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Metabolites 2013, 3(1), 144-154; doi:10.3390/metabo3010144
Abstract: In animals, cobalamin (Cbl) is a cofactor for methionine synthase and methylmalonyl-CoA mutase (MCM), which utilizes methylcobalamin and 5′-deoxyadenosylcobalamin (AdoCbl), respectively. The cblA complementation class of inborn errors of Cbl metabolism in humans is one of three known disorders that affect AdoCbl synthesis. The gene responsible for cblA has been identified in humans (MMAA) as well as its homolog (meaB) in Methylobacterium extorquens. Recently, it has been reported that human MMAA plays an important role in the protection and reactivation of MCM in vitro. However, the physiological function of MMAA is largely unknown. In the present study, we isolated the cDNA encoding MMAA from Euglena gracilis Z, a photosynthetic flagellate. The deduced amino acid sequence of the cDNA shows 79%, 79%, 79% and 80% similarity to human, mouse, Danio rerio MMAAs and M. extorquens MeaB, respectively. The level of the MCM transcript was higher in Cbl-deficient cultures of E. gracilis than in those supplemented with Cbl. In contrast, no significant differences were observed in the levels of the MMAA transcript under the same two conditions. No significant difference in MCM activity was observed between Escherichia coli that expressed either MCM together with MMAA or expressed MCM alone.
Vitamin B12, or cobalamin (Cbl), is an organometallic cofactor that supports the activities of enzymes in organisms, ranging from bacteria to humans [1,2]. In animals, Cbl is the cofactor for cytosolic methionine synthase (EC 126.96.36.199) and mitochondrial methylmalonyl-CoA mutase (MCM, EC 188.8.131.52), more specifically, methylcobalamin (MeCbl) and 5′-deoxyadenosylcobalamin (AdoCbl), respectively. Inhibition of Cbl transport or biochemical modifications of Cbl usually causes severe diseases . The cblA complementation class of inborn errors of Cbl metabolism is one of three known disorders that affect AdoCbl synthesis without affecting the synthesis of MeCbl . The gene responsible for cblA has been identified through the examination of prokaryotic gene arrangements and is called MMAA . The deduced amino acid sequences of human or mouse MMAA show homology with the periplasmic protein kinase ArgK of Escherichia coli . ArgK is a coupled ATPase of the lysine, arginine and ornithine (LAO) transport system , suggesting the possibility that MMAA is a component of a transporter or an accessory protein that is involved in the translocation of Cbl into mitochondria .
MCM and a homolog of MMAA (MeaB) are present in the genome of the methylotrophic bacterium Methylobacterium extorquens AM1 . This bacterium synthesizes AdoCbl and utilizes AdoCbl as the cofactor for MCM and meaA (ethylmalonyl-CoA mutase). The mutation in meaB has no effect on the function of meaA. However, total MCM activity was significantly reduced in meaB mutants compared with that of the wild-type, although the meaB mutants synthesized AdoCbl . These findings suggest that meaB is not involved in the biosynthesis of AdoCbl or the transport of Cbl in M. extorquens.
Diol and glycerol dehydratases, Cbl-dependent enzymes, undergo concomitant irreversible inactivation by glycerol during catalysis . This inactivation involves irreversible cleavage of the Co-C bond of AdoCbl, forming 5′-deoxyadenosine and an alkylcobalamin-like species. The Cbl species that is formed remains tightly bound to the enzyme, inactivating the enzyme irreversibly. Diol or glycerol dehydratase-reactivating factor participates in reactivation of the inactivated holoenzymes by mediating ATP-dependent exchange of the modified coenzyme for free intact coenzyme [9,10,11,12].
Korokova and Lidstrom  found that meaB forms a complex with MCM and stimulates MCM activity in vitro. However, neither cyanocobalamin (CNCbl) nor AdoCbl is released from MCM in the presence of meaB. Further, purified meaB did not restore MCM activity in the extracts prepared from the meaB mutant. Therefore, they proposed that meaB does not function as a reactivating factor, but is involved in protection of MCM from suicide inactivation by possibly providing a stabilization function. However, recently, it has been reported that meaB involved in AdoCbl trafficking to MCM functions as an editor, discriminating between inactive and active cofactor forms and permitting transfer only of AdoCbl, in a process that is gated by GTP hydrolysis . Furthermore, the editing function of meaB is also used for reactivating inactivated MCM formed occasionally during turnover. Takahashi-Íñiguez et al.  have reported that human MMAA plays as two important roles as both the “protectase” and reactivase of MCM. In E. coli, sleeping beauty mutase (sbm; MCM homolog) interacts with ygfD (the MMAA or meaB homolog) .
