Boosting isoprene production via heterologous expression of the Kudzu isoprene synthase gene (kIspS) into Bacillus spp. cell factory

Isoprene represents a key building block for the production of valuable materials such as latex, synthetic rubber or pharmaceutical precursors and serves as basis for advanced biofuel production. To enhance the production of the volatile natural hydrocarbon isoprene, released by plants, animals and bacteria, the Kudzu isoprene synthase (kIspS) gene has been heterologously expressed in Bacillus subtilis DSM 402 and Bacillus licheniformis DSM 13 using the pHT01 vector. As control, the heterologous expression of KIspS in E. coli BL21 (DE3) with the pET28b vector was used. Isoprene production was analyzed using Gas Chromatography Flame Ionization Detector. The highest isoprene production was observed by recombinant B. subtilis harboring the pHT01-kIspS plasmid which produced 1434.3 μg/L (1275 µg/L/OD) isoprene. This is threefold higher than the wild type which produced 388 μg/L (370 μg/L/OD) isoprene, when both incubated at 30 °C for 48 h and induced with 0.1 mM IPTG. Additionally, recombinant B. subtilis produced fivefold higher than the recombinant B. licheniformis, which produced 437.2 μg/L (249 μg/L/OD) isoprene when incubated at 37 °C for 48 h induced with 0.1 mM IPTG. This is the first report of optimized isoprene production in B. licheniformis. However, recombinant B. licheniformis showed less isoprene production. Therefore, recombinant B. subtilis is considered as a versatile host for heterologous production of isoprene.


Introduction
Isoprene is a small volatile hydrophobic molecule containing five carbon atoms and is also known as 2-methyl-1,3-butadiene. It is a colorless organic compound that is produced by animals, plants and bacteria. It has a low solubility in water as well as a low boiling point of 34 °C which enables withdrawal from the upper gas phase of a bioreactor when produced via biotechnological processes (Xue and Ahring 2011). This aspect turns it valuable for downstream chemical products. Isoprene as biofuel contains more energy, is not miscible in water and does not show corrosive effects compared to ethanol (Atsumi and Liao 2008;Lindberg et al. 2010). Companies develop bioisoprene production such as Genencor and Goodyear, published their efforts to develop a gas-phase bioprocess for production of isoprene (Whited et al. 2010). Their work involved metabolic engineering of E. coli capable of producing high yields of isoprene, in addition to developing a large-scale fermentation process with high rates of the isoprene recovered from the off-gas. They reported a titer of over 60 g/L, a yield of 11% isoprene from glucose and a volumetric productivity of 2 g/L/h (Chandran et al. 2011). Several researchers reported using isoprenol as anti-knock agent, in which branched C5 alcohols store more energy than ethanol and high octane numbers (RON,or research octane number,(92)(93)(94)(95)(96)(97)(98)(99)(100)(101)(102), that helps their use as gasoline alternatives and as anti-knock additives (Cann and Liao 2010;Mack et al. 2014). In addition, they have been verified in various engine types and they proved to have better gasoline-like properties than ethanol (Yang et al. 2010). All isoprenoids are known to be derived from the two universal five-carbon (C5) building blocks, isopentenyl diphosphate (IPP) and its isomer dimethylallyl diphosphate (DMAPP). These universal precursors are known to be produced by either one of the three identified pathways: the mevalonate (MVA) pathway and/or the pathway, which is also 1-deoxy-d-xylulose-5-phosphate (DXP) pathway. Additionally, an alternative MVA-independent pathway has been identified for the biosynthesis of IPP and DMAPP in bacteria, algae and plants which is named the methylerythritol 4-phosphate (MEP) pathway and lacks the first two steps of the DXP pathway (Rodríguez-Concepción and Boronat 2012). Bacillus subtilis uses the DXP pathway and was found to be the best naturally isoprene producing bacteria (Kuzma et al. 1995). It is known that the isoprene synthase utilize dimethylallyl diphosphate (DMAPP) as substrate (Withers et al. 2007). The isoprene synthase gene was not identified in bacteria yet, however it has been characterized from many plants such as Populus species, e.g. aspen, Poplar Alba (Beatty et al. 2014;Fortunati et al. 2008;Miller et al. 2001;Sasaki et al. 2005;Sharkey et al. 2005;Silver and Fall 1995;Chotani et al. 2013;Vickers et al. 2010), Pueraria Montana (kudzu) and/or Pueraria lobata (Beatty et al. 2014;Hayashi et al. 2015;Sharkey et al. 2005). The isoprene synthase gene from poplar was successfully isolated and heterologously expressed in E. coli. Moreover, isoprene synthase cDNA was isolated from Populus alba (PaIspS) and expressed in E. coli for enzymatic characterization (Sasaki et al. 2005). Previous studies failed to isolate the isoprene synthase from bacteria (Julsing et al. 2007;Sivy et al. 2002), thus the Kudzu isoprene synthase gene (kIspS) was codon optimized and heterologously expressed in E. coli . Previously, the codon optimized Mucuna bracteata IspS was engineered in S. cerevisiae and it only produced 16.1 μg/L (Hayashi et al. 2015). Additionally, when the codon optimized M. bracteata IspS was engineered in Pantoea ananatis, it produced 63 μg/L (Hayashi et al. 2015). Recent studies involved in overexpression of codon optimized kudzu IspS (kIspS) in E. coli using different constructs (Cervin et al. 2016). The E. coli best isoprene production yield was 10 μg/L. In addition, the codon optimized kudzu and poplar IspS genes were expressed in Yarrowia lipolytica using different methods; in which the isoprene yield was 0.5-1.0 μg/L from the headspace culture (Cervin et al. 2016). This study aimed to develop recombinant Bacillus strains (B. subtilis and B. licheniformis) with high level of isoprene production using the Kudzu isoprene synthase.

