Biotransformation of myrcene by Pseudomonas aeruginosa

Background Dihydrolinalool and terpineol are sources of fragrances that provide a unique volatile terpenoid alcohol of low toxicity and thus are widely used in the perfumery industry, in folk medicine, and in aromatherapy. They are important chemical constituents of the essential oil of many plants. Previous studies have concerned the biotransformation of limonene by Pseudomonas putida. The objective of this research was to study biotransformation of myrcene by Pseudomonas aeruginosa. The culture preparation was done using such variables as different microbial methods and incubation periods to obtain maximum cells of P. aeruginosa for myrcene biotransformation. Results It was found that myrcene was converted to dihydrolinalool and 2,6-dimethyloctane in high percentages. The biotransformation products were identified by Fourier-transform infrared spectroscopy (FT-IR), ultraviolet (UV) analysis, gas chromatography (GC), and gas chromatography-mass spectroscopy (GC-MS). Comparison of the different incubation times showed that 3 days was more effective, the major products being 2,6-dimethyloctane (90.0%) and α-terpineol (7.7%) and comprising 97.7%. In contrast, the main compounds derived for an incubation time of 1.5 days were dihydrolinalool (79.5%) and 2,6-dimethyloctane (9.3%), with a total yield of 88.8%.


Background
Dihydrolinalool and 2,6-dimethyloctane of low toxicity are widely used in the perfumery industry. They are important chemical constituents of the essential oil of many plants, with widespread applications in folk medicine and in aromatherapy [1].
In the course of work related to bioconversion of monoterpene by fungi, the biotransformation of myrcene by Pseudomonas aeruginosa (PTCC 1074) was investigated. The biotransformation of limonene by P. putida has been reported [2,3]. The bioconversion of neryl acetate by Aspergillus niger has also been described [4,5]. Some investigations have showed that the main reaction to liquefied A. niger was hydrolysis of terpene to 8-hydroxy derivatives [6].
Microorganisms and their enzymes have proven to be versatile biocatalysts [7] and are extensively used for biotransformation of various terpenoids [8,9].
The majority of biotransformations of terpenoids have been performed on monoterpenoids, which are the main constituents of many essential oils. The characteristic organoleptic properties of limonene and its usage in food and other applications have led to extensive work on its synthesis and microbial conversions [10][11][12][13]. However, most studies dealing with microbial conversion of limonene have reported low yields of products due to volatility of the substrate and the toxicity of limonene to most of the microorganisms [14,15]. The present study was aimed at the screening of microorganisms, and in the course of the survey a strain of P. aeruginosa was shown to successfully metabolize dihydrolinalool and 2,6-dimethyldoctane. Among the two bioconversion products, the alcohol compound is of particular importance, since it has been reported by several researchers that the alcohol compound derived from lavender (Lavandula angustifolia) has chemopreventive properties against liver, mammary, and lung carcinogenesis [16,17].
In 1964 the use of the sporulated surface cultures method suggested that geraniol was converted to dihydrolinalool and partially oxidized to citral [18]. Microbial transformation of geraniol and nerol by the sporulated surface cultures method using five A. niger strains and three Penicillium strains has been compared with the submerged liquid method [19]. Several researchers have used different fungi to bioconvert citral [20][21][22][23][24].

Experimental
Malt extract, peptone, and yeast extract were purchased from Merck & Co., USA. The substrate and the product myrcene were purchased from Sigma Chemicals Co., USA. Other chemicals of analytical grade were obtained from standard sources. A 0.1 M acetate buffer (pH 5.5) was prepared.

Microorganisms and cultural conditions
A strain of Pseudomonas aeruginosa identified according to the Persian Type Culture Collection (PTCC 1074) was purchased from Iranian Research Organization for Science & Technology, Tehran, Iran.