Euglena gracilis Z, a photosynthetic flagellate, possesses characteristics of both plant and animal cells  and requires Cbl for its growth [17,18]. It has been reported that E. gracilis has Cbl-dependent methionine synthase and ribonucleotide redactase [19,20]. Furthermore, the purification of aquacobalamin reductase form E. gracilis was reported . Recently, we reported that E. gracilis MCM is a homodimer and is present in mitochondria . Further, we isolated a full-length E. gracilis MCM cDNA whose deduced amino acid sequence indicates that it is a mitochondrial protein. These findings suggest the possibility that E. gracilis, human and M. extorquens MCMs share molecular properties. To explore the function of MMAA, we isolated a cDNA encoding MMAA from E. gracilis and measured MCM activity in E. coli that expressed MCM alone or together with MMAA.
2. Results and Discussion
2.1. Isolation and Characterization of a cDNA Encoding MMAA
To isolate a cDNA encoding E. gracilis MMAA, a BLASTP search was performed against the Euglena EST data base  using the amino acid sequence of human MMAA  as a query. This search revealed an EST clone (cluster ID ELL00001639) encoding a putative E. gracilis MMAA. Similar to other MMAA or meaB, this EST clone is annotated as a putative periplasmic protein kinase ArgK. The corresponding full-length cDNA was cloned using the rapid amplification of cDNA ends method, and its sequence was submitted to the DDBJ/GenBank/EMBL data base (accession number AB772316). In E. gracilis, the short sequences present at the 5′ end of small cytoplasmic mRNAs [24,25,26] are transferred to pre-mature mRNAs by a trans-splicing mechanism. The presence of a spliced leader sequence at the 5′ end of E. gracilis MMAA cDNA (5′-TTTTTTTTCG-3′) indicated that full-length MMAA cDNA was obtained. The cDNA contains 1,400 bp with an open reading frame of 1,056 bp predicted to encode 352 amino acids residues (with a calculated molecular mass of 39113.9 Da).
The deduced amino acid sequence of the E. gracilis MMAA cDNA shows 79%, 79%, 79% and 80% similarity to human (NP_758454), mouse (NP_598584), Danio rerio (NP_001098582) MMAAs and M. extorquens (AAL86727) meaB, respectively (Figure 1). The E. gracilis MMAA cDNA encodes a predicted protein of 352 amino acid residues and includes Walker A and Walker B motifs, as well as a GTP-binding sequence . The presence of a signal peptide and cleavage sites was predicted by the TargetP prediction program . However, the cleavage site is present in the relatively well-conserved region among the MMAAs of vertebrates (Figure 1), suggesting the possibility that the MMAA cleavage site in E. gracilis is located closer to its N-terminal region.
2.2. Expression of MMAA by E. gracilis
Although it is known that the levels of MCM protein and total MCM activity in the livers of Cbl-deficient rats are higher than those in the livers of rats whose diet was supplemented with Cbl, the level of the MCM transcript in the livers of rats fed a Cbl-deficient diet was lower than that in the livers of rats fed Cbl-supplemented diets . To explore the regulation of the expression of MCM and MMAA, we analyzed the levels of their respective transcripts in response to Cbl in Cbl-deficient E. gracilis.
Cells cultured (1 mL) for one week were transferred to CNCbl-free medium, cultured for another week and then transferred (1 mL) to CNCbl-free medium. After three days, CNCbl (5 µg/mL) was added, and the cells were cultured for another three days (closed circles; Figure 2). Under the Cbl deficient condition, the growth of E. gracilis cells was highly suppressed (open circles; Figure 2). The addition of CNCbl increased the cell growth.
In three-day cultured Cbl-deficient E. gracilis cells, total MCM activity was 8.54 nmol min−1 mg−1 protein. At three days after the addition of Cbl to Cbl-deficient cells, total MCM activity was decreased to 38%, while that in the Cbl-deficient cells remained high (89%). In Cbl-deficient E. gracilis cells, the level of the MCM transcript was 2.3-fold higher than that in the Cbl-supplemented E. gracilis cells (Figure 3).
In contrast, no significant differences in the levels of the MMAA transcript were observed between the Cbl-deficient and Cbl-supplemented E. gracilis, suggesting the possibility that MMAA is constitutively expressed these cells.
