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Electronic Journal of Biotechnology

versión On-line ISSN 0717-3458

Electron. J. Biotechnol. v.6 n.1 Valparaíso abr. 2003

 

Process Biotechnology

Electronic Journal of Biotechnology ISSN: 0717-3458 Vol. 6 No. 1, Issue of April 15, 2003
© 2003 by Universidad Católica de Valparaíso -- Chile Received October 29, 2002 / Accepted January 22, 2003
SHORT COMMUNICATION

Enzymatic synthesis of short chain citronellyl esters by a new lipase from Rhizopus sp

Gabriela Alves Macedo*
Faculdade de Engenharia de Alimentos
Universidade Estadual de Campinas
CP 6121, CEP 13083970, Campinas, SP, Brazil
Tel: 55 19 37882164
Fax : 55 19 32892832
E-mail: gmacedo@fea.unicamp.br

Maria Mercedez Soberón Lozano
Instituto de Bioquímica e Nutrição
Faculdade de Medicina
Universidade de San Marcos
Lima, Peru

Gláucia Maria Pastore
Faculdade de Engenharia de Alimentos
Universidade Estadual de Campinas
CP 6121, CEP 13083970, Campinas, SP, Brazil
Tel: 55 19 37883887
Fax: 55 19 37883887
E-mail: glaupast@fea.unicamp.br

*Corresponding author

Keywords: esters, flavor, lipases, synthesis.

Abstract Reprint (PDF)
Abstract
Article
References


Short chain citronellyl esters were synthesized by a new microbial lipase from Rhizopus sp strain isolated and lipase produced at UNICAMP, Brazil. Direct esterification and transesterification reactions have been performed to produce citronellyl acetate and butyrate in a free-solvent system and with n-hexane in reaction medium. Reaction mixture for direct esterification and transesterification was carried out at 45ºC in equimolar concentration of substrates: acid or ester and alcohol. Only citronellyl butyrate was synthesized by direct esterification with yields from 95 to 100% after 24 hrs. of reaction time, with or without n-hexane. Citronellyl acetate was synthesized by transesterification with ethyl acetate and cytronellol, with yield of 58% after 48 hrs. and 48% of conversion for reaction butyl acetate and cytronellol. The results suggest that the size of the aliphatic chain from acyl donor was importance to conversion rate. Acids with more than two carbons showed to be better substrate for Rhizopus sp lipase. Transesterification reaction showed different behaviour, ester substrate with four carbons was better than six carbon for citronellyl acetate synthesis.

Article
Abstract
Article

Materials and Methods
  • Chemicals
  • Lipase production and activity assay
  • Esterification reaction
  • Transesterification reaction
  • Analysis by gas chromatography
    Results and Discussion
  • Synthesis of citronellyl esters by direct...
  • Synthesis of citronellyl acetate by...
    Figure 1
    Figure 2
    References

  • Esters of short chain fatty acids and alcohols are known as flavour and fragrance compounds.

    Used in the food, beverage, cosmetic and pharmaceutical industries. Currently, most of the flavour compounds are provided by traditional methods as chemical synthesis or extraction from natural sources. The great recent interest for "natural" products pushed the flavour industry to seek new methods to obtain flavour compounds naturally. The use of Biotechnology specifically direct biosynthesis by fermentation has been described as potential source of esters (Christen and Munguia, 1994). However, the esters concentration and productivities obtained using fermentation are rather low. A new possibility to produce natural esters was opened by enzyme catalysis carried out in non-aqueous organic solvents or in free-solvent reaction medium (Gubicza et al. 2000). Direct esterification and transesterification reactions have been performed using lipases to produce, tailored triglycerides and numerous flavour esters. Many acetate and butyrate esters are components of natural flavours. However, reports on the production of acetate esters are scarce in various organic solvents. Due the toxicity of acetate on lipase activity in enzimic acetylation, the use of acetic acids an acyl donor in transesterification and direct esterification reactions was previously attempted with little or no success (Güvenç et al. 2002).