Fermentation procedure
Fermentation was carried out in 250-ml Erlenmeyer flasks containing 100 ml of medium and the microorganism P. aeruginosa PTCC 1074. The flasks were divided into three sets with four containing 1.0% (V/V) of myrcene to determine the optimum concentration. The flasks were incubated for 1.5 and 3 days at 30°C. Simultaneously, a control experiment was carried out without microorganisms by adding substrate directly into the sterile broth.

Agarose entrapment
An agarose solution was prepared by dissolving agarose (15% W/V) in water at 100°C, which was then cooled to 40°C and mixed with separated P. aeruginosa cells. The mixture was allowed to solidify by standing at 4°C. The hard gel was shredded in a Waring blender and the nonentrapped cells were removed by washing with saline [25].

Biotransformation
In this method 0.1 gl -1 methanol was used as a solubilising agent, added to 100 ml of medium containing 4.47 gl -1 myrcene.

Optimum conditions for biotransformation
For studying the optimum conditions necessary for biotransformation, 500-ml Erlenmeyer flasks were used for obtaining P. aeruginosa PTCC 1074 growth in 250 ml of media; 4.47 g l -1 myrcene with 0.1 gl -1 methanol was added to the medium, P. aeruginosa was entered into the media, and a suitable growth phase was determined after which cells could be harvested. This was done by employing different times of growth. An agitation speed of 150 rpm with biotransformation times of 3 days and 1.5 days were employed. The optimum values of pH and temperature for biotransformation were found to be in the area of pH 5.5 and 27°C for both incubation periods (see Figure 1).

Extraction of products
Extraction of bioconversion products of myrcene after treatment with P. aeruginosa was carried out after removing the bacterial cells by centrifugation (12,800 g, 10 min), and the supernatant was extracted with diethyl ether (3 × 25 ml). The combined extract was washed with distilled water (3 × 10 ml), dried over anhydrous sodium sulphate and filtered using Whatman No.1 filter paper. The solvent was removed under reduced pressure to give pure reaction products. The products were directly analyzed by FT-IR, UV, GC, and GC-MS.

Analysis of the samples with FT-IR, UV, GC, and GC-MS
The method described by Speelmans, Bijlsma, and Egglink [26] was employed with some modifications for analysis of the product on a gas chromatograph. The composition in relative percentages was computed by the normalization method from the GC peak areas, and percentage conversion was used as the performance criterion.
GC analysis was performed on a Shimadzu 15A gas chromatograph equipped with a DB5 capillary column (50 m × 0.2 mm, film thickness 0.32 μm). The split/splitless injector and flame ionization detector were heated at 250°C. N2 was used as the carrier gas (1 ml/min). The oven temperature was kept at 60°C for 3 min and then heated to 220°C at a 5°C/min rate and kept constant at 220°C for 5 min. The relative percentage amounts were calculated from the peak area using a Shimadzu C-R4A Chromatopac integrator without correction factor. GC-MS analysis was performed using a Hewlett-Packard 5973 equipped with an HP 5MS column (30 m × 0.25 mm, film thickness 0.25 μm). The oven temperature was kept at 60°C for 3 min and programmed to 220°C at a rate of 5°C/min and kept constant at 220°C for 5 min. The apparatus operated with helium as the carrier gas at a flow rate of 1 ml/min in an electronic impact mode of 70 eV. Identification of the constituents of the oil was made by comparison of their mass spectra and retention indices with those given in the literature and the authentic samples [27,28]. FT-IR mass spectra (6 main peaks) were recorded in CHCl 3 on a Perkin-Elmer 457 instrument. FT-IR (KBr) analysis in dihydrolinalool was ν max cm -1 : 3400 (C -OH), 1344 (-CH 3 or -CH 2 ). For 3 days FT-IR spectra showed for 2,6-dimethyloctane a peak in the region between 1344 and 2945 cm -1 (see Figure 2).
Products from the biotransformation of myrcene were extracted with diethyl ether (Et 2 O) three consecutive times and directly analyzed by FT-IR, UV, GC, and GC-MS.
The determination of a suitable culture age during growth of P. aeruginosa in medium for maximum product formation was accomplished by harvesting cells in various stages of growth and employing them for myrcene biotransformation. The results indicated the optimum cell culture age to be 3 days, with 97.7% product formation; the product formation for 1.5 days was 88.8%. Here, the cells were at the end of the exponential phase and had attained maximum cell concentration. The optimum substrate concentration to be employed for obtaining maximum product concentrations was done by adding different substrate concentrations to P. aeruginosa cell growth.