Construction of recombinant pET-28b plasmid with the kIspS for expression in E. coli
The Kudzu isoprene synthase from pBA2kIKmA2 plasmid was kindly obtained from Anastasios Melis (Addgene plasmid #39213) (Lindberg et al. 2010). The isoprene synthase gene from P. montana (kudzu) presented in Gen-Bank under Accession No. AY316691 (Sharkey et al. 2005). The kIspS orf (1.7 kb) was amplified using the specific primers; kIspS_NcoI_F: 5′-AACACCATGGATGCC GTGGATTT-GTGCTACGAGC-3′ and kIspS_NotI_R: 5′-ATCCGCGGCCGCCACGTACATTAGTT-GATTGA TTGG-3′ with added sites NcoI and NotI, respectively to facilitate the cloning process using phusion polymerase (NEB #M0530S). The amplification reaction was performed using PCR profile with an initial cycle at 95 °C for 5 min, followed by 30 cycles 95 °C for 30 s, 58 °C for 30 s, 72 °C for 2 min and a final extension at 72 °C or 5 min. Thereafter, PCR product was cleaned up using DNA, RNA and protein purification REF 740609.250 Gel and PCR clean up protocol (January 2012/Rev.02). The purified fragment was digested with NcoI and NotI and ligated (using T4 DNA ligase NEB #002025) at the corresponding sites of pET-28b, forming the constructed plasmid pET28b-kIspS (Fig. 1).

Construction of recombinant pHT01 plasmid with the kIspS for heterologous expression in Bacillus
The pHT01 plasmid (MoBiTec GmbH), which bears chloramphenicol resistance, was used for cloning and expressing the kIspS gene into two Bacillus strains; B. subtilis DSM 402 (https://www.dsmz.de/catalogues/ details/culture/DSM-402.html) and Bacillus licheniformis Fig. 1 Physical map of the constructed plasmid pET28b containing the kIspS gene DSM 13 (https://www.dsmz.de/catalogues/details/culture/DSM-13.html). Conducted B. subtilis antibiogram showed that no natural resistance to chloramphenicol is present. To facilitate the cloning into pHT01, two primers were designed to amplify the kIspS gene harboring BamHI and XbaI cloning site; named kIspS_BamHI_F: 5′-ATATGGATCCATGCCGTGGATTTGTGCTACG AGC-3′ and kIspS_XbaI_R: 5′-ATATTCTAGACACGTA CATTAGTTGATTGATTGG-3′, respectively with phusion polymerase (NEB #M0530S). The amplification reaction was performed using the same PCR profile as mentioned above and the PCR amplicon was cleaned as mentioned above. Following, the purified fragment was digested with BamHI and XbaI and ligated (using T4 DNA ligase NEB #002025) into the corresponding restriction sites of pHT01 vector, resulting in the recombinant plasmid pHT01-kIspS (Fig. 2).

