Construction and characterization of a functional chimeric laccase from metagenomes suitable as a biocatalyst

Screening of gene-specific amplicons from metagenomes (S-GAM) is an efficient technique for the isolation of homologous genes from metagenomes. Using the S-GAM approach, we targeted multi-copper oxidase (MCO) genes including laccase and bilirubin oxidase (BOX) in soil and compost metagenomes, and successfully isolated novel MCO core regions. These core enzyme genes shared approximately 70% identity with that of the putative MCO from Micromonospora sp. MP36. According to the principle of S-GAM, the N- and C-terminal regions of the deduced products of the mature gene come from the known parent gene, which should be homologous and compatible with the target gene. We constructed two different MCO hybrid genes using Bacillus subtilis BOX and Micromonospora sp. MP36 MCO, to give Bs-mg-mco and Mic-mg-mco, respectively. The constructed chimeric MCO genes were fused with the maltose-binding protein (MBP) gene at the N-terminus for expression in Escherichia coli cells. We found that MBP-Mic-mg-MCO/Mic-mg-MCO possessed the characteristic properties of laccase, although MBP-Bs-mg-MCO had no activity. This novel laccase (Mic-mg-MCO) demonstrated unique substrate specificity, sufficient activity at neutral pH, and high thermal stability, which are suitable properties for its use as a laccase biocatalyst. Supplementary Information The online version contains supplementary material available at 10.1186/s13568-021-01248-y.


Introduction
Multi-copper oxidases (MCOs) are a family of enzymes that contain copper as a prosthetic group to catalyze four one-electron oxidations of various compounds concomitantly with the reduction of molecular oxygen to water (Sakurai and Kataoka 2007). MCOs are found in a wide range of organisms including bacteria, fungi (mainly laccase), plants, insects, and vertebrates (Baldrian 2006;Aniszewski et al. 2008;Dwivedi et al. 2011;Chauhan et al. 2017). They can oxidize various aromatic and nonaromatic compounds by a radical-catalyzed reaction mechanism that can undergo further oxidation or radical coupling reactions (Riva 2006). They generally contain three types of copper, of which type 1 is responsible for the blue color, oxidation of substrates, and electron extraction. The extracted electrons are transferred to type 2 and/or type 3 copper sites, where molecular oxygen is reduced to water (Sakurai and Kataoka 2007).
The screening of gene-specific amplicons from metagenomes (S-GAM) approach we have developed is a powerful technique for the efficient isolation of target genes from metagenomes (Itoh et al. 2014(Itoh et al. , 2016bItoh 2017). This approach can overcome a major disadvantage of previous techniques, namely, low efficiency in obtaining target genes from metagenomes. S-GAM also permits the omission of time-consuming subcloning and expression-optimization procedures. Simply put, S-GAM is a unique shortcut to identify proteins hidden in nature. However, this method yields gene products that are all chimeric at the N-and C-terminal regions; thus, resulting in improper folding of the protein in some conditions and the need for further improvements of the enzymes by changing or optimizing these regions.
In this study, we describe the isolation of core DNA regions of novel MCO genes from soil metagenomes, optimization of the N-and C-terminal regions, expression of this chimeric Lcc gene in Escherichia coli, and characterization of this novel Lcc. Moreover, we present a series of modifications for the S-GAM approach to obtain a functional enzyme.

Preparation of metagenomes from soil samples
Metagenomic DNA was extracted from 14 environmental samples collected from soils, farm (35-45 °C) and bark (50-80 °C) composts, and activated sludge and its compost in Toyama and Kagoshima, Japan, using an ISOIL for Beads Beating ™ Kit (Nippon Gene, Tokyo, Japan) without further purification. Bark compost samples fermented at 50-80 °C were generously supplied by a compost-producing company (Hokuriku Port Service, Toyama, Japan). Successful extraction of DNA from soil and compost samples was confirmed using agarose gel electrophoresis, and DNA concentration was measured by NanoVue (GE Healthcare Life Sciences, Buckinghamshire, UK); these DNA samples served as templates for PCR.