    The Food Biochemistry Laboratory at UNICAMP, Brazil has isolated several microorganisms which producing lipases. One of the potent producer of lipases isolated is the strain Rhizopus sp. In our laboratory we have tested the ability of the lipase from Rhizopus sp to catalyse the formation of citronellyl esters with acetic and butyric acid by direct esterification and transesterification reactions.

    Materials and Methods

    Chemicals. (R,S) citronellyl were purchased from Fluka Chemika; acetic acid, butyric acid were obtained from Merck (Darmstadt, Germany), ethyl acetate, butyl acetate, n-hexane, decane were purchased from Aldrich Chemicals. Molecular sieves 4 Å obtained from Acros Organics (New Jersey, USA).

    Lipase production and activity assay. Lipase from Rhizopus sp was produced in a solid medium (60% wheat bran and 40% water) at 30ºC. After 72 hrs., water was added to the solid medium, followed by homogenization,1 hrs. of incubation followed by simple filtration. Supernatant were treated with ammonium sulphate (80% saturation). The precipitates were dialyzed in sodium phosphate buffer, pH 7.0, and lyophilized for use as crude lipase preparation in powder form. The lipase activities preparations were quantified by the hydrolysis of triolein (Macedo et al. 1997). One unit (U) of lipase activity was defined as one mmole of oleic acid released per minute at 40ºC. A Lowry method was employed to determinate the protein content in lipase crude power.

    Esterification reaction. (R,S) citronellyl alcohol was mixed with acetic acid and butyric acid  in equimolar (1:1) ratio, molecular sieves (4% w/w reactants) and lipase (10 Units). Ester synthesis was carried out in screw capped tubes incubated at 45ºC under constant agitation at 200 rpm. System #1 was solvent-free system and System #2, 2 mL of n-hexane was added. A control tube without lipase was prepared and incubated under the same conditions. Samples of 20 µL was withdrawn after 2, 5, 7, 10, 24, 48 and 72 hrs. of reaction time, and analysed by gas chromatography.

    Transesterification reaction. Citronellyl acetate synthesis was carried out in screw capped tubes containing equimolar ratio of citronellyl alcohol and ester (ethyl acetate, butyl acetate), molecular sieves (4% w/w reactants) and 10 lipase units. The experiments was conduced with and without n-hexane. Samples of 20 µL was withdrawn after 2, 5, 7, 10, 24, 48 and 72 hrs. of reaction time.

    Analysis by gas chromatography. At the end of incubation period, the reaction mixtures were cooled. Two hundred of internal standard (hexanol) was added to each sample. A one µL aliquot was injected in a split (1:100) mode into a CHROMPACK® CP9001 (Middle Burg, Holland) gas chromatograph equipped with a flame-ionisation detector. A CP WAX 52 CB (Chrompack®, Middle Burg, Holland) fused silica capillary column (30 m x 0.32 mm i.d.; film thickness 0.2 mm) was used. Injector and detector temperatures were set at 220ºC and 250ºC, respectively. Oven temperature ranged from 50ºC to 220ºC. The carrier gas was helium at 1ml/min. The extent of synthesis (yield) was determine calculated basis on the consume of alcohol injected and quantified with standard curves of alcohol. The results were calculated as the equation 1:

    Conversion rate (%) = Co – C / Co x 100 (1)

    Where:

    Co: initial concentration of (R,S) citronellyl

    C: concentration of alcohol at a given time

    Results and Discussion

    Synthesis of citronellyl esters by direct esterification

    Several lipases showed the ability in catalyse acetate and butyrate citronellyl esters by direct esterification. However, the synthesis of citronellyl acetate usually display very low yields (Claon and Akoh, 1994). Rhizopus sp lipase presented maximum yield of 10% after 24 hrs. of reaction time decreasing the yield after that time. Previous reports indicated an inhibitory effect of acetic acid on lipase-catalysed reactions (De Castro et al. 1997). The effect of acetic acid concentration on esterification reaction using lipase SP435 was investigated by Claon et al. 1994. In this study, increasing concentrations of acetic acid (0.4 to 0.7 M) inhibited SP435 lipase activity resulting in low conversion yields for acetate esters. According to Claon and Akoh, 1994 the presence of acetic acid can damage the hydration layer-protein interaction of the enzyme structure causing lipase deactivating during the esterification process. Probably Rhizopus sp lipase is vulnerable to acetic acid in reaction medium as other lipases reported.

