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"a2   `?dyd @? #"    <H' " D   T Click to edit Master title style! !  0 " X  W#Click to edit Master subtitle style$ $  6w #" `|  Z*   6 #" `    \*   6) #" `|   \* `  H|yd޽h @ ? ff[[ffRR|80___PPT10. 0)24K0 11 ,k1(     `d,lxlx3?" 8 UOPTIMISATION OF MONOOLEIN CONCENTRATION IN A LIPASE CATALYSED REACTION ESTERIFICATION4V0 UU L''LLss:  Hplxlx@^ 1Department of Chemistry and Biochemistry, Medical Faculty of Rijeka, Brae Branchetta 20, HR-51000 Rijeka; 2Adria-PI, HR-51513 Omiaalj; 3Department of Reaction Engineering and Catalysis, Faculty of Chemical Engineering & Technology, University of Zagreb, Savska cesta 16, HR-10000 Zagreb, Croatia. *jasminka@mamed.medri.hrlE0  k   L''LLssT  T`Xlxlx;d  Jasminka Giacometti1*, Fabio Giacometti2, edomila Milin1, ura Vasi-Ra ki3N0              \    L''LLssX  0A?-0L   <X`] ` Introduction        `(,k s)?" 0A  Monoglycerides and mixture of the mono- and diglycerides of long chain fatty acids are food additives (E471) in products such as bread, ice cream, and margarine. On an industrial scale, these food-grade surfactants are normally manufactured by chemical glycerolysis of fats and oils1. An important application of enzyme catalysis in low-water organic media is the synthesis of esters catalysed by lipase2. Regarding of the 1,3-specificity, immobilised lipase from Mucor miehei was use for production of monoolein (MO) and diolein (DO) mixtures. The effect of hydrophobic organic solvents, the presence of molecular sieves3 and reaction temperatures were investigated for the synthesis optimisation of MO and DO mixture in a batch stirrer tank reactor (BSTR).  x; &    ,     x <          \    <B ] ` Experimental       `Ȝ s?" fx 8Lipase catalyzed esterification of glycerol with oleic acid in a solvent system was carried out with 6.67 mg ml-1 immobilized 1,3-specific Mucor miehei lipase at 25, 37 and 50oC, using n-hexane, cyclohexane and isooctane, without and by adding 40 mg ml-1 of 5 molecular sieves at the start of esterification, at 100 rpm, in a batch stirrer-tank reactor (BSTR). The reactions were followed and simultaneously monitored by the determination of free oleic acid and monoolein by the gas chromatographic method during 45 hrs. Diolein was calculated in the mass balance.9 o  B;    ,   4    3  $ >  H422LԔ,kX)?` (Figure 1. Final concentrations of monoolein in the solvent system with and without (u) molecular sieves in the presence of various organic solvents.l0  I>  TA M?$$6ԔȜX?"` `  M  # lA Y?$$6Ԕ,kX)??S"`?`  , Y@ # H$$6ԔȜX?`  Figure 2. Concentrations of monoolein after 45 hrs followed reaction esterification, in the solvent system with n-hexane in the presence of molecular sieves at various temperatures: red symbols  25oC; yellow symbols  37oC; green symbols  50oC.0  fV    $  fA [?$$6$$6Ԕ,kX)??C"?` $ [ % <4c` [Results   & Z_f,k s)?" /` kAfter 45 hrs followed reaction esterification, the amounts of MO were higher in the presence of n-hexane in the system without molecular sieves. In the system with molecular sieves, the amount of MO was higher in the presence of isooctane. A higher amount of MO was found at 37oC and DO at 50oC in the presence of molecular sieves and n-hexane. The enzyme activity, as function of hydrophobicity of organic solvents, affected DO/MO ratio. In the system without molecular sieves, the solvent hydrophobicity did not affect DO/MO ratio, but by adding of molecular sieves in the system, the ratio depended on solvent hydrophobicity. The all examined conditions show the different initial reaction rates. The presence of molecular sieves and examined reaction temperatures affected on final MO and DO concentrations. In the examined conditions, DO concentration did not exceed 69% (w/w) and MO 46% (w/w).  `*6 ' HFFj$$6ԔȜX?p  vFigure 3. Concentrations of monoolein after 45 hrs followed reaction esterification, in the solvent system with molecular sieves in the presence of organic solvents: red symbols  isooctane; yellow symbols  n-hexane; blue symbols  cyclohexane.Z0  % ( 0L.P L[1] Stevenson, D.E., Stanley, R.A. & Furneaux, R.H., Biotechnol.Lett. 1993, 15, 1043-1048. [2] A. Zaks, A. M. Klibanov, J. Biol. Chem.,1988, 263, 3194-3201. [3] J.Giacometti, F. Giacometti, . Milin, . Vasi-Ra ki, J. Mol. Catal. B-Enzym. 2001, 11, 921-928. 0  3   8 t X A g  ) <M ^ References     *  `A ]?$$6$$6Ԕ,kX)?C"?Lh \ ]F + N6FFj$$699Up99p?l8___PPT10N___PPT90( "Figure 4. Effect of hydrophobicity (versus log P value) on DO/MO ratio after 45 hrs followed reaction esterification, in the solvent system with n-hexane, with (%) and without (u) molecular sieves at 37oC. 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