Genome database homology search and design of PCR primers
A database homology search was performed using BLAST (National Center for Biotechnology Information, Bethesda, MD, USA). Bacterial BOX genes whose products shared 40-80% amino acid sequence identity with Bacillus subtilis CotA (Lcc/BOX, accession no. CAB12449.1) (Hullo et al. 2001) were selected from databases, and the homologous regions as near as possible to the N-and C-terminal regions were determined (Fig. 1). Subsequently, two sets of forward and reverse degenerate primers were designed: BacBOXdgFw1, BacBOXdgFw2, BacBOXdgRv1, and BacBOXdgRv2 (Table 1). The following GAM primers for PCR were designed to introduce 15-bp fusion sites to both 5′-ends: BacBOXdgFw1GAM, BacBOXdgFw2GAM, mgBOXInfFw, and mgBOXInfRv (Table 1).

PCR amplification of target genes
Standard techniques were used for DNA manipulation (Sambrook and Russell 2001). E. coli JM109, E. coli BL21 (DE3), and E. coli 10-β (New England Biolabs, Tokyo, Japan) were used to host mco and lcc genes. PCR was performed using KOD FX Neo DNA polymerase (Toyobo, Osaka, Japan). Hot-start and step-down PCR protocols were used to avoid non-specific amplification. Each reaction mixture contained 10 µL of 2× buffer from the KOD FX Neo kit, 2 nmol of each dNTP, 8 pmol of each primer, 10-50 ng metagenomic DNA, and 0.4 U DNA polymerase in a total volume of 20 µL. PCR commenced at 94 °C for 2 min, followed by a step-down protocol: 4 cycles at 94 °C for 10 s, 56 °C for 30 s, and 68 °C for 1 min; 4 cycles at 94 °C for 10 s, 54 °C for 30 s, and 68 °C for 1 min; 4 cycles at 94 °C for 10 s, 52 °C for 30 s, and 68 °C for 1 min; 4 cycles at 94 °C for 10 s, 50 °C for 30 s, and 68 °C for 1 min; 20 cycles at 94 °C for 10 s, 48 °C for 30 s, and 68 °C for 1 min; and finally the sample was maintained at 68 °C for 5 min. The obtained amplicons were analyzed by agarose gel electrophoresis. Following confirmation of the proper amplification of the target genes, the GAMprimer sets were applied to these positive metagenomic samples. The same PCR conditions were used for the GAM-primer sets, except that the following step-down annealing temperatures were applied: 58 °C, 56 °C, 54 °C, 52 °C, and 50 °C. The gene-specific amplicons obtained with the GAM-primer sets were purified using a Fast-Gene Gel/PCR Extraction Kit (Nippon Genetics, Tokyo, Japan) from the agarose gel after electrophoresis.
Approximately 900 bp was deleted from the inner part of Bsbox in pUC57-Kan-BsBOX and Micmco in pUC57-Kan-MicMCO by inverse PCR using a KOD-Plus-Mutagenesis Kit (Toyobo). After amplification by inverse PCR, the linearized plasmids were self-ligated, and they were transformed into E. coli JM109 by electroporation. Following cultivation in LB medium (pH 7.0) with 50 µg/mL kanamycin at 37 °C overnight, the plasmids were extracted from the recombinant cells, the deleted DNA fragment of Bsbox or Micmco treated with NdeI and BamHI was separated by agarose gel electrophoresis and purified from the gel using a FastGene Gel/PCR Extraction Kit. The purified DNA fragments (ca. 400 bp) were ligated between the same restriction enzyme sites of pMAL-c5x to generate pMAL-c5x-delBsBOX and pMAL-c5x-delMicMCO, respectively.
Using pMAL-c5x-delBsBOX or pMAL-c5x-delMic-MCO as a template, inverse PCR was carried out to linearize and insert 15 nucleotides at both 5′-ends for the In-Fusion reaction using the following primer sets: BacBOXInfFw and BacBOXInfRv for pMAL-c5x-delBsBOX; and MicMCOInfFw and MicMCOInfRv for pMAL-c5x-delMicMCO. After PCR amplification, the linearized plasmids were purified using a FastGene Gel/ PCR Extraction Kit and used for the In-Fusion reaction.
The gene-specific amplicons containing the core BOX/ MCO gene were fused between the same compatible sites of linearized pMAL-c5x-delBsBOX or pMAL-c5x-delMicMCO using an In-Fusion ® HD Cloning Kit (Clontech, Mountain View, CA, USA) to generate each expression vector. The reaction mixture consisted of 2 µL In-Fusion HD enzyme premix, 2 µL DNA fragment amplified from pMAL-c5x-delBsBOX or pMAL-c5x-delMicMCO (ca. 50 ng in total), 2 µL DNA from metagenomes (ca. 50 ng in total), 2 µL In-Fusion enzyme, and 2 µL sterilized water in a total volume of 10 µL, and the mixture was incubated at 50 °C for 15 min. In accordance with the manufacturer's protocol, the obtained plasmids (2 µL) were transformed into a suspension of E. coli 10-β (50 µL) by heat-shock (pre-incubation at 0 °C for 30 min, 42 °C for 30 s, and incubation at 0 °C for 5 min), and recovered in New England Biolabs 10-β stable outgrowth medium at 37 °C for 1 h. The clones were grown overnight at 37 °C on agar plates containing LB medium (pH 7.0) with 50 µg/mL ampicillin. Clones grown on the agar plates were selected randomly and the plasmids were extracted. The plasmids, designated as pMAL-c5x-Bs-mg-MCO and pMAL-c5x-Mic-mg-MCO, were transformed into E. coli BL21 (DE3)/pG-KJE8 (chaperone plasmid; Takara Bio Inc., Shiga, Japan) by electroporation.
To construct the MBP-deleted Mic-mg-MCO (Micmg-MCOΔMBP), inverse PCR was performed using pMAL-c5x-Mic-mg-MCO120-3 as a template with the MicMCOFw2 and pMALdelMBPRv primer set ( Table 1). The amplified fragment was treated with DpnI and selfligated to give pMAL-c5x-Mic-mg-MCO120-3ΔMBP. The deletion of MBP was confirmed by plasmid analysis on agarose gel electrophoresis and DNA sequencing.
DNA sequences were determined for both strands using a capillary DNA sequencer (ABI PRISM 310; Applied Biosystems ® Life Technologies, Carlsbad, CA, USA).