Discussion
The purpose of this research was to study the microbial transformation of myrcene by P. aeruginosa.
In a previous study of biotransformation of menthol by sporulated surface cultures of A. niger and P. sp., the main bioconversion product obtained from menthol of A. niger was cis-p-menthan-7-ol, and the main products obtained by sporulated surface cultures of P. sp. were limonene, p-cymene, and γ-terpinene [31]. Leuenberger (1984) reported that product yields could be effectively increased by solubilizing/emulsifying immiscible substrates. However, careful selection of the nature and concentration of the solvent is necessary because many miscible solvents are cytotoxic at lower concentrations [31]. The biotransformation of volatile monoterpenoids by fungi was examined. Using 1.5 days and 3 days for biotransformation, we identified two components for each incubation period, representing 88.8% and 97.7% respectively (see Figure 3).
Comparing samples of IR spectra showed a peak for 1.5 days in the 3400 cm -1 region, while 3 days did not have signals in the >3000 cm -1 region for -OH protons (see Figure 2).
It can be concluded that myrcene was converted primarily to dihydrolinalool, 2,6-dimethyloctane and α-terpineol. The reduction of the C = C bonds and the formation of an OH group of α-terpineol is achieved by epoxidation of a double bond followed by a reductive ring opening of the epoxide. Myrcene was reduced by P. aeruginosa and formed α-terpineol (see Figure 4). The GC pattern showed that in 1.5 and 3 days volatile components and monoterpene components mostly exit the column first. Figures 5 and 6 show GC-MS analysis for bioconversion of 1.5 and 3 days. The best results were obtained at 1.5 and 3 days. In the other incubation periods, the percentage of the components was small and could not be identified.
Of the various values of pHs tested, pH 5.5 had the best result.
The cited results suggest that microbial transformation of monoterpenes with Penicillium and Aspergillus  involve an oxidation reaction and result in a more stable product. But bioconversion of Penicillium using the sporulated surface cultures and liquid methods demonstrated that it was possible to obtain similar products with high yield and selectivity.
Thymol can be produced by removal of hydrogen and rearrangement of citral. Thymol is present in the essential oils from herbs and spices [32]. It is produced by these plant species as a chemical defense against phytopathogenic microorganisms. Therefore, these compounds have attracted great attention in food industry. They have been used as natural preservatives in foods such as cheese to prevent fungal growth.

Conclusions
Biosynthesis of myrcene was investigated. The major bioconversion products were confirmed by analysis using FT-IR, UV, GC, and GC-MS. The major components of the microbial transformation of myrcene with P. aeruginosa were derived most effectively over a period of 3 days, the major products being 2,6-dimethyldoctane (90.0%) and a-terpineol (7.7%) and comprising (97.7%). An incubation period of 1.5 days yielded dihydrolinalool (79.5%) and 2,6-dimethyloctane (9.3%), with the main compounds comprising 88.8%.
Dihydrolinalool, 2,6-dimethyloctane, and terpineol are the major products in this method. They have many Esmaeili and Hashemi Chemistry Central Journal 2011, 5:26 http://journal.chemistrycentral.com/content/5/1/26 applications in flavoring, extracts, food and drug manufacturing, and as a fragrance ingredient used in decorative cosmetics, fine fragrances, shampoos, toilet soaps, and other toiletries, as well as in noncosmetic products such as household cleaners and detergents. Their use worldwide is in the region of greater than 1,000 metric tons per annum.