Transformation and screening of the recombinant plasmid pET28b-kIspS in E. coli BL21 (DE3)
Chemical transformation was carried out for heterologous expression of pET28b-kIspS-C-term in BL21 (DE3) (Mamiatis et al. 1985). Colony PCR strategy was performed to screen the pET28b-kIspS-C-term in BL21 (DE3) using the kIspS specific primers with the same amplification conditions as mentioned previously.

Transformation and screening of the recombinant plasmid pHT01-kIspS into B. subtilis and B. licheniformis
Preparation of electro-competent cells as well as transformation protocol was carried out according to (Xue et al. 1999) with minor modifications. In the preparation of washing and/or electroporation solution, 20% glycerol was used instead of 10% glycerol. Additionally, electroporation of the cells was performed using Micropulser electroporator BioRad catalog #165-2100 and cuvette 1 mm gap for both Bacillus strains. In the case of B. subtilis, 180 ng of plasmid DNA (pHT01-kIspS) was added to 60 µL of electro-competent cells using program EC1; voltage: 1.8 kV and time constant: 5.7 m/s as 1 pulse. In case of B. licheniformis, 290 ng of the plasmid DNA (pHT01-kIspS) was added to 60 µL of electro-competent cells. While for electroporation of cells mode: Ag, voltage: 2.2 kV and time constant 5.6 m/s as 1 pulse. For selection LB agar plates with 34 µg/mL chloramphenicol was used. In case of B. subtilis, plates were incubated on 30 °C O/N, while for B. licheniformis plates were incubated on 37 °C O/N. pHT01-kIspS plasmid mini preparation was performed (Gene JET plasmid Miniprep kit Thermo-scientific #k0503) from both Bacillus spp., in which lysozyme (20 mg/mL) was added as 5 mg/250 resuspension solution then samples were incubated for 1 h at 37 °C with shaking for each sample. PCR was carried out for the screening of the cells harboring the recombinant the pHT01-kIspS plasmid using the same primers and amplification conditions as mentioned above.

Gas Chromatography-Flame Ionization Detector (GC-FID) analysis
Analysis of the produced isoprene was carried out using GC-FID. In this assay, an overnight grown culture was transferred to a 10 mL GC headspace vial (Macherey-Nagel, Germany) resulting in a 2 mL culture with an OD 600 of 0.1. After incubation using an orbital shaker at 150 rpm, the GC vials were placed on the RSH Plus autosampler (Thermo Fisher) and injected onto a Trace 1310 gas chromatograph equipped with a flame ionization detector (FID). The column used to detect isoprene was a Bond-U-Rt column 30 m, 0.25 mm as column ID, 8 µm df from Restek GmbH (Germany). Amounts of isoprene produced were estimated by comparison with a dilution of isoprene in ethyl acetate (Sigma-Aldrich). The response of the detector was linear at a range from 1 to 4 µM of isoprene, giving the calibration Eq. (1) with an R 2 of 1.
Different parameters were evaluated to study the level of isoprene production, including the effect of different time intervals and IPTG induction on isoprene production.
Bacillus subtilis samples were incubated at 30 °C and in case of E. coli samples were incubated at 37 °C for 4, 8, 12, 24 and 48 h with and without 0.1 mM IPTG induction. While, B. licheniformis WT and recombinant B. licheniformis harboring pHT01-KIspS samples were incubated at 37 °C for 4, 8, and 48 h upon induction with 0.1 M IPTG and without induction.

