Patent Grant
7341857
The present invention relates to a novel esterase, a microorganism producing said enzyme and a method of producing said enzyme. This enzyme has an effect of restraining pathogenic expression of Ralstonia solanacearum.
Bacterial wilt, which brings down serious damages to agricultural crops, is known to be a disease that is difficult to prevent. Methods of preventing bacterial wilt thus far developed include mainly a technology aimed at killing Ralstonia solanacearum, pathogen, with antibiotics and the like (Study Reports of Agricultural Experiment Station, Okayama Prefectural Center for General Agriculture, No. 19, p. 29-35 (2001-12)), or a technology aimed at restraining the growth of the pathogen by grafting using a variety that is resistant to the disease as a rootstock (Journal of Phytopathological Society of Japan, Vol. 63, No. 2, p. 83-88 (1997-4)).
However, the method that involves use of antibiotics has a problem that the method gives the pathogen a stress to exist and a microorganism resistant to the stress will appear. On the other hand, the method that involves using a variety that is resistant to the disease as a rootstock takes many troubles and much time and hence tends to be avoided in a large-scale cultivation.
Incidentally, it has revealed that methyl 3-hydroxypalmitate represented by the general formula (I)
functions as a regulator for the pathogenic expression of Ralstonia solanacearum (Flavier, A. B., Clough, S. J., Schell, M. A., and Denny, T. P. (1997) Mol. Microbiol. 26, 251-259). Therefore, as Ralstonia solanacearum invades into crops and grows therein, the concentration of the compound increases, thereby developing pathogenicity.
Accordingly, the above-mentioned compound is expected to be used as a precursor for developing agricultural chemicals that are effective to bacterial wilt. The enzyme activity to decompose the compound is supposed to be applicable to a new breeding method for restraining the bacterial wilt.
However, only a chemical method such as an alkaline hydrolysis used for general fatty acid esters has been available as a reaction of decomposing the compound, for example, a method of hydrolyzing the compound into 3-hydroxypalmitic acid and methanol, represented by the general formula (II)
Therefore, the reaction must have been performed under strong reaction conditions, including, for example, use of a strong alkali.
If an enzyme activity that catalyzes this reaction is found, hydrolysis of methyl 3-hydroxypalmitate can be carried out under mild reaction conditions unlike the chemical methods. In addition, even if other fatty acids coexist, use of an appropriate enzyme activity enables selective hydrolysis of methyl 3-hydroxypalmitate utilizing substrate specificity of the enzyme. However, no reports on the enzyme activity to hydrolyze methyl 3-hydroxypalmitate have been available.
Accordingly, it is an object of the present invention to provide an enzyme that hydrolyzes methyl 3-hydroxypalmitate, a microorganism that produces the enzyme, and a method of producing the enzyme.
The inventors of the present invention have made extensive studies with a view to achieving the above-mentioned object, and as a result, they have found that a microorganism isolated from soil has an ability to produce the above-mentioned enzyme, esterase; the present invention has been completed based on this finding.
That is, a first aspect of the present invention relates to a novel esterase, which is derived from Ideonella sp. 0-0013 strain (FERM BP-08660) and has the following properties.
Further, a second aspect of the present invention relates to Ideonella sp. 0-0013 strain (FERM BP-08660), which has an ability to produce a substance that hydrolyzes methyl 3-hydroxypalmitate to generate 3-hydroxypalmitic acid and methanol.
Furthermore, a third aspect of the present invention relates to a method of producing the novel esterase described above, characterized by comprising: cultivating Ideonella sp. 0-0013 strain (FERM BP-08660) in a medium; and collecting the esterase from the culture broth.
Thus, according to the present invention, an enzyme that hydrolyzes methyl 3-hydroxypalmitate, a microorganism that produces the enzyme, and a method of producing the enzyme are provided.
Since methyl 3-hydroxypalmitate acts as a regulator of expression of the pathogenicity in Ralstonia solanacearum, the novel esterase of the present invention that hydrolyzes methyl 3-hydroxypalmitate is useful for effectively restraining the bacterial wilt.
