Biochemical Characterization of a First Fungal Esterase from Rhizomucor miehei Showing High Efficiency of Ester Synthesis

Background Esterases with excellent merits suitable for commercial use in ester production field are still insufficient. The aim of this research is to advance our understanding by seeking for more unusual esterases and revealing their characterizations for ester synthesis. Methodology/Principal Findings A novel esterase-encoding gene from Rhizomucor miehei (RmEstA) was cloned and expressed in Escherichia coli. Sequence analysis revealed a 975-bp ORF encoding a 324-amino-acid polypeptide belonging to the hormone-sensitive lipase (HSL) family IV and showing highest similarity (44%) to the Paenibacillus mucilaginosus esterase/lipase. Recombinant RmEstA was purified to homogeneity: it was 34 kDa by SDS-PAGE and showed optimal pH and temperature of 6.5 and 45°C, respectively. The enzyme was stable to 50°C, under a broad pH range (5.0–10.6). RmEstA exhibited broad substrate specificity toward p-nitrophenol esters and short-acyl-chain triglycerols, with highest activities (1,480 U mg−1 and 228 U mg−1) for p-nitrophenyl hexanoate and tributyrin, respectively. RmEstA efficiently synthesized butyl butyrate (92% conversion yield) when immobilized on AOT-based organogel. Conclusion RmEstA has great potential for industrial applications. RmEstA is the first reported esterase from Rhizomucor miehei.


Introduction
Esterase (carboxylesterase, EC 3.1.1.1) and lipase (EC 3.1.1.3) are usually known as lipolytic enzymes catalyzing the cleavage and formation of ester bonds. Esterases mainly catalyze the hydrolysis of ester bonds of short-chain triglycerides or esters (,10 carbon atoms), whereas lipases favor the hydrolysis of water-insoluble triglycerides bearing long-chain fatty acids (.10 carbon atoms) [1]. Under certain conditions (anhydrous organic solvent systems), both types of enzymes can catalyze the reverse reaction, esterification, as well as transesterification and enantioselective hydrolysis reactions [2]. The most significant difference between esterases and lipases is in their ability to act on surface display: lipases exhibit interfacial activation whereas esterases do not [3].
Due to their unique properties, such as a broad range of nonnatural substrate specificity, high stability in organic solvents and high enantioselectivity (for some of them), esterases are useful for a variety of industrial applications: as additives in fat and oil processing, in laundry detergents, for the synthesis of fine chemicals and pharmaceuticals, in paper making and in the manufacture of cosmetics, among others [2][3][4]. In the food industry in particular, they exhibit numerous potential applications in flavor-ester producing processes, since flavorings represent over a quarter of the world market for food additives, consumers have been shown to prefer foodstuff that can be labeled as ''natural'', and the enzyme-based biochemically produced flavor esters excel, with better odors and flavors than their chemical counterparts [5]. To date, various flavor esters have been synthesized by esterification reaction using microbial lipolytic enzymes [5,6]. However, esterases seem to be less popular than lipases, mainly due to lack of availability despite their commercial value. Accordingly, identification, isolation and characterization of novel esterases with unique properties are of great value for application in the industry.
Rhizomucor miehei is a thermophilic zygomycete that secretes multiple hydrolytic enzymes, such as lipase [2], milk clotting protease [23] and b-glucanase [24]. However, no esterases have been characterized from this species. In this paper, we describe the first molecular cloning and expression of a novel esterase gene from R. miehei CAU432 and characterize the recombinant enzyme. In addition, the potential for application of this esterase to flavorester synthesis was investigated.