2.3. Effect of Coexpression of MMAA on MCM Activity in E. coli
As noted above, MCM activity is significantly decreased in meaB mutants of M. extorquens . To examine the effect of the expression of MMAA on MCM activity, the expression vectors pET/Eg.MCM and pCDF/Eg.MMAA were transformed together or individually in E. coli using the expression vectors described below. In cells transformed with either the combinations of pET-16b and pCDF/Eg.MMAA or pET-16b and pCDF-1b, MCM activity was below the detection limit of the assay (5 pmol min−1 mg−1 protein) (Table 1). No significant difference in MCM activity was detected between cells expressing MCM alone or together with MMAA . We checked E. gracilis MMAA protein in E. coli cells using anti His-tag antibody. E. gracilis MMAA protein was slightly expressed in the soluble fraction in the pCDF-1b/Eg.MMAA transformed E. coli, suggesting that the expression level of E. gracilis MMAA protein was very low.
|Vector pairs||MCM activity (nmol min−1 mg−1 protein)|
|pET/Eg.MCM - pCDF-1b||12.1 ± 2.0|
|pET-16b - pCDF-1b/Eg.MMAA||< 0.005|
|pET-16b - pCDF-1b||< 0.005|
|pET/Eg.MCM - pCDF/Eg.MMAA||11.6 ± 1.8|
Data are mean values ± standard deviation from three assays.
E. coli sbm and ygfD genes are contained in an operon comprising sbm-ygfD-ygfG-ygfH . E. coli sbm forms a homodimer  as its E. gracilis homolog. Further, the deduced amino acid sequence of E. coli sbm is 89% similar to that of E. gracilis MCM. These findings suggest the possibility that ygfD functions to protect E. gracilis MCM from inactivation and acts to reactivate it in E. coli. Previous findings, and our presented data suggests the possibility that the function of E. gracilis MMAA was similar to those of human MMAA and meaB.
In Caenorhabditis elegans, the suppression of MMAA, MMAB [co(I)balamin adenosyltransferase] or MCM expression using RNAi technology caused the increase of methylmalonic acid . To clarify the Cbl metabolism, including the function of MMAA in E. gracilis, analyses using recombinant proteins and RNAi technology are necessary.
3. Experimental Section
3.1. E. gracilis and Culture Conditions
E. gracilis strain Z was grown in Koren–Hutner medium under continuous illumination at a photosynthetic photon flux density of 24 µmol m−2 s−1 at 26 °C until the cells reached stationary phase (6 days) 
3.2. RT-PCR-Amplification and Sequence Analysis
Based on analysis of the Euglena EST database using the Protest EST Program , a gene-specific primer was designed to amplify the missing 3′ and 5′ ends of the MMAA EST sequence (ELL00001639). Total RNA was isolated from E. gracilis using Sepasol-RNA I (Nakalai Tesque, Kyoto, Japan). The primers 5′-TGGTGGAGTCAAACCACATG-3′ and 5′- TCAGACACTTCCACAATGCC -3′ were used sequentially for 3′-rapid amplification of cDNA ends (3′-RACE) or 5′-RACE with a GeneRacerTM Kit (Life Technologies, Carlsbad, CA, USA). Amplified fragments were cloned into pSTBlue-1, and the nucleotide sequences of the 3′- or 5′-extended fragments were determined using an ABI Prism 3100 Genetic Analyzer (Applied Biosystems, Foster City, CA, USA). The full-length coding sequence of Euglena MMAA was amplified using PCR primed by Eg.MMAA-F (5′-ATTCCATGCAACGCCGCCCA-3′) and Eg.MMAA-R (5′-CCACGTATGCTTTCCTCCTT-3′). PCR amplification was carried out using PrimeSTAR (Takara Shuzo, Kyoto, Japan). A single-stranded cDNA prepared from 3-day Euglena cultures was used as template. The amplified product was cloned into pZErO-2 (Life Technologies), and the sequence was verified using an ABI Prism 3100 Genetic Analyzer (Applied Biosystems).
3.3. Semi-Quantitative RT-PCR Analysis
Semi-quantitative RT-PCR analysis was performed according to Ishikawa et al. . Primer pairs were as follows: EF1-α-F (5′-GTTGACCCTCATTGGTGCTT-3′); EF1-α-R (5′-CTTGGTCACCTTCCCAGTGT-3′); Eg.MCM-F (5′-GTCCATCGACAACACCATTG -3′); Eg.MCM-R (5′-CGACTTCAGCTCGTTGATGA -3′); and Eg.MMAA-F (5′-ATTCCATGCAACGCCGCCCA-3′); Eg.MMAA-R (5′-TCAGACACTTCCACAATGCC-3′). The experiments were repeated at least three times with cDNA prepared from three batches of E. gracilis cultures. The quantitative intensity was determined by applying densitometry to images of the blots .