The influence of different IPTG concentrations on isoprene production
The level of isoprene production for B. subtilis and B. licheniformis harboring the recombinant plasmid pHT01-kIspS, in addition to E. coli BL21(DE3) harboring the recombinant plasmid pET28b-kIspS were investigated using different IPTG concentrations (i.e., 0.1, 0.5, 1 and 2 mM) for 4 h incubation at the suitable temperature for each.

The effect of 0.3 M NaCl on B. subtilis and B. licheniformis isoprene production
Cultures of the B. subtilis and B. licheniformis were grown in Free LB and LB treated by 0.3 M NaCl with and without 0.1 mM IPTG induction for 4 h incubation at the suitable temperature for each.

The effect of utilizing an extra carbon source on B. subtilis and B. licheniformis isoprene production
Cultures of B. subtilis and B. licheniformis were grown in Free LB and LB containing 5 g/L glucose and 5 g/L (1) y = 3.113 * x + 0.0003 glycerol were investigated. Cultures were also grown for 4 h at the suitable temperature for each.

Codon usage analysis for B. subtilis and B. licheniformis
Codon usage analysis was performed, in which the codon usage preference table for each Bacillus spp. (B. subtilis DSM and B. licheniformis) was determined using codon usage database (http://www.kazusa.or.jp/codon/). Then the P. montana (kudzu) isoprene synthase (kIspS) original sequence of GenBank Accession No. AY316691 was optimized using the online tool optimizer (http://genomes. urv.es/OPTIMIZER/). Comparison between the kIspS original sequence, the codon optimized kIspS sequence for B. subtilis and B. licheniformis showed that there are differences in the preferred codon and that could explain the differences in the level of kIspS in the two species.

Generation of recombinant plasmid pET-28b-kIspS for heterologous expression into E. coli
The pET-28b plasmid and the amplified kIspS fragment were digested using NcoI and NotI enzymes. Agarose gel electrophoresis for the digested DNA showed the two linearized DNA strands, one at 5.2 kb which represent the expected band of the linearized pET-28 backbone and another band at 1.7 kb, which represent the kIspS gene (Additional file 1: Figure S1). The two bands were cut from the gel, cleaned up and ligated, together forming the recombinant plasmid pET28b-kIspS for heterologous expression into E. coli BL21 (DE3). Bacterial cells with and without the recombinant plasmid were used to measure isoprene production. For screening of the recombinant plasmid, colony PCR was carried out using isoprene specific primers. Positive clones showed a band at 1.7 kb (Additional file 2: Figure S2).

Generation of recombinant pHT01-kIspS plasmid for heterologous expression into B. subtilis and B. licheniformis
The pHT01 plasmid and the amplified kIspS gene were digested using BamHI and XbaI restriction enzymes. Agarose gel electrophoresis of the digested DNA showed bands at 7.9 and 1.7 kb, which represent the linearized pHT01 plasmid and the kIspS gene, respectively (Additional file 3: Figure S3). The two fragments were cut from the gel, cleaned up and ligated together to form the recombinant plasmid pHT01-kIspS. Transformation was carried out for B. subtilis and B. licheniformis transformation with the recombinant plasmid pHT01-kIspS. For screening of recombinant cells, plasmid was purified and subjected to PCR analysis using the specific primers, which were mentioned above. PCR amplification of the pHT01-kIspS plasmid displayed a band at 1.7 kb; which represents the expected size of the kIspS amplicon (Additional file 4: Figure S4).