Strains and Plasmids
The Rhizomucor miehei strain CAU432 used in this study has been deposited in the China General Microbiological Culture Collection Center (CGMCC, accession No. 4967). E. coli strain DH5a was used to propagate plasmids and strain BL21 (DE3) was used as the host for expression of the esterase gene. pET-30a(+) was obtained from Novagen (Madison, WI, USA). pMD18-T was purchased from TaKaRa.
Cloning of the Full-length Esterase cDNA and Sequence Analysis DNA manipulations were performed as described by Sambrook and Russell [25]. Genomic DNA was isolated from R. miehei CAU432 mycelia using the CTAB (Hexadecyltrimethy Ammonium Bromide) method. For mycelium collection, R. miehei CAU432 was cultivated at 50uC for 2 days in medium containing (g L 21 ): oat flour 10, tryptone 10, yeast extract 10, MgSO 4 ?7H 2 O 0.3, FeSO 4 0.3 and CaCl 2 0.3, then the fungal mycelia were collected by centrifugation (5,0006g, 10 min) and washed twice with sterilized water at 4uC. Total RNA was isolated using the Trizol Kit (Invitrogen, Carlsbad, CA, USA), and mRNAs were purified using the Oligotex mRNA Midi Kit (Qiagen, Dusseldorf, Germany).
Genomic DNA of R. miehei CAU432 was used as the template for subsequent polymerase chain reaction (PCR) amplification. To clone the esterase gene, degenerate primers EstDF and EstDR (Table 1) were designed based on the conserved blocks of amino acid residues (LAVAGDSAG and DVLRDEGE) from other known esterases using the CODEHOP algorithm [26]. A putative homologous consensus region of the esterase gene was amplified using the degenerate primers and analyzed by sequencing the PCR products. PCR conditions were as follows: a hot start at 94uC for 5 min followed by 10 cycles of 94uC for 30 s, 60uC for 30 s and 72uC for 1 min, with 0.5uC decrease in annealing temperature per cycle, then 20 cycles of 94uC for 30 s, 55uC for 30 s and 72uC for 1 min. The PCR product was purified, ligated to pMD18-T vector, transformed into E. coli DH5a competent cells and sequenced.
The full-length cDNA sequence of the esterase was obtained by 59 and 39 rapid amplification of cDNA ends (RACE) using a BD SMART TM RACE cDNA Amplification Kit (Clontech, Palo Alto, CA, USA). The PCR conditions for RACE were as follows: a hot start at 94uC for 1 min, followed by 30 cycles of 30 s at 94uC, 30 s at 68uC and 1 min at 72uC, and finally 10 min at 72uC. PCR was performed with the following primer pairs (Table 1): Est59GSP and Universal Primer A Mix for the first PCR, followed by a nested PCR with the primers Est59NGSP and Nested Universal Primer A for 59 RACE. Similarly, 39 RACE was performed with Est39GSP and Universal Primer A Mix, followed by nested PCR with Est39NGSP and Nested Universal Primer A. The obtained PCR product was purified, cloned and sequenced. The 59 and 39 flanking sequences obtained by 59 and 39 RACE were assembled with that of the consensus region to form the full-length cDNA sequence containing the open reading frame (ORF) of the esterase gene. To amplify this region from the genomic DNA of R. miehei CAU432, the same PCR conditions were used with the specific primers EstDNAF and EstDNAR ( Table 1). The purified PCR product was ligated with pMD18-T vector and transformed into E. coli DH5a for sequencing.

Expression of the Esterase Gene in E. coli
The ORF encoding the esterase (designated RmEstA) was amplified by PCR from the cDNA of R. miehei CAU432 with primers RmEstAF and RmEstAR (Table 1). NdeI and XhoI sites (underlined) were added to the forward and reverse primers, respectively, and the expressed protein carried a C-terminal His  tag encoded by the vector. PCR conditions were as follows: a hot start at 94uC for 5 min, 30 cycles of 94uC for 30 s, 55uC for 30 s and 72uC for 1 min, followed by one cycle of 72uC for 10 min. The purified PCR product was digested by NdeI and XhoI, subcloned into the similarly digested pET-30a(+) vector, and transformed into E. coli BL21 competent cells for protein expression. A single colony of E. coli BL21 harboring RmEstA in pET-30a(+) was inoculated into LB medium containing kanamycin (50 mg mL 21 ) and incubated on a rotary shaker (200 rpm, 37uC) until the optical density at 600 nm (OD 600 ) reached about 0.6-0.8. Isopropyl b-D-thiogalactopyranoside (IPTG) was added to a final concentration of 1 mM, and the culture was then grown at 30uC for 12 h in a rotary shaker at 200 rpm.

Purification of the Recombinant Esterase (RmEstA)
The cells (from 1 L of culture) were harvested by centrifugation and homogenized in 10 mL buffer A (50 mM pH 8.0 Tris-HCl buffer containing 500 mM NaCl and 30 mM imidazole) and disrupted by ultrasonication. Cell debris was removed by centrifugation at 8,0006g for 20 min at 4uC. The supernatant was loaded onto a Ni-IDA column (1 cm65 cm) pre-equilibrated with buffer A. After the column had been washed with 15 column volumes (CV) of buffer A followed by 5 CV of buffer B (50 mM Tris-HCl pH 8.0 containing 500 mM NaCl and 50 mM imidazole), the bound proteins were eluted with buffer C (50 mM Tris-HCl pH 8.0, 500 mM NaCl, 200 mM imidazole). The elution rates were all adjusted to 1.0 mL min 21 . The protein fractions  with esterase activity were pooled and concentrated, and the buffer was exchanged (50 mM phosphate buffer pH 6.5) using a 10-kDa MW cut-off ultrafiltration membrane.

