scholarly journals Copper Storage Protein From Streptomyces Lividans

Author(s):  
Jonathan AR Worrall
Metallomics ◽  
2018 ◽  
Vol 10 (1) ◽  
pp. 180-193 ◽  
Author(s):  
Megan L. Straw ◽  
Amanda K. Chaplin ◽  
Michael A. Hough ◽  
Jordi Paps ◽  
Vassiliy N. Bavro ◽  
...  

A cytosolic copper storage protein has been identified inStreptomyces lividansand plays a role in copper tolerance once the first layer of copper resistance becomes saturated.


ACS Catalysis ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 5847-5859 ◽  
Author(s):  
Dhanashree Selvan ◽  
Pallavi Prasad ◽  
Erik R. Farquhar ◽  
Yelu Shi ◽  
Skyler Crane ◽  
...  

2020 ◽  
Vol 49 (6) ◽  
pp. 1928-1934
Author(s):  
Dhanashree Selvan ◽  
Yelu Shi ◽  
Pallavi Prasad ◽  
Skyler Crane ◽  
Yong Zhang ◽  
...  

The O2 reactivity of an artificial biomolecular hydrogenase, the nickel binding protein (NBP) is investigated.


The Analyst ◽  
2019 ◽  
Vol 144 (13) ◽  
pp. 3949-3958 ◽  
Author(s):  
Dhanashree Selvan ◽  
Pallavi Prasad ◽  
Skyler Crane ◽  
Abubkr Abuhagr ◽  
Richard Covington ◽  
...  

A copper storage protein is used to synthesize gold clusters with tunable emission that follow the Irving–Williams series for metal detection.


Author(s):  
Hsin-Kan Wu ◽  
Mei-Chu Chung

In one of our earlier papers (Wu et al. 1978), we suggested that glutelin is the major composition of the round storage protein bodies although they also contain relatively more prolamine than the angular one does. Immunochemical studies of Krishnan et al. (1986) later showed the presence of glutelin in the irregularly-shaped (angular) protein bodies while the prolamines were found in the round ones. Our recent experiment using protein A-gold technique found that prolamine is mainly deposited into the angular protein bodies.Small blocks (1 mm3) of 7 DAF (days after flowering) caryopsis of Orvza perennis were fixed with 3% paraformaldehyde and 3% glutaraldehyde in 0.1M sodium phosphate, pH7.4, dehydrated in a graded ethanol series and infiltrated with Spurr’s resin. Thin sections, after gold labeling, were stained with uranyl acetate and lead citrate. Rabbit antibodies were raised against purified prolamine. Protein A-gold sol complex was prepared based on the technique of Horisberger et al. (1977).


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