Isoprene production by different bacterial strains
The concentrations of isoprene produced from different strains were measured using GC-FID and the results indicated that the recombinant B. subtilis harboring pHT01-kIspS has the highest isoprene production of 1434.3 μg/L (1275 µg/L/OD isoprene). This is threefold higher than the wild type which produced 388 μg/L (370 μg/L/OD isoprene), when both incubated at 30 °C for 48 h and induced with 0.1 mM IPTG (Fig. 3a). While recombinant B. licheniformis, showed less isoprene production. Compared to the control (recombinant BL21 cells harboring pET28b-kIspS), which produced 53 µg/L/OD isoprene when incubated at 37 °C for 48 h and induced by 0.1 mM IPTG. Results revealed that recombinant B. licheniformis harboring pHT01-kIspS showed no significant differences in the isoprene production compared to the B. licheniformis WT during different time intervals (4, 8 and 48 h) of incubation at 37 °C and induction by 0.1 mM IPTG. Recombinant B. licheniformis harboring pHT01-kIspS produced 249 µg/L/OD when incubated at 37 °C for 48 h (Fig. 3b). The comparison between the expression of isoprene in the recombinant bacteria at 48 h incubation and 0.1 mM IPTG induction indicated that the two B. subtilis strains harboring pHT0-kIspS produced fivefold higher isoprene production than the recombinant B. licheniformis harboring pHT0-kIspS. To the best of our knowledge this is the first attempt of enhancing isoprene production in B. licheniformis.

Influence of different IPTG concentrations on isoprene production
The concentrations of isoprene produced from different strains under induction with 0.1, 0.5, 1 and 2 mM IPTG were measured using GC-FID. Results showed insignificant difference in isoprene production of the recombinant B. subtilis harboring pHT01-kIspS upon different IPTG induction at 30 °C incubation for 4 h (Fig. 4a). While in case of recombinant B. licheniformis harboring pHT01-kIspS, results also showed insignificant differences in isoprene production by induction using different IPTG concentrations at 37 °C incubation for 4 h (Fig. 4b).
Although recombinant E. coli BL21 (DE3) harboring pET28b-kIspS showed highest isoprene production (76 µg/L/OD) at 37 °C for 4 h incubation when induced by 0.5 mM IPTG, no isoprene production was detected for the recombinant BL21 grown in LB media induced by 0.1 mM IPTG at 37 °C incubation for 4 h (Fig. 4c).

The effect of 0.3 M NaCl on isoprene production
Our results demonstrated that 0.3 M NaCl did not enhance the isoprene production for B. subtilis WT, recombinant B. subtilis and B. licheniformis harboring pHT01-kIspS. However, 0.3 M NaCl enhanced B. licheniformis WT isoprene production. In this respect (Xue and Ahring 2011) reported that some external factors, such as heat 48 °C, 0.3 M NaCl and H 2 O 2 (0.005%) induce isoprene production, while 1% ethanol inhibits isoprene production. Results revealed that B. subtilis harboring pHT01-klspS produced 243 µg/L/OD, while B. subtilis WT produced only 94 µg/L/OD isoprene, when both treated with 0.3 M NaCl and 0.1 mM IPTG for 4 h incubation at 30 °C. Thus, 0.3 M NaCl did not enhance the isoprene production for the recombinant B. subtilis harboring pHT01-klspS, in which it produced 338 µg/L/OD for 4 h incubation at 30 °C without NaCl and with 0.1 mM IPTG induction (Fig. 5a). While for B. licheniformis the WT isoprene production was slightly enhanced by 0.3 M NaCl and 0.1 mM IPTG induction, as it produced 191 µg/L/OD, compared to the B. licheniformis WT that produced 108.5 µg/L/OD without 0.3 M NaCl and by 0.1 mM IPTG induction at 37 °C incubation for 4 h. Recombinant B. licheniformis harboring pHT01-klspS without 0.3 M NaCl and by 0.1 mM IPTG induction, it produced 143 µg/L/OD, while when induced by Fig. 4 Influence of IPTG concentration on isoprene production of the different strains used in this study. The average concentrations (µg/L/OD 600 ) were obtained from three independent cultures starting with the standard OD 600 nm of 0.1. Error bars indicate standard deviation between replicate data 0.3 M NaCl and 0.1 mM IPTG it produced 178.5 µg/L/ OD (Fig. 5b).