Enzyme Assay and Protein Determination
Esterase activity was determined spectrophotometrically using pNPH as the substrate according to the method of Sumby et al. [12] with minor modifications: 50 mL of suitably diluted enzyme was prepared in 400 mL of 50 mM phosphate buffer (pH 6.5) and after preheating for 2 min, 50 mL of 20 mM pNPH substrate (in pure isopropanol) was added. The mixture was incubated at 45uC for 10 min, and then 500 mL of 300 mM sodium phosphate buffer (pH 7.0) containing 5% (w/v) SDS was added. The liberated pNP was quantified by measuring the absorbance at 410 nm. One unit of enzyme activity was defined as the amount of enzyme required to liberate 1 mmol pNP per minute under the above conditions. The assay of interfacial activation was performed according to the methods of Martinelle et al. [27].
Protein concentration was measured by the method of Lowry et al. [28] using bovine serum albumin as the standard. Specific activity was expressed as units per milligram protein. used. Esterase activity staining was performed as described by Karpushova et al. [30].

SDS-PAGE and Zymogram Analysis
Effect of pH and Temperature on the Activity and Stability of the Purified Esterase The effect of pH on enzyme activity was determined by measuring esterase activity in different buffers (50 mM) from pH 2.5 to 10.6 using the standard enzyme assay. The following buffers were used: glycine-HCl (pH 2.5-3.5), citrate buffer (pH 3.0-6.0), 2-(N-morpholino)ethanesulfonic acid (MES) buffer (pH 5.5-6.5), phosphate buffer (pH 6.0-8.0), Tris-HCl buffer (pH 7.5-9.0) and glycine-NaOH (pH 8.6-10.6). To determine its pH stability, the purified enzyme was incubated in the listed buffers at 45uC for 30 min, and then residual activity was measured at 45uC in 50 mM sodium phosphate buffer (pH 6.5).
The optimal temperature for the purified esterase's activity was examined by measuring the enzyme activity at temperatures ranging from 30uC to 80uC in 50 mM phosphate buffer (pH 6.5). Thermostability of the esterase was investigated by incubating the enzyme (in 50 mM pH 6.5 phosphate buffer) at various temperatures (30-80uC) for 30 min. Then the residual activities of the samples withdrawn at different time intervals were measured at 45uC in 50 mM phosphate buffer (pH 6.5).
The effect of metal ions on the enzyme stability was evaluated by incubating the enzyme (40 mg mL 21 ) in 50 mM phosphate buffer (pH 6.5) at 30uC for 1 h in the presence of 10 mM various metal ions. Then the residual activity was measured.

