Ashish Sachan

Dr. Ashish Sachan


Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

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

Representative Publications

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12 August 2014 in Reviews in Environmental Science and Bio/Technology
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Journal Article
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SMShashank Mishra
Shashank Mishra
ASAshish Sachan
Ashish Sachan
AVAmbarish Sharan Vidyarthi
Ambarish Sharan Vidyarthi
SSShashwati Ghosh Sachan
Shashwati Ghosh Sachan

17 October 2006 in Journal of Industrial Microbiology and Biotechnology
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Journal Article
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SGShashwati Ghosh
Shashwati Ghosh
ASAshish Sachan
Ashish Sachan
SSSukanta Kumar Sen
Sukanta Kumar Sen
AMAdinpunya Mitra
Adinpunya Mitra
Streptomyces sannanensis MTCC 6637 was examined for its potentiality to transform ferulic acid into its corresponding hydroxybenzoate-derivatives. Cultures of S. sannanensis when grown on minimal medium containing ferulic acid as sole carbon source, vanillic acid accumulation was observed in the medium as the major biotransformed product along with transient formation of vanillin. A maximum amount of 400 mg/l vanillic acid accumulation was observed, when cultures were grown on 5 mM ferulic acid at 28°C. This accumulation of vanillic acid was found to be stable in the culture media for a long period of time, thus facilitating its recovery. Purification of vanillic acid was achieved by gel filtration chromatography using Sephadex™ LH-20 matrix. Catabolic route of ferulic acid biotransformation by S. sannanensis has also been demonstrated. The metabolic inhibitor experiment [by supplementation of 3,4 methylenedioxy-cinnamic acid (MDCA), a metabolic inhibitor of phenylpropanoid enzyme 4-hydroxycinnamoyl-CoA ligase (4-CL) along with ferulic acid] suggested that biotransformation of ferulic acid into vanillic acid mainly proceeds via CoA-dependent route. In vitro conversions of ferulic acid to vanillin, vanillic acid and vanillin to vanillic acid were also demonstrated with cell extract of S. sannanensis. Further degradation of vanillic acid to other intermediates such as, protocatechuic acid and guaiacol was not observed, which was also confirmed in vitro with cell extract.

1 June 2013 in Journal of Industrial Microbiology and Biotechnology
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Journal Article
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SMShashank Mishra
Shashank Mishra
ASAshish Sachan
Ashish Sachan
SSShashwati Ghosh Sachan
Shashwati Ghosh Sachan
During the past few years, the production of natural value-added compounds from microbial sources has gained tremendous importance. Due to an increase in consumer demand for natural products, various food and pharmaceutical industries are continuously in search of novel metabolites obtained from microbial biotransformation. The exploitation of microbial biosynthetic pathways is both feasible and cost effective in the production of natural compounds. The environmentally compatible nature of these products is one major reason for their increasing demand. Novel approaches for natural product biogeneration will take advantage of the current studies on biotechnology, biochemical pathways and microbiology. The interest of the scientific community has shifted toward the use of microbial bioconversion for the production of valuable compounds from natural substrates. The present review focuses on eugenol biotransformation by microorganisms resulting in the formation of various value-added products such as ferulic acid, coniferyl alcohol, vanillin and vanillic acid.

1 September 2012 in Renewable and Sustainable Energy Reviews
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Journal Article
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PGPriyanka Gupta
Priyanka Gupta
RSRaj Shekhar Singh
Raj Shekhar Singh
ASAshish Sachan
Ashish Sachan
AVAmbarish S. Vidyarthi
Ambarish S. Vidyarthi
AGAsha Gupta
Asha Gupta

1 June 2014 in Annals of Microbiology
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NPNeha Panjiar
Neha Panjiar
SSShashwati Ghosh Sachan
Shashwati Ghosh Sachan
ASAshish Sachan
Ashish Sachan

16 November 2005 in Applied Microbiology and Biotechnology
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Journal Article
Closed access
PDF file
ASAshish Sachan
Ashish Sachan
SGShashwati Ghosh
Shashwati Ghosh
SSSukanta Kumar Sen
Sukanta Kumar Sen
AMAdinpunya Mitra
Adinpunya Mitra