Purification and physicochemical characterization of chimeric Lcc
Mic-mg-MCO120-3 was purified at 0-4 °C in 20 mM KPB (pH 7.0) unless otherwise stated. Washed recombinant E. coli BL21 (DE3)/pMAL-c5x-Mic-mg-MCO120-3ΔMBP/pG-KJE8 cells from 500 mL culture, which were cultured at 37 °C for 17 h in LB medium in a 2-L shake flask and then at 18 °C for a further 16 h with 0.1 mM IPTG and 1 mM CuSO 4 , were washed with the buffer, suspended in 30 mL buffer, and disrupted using an ultrasonic oscillator (Ultra Sonic Disrupter UD-200; Tomy Corp., Tokyo, Japan) for 150 s (5 disruption sequences of 30 s followed by a 60-s interval for cooling). After centrifugation (12,000×g, 15 min), the cell-free extract was fractionated with solid ammonium sulfate. The precipitate with 0 to 40% saturation of ammonium sulfate was collected, dialyzed against the buffer, and then applied to a DEAE-Toyopearl 650 M (Tosoh Co., Ltd., Tokyo, Japan) column (20 × 100 mm) equilibrated with the buffer. The column was washed with 10 column volumes of the buffer. Mic-mg-MCO120-3 was eluted with a linear 0-0.5 M NaCl gradient in the same buffer. Fractions exhibiting high levels of enzyme activity at approximately 0.2 M NaCl were collected and dialyzed against the buffer. The enzyme solution obtained was used as purified enzyme.
Protein concentration was estimated by measuring the absorbance of protein-containing solutions at 280 nm or by the method of Bradford using bovine serum albumin as a standard (Protein Assay Kit; Bio-Rad, Hercules, CA, USA). Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) was performed using 12% (w/v) polyacrylamide slab gels and the Tris-glycine buffer system of Laemmli (1970). The molecular weight of the purified enzymes was determined by analytical high-performance liquid chromatography using a TSK-Gel G3000SW XL (Tosoh, Tokyo, Japan) column (7.8 mm × 30 cm) and an elution flow rate of 0.5 mL/ min in 50 mM Tris-HCl (pH 7.0) with 0.1 M NaCl. The molecular mass of the enzyme was determined by comparing its retention time with those of standard proteins.

Nucleotide sequence accession number
The lcc120-3 (Mic-mg-mco120-3Δmbp) sequence was registered at the DNA Data Bank of Japan under the accession number LC624142.