Influence of utilizing an extra carbon source on isoprene production by B. subtilis and B. licheniformis
The highest isoprene production was observed for the recombinant B. subtilis harboring pHT01-kIspS upon utilizing 5 g/L glucose as an extra carbon source, in which it produced 359 µg/L/OD isoprene (Fig. 6a). While upon utilizing 5 g/L glycerol it produced 261.4 µg/L/OD isoprene when incubated at 30 °C for 4 h and induced by 0.1 mM IPTG (Fig. 6b). In contrary results revealed that B. licheniformis WT and recombinant B. licheniformis harboring pHT01-kIspS showed insignificant difference in isoprene production upon utilizing glucose (Fig. 7a) and glycerol (Fig. 7b) as an extra carbon source.

Codon usage analysis
To clarify the reason for the difference in isoprene production in B. licheniformis and B. subtilis, bioinformatics study was carried out to predict the best codon usage for both strains using software for Codon Usage Data-Base. Comparison between the kIspS and the optimized IspS sequence for B. subtilis and B. licheniformis were performed and results showed differences in the codon usage between them as shown in Additional file 5: Table  S1 as shaded sequences. These differences may be the cause in the level of expression of the same gene in the different species.

Discussion
In this study, we developed recombinant Bacillus strains (B. subtilis DSM 402 and B. licheniformis DSM 13) in an attempt to enhance isoprene production using the kudzu isoprene synthase. Interestingly, B. subtilis harboring the pHT01-kIspS plasmid showed a higher production of isoprene than B. licheniformis harboring the same plasmid. Recombinant B. subtilis produced 1434.3 μg/L (1275 μg/L/ OD isoprene), which is threefold higher than the wild type that produced 388 μg/L (370 μg/L/OD) isoprene, when both incubated at 30 °C for 48 h by 0.1 mM IPTG induction. Our results are in accordance with a recent study for expression of kIspS in B. subtilis, in which the isoprene production levels were increased also with threefold in comparison to the wild type, from 400 μg/L to 1.2 mg/L in batch culture (Vickers and Sabri 2015). To the best of our knowledge no previous work was done for enhancing isoprene production in B. licheniformis, where this is the first report of optimized isoprene production in B. licheniformis. Since recombinant B. subtilis harboring pHT01-kIspS produce a fivefold higher isoprene production than recombinant B. licheniformis harboring pHT01-kIspS at 48 h incubation with induction by 0.1 mM IPTG. Thus, B. licheniformis seems to be not of significant importance for further studies on isoprene production. Additionally, multiple sequence alignment results showed differences in the codon usage of kIspS optimization for B. subtilis and B. licheniformis, which might be the reason that there is difference in isoprene production for both recombinant bacteria. For isoprene production optimization in our study, on one hand we found that induction by different IPTG concentrations (0.1, 0.5, 1 and 2 mM) did not change the level of isoprene production in B. subtilis and B. licheniformis. Recombinant E. coli BL21 (DE3) harboring pET28b-kIspS showed higher isoprene production (76 µg/L/OD) at 37 °C for 4 h incubation when induced by 0.5 mM IPTG. On the other hand for the effect of NaCl on isoprene production, our results demonstrated that 0.3 M NaCl did not enhance the isoprene production for all strains under study except the wild type B. licheniformis. However, it was revealed that NaCl and heat can induce isoprene production, (Xue and Ahring 2011), in which isoprene increases at temperature ranging between 25 and 45 °C then decreases until it reaches 0 at 65 °C in another study, optimum bacterial isoprene production was obtained at 45 °C (Kuzma et al. 1995). Moreover, when utilizing extra carbon sources to the media, i.e. glucose and/or glycerol, highest isoprene production was observed for the recombinant B. subtilis at 5 g/L glucose as an extra substrate. This result is in contrary to the previous observation  for E. coli transformed with kIspS, in which glycerol provided higher yields of isoprene compared to glucose, fructose, xylose, or LB media. In addition, isoprene production assays demonstrated that kIspS expression in E. coli best activity were obtained at 37 °C for 6 h when induced by 0.1 mM IPTG . Previous studies demonstrated