Direct observation of redox reactions in Candida parapsilosis ATCC 7330 by Confocal microscopic studies
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep34344.pdf
Reference47 articles.
1. Kaliaperumal, T., Kumar, S., Gummadi, S. & Chadha, A. Asymmetric synthesis of (S)-ethyl-4-chloro-3-hydroxybutanoate using Candida parapsilosis ATCC 7330. J. Ind. Microbiol. Biotechnol. 37, 159–165 (2010).
2. Mahajabeen, P. & Chadha, A. One-pot synthesis of enantiomerically pure 1,2-diols: Asymmetric reduction of aromatic α-oxo aldehydes catalyzed by Candida parapsilosis ATCC 7330. Tetrahedron: Asymmetry 22, 2156–2160 (2011).
3. Venkataraman, S., Roy, R. K. & Chadha, A. Asymmetric reduction of alkyl-3-oxobutanoates by Candida parapsilosis ATCC 7330: Insights into solvent and substrate optimisation of the biocatalytic reaction. Appl. Biochem. Biotechnol. 171, 756–770 (2013).
4. Baskar, B., Pandian, N. G., Priya, K. & Chadha, A. Deracemisation of aryl substituted α-hydroxy esters using Candida parapsilosis ATCC 7330: Effect of substrate structure and mechanism. Tetrahedron 61, 12296–12306 (2005).
5. Padhi, S. K. & Chadha, A. Deracemisation of aromatic β-hydroxy esters using immobilised whole cells of Candida parapsilosis ATCC 7330 and determination of absolute configuration by 1H NMR. Tetrahedron: Asymmetry 16, 2790–2798 (2005).
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