Evaluation of UV-B protection efficiency of mycosporine like amino acid extracted from the cyanobacteria Anabaenopsis sp. SLCyA isolated from a hypersaline lake

2021 ◽  
pp. 100749
Author(s):  
Himanshu Kumar Bairwa ◽  
Ganshyam Prajapat ◽  
Shikha Jain ◽  
Inshad Ali Khan ◽  
Lalita Ledwani ◽  
...  
2019 ◽  
Vol 2019 ◽  
pp. 1-11
Author(s):  
Hwa Sung Ryu ◽  
Chang Gil Lim ◽  
Tae Won Kang ◽  
Seungmin Lim ◽  
Hong Tae Kim ◽  
...  

Reinforcing steel maintains passivity in an alkaline concrete environment. However, the passive film on the steel can be destroyed as the concrete becomes acidic, which could induce the corrosion of reinforcing steel. Carbonates and sulfates destroy the concrete matrix and accelerate the penetration of hazardous ions, thereby deteriorating the structure. To alleviate the corrosion of internal reinforcing steel within concrete, corrosion inhibitors are most widely used. In this study, the effects of inorganic nitrite (lithium nitrite) and amino acid corrosion inhibitors (diethanolamine, methyl diethanolamine, and 4-aminobutyric) on corrosion resistance and the pH of the solution with various concentrations of Na2SO4 (0.89, 1.77 g/L) in saturated Ca(OH)2 that contained NaCl (0.98 g/L), which simulated the concrete environment, were investigated. The corrosion resistance of inhibitors was evaluated by corrosion potential, electrochemical impedance spectroscopy, and potentiodynamic techniques. The results indicated improvement of corrosion resistance by the addition of amino acid corrosion inhibitors. It was confirmed that the inhibitor adsorbed on the surface of the specimen and passivated to reduce the corrosion reaction. In addition, the 4-aminobutyric acid corrosion inhibitors had the corrosion protection efficiency of 67.87–77.80%, which is a higher value than that of the inorganic nitrite corrosion inhibitor (lithium nitrite: 69.36–75.93%) and other amino acid corrosion inhibitors (diethanolamine: 35.69–39.91%; methyl diethanolamine: 66.07–69.09%).


Author(s):  
M.K. Lamvik ◽  
L.L. Klatt

Tropomyosin paracrystals have been used extensively as test specimens and magnification standards due to their clear periodic banding patterns. The paracrystal type discovered by Ohtsuki1 has been of particular interest as a test of unstained specimens because of alternating bands that differ by 50% in mass thickness. While producing specimens of this type, we came across a new paracrystal form. Since this new form displays aligned tropomyosin molecules without the overlaps that are characteristic of the Ohtsuki-type paracrystal, it presents a staining pattern that corresponds to the amino acid sequence of the molecule.


Author(s):  
A. J. Tousimis

The elemental composition of amino acids is similar to that of the major structural components of the epithelial cells of the small intestine and other tissues. Therefore, their subcellular localization and concentration measurements are not possible by x-ray microanalysis. Radioactive isotope labeling: I131-tyrosine, Se75-methionine and S35-methionine have been successfully employed in numerous absorption and transport studies. The latter two have been utilized both in vitro and vivo, with similar results in the hamster and human small intestine. Non-radioactive Selenomethionine, since its absorption/transport behavior is assumed to be the same as that of Se75- methionine and S75-methionine could serve as a compound tracer for this amino acid.


Author(s):  
Chi-Ming Wei ◽  
Margaret Hukee ◽  
Christopher G.A. McGregor ◽  
John C. Burnett

C-type natriuretic peptide (CNP) is a newly identified peptide that is structurally related to atrial (ANP) and brain natriuretic peptide (BNP). CNP exists as a 22-amino acid peptide and like ANP and BNP has a 17-amino acid ring formed by a disulfide bond. Unlike these two previously identified cardiac peptides, CNP lacks the COOH-terminal amino acid extension from the ring structure. ANP, BNP and CNP decrease cardiac preload, but unlike ANP and BNP, CNP is not natriuretic. While ANP and BNP have been localized to the heart, recent investigations have failed to detect CNP mRNA in the myocardium although small concentrations of CNP are detectable in the porcine myocardium. While originally localized to the brain, recent investigations have localized CNP to endothelial cells consistent with a paracrine role for CNP in the control of vascular tone. While CNP has been detected in cardiac tissue by radioimmunoassay, no studies have demonstrated CNP localization in normal human heart by immunoelectron microscopy.


1979 ◽  
Vol 7 (1) ◽  
pp. 261-262
Author(s):  
E. V. ROWSELL

2001 ◽  
Vol 120 (5) ◽  
pp. A153-A153
Author(s):  
S MIYAMOTO ◽  
K KATO ◽  
Y ISHII ◽  
S ASAI ◽  
T NAGAISHI ◽  
...  

1950 ◽  
Vol 16 (4) ◽  
pp. 757-763 ◽  
Author(s):  
A. Leonard Sheffner ◽  
Joseph B. Kirsner ◽  
Walter L. Palmer

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