Author： Park S.J.
Publisher： Springer Publishing Company
ISSN： 0141-5492
Source： Biotechnology Letters, Vol.24, Iss.3, 2002-02, pp. : 181-184
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
Monooctanoyl phloroglucinol with anti-microbial activities was synthesized from phloroglucinol (50 mM) and vinyl octanoate (150 mM) with agitation at 40 °C using 10 mg lipase AK (Pseudomonas fluorescens) in acetonitrile (1 ml, aw=0.07). The yield was approximately 70% as conversion rate of phloroglucinol over 3 days. The product, at 205 μg ml^−1, was bacteriocidal against Escherichia coli and Staphylococcus epidermidis.
Related content
Access to resources
Recommend
By Miyazawa T.
Biotechnology Letters, Vol. 21, Iss. 11, 1999-11 ,pp. :
Enzymatic Synthesis of Cinnamic Acid Derivatives
By Lee Gia-Sheu Widjaja Arief Ju Yi-Hsu
Biotechnology Letters, Vol. 28, Iss. 8, 2006-04 ,pp. :
Lipase-catalyzed synthesis of 6-O-vinylacetyl glucose in acetonitrile
By Zhang X.
Biotechnology Letters, Vol. 24, Iss. 13, 2002-07 ,pp. :