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Dinesh C. Indurthi

Researcher at University of Sydney

Publications -  27
Citations -  895

Dinesh C. Indurthi is an academic researcher from University of Sydney. The author has contributed to research in topics: Nicotinic agonist & Agonist. The author has an hindex of 10, co-authored 22 publications receiving 784 citations. Previous affiliations of Dinesh C. Indurthi include University of Delaware & Delaware Biotechnology Institute.

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Clostridia: the importance of their exceptional substrate and metabolite diversity for biofuel and biorefinery applications.

TL;DR: Pathway engineering to combine established substrate-utilization programs, such as for cellulose, CO2/H2 or CO, with desirable metabolic programs could lead to modular design of strains suitable for many applications.
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Resolving the TCA cycle and pentose-phosphate pathway of Clostridium acetobutylicum ATCC 824: Isotopomer analysis, in vitro activities and expression analysis

TL;DR: Dynamic gene expression analysis of the putative Re-CS gene (CAC0970), its operon, and all glycolysis, pentose-phosphate pathway, and TCA cycle genes identify genes and their degree of involvement in these core pathways that support the powerful primary metabolism of this industrial organism.
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Synthetic tolerance: three noncoding small RNAs, DsrA, ArcZ and RprA, acting supra-additively against acid stress

TL;DR: It is shown that simultaneous overexpression of noncoding small RNAs, DsrA, RprA and ArcZ, which are translational RpoS activators, increased acid tolerance supra-additively up to 8500-fold during active cell growth, and provided protection against carboxylic acid and oxidative stress.
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Small RNAs in the Genus Clostridium

TL;DR: A conserved, novel sRNA is identified which, together with the downstream gene coding for an ATP-binding cassette (ABC) transporter gene, responds to the antibiotic clindamycin.
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A genomic-library based discovery of a novel, possibly synthetic, acid-tolerance mechanism in Clostridium acetobutylicum involving non-coding RNAs and ribosomal RNA processing.

TL;DR: By hybridizing against unprocessed rRNA precursors, ncRNA(RD7) alters rRNA processing, and these alterations result in acid tolerance, possibly through a mechanism involving the Ffh protein.