Substrate Specificity and Kinetic Parameters
Substrate specificity of the purified esterase toward pNP esters was determined using pNPA, pNPB, pNPH, pNPC, pNPD, pNPL, pNPM and pNPP as the substrates. The reaction mixture was the same as described in the enzyme assay, except that it contained 0.1% (v/v) Triton X-100, 0.1% (w/v) arabic gum and different substrates. After incubating at 45uC for 10 min, the reaction was stopped by adding 0.5 mL chilled stop reagent (300 mM sodium phosphate buffer pH 7.0 containing 5% SDS), the mixture was centrifuged at 12,0006g for 3 min, and the absorbance of the supernatant was immediately measured at 410 nm [12]. Substrate specificity for synthetic triacylglycerols (triacetin, tributyrin, tricaproin, tricaprylin and tricaprin) and for olive oil was analyzed titrimetrically at 45uC for 10 min using 10 mM NaOH for titration according to the method of Eggert et al. [8]. The substrates at 10 mM (8.72 g L 21 for olive oil) were emulsified in 20 mL reaction buffer containing 2.5 mM phosphate buffer (pH 6.5) and 1% arabic gum. The reaction was initiated with the addition of 10 mL purified enzyme, and NaOH consumption was recorded. One unit of enzyme activity was defined as the amount of enzyme releasing 1.0 mmol fatty acid per minute.
The kinetic parameters of the purified esterase toward pNPA, pNPB, pNPC, pNPD, pNPH and pNPL were determined by measuring the enzyme activities with different substrate concentrations in 50 mM sodium phosphate buffer (pH 6.5) at 45uC for 5 min. The constant kinetic parameters of K m and V max were calculated using ''GraFit'' software.  Synthesis of Butyl Butyrate using Immobilized RmEstA The purified RmEstA was immobilized on sodium bis(2ethylhexyl) sulfosuccinate (AOT)-based organogels as described by Dandavate and Madamwar [31]. The immobilized RmEstA was used to synthesize butyl butyrate. The synthetic reaction was performed in 10 mL of mixture containing butyric acid, 1-butanol and immobilized esterase at 45uC for 7 days in an orbital shaker with rotation speed of 150 rpm. A 50-mL aliquot of the reaction mixture was withdrawn every 24 h and immediately analyzed by gas chromatography. Gas chromatography analysis was performed using an Agilent GC model 7890A, equipped with a Varian CP-Dex CB capillary column (25 m60.25 mm60.25 mm) and a flame ionization detector (FID) according to the method of De Barros et al. [32]. In all cases, hydrogen was used as carrier gas. The injector and detector temperature were set at 200uC and 250uC, respectively. The oven temperature was raised to 150uC at a rate of 15uC per minute after it was held at 50uC for 4 min.
To determine the effect of substrate concentration and ratio on esterification efficiency, the concentration of one substrate was held constant while that of the other was varied. In the first set of reactions, butyric acid concentration was held constant at 100 mM and that of 1-butanol was varied from 50 to 200 mM. In the second set of reactions, butyric acid concentration was varied from 50 to 200 mM while that of 1-butanol was held constant at the optimal concentration obtained in the first experiment.

Cloning and Sequence Analysis of the Esterase Gene from R. miehei
Based on the conserved amino-acid sequences of known esterase genes, a 407-bp fragment from R. miehei was amplified with degenerate primers ( Table 1). The fragment shared highest nucleotide sequence identity (50%) with the esterase gene from Herbaspirillum sp. CF444 (EJL92844). Thus, this partial sequence   According to the sequence similarity results from the BLAST search, the amino-acid sequence similarities of RmEstA to esterases/lipases from the bacteria Pseudomonas mandelii (AEW10549), Paenibacillus mucilaginosus (AFH64822), P. syringae (AAZ35718), Bacillus amyloliquefaciens (AEB22650) and P. fluorescens (AEV61721) were 44%, 43%, 42%, 42% and 41%, respectively; RmEstA shared only 43% identity with a putative esterase (EIE77101) from the fungus Rhizopus delemar (Figure 2A). A phylogenetic tree comprising all of these members was constructed ( Figure 2B). Results showed that RmEstA is much more closely related to the fungal esterase (R. delemar gb|EIE77101) than to those from bacteria, thus indicating that it is a novel fungal esterase. BLAST homology search of the sequence of RmEstA   identified it as belonging to the a/b hydrolase superfamily. RmEstA contained the esterase-conserved catalytic nucleophile S161 in the consensus pentapeptide GDSAG. The other two amino acids of the enzyme's catalytic triad were predicted as D262 and H292. A conserved HGGG motif was found upstream of the active-site conserved motif from amino acid 87 to 90, which indicated that RmEstA belongs to the hormone-sensitive lipase (HSL) family (family IV) [18,33]. Nucleotide sequencing of RmEstA revealed a 975-bp ORF encoding a protein of 324 amino acids. The sequence of RmEstA contained the typical conserved esterase/lipase motif, GXSXG ( Figure 1). Multiple amino-acid-sequence alignment indicated that the present esterase sequence shares relatively low identity (less than 44%) with those of other reported bacterial esterases, and 43% identity with only one putative fungal esterase from Rhizopus delemar (EIE77101), indicating that RmEstA should be considered a novel member of the esterases.

Expression and Purification of the Recombinant Esterase (RmEstA)
RmEstA was expressed in E. coli BL21 as a soluble intracellular enzyme. RmEstA was purified to homogeneity by Ni-IDA chromatography with 12-fold purification and an overall yield of 75%. The specific activity of RmEstA was increased to 1,480 U mg 21 (data not shown). The purified enzyme migrated on an SDSpolyacrylamide gel as a single homogeneous band of 34 kDa, matching the molecular mass (34,989 Da) calculated from the deduced amino-acid sequence (Figure 3).