that Synechocystis PCC6803 and E. coli are responsive strains for heterologous transformation by the IspS gene, in which they express and store the isoprene protein into their cytosol (Lindberg et al. 2010). Recent studies involved in overexpression of codon optimized kudzu IspS (kIspS) in E. coli using different constructs (Cervin et al. 2016). In This study, the E. coli best isoprene production yield was 10 μg/L. Moreover, the codon optimized kudzu and poplar IspS genes were expressed in Y. lipolytica using different methods; in which the isoprene yield was 0.5-1.0 μg/L from the headspace culture (Cervin  (Hayashi et al. 2015). Moreover, the kIspS was expressed in Trichoderma reesei; in which it yields 0.5 μg/L isoprene. Also, the synthetic tagged kIspS gene was introduced into Synechocystis sp. PC6803 (Lindberg et al. 2010). Results revealed that low levels of IspS protein were detected, in addition to the codon optimization that significantly enhanced protein production, in which latter strain produced 50 μg isoprene per gram dry cell weight per day, which is equivalent to 4 μg isoprene/L culture/h −1 (Hong et al. 2012). The same kIspS construct was used with a glucose-sensitive version of Synechocystis sp. PC6803; which produced isoprene that peaked at 100-130 μg/L culture (Bentley et al. 2014;Bentley and Melis 2012). Additionally, the isoprene production was slightly improved to 300 μg/L culture by introducing a heterologous MVA pathway (Bentley et al. 2014). There are previous studies on expression of more than one isoprene synthase, which shows are highly production of isoprene.
In which the expression of ten isoprene synthase genes from Arachishypogaea together with the MVA pathway in E. coli resulted in the production of up to 35 mg/L/h/ OD of isoprene (Beatty et al. 2014). Also, it was shown that heterologous expression of P. alba IspS and S. cerevisiae MVA pathway in E. coli, yield 532 mg/L isoprene in a fed-batch fermentation (Yang et al. 2012). Previous study on enhancing isoprene production through heterologous expression of B. subtilis DXS and DXR yield 314 mg/L isoprene, while over expression endogenous DXS and DXR in E. coli harboring P. nigra IspS gene enhanced isoprene production from 94 to 160 mg/L (Zhao et al. 2011). Additionally, by introducing RBS and nucleotide spacers provide the maximum isoprene expression in E. coli batch cultures from 0.4 mg/L isoprene of the control culture to 5 mg/L isoprene per of MEP super-operon transformants culture and up to 320 mg/L isoprene of MVA superoperon transformants culture . It was demonstrated that B. subtilis bears an isoprene synthase activity which utilizes the dimethylallyl diphosphate (DMAPP) as a substrate for isoprene production. Additionally, the isoprene synthase activity was optimal at pH 6.2 as well as it requires low levels of divalent ions and it was found to be separated from the chloroplast isoprene synthase (Sivy et al. 2002). Recently, 1-deoxy-d-xylulose-5-phosphate synthase (Dxs) and 1-deoxy-d-xylulose-5-phosphate reductoisomerase (Dxr) were overexpressed separately in B. subtilis DSM 10 strain. Over expression of Dxs increased the yield of isoprene by 40%. While over expression of Dxr had no change on the level of isoprene production (Xue and Ahring 2011). Concerning the control we have successful results in transformation of recombinant plasmid pET28b-kIspS-C-term in BL21 cells and the highest isoprene production for the recombinant BL21 cells harboring pET28b-kIspS-C-term was 70 μg/L/OD whenincubated at 37 °C for 24 h induced by 0.1 mM IPTG. Previous assays for kIspS expression in E. coli, revealed that the best isoprene production activity were obtained at 37 °C for 6 h with 0.1 mM IPTG induction . Moreover, heterologous expression of the codon optimized kIspS in E. coli has been carried out and results showed that there is no significant difference of kIspS gene expression in recombinant and non-recombinant E. coli ). It can be concluded from the obtained results that recombinant B. subtilis is a better host than B. licheniformis and E. coli for expressing isoprene and is considered as a versatile host for heterologous production of isoprene. It is recommended in the future research to give more attention for synthetic biology as well as substrate utilization pathways that would aid enzyme optimization and production improvement.