The novel esterase of the present invention, which has the above-mentioned properties, is a monomeric enzyme composed of a single subunit judging from the value of its molecular weight. This enzyme can be obtained by cultivating Ideonella sp. 0-0013 strain in a medium. The Ideonella sp. 0-0013 strain, a novel esterase-producing microorganism, was isolated from the soil collected in Aichi by the inventors of the present invention. More specifically, the strain was isolated using an isolation medium that contains methyl 3-hydroxypalmitate as a single carbon source.
This microorganism was identified to belong to the genus Ideonella by analyzing the entire base sequence of 16S rDNA. The results are as follows.
When the base sequence of 16S rDNA of 1,158 bp was determined and BLAST search was performed, it revealed that the strain of the present invention had a high homology with microorganisms belonging to the genus Ideonella, with a 99% homology with the Ideonella sp. B513 strain (a strain derived from a rice plant) and the like and with a 98% homology with Ideonella dechloratans.
From the above-mentioned results, the Ideonella sp. strain of the present invention isolated from the soil as having a high activity to hydrolyze methyl 3-hydroxypalmitate was identified as the Ideonella sp.
The mycological properties of the strain of the present invention are as follows.
The strain grows well at 30 to 43° C. on Nissui standard medium (manufactured by Nissui Pharmaceutical) to form white colonies. It also grows on an LB medium but slightly poorly. On an agar medium containing methyl 3-hydroxypalmitate as a single carbon source, it grows at 43° C. It does not grow well on agar media that contain methyl palmitate or methanol as a single carbon source, respectively.
The Ideonella sp. Strain of the present invention was recognized by 16S rDNA sequencing to be a new species and deposited under the Budapest Treaty on Mar. 12, 2003 at the International Patent Organism Depositary, National Institute of Advanced Industrial Science and Technology at Tsukuba Central 6, 1-1, Higashi 1-Chome, Tsukuba-shi, Ibaraki-ken, Japan with an Accession Number: FERM BP-08660 (transferred from FERM P-19248). As described by 37 CFR 1.808, upon granting of the patent, all restrictions imposed by the depositor, subject to paragraph (b), on the availability to the public of the deposited material will be irrevocably removed for the term of the patent. In the present invention, those variants that are obtained by mutating the strain of the present invention naturally or with artificial means can also be used as far as they have an ability to produce the target esterase.
The microorganisms that produce the novel enzyme of the present invention that can be used include besides the above strain of the present invention, genetically engineered microorganisms or plants obtained by incorporating an enzyme gene isolated from the strain of the present invention into various host vector systems.
As the enzyme described in claim 1, the culture broths obtained by cultivating the above-mentioned microorganisms or the like in a medium can be used as they are. Alternatively, supernatants or microbial cells recovered from the culture broths, or their treated products can be used as a crude enzyme.
The treated microbial cells include, for example, crushed microbial cells, cell-free extracts obtained by crushing microbial cells, and microbial cells treated with organic solvents such as acetone, toluene, etc. Examples of the enzyme that can be used include in addition to those described above, a crude enzyme or a purified enzyme separated from the microbial cells, immobilized microbial cells or immobilized enzyme.
When using the enzyme, it is convenient to immobilize the enzyme to an appropriate carrier before it can be used. This facilitates separation and recovery of the enzyme from the reaction mixture after completion of the reaction and also reuse of the enzyme. Examples of the carrier that can be used include polyacrylamide and hydroxyapatite.
In the present invention, usually one kind of the crude enzyme such as microbial cells culture broth, microbial cells, or treated microbial cells or a purified enzyme can be used. However, two or more kinds having similar abilities can be used in combination as desired.