Effect of pH and Temperature on the Activity and Stability of RmEstA
RmEstA exhibited optimal activity at pH 6.5 in 50 mM phosphate buffer ( Figure 4A). The enzyme was fairly stable over a broad range of pHs (5.0-10.6), retaining more than 90% of its activity ( Figure 4B). The optimal temperature for RmEstA activity was 45uC (Figure 4C), and it was stable at up to 50uC, with more than 90% of its activity remaining ( Figure 4D). The thermal denaturing half life of the enzyme at 40, 55 and 60uC was 219, 156 and 15 min, respectively (data not shown).
The influence of metal ions on enzyme stability is presented in Table 2. The esterase's activity was strongly inhibited by Cu 2+ , Mg 2+ , Fe 2+ , Ag + , Hg 2+ , but only moderately inhibited by Sn 2+ . In contrast, the enzyme was markedly activated by Zn 2+ , Mn 2+ , Co 2+ and Ba 2+ , and moderately activated by Na + and Cr 2+ . No significant effect of Ca 2+ and Ni 2+ was observed on enzyme activity.

Substrate Specificity and Kinetic Parameters of RmEstA
Specific activities of RmEstA on different substrates are shown in Table 3. The enzyme hydrolyzed pNP derivatives with acylchain lengths ranging from C 2 to C 16 ; the highest hydrolysis rate was observed with pNPH (1,480 U mg 21 ), followed by pNPB (1250 U mg 21 ), pNPC (850 U mg 21 ) and pNPD (380 U mg 21 ). RmEstA showed relatively low activity on various emulsified synthetic triglycerides, displaying its highest activity of 228 U mg 21 with tributyrin as the substrate. When the carbon chain length of the substrate increased to above 4 or decreased, the specific activity declined dramatically (Table 3). RmEstA displayed no interfacial activation using pNPB as no sharp increase of enzyme activity was observed when the concentration of substrate increased from 0 to 4 mM (form soluble to insoluble) (data not shown). The Michaelis-Menten constant (K m ) for pNPA (C 2 ), pNPB (C 4 ), pNPH (C 6 ), pNPC (C 8 ), pNPD (C 10 ) and pNPL (C 12 ) was determined to be 1.0, 0.17, 0.12, 0.82, 0.28 and 0.3 mM, respectively ( Table 4).

Synthesis of Butyl Butyrate Using RmEstA
RmEstA in free form showed significant esterification efficiency (56%) in the synthesis of butyl butyrate from 1-butanol and butyric acid. However, when the free enzyme was immobilized on an AOT-based organogel, a 1.3-fold higher (73%) esterification efficiency was obtained for butyl butyrate synthesis ( Figure 5). The optimal ratio of the two substrates for butyl butyrate synthesis was investigated. Holding the concentration of butyric acid constant at 100 mM and varying that of 1-butanol from 50-175 mM gave the highest esterification yield of 87% with 125 mM 1-butanol on day 5 (Table 5). 1-Butanol was then held at a constant 125 mM, and the concentration of butyric acid was varied from 50 to 175 mM. The highest esterification yield of 92% was achieved with 150 mM butyric acid (Table 5).

