Shrinivas Nageshwar Rao Dangeti

Shrinivas Nageshwar Rao Dangeti
  • Doctor of Philosophy
  • Researcher at Advanced Enzymes

About

5
Publications
1,113
Reads
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194
Citations
Current institution
Advanced Enzymes
Current position
  • Researcher
Additional affiliations
November 2011 - January 2013
Karnataka State Women's University
Position
  • Research Associate
January 2013 - present
Advanced Enzymes
Position
  • Researcher
Education
March 2008 - February 2012
Gulbarga University
Field of study
  • Biotechnology
April 2005 - May 2007
Gulbarga University
Field of study
  • Biotechnology
May 2003 - April 2005
University of Mumbai
Field of study
  • Microbiology and Biotechnology

Publications

Publications (5)
Article
Full-text available
Trichoderma species are widely used as production hosts for industrial enzymes. Identification of Trichoderma species requires a complex molecular biology based identification involving amplification and sequencing of multiple genes. Industrial laboratories are required to run identification tests repeatedly in cell banking procedures and also to p...
Article
Full-text available
Pigeonpea (Cajanus cajan (L) Millsp.) is a drought tolerant legume widely grown in the arid and semi-arid tropics of the world which possesses a deep and extensive root system that succors a number of important physiological and metabolic functions to cope with drought. Application of available functional genomics approaches to improve productivity...
Article
Full-text available
The thermoalkalophilic Bacillus halodurans JB 99 cells known for production of novel thermostable alkaline keratinolytic protease were immobilized in calcium alginate matrix. Batch and repeated batch cultivation using calcium alginate immobilized cells were studied for alkaline protease production in submerged fermentation. Immobilized cells with 2...
Article
A thermostable alkaline protease produced from Bacillus sp. JB 99 exhibited significant keratinolytic and dehairing activity. The enzyme was purified by ammonium sulphate precipitation followed by CM-cellulose and Sephadex G-100 chromatography and resulted in 13.6 fold purification with 23.8% of recovery. The specific activity of purified enzyme wa...
Article
A highly thermostable alkaline xylanase was purified to homogeneity from culture supernatant of Bacillus sp. JB 99 using DEAE-Sepharose and Sephadex G-100 gel filtration with 25.7-fold increase in activity and 43.5% recovery. The molecular weight of the purified xylanase was found to be 20 kDA by SDS-PAGE and zymogram analysis. The enzyme was optim...

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