Dergiler / Turkish Journal of Biology / 2010 / Cilt: 34 - Sayı: 1

Production of (S)-2'-fluorophenylethan-1-ol and (S)-3'- fluorophenylethan-1-ol by Alternaria alternata using ram horn peptone in microbial growth medium

Sayfa
39–46
Yayın Tarihi
2010-01-01
DOI
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As a result, 2 important chiral intermediates for the pharmaceutical industry using A. alternata EBK-6 in the submerged culture containing RHP from waste material were scaled up to gram scale with excellent ee.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Enantiomerically pure, fluorinated compounds have an important role in medicinal chemistry.
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Temel Bulgular & Veri:Alternaria alternata isolates were used for the synthesis of (S)-2'-fluorophenylethan-1-ol 1b and (S)-3'-fluorophenylethan-1-ol 2b.
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Sonuç & Katkı:As a result, 2 important chiral intermediates for the pharmaceutical industry using A. alternata EBK-6 in the submerged culture containing RHP from waste material were scaled up to gram scale with excellent ee.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Key words: Alternaria alternata · bioconversion · fluoroacetophenone

Özet

Enantiomerically pure, fluorinated compounds have an important role in medicinal chemistry. Alternaria alternata isolates were used for the synthesis of (S)-2'-fluorophenylethan-1-ol 1b and (S)-3'-fluorophenylethan-1-ol 2b. Biocatalytic syntheses of optically active 1b and 2b were achieved by asymmetric reduction of 2'-fluoroacetophenone 1a and 3'-fluoroacetophenone 2a in the batch culture of A. alternata containing ram horn peptone (RHP). The reaction conditions (pH, temperature, and agitation) that improve the conversion of the substrates were studied. The optimal reaction conditions were found as pH 6.0, agitation 250, temperature 32 °C and substrate 3 mmol/100 mL. The gram scale productions of 1b and 2b by the most effective biocatalyst A. alternata EBK-6 using RHP was carried out in a fermenter with 1-L working volume. The results showed that the yields with >99% enantiomeric excess (ee) of both 1b and 2b reached 75% for 1b and 66% for 2b. The concentrations of products 1b and 2b at the end of fermentation were 3.1 g/L and 2.8 g/L, respectively. As a result, 2 important chiral intermediates for the pharmaceutical industry using A. alternata EBK-6 in the submerged culture containing RHP from waste material were scaled up to gram scale with excellent ee.

Abstract

Enantiomerically pure, fluorinated compounds have an important role in medicinal chemistry. Alternaria alternata isolates were used for the synthesis of (S)-2'-fluorophenylethan-1-ol 1b and (S)-3'-fluorophenylethan-1-ol 2b. Biocatalytic syntheses of optically active 1b and 2b were achieved by asymmetric reduction of 2'-fluoroacetophenone 1a and 3'-fluoroacetophenone 2a in the batch culture of A. alternata containing ram horn peptone (RHP). The reaction conditions (pH, temperature, and agitation) that improve the conversion of the substrates were studied. The optimal reaction conditions were found as pH 6.0, agitation 250, temperature 32 °C and substrate 3 mmol/100 mL. The gram scale productions of 1b and 2b by the most effective biocatalyst A. alternata EBK-6 using RHP was carried out in a fermenter with 1-L working volume. The results showed that the yields with >99% enantiomeric excess (ee) of both 1b and 2b reached 75% for 1b and 66% for 2b. The concentrations of products 1b and 2b at the end of fermentation were 3.1 g/L and 2.8 g/L, respectively. As a result, 2 important chiral intermediates for the pharmaceutical industry using A. alternata EBK-6 in the submerged culture containing RHP from waste material were scaled up to gram scale with excellent ee.

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Bu Makaleye Atıf Yap

KURBANOĞLU, E. B., *, -., KURBANOĞLU, N. İ., ZILBEYAZ, K. (2010). Production of (S)-2'-fluorophenylethan-1-ol and (S)-3'- fluorophenylethan-1-ol by Alternaria alternata using ram horn peptone in microbial growth medium. Turkish Journal of Biology, Cilt: 34 - Sayı: 1, 39–46. https://ajindex.com/articles/182444

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Kaynakça (13)

  1. Gladysz JA, Curran DP, Horvath IT. Handbook of fluorous chemistry, Wiley-VCH, Weinheim, 2004.
  2. Soni P, Banerjee U.C. Enantioselective reduction of acetophenone and its derivatives with a new yeast isolate Candida tropicalis PBR-2 MTCC 5158. Biotechnol J 1: 80-85, 2006. 8. Nakamura K, Matsuda T. Asymmetric reduction of ketones by the acetone powder of Geotrichum candidum. J Org Chem 63: 8957-8964, 1998. 9. Lee B, Pometto AL, Demirci A et al. Media evaluation for the production of microbial enzymes. J Agric Food Chem 46: 4775- 4778, 1998.
  3. Kurbanoglu EB, Zilbeyaz K, Kurbanoglu NI et al. Highly enantioselective reduction of acetophenone by locally isolated Alternaria alternata using ram horn peptone. Tetrahedron: Asym 18: 1529-1532, 2007.
  4. Kurbanoglu EB, Kurbanoglu NI. Ram horn peptone as a source of citric acid production by Aspergillus niger, with a process. J Ind Microbiol Biotechnol 131: 289-294, 2004. Kurbanoglu EB. Enhancement of glycerol production with ram horn hydrolysate by yeast. Energy Conv Mngt 44: 2125-2133, 2003.
  5. Kurbanoglu EB, Algur OF, Zulkadir A. Submerged production of edible mushroom Agaricus bisporus mycelium in ram horn hydrolysate. Ind Crop Prod 19: 225-230, 2004.
  6. Kurbanoglu EB, Kurbanoglu NI. Production of citric acid from ram horn hydrolysate by Aspergillus niger. Process Biochem 38: 1421-1424, 2003.
  7. Kurbanoglu EB, Zilbeyaz K. Kurbanoglu NI et al. Asymmetric reduction of acetophenone analogues by Alternaria alternata using ram horn peptone. Tetrahedron: Asym 18: 2332-2335, 2007.
  8. Nie Y, Xu Y, Mu XQ. Highly enantioselective conversion of racemic 1-phenyl-1,2-ethanediol by stereoinversion involving a novel cofactor-dependent oxidoreduction system of Candida parapsilosis CCTCC M203011. Org Proc Res Develop 8: 246- 251, 2004.
  9. He JY, Sun ZH, Ruan WQ et al. Biocatalytic synthesis of ethyl (S)-4-chloro-3-hydroxy-butanoate in an aqueous-organic solvent biphasic system using Aureobasidium pullulans CGMCC 1244. Proceses Biochem 41: 244-249, 2006.
  10. Singh RS, Sooch BS. Puri M. Optimization of medium and process parameters for the production of inulinase from a newly isolated Kluyveromyces marxianus YS-1. Biores Technol 98: 2518-2525, 2007.
  11. Pfruender H, Jones R, Weuster-Botz D. Water immiscible ionic liquids as solvents for whole cell biocatalysis. J Biotechnol 124: 182-190, 2006.
  12. Xie Q, Wu J, Xu G et al. Asymmetric reduction of o- chloroacetophenone with Candida pseudotropicalis 104. Biotechnol Prog 22: 1301-1304, 2006.
  13. Chanda S, Chagrabarti S. Plant