Discussion
Lipolytic enzymes have been classified into eight families (families I to VIII) based on their conserved sequence motifs and biological properties [33]. Evidence for the existence of more additional lipolytic enzyme families, i.e. family IX [34], family X [35] and family XIII [36] has been further published. Family IX is also known as the HSL family since lipolytic enzymes from this family display a striking amino-acid-sequence similarity to the mammalian HSL [33]. To date, all reported microbial HSL esterases have been from bacteria, such as Archaeoglobus fulgidus [37], Rheinheimera sp. [38] and Geobacillus thermodenitrificans T2 [16]. RmEstA is the first reported fungal HSL esterase.
Although esterases are gaining attention for their wide range of applications, to date very few esterases have been characterized from fungi, in contrast to the number of esterases which have been characterized from bacteria [7]. Moreover, few fungal esterase genes have been cloned and expressed. Here we identified and cloned a novel esterase gene (RmEstA) from R. miehei CAU432, and successfully expressed it in E. coli. Fungi provide promising sources for the discovery of novel esterases. RmEstA is the first esterase to be characterized from a thermophilic fungus. The recombinant RmEstA was purified to homogeneity, with a molecular mass of 34 kDa as determined by SDS-PAGE (Figure 3), and a specific activity of 1,480 U mg 21 protein. The molecular mass of RmEstA is in accordance with most other reported microbial esterases, which range from 20 to 60 kDa [4,12,14,17]. Most esterases show optimal activity at pH values above 7.0 and are stable in a narrow alkaline pH range [4,12,17]. RmEstA's optimal pH of 6.5 ( Figure 4A) is lower than that of most other reported esterases, such as from Pseudoalteromonas arctica (pH 7.5) [13], Bacillus licheniformis (pH 8.0) [9], Pseudoalteromonas sp. (pH 8.0) [4], B. pseudofirmus (pH 8.5) [14] and Rhodococcus sp. LKE-028 (pH 11.0) [10], but it is higher than that of the esterases from Oenococcus oeni (pH 5.0) [12] and Pleurotus sapidus (pH 6.0) [11]. RmEstA showed excellent stability across a broad range of pHs from 5.0 to 10.6 ( Figure 4B), which is much wider than most other esterases [4,9,17,30]. RmEstA exhibited maximal activity at 45uC, i.e. at a temperature that is lower than that of most other esterases from bacteria, including B. pseudofirmus (50uC) [36], P. sapidus (50uC) [11], B. licheniformis (60-65uC) [9], Thermoanaerobacter tengcongensis (70uC) [14] and Rhodococcus sp. LKE-028 (70uC) [10], comparable to that of esterases from Pelagibacterium halotolerans B2 (45uC) [39] and O. oeni (45uC) [12], and clearly higher than that of the cold-adapted esterases from P. arctica (25uC) and Pseudoalteromonas sp. (35uC) [13]. An enzyme with a relatively low optimal reaction temperature can potentially improve the efficiency of industrial processes that should be carried out at low temperatures, such as cheese ripening, and offers possible economic benefits through potential energy savings [13].
Substrate specificity of RmEstA was determined using pNPlinked esters of various acryl chain lengths (C 2 to C 16 ), triglycerides (C 2 to C 10 ) and olive oil ( Table 3). The enzyme was most active on pNP-linked esters with a chain length of up to C 10 , whereas low activity was detected for substrates with longer chain lengths. Highest activity was also observed for pNP-linked esters and triglycerides with carbon chain lengths of C 6 and C 4 , indicating that RmEstA is a typical esterase rather than a lipase, since esterases favor esters with carbon chain lengths shorter than 10 for hydrolysis, while lipase acts more efficiently on esters with long carbon chain lengths [3]. It should be noted that the esterase in the present study could hydrolyze pNP esters with chain lengths longer than C 14 , which is different from most other reported esterases, such as the enzymes from Oenococcus oeni [12], Geobacillus thermodenitrificans T2 [16] and Rhodococcus sp. LKE-028 [10]. The present esterase could also degrade olive oil, a property characteristic of lipases. The remarkably broad substrate specificity offers great potential for the use of this esterase in the production of a diverse range of high-value products.
K m values were comparable to or lower than those of most bacterial esterases. An increase in chain length from C 2 to C 4 resulted in a slight decrease in the respective K m values, and a significant increase in catalytic efficiency (k cat /K m ). On the other hand, V max values were not obviously affected, indicating a preference of RmEstA for pNP esters with a chain length of C 4 . However, the K m values for both pNPB (C 2 ) and pNPH (C 4 ) were lower than those reported for other bacterial esterases [9,10,14].
Flavor compounds are one of the most important additives in today's food industry, and biocatalysts play an important role in their synthesis [5]. Among the various enzymes, lipases have demonstrated unique properties that can be exploited for the synthesis of flavor esters [5,6,9], and several flavor esters, such as ethyl butyrate, ethyl acetate, ethyl isovalerate, isoamyl acetate and ethyl caprylate have been synthesized by various lipases [5,6]. The esterase in the present study exhibited the same synthetic ability. RmEstA in free form converted butyric acid and 1-butanol to butyl butyrate with an esterification efficiency of 56%. When RmEstA was immobilized on an AOT-based organogel, the immobilized enzyme showed much higher esterification efficiency (92%) than the free enzyme (Table 5) after 7 days of incubation. Similar enhancement of ester synthesis by immobilized enzyme was also obtained with a lipase from Burkholderia multivorans [6]. This might have been due to immobilization of the enzyme on a support matrix which can improve the catalytic activity of the enzyme by providing protection against the inhibitory effect of organic solvents [6]. In addition, enzyme immobilization can cut enzyme costs by improving its reusability based on the easy recovery protocol in commercial use. The high esterification efficiency and reusability are very important from an economical point of view, making this enzyme attractive for possible practical application in the synthesis of flavor esters.