Any medium can be used as the medium for cultivating the above-mentioned microorganisms as far as the microorganism can grow. Preferable examples of the medium include Nissui Standard Medium (manufactured by Nissui Pharmaceutical), and SCD medium (manufactured by Nihon Pharmaceutical). The microorganisms can grow well in these medium. To obtain higher enzyme activities, it is effective to add compounds having skeleton of ester of fatty acid such as methyl 3-hydroxypalmitate and methyl palmitate to the medium and utilize the compounds as an induction substance for producing the enzyme.
Cultivation can be performed by a conventional method. For example, cultivation is performed at pH 4 to 10, preferably 6 to 8, at a temperature in the range of 15 to 50° C., preferably 30 to 45° C., for 6 to 96 hours, preferably 12 to 30 hours aerobically. Sometimes, a higher enzyme activity can be obtained by stationary culture in a similar manner.
After completion of the cultivation, when the enzyme is separated and collected from the culture broth, and purified, a conventional method may be followed. For example, the enzyme can be purified from: a supernatant obtained by a solid-liquid separating means such as centrifugation, from the culture broth; a cell-free extract obtained by crushing the microbial cells; or an extract with solvent such as acetone, toluene, etc., by a conventional method such as concentration, filtration, or chromatography, etc.
The esterase of the present invention has the following properties.
Methyl 3-hydroxypalmitate is detected by gas chromatography with a column of Stabilwax-DA, 30 m×0.53 mm×0.25 μm. The 3-hydroxypalmitic acid generated by hydrolysis of the ester can be detected by the same gas chromatography as described above.
Hereinafter, the present invention is explained in more detail by way of examples. However, the present invention is not limited by them.
200 mL of a medium containing 2.5 g/L yeast extract, 5.0 g/L peptone, and 1.0 g/L glucose was dispensed in a 500-mL Erlenmeyer flask and heated at 121° C. for 25 minutes to sterilize it. Then the Ideonella sp. 0-0013 strain (FERM BP-08660) was inoculated and cultivated with shaking at 43° C. for 20 hours.
After completion of the cultivation, the culture broth was centrifuged to obtain a supernatant, which was used as a crude enzyme. For purifying the enzyme, 70% ammonium sulfate fractionation was performed.
The culture broth obtained by cultivating the strain in the same manner as that in Example 1 was centrifuged to obtain a supernatant and microbial cells. The supernatant or the microbial cells were suspended in 200 μL of 10 mM potassium phosphate buffer (pH 7.0) containing 0.5 mg of methyl 3-hydroxypalmitate, and the resultant was allowed to react at 43° C. for 12 hours.
After completion of the reaction, 500 μL of dichloromethane was added to the reaction mixture to extract 3-hydroxypalmitic acid. The extract was subjected to gas chromatography (Stabilwax-DA, 30 m×0.53 mm×0.25 μm) to measure the decomposing activity of methyl 3-hydroxypalmitate. The results obtained are shown in Table 1.
0.5 mg of methyl palmitate or methyl 3-hydroxypalmitate was reacted and analyzed in the same manner as that in Example 1 and the decomposing activities of the compounds were measured in each case. The results obtained are shown in Table 2.
The table shows that the hydrolytic activity for methyl 3-hydroxypalmitate is about 5 times as high as that for methyl palmitate. This indicates that the enzyme activity of the present invention is selective to methyl 3-hydroxypalmitate.
According to the present invention, an enzyme that hydrolyzes methyl 3-hydroxypalmitate is provided. Methyl 3-hydroxypalmitate acts as a regulator for the expression of pathogenicity in Ralstonia solanacearum. The enzyme of the present invention that hydrolyzes said compound is useful for effectively restraining bacterial wilt.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2003-071376 | Mar 2003 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2004/003472 | 3/16/2004 | WO | 00 | 9/14/2005 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2004/083420 | 9/30/2004 | WO | A |
| Number | Date | Country |
|---|---|---|
| 11-56349 | Mar 1999 | JP |
| 11-56364 | Mar 1999 | JP |
| Number | Date | Country | |
|---|---|---|---|
| 20060194295 A1 | Aug 2006 | US |