Design of primers and amplification of mco genes by S-GAM
Degenerate primers were designed according to the Nand C-terminal regions of bacterial BOX and its related genes, belonging to the MCO family, which shared 40-80% identity with B. subtilis CotA (BOX/Lcc), and are proteins of approximately 513 amino acid residues (Fig. 1). However, alignment of several MCOs at the terminal regions showed quite low identity to each other, and the well-conserved regions were located in the more inner regions from the N-and C-termini (Fig. 1), which were TWG(Y/V)NGS in the N-terminal region and (F/Y) MYHCH(I/L) and HED(G/N)GMM in the C-terminal region. Primers of approximately 20 bp (BacBOXdgFw1/ Fw2, BacBOXRv1, and BacBOXRv2) were designed based on these sequences. GAM-primers of approximately 35 bp (BacBOXdgFw1GAM, BacBOXdgFw2GAM, BacBOXdgRv1GAM, and BacBOXdgRv2GAM), containing the regions for fusion with the pMAL-c5x-delBsBOX expression vector, were also designed (Table 1). First, a combination of the primers BacBOXdgFw1/Fw2 and BacBOXRv1/BacBOXRv2 was tested to amplify the core genes for some metagenomes. Adjustments were made to the primer set combinations and to optimize other PCR conditions, especially annealing temperatures. We used hot-start and step-down PCR protocols to avoid nonspecific amplification and to support the sufficient amplification of DNA using KOD FX Neo DNA polymerase. Under the optimized conditions, we observed the amplification of target genes from 8 samples among 14 metagenomic samples, which were mainly isolated from bark composts under fermentation collected in Japan. Second, we carried out amplification using the optimized GAM-primer set (BacBOXdgFw1GAM and BacBOXdgRv2GAM) based on the first amplification results to isolate the core DNAs of the target genes and to fuse them to the expression vector. This simple method was effective to determine which metagenomic samples should be used to amplify the target genes with the GAM-primer set.

Screening and analyses of mco genes from the metagenomic library
PCR-amplified genes with the GAM-primer set were fused with the parent gene, Babox, at both terminal regions using a linearized DNA fragment amplified from pMAL-c5x-delBsBOX. They were transferred into E. coli and expressed as MBP-fusion proteins because it is difficult to express many mco genes normally in E. coli cells. In advance of this experiment, we had confirmed that MBP-BsBOX can be expressed as an active form in E. coli BL21 (DE3) with the pMAL-c5x-BsBOX/pG-KJE8 system. Approximately 2000 colonies obtained from 4 compost metagenomes were measured directly using their enzyme activity for two substrates, DMP on agar plates and ABTS in liquid medium. However, all clones were null for enzymatic activity, despite observing normal protein expression in some clones by SDS-PAGE (data not shown). Therefore, we analyzed the 12 DNA sequences of the potential mco genes obtained from 4 compost metagenomes, and the results indicated that most core DNAs had high similarity with the putative MCOs of Micromonospora sp. MP36 (ca. 70% amino acid identity) and Comamonadaceae (accession no. TY22925.1) (ca. 60% amino acid identity), but relatively low similarity with that of BsBOX (ca. 30% amino acid identity) ( Table 2). The chimeric enzymes, except MBP, consisted of 49 amino acid residues of BsBOX at the N-terminus, 387 residues of the core region, and 22 residues of BsBOX at the C-terminus in a total of 458 amino acid residues, suggesting that the N-and C-amino acid residues are incompatible with the core region of the enzymes.
To obtain an active form of MCO, we substituted the N-and C-terminal regions of BsBOX with those of Mic-MCO. Eight clones shown in Table 2 isolated from three bark compost samples (s-120, s-121, and s-123) and eliminated the sequence-duplicated ones, which showed high similarity with MicMCO, were PCR-amplified using the mgBOXInfFw and mgBOXInfRv primer set (Table 1), and fused to the linearized DNA fragment amplified from pMAL-c5x-delMicMCO. Amino acid sequence identity, as compared to that of MicMCO, for the core regions by BLASTP analysis is summarized in Table 2. The hybrid genes were given the descriptor mbp-Micmg-mco to indicate the chimeric MCO of Micromonospora sp. and metagenomic MCO. The chimeric enzymes, except MBP, consisted of 98 amino acid residues of Mic-MCO at the N-terminus, 387 residues of the core region, and 54 residues of MicMCO at the C-terminus in a total of 539 amino acid residues. The core regions had 98-99% amino acid identity to each other except 123-3 (Additional file 1). The activity of these clones after inducing gene expression was measured spectrophotometrically using cell-free extracts from recombinant E. coli. We confirmed they had measurable Lcc activity, although there was a large difference among their activity (Table 3). We observed that the MBP-Mic-Mg-MCO120-3 clone possessed fourfold higher activity than MBP-MicMCO. Moreover, some amino acid substitutions (Additional file 1) in the core region significantly affected the enzyme activity of MBP-Mic-mg-MCOs.
The enzyme was relatively stable during purification, and also towards concentrated NaCl. Therefore, the process of purifying Lcc120-3 (Mic-mg-MCO120-3) from the crude extract was conducted by ammonium sulfate fractionation and anion-exchange chromatography using DEAE-Toyopearl. However, total enzymatic activity was largely lost with anion-exchange chromatography including DEAE-or QAE-resin. The reason for this phenomenon is unclear. The enzyme was purified by 10.8-fold, and the yield was 13.2%. SDS-PAGE indicated the purified enzyme preparation was almost homogeneous (Fig. 2).

