EC 3.5.1.11

  • CAT Number: M017563
  • CAS Number: 9014-06-6
  • Purity: ≥95%
Inquiry Now

EC 3.5.1.11 (Cat.No:M017563), also known as&nbsp;</font><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”><font face=”arial, helvetica, sans-serif”>Penicillin amidase,&nbsp;</font><span style=”font-variant-ligatures: normal;”><font face=”arial, helvetica, sans-serif”>&nbsp;is the enzyme used commercially for the production of semisynthetic penicillins. It</font><font face=”Arial, sans-serif” size=”2″>&nbsp;</font></span></span><span style=”font-family: arial, helvetica, sans-serif; font-size: 12px; font-variant-ligatures: normal; orphans: 2; widows: 2;”>was used to study its effect in release of fatty acid and HSL (homoserine lactone) from AHLs (N-acylhomoserine lactones) in degradation of antibiotics. It was used as positive control for assaying penicillin G acylase activity in the study of functional analysis of bile salt hydrolase and penicillin acylase family members in Lactobacillus sp. Penicillin amidase may be used for synthesis of 6-aminopenicillanic acid from penicillin-G and for the industrial production of &beta;-lactam antibiotics.

Catalog Number M017563
CAS Number 9014-06-6
Purity 95%
Storage 2-8°C
Reference

<div class=”pubauthors” style=”font-size: 16px; box-sizing: inherit; margin: 0px; padding: 0px; background-color: rgb(254, 254, 254); color: rgb(10, 10, 10); font-family: &quot;Helvetica Neue&quot;, Helvetica, Roboto, Arial, sans-serif; font-variant-ligatures: normal; orphans: 2; widows: 2;”>
<span style=”color:#000000;”><span style=”font-family:arial,helvetica,sans-serif;”><span style=”font-size:12px;”>1.Sakaguchi, K. and Murao, S.A preliminary report on a new enzyme, &quot;penicillin-amidase&quot;.</span></span></span></div>
<div class=”pubjournal” style=”font-size: 16px; box-sizing: inherit; margin: 0px; padding: 0px; background-color: rgb(254, 254, 254); color: rgb(10, 10, 10); font-family: &quot;Helvetica Neue&quot;, Helvetica, Roboto, Arial, sans-serif; font-variant-ligatures: normal; orphans: 2; widows: 2;”>
<span style=”color:#000000;”><span style=”font-family:arial,helvetica,sans-serif;”><span style=”font-size:12px;”><span class=”pubName” style=”box-sizing: inherit; font-style: italic !important;”>J. Agric. Chem. Soc. Jpn.</span>&nbsp;23: 411 (1950).<br />
2.<span style=”background-color: rgb(255, 255, 255); font-variant-ligatures: normal;”>Mali, R. S., V. K. Sudhakaran, and J. G. Shewale. &quot;Affinity and hydrophobic interactions of penicillin amidase.&quot;&nbsp;</span><i style=”color: rgb(34, 34, 34); background-color: rgb(255, 255, 255); font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal;”>Hindustan Antibiotics Bulletin</i><span style=”background-color: rgb(255, 255, 255); font-variant-ligatures: normal;”>&nbsp;31.1-2 (1989): 25-28.<br />
3.</span><span style=”background-color: rgb(255, 255, 255); font-variant-ligatures: normal;”>Valle, Fernando, et al. &quot;The role of penicillin amidases in nature and in industry.&quot;&nbsp;</span><i style=”color: rgb(34, 34, 34); background-color: rgb(255, 255, 255); font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal;”>Trends in biochemical sciences</i><span style=”background-color: rgb(255, 255, 255); font-variant-ligatures: normal;”>&nbsp;16 (1991): 36-40.<br />
4.</span><span style=”background-color: rgb(255, 255, 255); font-variant-ligatures: normal;”>Lin, Yi‐Han, et al. &quot;Acyl‐homoserine lactone acylase from Ralstonia strain XJ12B represents a novel and potent class of quorum‐quenching enzymes.&quot;&nbsp;</span><i style=”color: rgb(34, 34, 34); background-color: rgb(255, 255, 255); font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal;”>Molecular microbiology</i><span style=”background-color: rgb(255, 255, 255); font-variant-ligatures: normal;”>&nbsp;47.3 (2003): 849-860.<br />
5.</span></span></span></span><span style=”color: rgb(34, 34, 34); background-color: rgb(255, 255, 255); font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal;”>Lambert, Jolanda M., et al. &quot;Functional analysis of four bile salt hydrolase and penicillin acylase family members in Lactobacillus plantarum WCFS1.&quot;&nbsp;</span><i style=”color: rgb(34, 34, 34); background-color: rgb(255, 255, 255); font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal;”>Applied and environmental microbiology</i><span style=”color: rgb(34, 34, 34); background-color: rgb(255, 255, 255); font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal;”>&nbsp;74.15 (2008): 4719-4726.</span></div>

Request a Quote

Contact Us at MuseChem

We are committed to providing you with reliable, cost-effective solutions for your chemical needs, while ensuring your safety and comfort. Our team of experts is always available to answer your questions and help you navigate the complexities of the chemical industry.

Whether you're looking for a specific product or need help with a custom synthesis project, we're here to help you discover a new world of chemical possibilities. Contact us today to learn more about how we can assist you with all of your chemical needs.

Our goal is to make the process of ordering chemicals as seamless and hassle-free as possible. Let us know how we can assist you, and we'll get back to you as soon as possible. We look forward to hearing from you!