Advanced search
Publication Cover
Biocatalysis and Biotransformation Volume 29, 2011 - Issue 5
Submit an article Journal homepage
67
Views
0
CrossRef citations to date
0
Altmetric
Short Communication

Cis-GPRA synthesis by enzymatic removal of a p-methoxybenzyl protecting group from p-methoxybenzyl-7-phenylacetylamino-3-propenyl-3-cephem-4-carboxylate

Jia-Wei RongSchool of Bioscience and Bioengineering, South China University of Technology, Guangzhou, People's Republic of China
,
Ming-Jun ZhuSchool of Bioscience and Bioengineering, South China University of Technology, Guangzhou, People's Republic of ChinaCorrespondence[email protected]
,
Sheng-Xi FengGuangzhou Baiyunshan Pharmaceutical Co. Ltd, Guangzhou, People's Republic of China
&
Shi-Zhong LiangSchool of Bioscience and Bioengineering, South China University of Technology, Guangzhou, People's Republic of China
Pages 217-221 | Received 22 Oct 2010, Accepted 06 Jun 2011, Published online: 05 Aug 2011

References

  • Barbhaiya RH, Shukla UA, Gleason CR, Shyu WC, Wilber RB, Pittman KA. 1990. Comparison of cefprozil and Cefaclor pharmacokinetics and tissue penetration. Antimicrob Agents Chemother 34:1204–1209.
  • Brannon DR. 1976. Enzymatic de-esterification of cephalosporin para-nitrobenzyl esters. US Patent 3, 972,774. Aug 3.
  • Chen YR, Usui S, Queener SW, Yu CA. 1995. Purification and properties of p-nitrobenzyl esterase from Bacillus subtilis. J Ind Microbiol Biotechnol 15:10–18.
  • Davis BG, Boyer V, 2001. Biocatalysis and enzymes in organic synthesis. Nat Prod Rep 18:618–640.
  • Feng SX, Liang SZ, Lou WY. 2008. Two-step, one-pot enzymatic synthesis of cefprozil from 7-phenylacetamido-3-propenyl-cephalosporanic acid (GPRA). Biocatal Biotransformation 26:321–326.
  • Fotakopoulou I, Barbayianni E, Constantinou-Kokotou V, Bornscheuer UT, Kokotos G. 2007. Enzymatic removal of carboxyl protecting groups. III. Fast removal of allyl and chloroethyl esters by Bacillus subtilis esterase (BS2). J Org Chem 72:782–786.
  • Hussain W, Pollard DJ, Truppo M, Lye GJ. 2008 Enzymatic ketone reductions with co-factor recycling: improved reactions with ionic liquid co-solvents. J. Mol. Catal. B: Enzym 55:19–29.
  • Kadereit D, H Waldmann. 2001. Enzymatic protecting group techniques. Chemical Reviews 101:3367–3396.
  • Moore JC, Arnold FH 1996. Directed evolution of a para-nitrobenzyl esterase for aqueous–organic solvents. Nat Biotechnol 14:432–436.
  • Schmidt M, Henke Erik, Heinze B, Kourist R, Hidalgo A, Bornscheuer UT. 2007. Versatile esterase from Bacillus subtilis: cloning, expression, characterization, and its application in biocatalysis. Biotechnol J 2:249–253.
  • Torii S, Tanaka H, Taniguchi M, Kameyama Y, Sasaokam M, Shiroi T, Kikuchi R, Kawahara I, Shimabayashi A, Nagao S. 1991. Deprotection of caboxylic ester of beta-lactam homologs. Cleavage of p-methoxybenzyl, diphenylmethyl and tert-butyl esters effected by phenolic matrix. J Org Chem 56: 3363–3637.
  • Walker JM. 1996. The protein protocols handbook. Totowa (NJ): Humana Press.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.