c parapsilosis atcc 7330 proceeds (ATCC)
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c parapsilosis atcc 7330 proceeds
C Parapsilosis Atcc 7330 Proceeds, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 253 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/c+parapsilosis+atcc+7330+proceeds/Candida+parapsilosis+(Ashford)+Langeron+et+Talice/10__1039_slash_c5ra18532g-22-40-42
Average 95 stars, based on 253 article reviews
C Parapsilosis Atcc 7330 Proceeds, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 253 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/c+parapsilosis+atcc+7330+proceeds/Candida+parapsilosis+(Ashford)+Langeron+et+Talice/10__1039_slash_c5ra18532g-22-40-42
Average 95 stars, based on 253 article reviews
c parapsilosis atcc 7330 proceeds - by Bioz Stars,
2026-10
95/100 stars
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Yeast:Article Title: Candida parapsilosis ATCC 7330 mediated oxidation of aromatic (activated) primary alcohols to aldehydes Article Snippet: Aldehydes are useful precursors in the synthesis of a variety of pharmaceuticals e.g. anti-malarial drugs, anti-cancer drugs, antioxidants and anti-bacterials, anti-amoebics, drugs for the treatment of iron overload and iron de ciency and antipsychotic drugs among others.. Several chemical reagents have been reported so far for the oxidation of primary alcohols to aldehydes.. The limitations that are associated with the chemical reagents, (e.g. removal of metallic by-products, formation of side products, difficulty in handling of hygroscopic reagents, requirements of low or high temperature which is an additional setup to maintain the temperature) make it important to develop alternate green methods for this oxidation. High Performance Liquid Chromatography:Article Title: Regio- and enantio-selective oxidation of diols by Candida parapsilosis ATCC 7330 Article Snippet: Selectivity between primary and secondary alcohols was observed in oxidation using whole cells ofCandida parapsilosis ATCC 7330, where the secondary alcohol was preferentially oxidized.. In racemic sec alcohols, the ‘R’ enantiomer was selectively oxidized to the corresponding keto alcohol (yield 1⁄4 18–54%) leaving the ‘S’ diol (yield 1⁄4 31–69% and enantiomeric excess from 14% to >99%).. A biphasic system consisting of isooctane–water (48 : 2 v/v) was used as a medium for biotransformation at 25 C. This is the first report of the regioand enantio-selective oxidation of diols using C. parapsilosis ATCC 7330. |