Molecular mass and subunit structure
The molecular mass of Lcc120-3 (Mic-mg-MCO120-3) was estimated to be 57 kDa according to analytical highperformance liquid chromatography with a TSK-Gel G3000SW column. SDS-PAGE revealed an almost single band corresponding to a molecular mass of 50 kDa (Fig. 2), indicating that Lcc120-3 is a monomeric enzyme. As described, the enzyme consisted of 539 amino acid residues. Therefore, the theoretical molecular mass of Lcc120-3 was inferred to be 58.4 kDa. The pI value of Lcc120-3 estimated from the amino acid sequence was 5.92. On the other hand, the theoretical molecular mass of MBP-LCC120-3 was estimated to be 106.6 kDa, including MBP (48.2 kDa) and chimeric Mic-mg-MCO (58.4 kDa). The molecular mass observed on SDS-PAGE matched the theoretical one (Fig. 2).

Effect of temperature on enzyme stability
The thermal stability of Lcc120-3 and MBP-Lcc120-3 was measured by incubating the purified or crude enzyme at each tested temperature for 30 min in 50 mM KPB (pH 7.0). Lcc120-3 was stable after incubation below 50 °C, and 47% and 9% of its original activity was maintained after incubation at 65 °C and 70 °C, respectively (Fig. 4), indicating sufficient thermal stability. The data showed that MBP-Lcc120-3 had slightly lower thermal stability than Lcc120-3.

Substrate specificity and kinetic parameters
The activity and kinetic parameters of purified Lcc120-3 were measured for various substrates (Table 4). The enzyme showed relatively high activity toward pyrogallol, o-catechol, DMP, and ABTS, which are well-known substrates of Lcc. Conversely, activity toward guaiacol and gallic acid was low compared with the other substrates. l-tyrosine, l-DOPA, bilirubin, syringaldazine, and iodide ions were not substrates of Lcc120-3. Because syringaldazine is an Lcc-specific compound, the lack of this activity in Lcc120-3 was characteristic of this enzyme (Baldrian 2006;Mano 2012), suggesting that Lcc120-3 is an Lcc-like enzyme and not a tyrosinase-, BOX-, and iodide oxidase-like enzyme. As summarized in Table 4, the specific activity of Lcc120-3 toward DMP (2.0 U/ mg, k cat : ca. 2.3 s −1 ) was much lower than that of Lccs reported in basidiomycetes, for example, 165 U/mg (k cat : 185 s −1 ) of Lcc2 from Hericium coralloides (Itoh et al. 2016a), but was comparable with those ranging from 3 to 57 s −1 of bacteria such as Bacillus sp. CotAs (Mano 2012). The K m and V max values toward DMP calculated from a Lineweaver-Burk plot were 10.5 mM and 2.3 U/ mg, respectively. Such a high K m value for DMP has not been reported for known Lccs, suggesting that Lcc120-3 might possess a rather different substrate specificity from known Lccs. Notably, chimeric MBP-Lcc120-3 (MBP-Mic-mg-MCO) had fourfold higher activity for ABTS    (Table 3). This means that the core region isolated from the metagenomes possesses a positive effect increasing Lcc activity.

