Team:Tokyo-NoKoGen/g3dh

About G3DH

　The enzyme, glucoside 3-dehydrogenase (E.C.1.1.99.13) or glucose-3-dehydrogenase (G3DH) catalyzes the oxidation of the C-3 hydroxyl group of the glucosides and converting them to corresponding 3-ketoglucosides (1). Because G3DH has wide substrate specificity, it can convert not only monosaccharides but disaccharides, including trehalose.

　G3DH is composed of three subunits: catalytic subunit, cytochrome c subunit, and small subunit. The catalytic subunit has a flavin adenine dinucleotide (FAD) as cofactor, and the cytochrome c subunit is bound to the cytoplasmic membrane in the periplasm.

　In our project, we used G3DH derived from Rhizobium tumefaciens EHA101, formerly known as Agrobacterium tumefaciens. The enzymatic activity of G3DH in this microorganism was first reported in 1967 (2). The gene encoding this enzyme was found from a putative proteins which is homologous to G3DH derived from Halomonas sp. α-15 (3), which was reported to convert trehalose to 3,3’dkT (see below). The functional expression of R.tumefaciens derived putative enzyme confirmed that the gene encodes the G3DH complex (unpublished data from Sode laboratory, Tokyo univ. of Agric. and Technol.).

About 3,3'-diketotrehalose (3,3'-dkT)

　3,3’-dkT is a novel trehalose derivative in which the third hydroxyl group of both glucose moieties are oxidized. It was already reported that 3,3-dkT showed an inhibitory effect toward the trehalase from pig-kidney and Bombyx mori (silkworm)(3).

Construction of Biobrick

　We amplified G3DH gene from Rhizobium tumefacience by PCR. PCR products were inserted in pSB1C3. Original G3DH gene has two EcoRI restriction sites, which is incompatible with BioBrick parts. These restriction sites was removed by overlap extension PCR using designed primers.

Fig.1. The schematic image to remove internal EcoRI sites in G3DH.

　　G3DH gene fragments were amplified and three PCR products were connected. Then, G3DH (removed illegal restriction sites) were ligated with four promoters and double terminator (BBa_B0010 and BBa_B0012).

Fig 2. BioBrick parts containing G3DH.

　One of those promoters is arabinose inducible, and the others are constitutive promoter.

Table 1. Promoter connected with G3DH genes.

Evaluation

　This G3DH needs the maturation of cytochrome c subunit to have catalytic activity. Therefore, we transformed E. coli TOP 10 with the constructed plasmids and pEC86, which expresses cytochrome c maturation (CCM) enzymes (3).

This is the method of culturing and extraction of production (Fig. 3).

We cultured TOP10 transformed with below plasmids in LB medium containing 20 mM Trehalose. P_high, _medium-RBS-G3DH-DT and P_BAD-RBS-G3DH-DT were cultured at 80 rpm, 37 ℃, for 24 hours and at 150 rpm, 37 ℃ respectively.

When OD₆₆₀ achieves 0.6, 0.2 % arabinose was added to the medium for induction (PEC86,P_BAD-RBS-G3DH-DT). The transformants were harvested, suspended in 10 mM sodium phosphate buffer (SPB) and pellet was obtained by centrifugation.

　First, we investigated expression of G3DH by SDS-PAGE analysis. Second, we measured the glucose dehydrogenase activity of G3DH. Finally we tried to detect 3,3’-dkT by thin-layer chromatography (TLC).

Fig. 3 Evaluation of G3DH

SDS-PAGE

　By SDS-PAGE analysis, there was the band which showed about 68 kDa on G3DH under the constitutive promoter P_medium and P_high, P_BAD. Therefore, we confirmed the expression of G3DH (Fig. 2).

Fig. 4 SDS-PAGE analysis of G3DH expression.

Measurement of glucose dehydrogenase activity

　We measured the oxidase activity of G3DH by PMS-DCIP assay (Fig. 5). On this assay, we measured the decrease in absorbance of DCIP at 600 nm. Substrates were glucose and trehalose. PMS stands for phenazine methosulfate, and DCIP stands for 2,6-dichlorophenol-indophenol.

Fig.5 The scheme of PMS-DCIP assay.

P_high had highest productivity. It is reason that we confirmed expression of Phigh-G3DH by SDS-PAGE.

Both of P_BAD-G3DH(+) and (-) had comparatively high productivity. Increase of PBAD(-) productivity results that regulation by non-arabinose was not enough.

We confirmed high expression of P_medium-G3DH by SDS-PAGE, but productivity was very low level. This result indicates expressed protein misfolded.

We performed glucose dehydrogenase activity assay. Productivity was calculated by total activity. Productivity of P_high was the highest (370 U/L culture)

Trehalase inhibition measurement

　This is the result of trehalase inhibition activity assay(Fig. 6). Each value of activity was normalized at the value of activity of empty vector which were not induced by arabinose. Samples of G3DH which induced by P_high and P_medium activity was lower than that of empty vector.

　We concluded that G3DH which induced by P_high and P_medium expressed G3DH. And G3DH converted trehalose to 3,3’-dkT.

Fig. 6 Trehalose inhibition activity assay

Reference

(1) K Kojima et al., (2001) Cloning and Expression of Glucose 3-Dehydrogenase from Halomonas sp. α-15 in Escherichia coli. Biochem Biophys Res Commun, 282, 21-27

(2) K Hayano et al., (1967) Purification und properties of 3-ketosucrose-forming enzyme from the cells of Agrobacterium tumefaciens. J. Biol. Chem.,　242, 3665-3672

(3) K Sode et al., (2001) Enzymatic synthesis of a novel trehalose derivative, 3,3’-diketotrehalose, and its potential application as the trehalase enzyme inhibitor. FEBS Letters, 489, 42-45

(4) E Arslan et al., (1998) Overproduction of the Bradyrhizobium japonicum c-Type Cytochrome Subunits of the cbb3 Oxidase in Escherichia coli. Biochem Biophys Res Commun, 251, 744-747

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Future work

　We could confirm the production of trehalose and 3,3’-dkT respectively. Therefore, we are going to cotransform E. coli with 3 different plasmids each expresses OtsA+OtsB, G3DH and cytochrome c maturation enzymes. By doing this, E. coli can directly produce 3,3’-dkT from glucose.

　We thought that low productivity of 3,3’-dkT was caused by low amount of precursor (trehalose). To increase the production of trehalose, we’re planning to use other kind of enzyme to produce trehalose. In our project, we used OtsA and OtsB derived from E. coli to produce trehalose, but E. coli and other microorganisms have different kind of pathway to produce trehalose. If we introduce other pathway into E. coli productivity of trehalose may increase.

Further improvement

　To improve the specificity of Exterminator coli, we are going to introduce cockroach pheromone expression system to it. And if we want to create an Exterminator coli for other insects, we can engineered it by introducing specific pheromone for each insect.