RAJESH K SANI

Prof. RAJESH K SANI

Chemical & Biological Engineering and Chemistry, Biology, and Health sciences, South Dakota School of Mines and Technology, Rapid City, South Dakota, USA
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Research Focus & Metrics

Academic Career Length

32Years (1995-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2013 in Bioresource Technology
Verified
Journal Article
Closed access
ABAditya Bhalla
Aditya Bhalla
NBNamita Bansal
Namita Bansal
SKSudhir Kumar
Sudhir Kumar
KBKenneth M. Bischoff
Kenneth M. Bischoff
RAJESH K SANIRAJESH K SANI
RAJESH K SANI

1 February 1998 in Enzyme and Microbial Technology
Verified
Journal Article
Closed access
WAWamik Azmi
Wamik Azmi
RAJESH K SANIRAJESH K SANI
RAJESH K SANI
UBUttam Chand Banerjee
Uttam Chand Banerjee

1 November 2010 in Bioresource Technology
Verified
Journal Article
Closed access
GRGurdeep Rastogi
Gurdeep Rastogi
ABAditya Bhalla
Aditya Bhalla
AAAkash Adhikari
Akash Adhikari
KBKenneth M. Bischoff
Kenneth M. Bischoff
SHStephen R. Hughes
Stephen R. Hughes
RAJESH K SANIRAJESH K SANI
RAJESH K SANI

1 May 1999 in Enzyme and Microbial Technology
Verified
Journal Article
Closed access
RAJESH K SANIRAJESH K SANI
RAJESH K SANI
UBUttam Chand Banerjee
Uttam Chand Banerjee


1 October 2001 in Applied and Environmental Microbiology
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Journal Article
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RAJESH K SANIRAJESH K SANI
RAJESH K SANI
BPBrent M. Peyton
Brent M. Peyton
LBLaura T. Brown
Laura T. Brown
The toxicity of copper [Cu(II)] to sulfate-reducing bacteria (SRB) was studied by using Desulfovibrio desulfuricans G20 in a medium (MTM) developed specifically to test metal toxicity to SRB (R. K. Sani, G. Geesey, and B. M. Peyton, Adv. Environ. Res. 5:269–276, 2001). The effects of Cu(II) toxicity were observed in terms of inhibition in total cell protein, longer lag times, lower specific growth rates, and in some cases no measurable growth. At only 6 μM, Cu(II) reduced the maximum specific growth rate by 25% and the final cell protein concentration by 18% compared to the copper-free control. Inhibition by Cu(II) of cell yield and maximum specific growth rate increased with increasing concentrations. The Cu(II) concentration causing 50% inhibition in final cell protein was evaluated to be 16 μM. A Cu(II) concentration of 13.3 μM showed 50% inhibition in maximum specific growth rate. These results clearly show significant Cu(II) toxicity to SRB at concentrations that are 100 times lower than previously reported. No measurable growth was observed at 30 μM Cu(II) even after a prolonged incubation of 384 h. In contrast, Zn(II) and Pb(II), at 16 and 5 μM, increased lag times by 48 and 72 h, respectively, but yielded final cell protein concentrations equivalent to those of the zinc- and lead-free controls. Live/dead staining, based on membrane integrity, indicated that while Cu(II), Zn(II), and Pb(II) inhibited growth, these metals did not cause a loss of D. desulfuricans membrane integrity. The results show that D. desulfuricans in the presence of Cu(II) follows a growth pattern clearly different from the pattern followed in the presence of Zn(II) or Pb(II). It is therefore likely that Cu(II) toxicity proceeds by a mechanism different from that of Zn(II) or Pb(II) toxicity.