Discussion
Eukaryote Lccs mainly isolated from basidiomycetes have been heterologously expressed in Saccharomyces cerevisiae (Hoshida et al. 2005), the methylotrophic yeast Pichia pastoris (Hong et al. 2007), and the filamentous fungi Aspergillus niger, Aspergillus oryzae (Hoshida et al. 2005;Sigoillot et al. 2002), and Trichoderma reesei (Kiiskinen et al. 2004). However, it is difficult to sufficiently express the eukaryote Lcc genes in E. coli cells except in some special cases (Zelena et al. 2014;Ma et al. 2018). On the other hand, prokaryote MCOs such as from Bacillus subtilis (Enguita et al. 2003), Bacillus licheniformis (Koschorreck et al. 2008), and Bacillus pumilus (Reiss et al. 2011) have been overproduced in E. coli, especially B. licheniformis Lcc (Koschorreck et al. 2008). Based on this information, we focused on Bacillus sp. CotA genes, which are similar to the genes of the target MCO. Moreover, we adopted the MBP tag (di Guan et al. 1988) and E. coli chaperone system to support the soluble expression of mco genes in E. coli. The S-GAM method we have developed includes the following steps (Itoh 2017): (1) Design of degenerate PCR primers (GAM primers) based on the conserved regions as near as possible to the N-and C-terminal regions in alignments constructed from the target gene; these primers are 25-30 bp in length and contain 15-bp regions that match the sequences of the known target enzyme gene. The 15-bp long regions are used to ligate the terminal regions with the expression vector using the In-Fusion method.
(2) PCR using the GAM-primer set for various metagenomic samples. (3) Connection of the amplified amplicons with the linearized expression vector, and construction of E. coli libraries. (4) Screening of the libraries by simple enzyme activity or another high-throughput screening method. The obtained enzymes are all chimeric proteins with N-and C-terminal regions matching the known target enzyme. (5) If necessary, follow-up sequence analysis is performed. S-GAM is defined by steps 1 and 3, which enable omission of time-consuming subcloning and expression optimization procedures. To date, at least three enzyme genes including short-chain alcohol dehydrogenase (Itoh et al. 2014), zinc-dependent medium-chain alcohol dehydrogenase (Itoh et al. 2016b), and styrene monooxygenase genes have been isolated by this method and characterized. In this study, we applied this approach to bacterial MCO genes in the soil environment because bacterial MCOs represented by Bacillus sp. CotA (Lcc/BOX) have superior enzymatic properties and especially sufficient activity around neutral pH. However, we were unable to find suitable conserved regions matching the known bacterial MCO genes at the N-and C-terminal regions (Fig. 1). Thus, the isolation, expression, and detection of mco/lcc genes by the S-GAM technique using E. coli as a host cell is challenging. First, we modified this technique to select metagenomic samples from which the target genes can be amplified using normal degenerate primer sets and optimized the amplification conditions. Then, we used the GAM-primer set to amplify the core region of target genes from specific metagenomic samples. This modified technique functioned sufficiently well and the targeted mco genes were amplified by the GAM-primer set. Moreover, we expected that the chimeric MCOs/Lccs constructed possessing long flanking regions at the N-and C-termini might be inactive because they would be incompatible with the core regions isolated from the metagenomes. In fact, approximately 2000 clones constructed with the core genes and flanking regions of BsMCO were all inactive in E. coli. Accordingly, we changed the strategy from isolating diverse mco genes from metagenomes to optimizing or changing the N-and C-termini to match the specific core gene. Sequence analysis of major isolates indicated high similarity with the putative mco of Micromonospora sp. MP36 (ca. 70% amino acid identity) and that of Comamonadaceae (accession no. TY22925.1) (ca. 60% amino acid identity). Therefore, we substituted the N-and C-terminal regions of BsMCO (MBP-Bs-mg-MCO) with Micromonospora sp. MP36 MCO by using a different expression vector (pMAL-c5x-delMicMCO) to give MBP-Mic-mg-MCO.
As described in the Results, the chimeric enzyme (MBP-Mic-mg-MCO/Mic-mg-MCO) was active and demonstrated Lcc-specific characteristics, especially sufficient activity at neutral pH, a medium range of substrate specificity, and thermal stability. Interestingly, the constructed chimeric MBP-Lcc120-3 (MBP-Mic-mg-MCO) had much higher enzymatic activity than the original MBP-MicMCO (Table 3), although the effect of the MBP tag is not completely negligible. This suggested that using the S-GAM method to produce a chimeric enzyme can result in the generation of a superior enzyme as a protein engineering tool. Although the enzyme production level (0.09-0.16 U/ mL-culture for ABTS) in E. coli was slightly lower than in a previous report using E. coli as a host, for example, 0.37 U/mL-culture for ABTS of B. licheniformis CotA (Lcc) (Koschorreck et al. 2008), further optimization of enzyme production should increase productivity. Chimeric Lcc120-3 (Mic-mg-MCO) was identified as a novel and unique Lcc in terms of its enzymatic properties, which could be applied as a biocatalyst in several reactions at neutral pH.