EC 3.5.1.11

For research use only. Not for therapeutic Use.

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

E-PCA;EC 3.5.1.11;PENICILLIN ACYLASE;PENICILLIN AMIDASE;PENICILLIN AMIDASE, IMMOBILIZED ON EUPERGIT(R) C;PENICILLIN AMIDOHYDROLASE;PENICILLIN G AMIDASE;PENICILLIN G AMIDASE, CARRIER-FIXED

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>

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