Na Su ◽  
Li-Li Gong ◽  
Wei-Wei Yang ◽  
Juan Chen ◽  
...  

Author(s):  
E. Naranjo

Equilibrium vesicles, those which are the stable form of aggregation and form spontaneously on mixing surfactant with water, have never been demonstrated in single component bilayers and only rarely in lipid or surfactant mixtures. Designing a simple and general method for producing spontaneous and stable vesicles depends on a better understanding of the thermodynamics of aggregation, the interplay of intermolecular forces in surfactants, and an efficient way of doing structural characterization in dynamic systems.


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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