3.4. Construction of MMAA and MCM Expression Plasmids
To construct MMAA and MCM expression vectors, their open reading frames were amplified from the first strand cDNAs, using the primer sets as follows: MMAA-Pma CI-F (5′-TCACCACCACCATCACGTGATGCAACGCCGCCCATGCAA-3′), MMAA-Pma CI-R (5′-TCGAACCGGTACCCACGTGCTACAGGCTGCAGCCCTCCA-3′), MCM-Nde I-F (5′-CATATGATCGACCTTCCACCAAAGTG-3′) and MCM-Bam HI-F(5′-GGATCCTCAGAGTTTGTTCAGGACCT-3′). The amplified DNA fragments were ligated into the vector pZErO-2 (Life Technologies), and the sequence was verified using an ABI Prism 3100 Genetic Analyzer (Applied Biosystems). The resulting constructs were digested with Pma CI for MMAA or Nde I/Bam HI for MCM and ligated into the expression vectors pCDF-1b (Novagen, Madison, WI) or pET16b (Novagen) to produce histidine-tagged proteins. The resulting constructs were designated pCDF/Eg.MMAA and pET/Eg.MCM, respectively.
3.5. Expression of Recombinant MMAA or MCM Proteins
To explore the effect of the expression of Eg.MMAA on MCA activity in E. coli, four plasmids sets (pET16-b and pCDF-1b, pET/Eg.MCM and pCDF-1b, pET16-b and pCDF/Eg.MMAA and pET/Eg.MCM and pCDF/Eg.MMAA) were introduced into E. coli strain BL21 Star (DE3) (Life Technologies). Transformed E. coli were cultured in 50 mL LB medium supplemented with ampicillin (50 µg mL−1) and chloramphenicol (34 µg mL−1) at 37 °C overnight. The culture was then transferred to Luria–Bertani medium (1 l). When the culture reached an absorbance of 0.6 at 600 nm, 0.4 mM isopropyl β-D-thiogalactopyranoside was added, and the bacteria were grown for another 6 h at 37 °C. The cells were harvested by centrifugation at 6,000 × g for 10 min, and the pellets were kept frozen at −20 °C.
3.6. Enzyme Extraction and Assay
E. coli pellets were resuspended in 100 mM Tris-HCl, pH 7.5, sonicated (Tomy, Tokyo, Japan) (10 kHz) using 20 s strokes with 30 s intervals and centrifuged at 15,000 × g for 15 min. MCM activity was assayed by a modified HPLC method described by Gaire et al. (1999). Briefly, the assay mixture (0.15 mL) for determining total MCM activity contained 100 mM potassium phosphate buffer (pH 7.5), 30 µM AdoCbl, 0.15 mM (R, S)-methylmalonyl-CoA and enzyme. The components, except for (R, S)-methylmalonyl-CoA, were mixed in microcentrifuge tubes in the dark, and the temperature was equilibrated by incubation in a heating bucket (e-Heating Bucket EHB, TAITEC Cop., Saitama, Japan) maintained at 3 °C. The reaction mixture was preincubated for 5 min, and the reaction was started by the addition of (R, S)-methylmalonyl-CoA and maintained for 5 min. The enzyme reaction was stopped by the addition of 50 µL of 10% (w/v) trichloroacetic acid. The reaction mixture was filtered through a 0.45 µM membrane filter (Millex Syringe Driven Filter Unit, LH-type, Milli-pore, USA). An aliquot (20 µL) of the filtrate was analyzed using a Shimadzu HPLC apparatus (two LC-10ADvp pumps, DGV-12A degasser, SCL-10Avp system controller, SPD-10Avvp ultraviolet-visible detector, CTO-10Avp column oven, 100 µL sample loop and C-R6A Chromatopac Integrator). The sample (20 µL) was loaded onto a reversed-phase HPLC column (Cosmosil 5C18-AR-II, Φ3.0 × 150 mm) equilibrated with 50% solvent A (100 mM acetic acid in 100 mM potassium phosphate buffer, pH 7.0) and 50% solvent B [18% (v/v) methanol in solvent A]. (R, S)-methylmalonyl-CoA and succinyl-CoA were eluted with a linear gradient of methanol (50%–100% solvent B) for 7.0 min at 40 °C and monitored by measuring the absorbance at 254 nm. The flow rate was 1.0 mL min−1. MCM activity was calculated from the amount of succinyl-CoA formed. Protein concentrations were determination using a Quant-iT™ Protein Assay and a Qubit fluorometer (Life Technologies).
E. gracilis MMAA cDNA contained an open reading frame encoding the protein of 352 amino acids with a calculated molecular mass of 39113.9 Da, preceded by a putative mitochondrial targeting signal consisting of 41 amino acid residues. No significant differences in the levels of the MMAA transcript were observed between the Cbl-deficient and Cbl-supplemented E. gracilis. No significant difference in MCM activity was observed between E. coli that expressed either MCM together with MMAA or expressed MCM alone. Previous findings, and our presented data suggests the possibility that the function of E. gracilis MMAA was similar to those of human MMAA and meaB.
The authors would like to thank Enago  for the English language review.
Conflict of Interest
The authors declare no conflict of interest.
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