    Synthesis of citronellyl butyrate exhibited better yields. The maximum ester conversion achieved was 95% after only 24 hrs. of reaction time. In Figure 1 the experimental results are shown for solvent-free system and n-hexane reaction system. Ester conversion obtained without n-hexane was not much lower than the yields observed using n-hexane as organic solvent during esterification reaction. The results suggest that n-hexane is not necessary for citronellyl butyrate direct synthesis using Rhizopus sp lipase. This fact is of great interest for food industry since the step of solvents recovery (that are toxic) could be eliminate reducing costs and pollution concerns.

    Synthesis of citronellyl acetate by transesterification

    As direct esterification does not produced satisfactory yields for citronellyl acetate ester, transesterification was tested. The reaction mixture was composed by ester as acyl donor (ethyl acetate or butyl acetate) and alcohol citronellyl. Figure 2 shows the results obtained for both preparations. Since the presence of n-hexane was not significant in the yields obtained, transesterification reaction was carried out without n-hexane. Rhizopus sp lipase catalysed acetate ester with maximum yield of 60% after 48 hrs. using ethyl acetate as substrate. Mucor miehei lipase also showed affinity for lower molecular mass acyl donor for geranyl acetate synthesis according to Chulalaksananukul et al. 1992. The chain length of acyl donor could be affecting the yield of ester synthesis either in direct esterification or transesterification reaction using Rhizopus sp lipase. Thus, findings indicate that overall a higher affinity was shown for butyrate than for acetate and that the chain length of the acyl donor could have an effect on the yield of cytronellol esters. Rhizopus sp lipase showed promising results and immobilizing the enzyme could also improve yields as well as reduce costs. Therefore, reaction conditions and parameters need to be studied more extensively to develop optimum product yields.

    References

    CLAON, P and AKOH, C. Effect of reaction parameters on SP435 lipase-catalyzed synthesis of citronellyl acetate in organic solvent. Enzyme and Microbial Technology, 1994, vol. 16, p. 835-838.        [ Links ]

    CHULALAKSANANUKUL, W.; CONDORET, J.S. and COMBES, D. Kinetics of geranyl acetate synthesis by lipase-catalyzed transesterification. Enzyme and Microbial Technology, 1992, vol. 14, p. 293-298.        [ Links ]

    CHRISTEN, P. and MUNGUIA, L.A. Enzymes and food flavour a review. Food Biotechnology, 1994, vol. 8, p. 167-190.        [ Links ]

    DE CASTRO, H.F.; DE OLIVEIRA, P.C. and PEREIRA, E.B. Evaluation of different approaches for lipase catalysed synthesis of citronellyl acetate. Biotechnology Letters, 1997, vol. 19, p. 229-232.        [ Links ]

    GUBICZA, L.; KABIRI-BADR, A.; KEOVES, E. and BELAFI-BAKO, K. Large-scale enzymatic production of natural flavour esters in organic solvent with continuous water removal. Journal of Biotechnology, 2000, vol. 84, p. 193-196.        [ Links ]

    GÜVENÇ, A.; KAPUCU, N. and MEHMETOGLU, Ü. The production of isoamil acetate using immobilized lipases in a solvent-free system. Process Biochemistry, 2002, vol. 38, p. 379-386.        [ Links ]

    MACEDO, G. and PASTORE, G.M. Lipases microbianas na produção de ésteres formadores de aroma. Revista da Sociedade Brasileira de Ciência e Tecnologia de Alimentos, 1997, vol. 17, no. 2, p. 115-119.        [ Links ]

    Note: Electronic Journal of Biotechnology is not responsible if on-line references cited on manuscripts are not available any more after the date of publication.

     
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