Microbiological process for the production of hydroxylated pyrazine derivatives

Abstract

Microorganisms, which are capable of growing with pyrazine as the sole carbon, nitrogen and energy source. These microorganisms hydroxylate pyrazine derivatives of general formula: ##STR1## to hydroxylated pyrazine derivatives of general formula: ##STR2## and the latter are accumulated in the growth medium.

Description

BACKGROUND OF THE INVENTION

1. Field Of The Invention

The invention relates to new microorganisms, which grow with pyrazine, and hydroxylate pyrazine derivatives of the general formula: ##STR3## wherein R.sub.1 means a hydrogen atom or a halogen atom and R.sub.2 and R.sub.3 are the same or different and mean a hydrogen atom or a C.sub.1 -C.sub.4 alkyl group, but R.sub.1,R.sub.2 and R.sub.3 do not all simultaneously mean hydrogen, as well as to a process for the production of hydroxylated pyrazine derivatives.

2. Background Art

Hydroxylated pyrazine derivatives are, for example, important intermediate products for the production of methoxyalkylpyrazines. Methoxyalkylpyrazines are essential components of aromatic substances [Maga and Sizer, J. Agric., Food Chem., 21, (1973), pages 22 to 30].

So far, only chemical processes for the production of hydroxylated pyrazines have been known, such as, the one described by Karmas and Spoerri, in J. Amer. Chem. Soc., 74, (1952), pages 1580 to 1584, in which, for example, 2-hydroxy-5-methylpyrazine is synthesized starting from methylglyoxal and glycinamide hydrochloride. But this process has the drawback that the product is greatly contaminated.

In addition, studies on the biological catabolism of 2-hydroxypyrazine are described in Matley and Harle, Biochem. Soc. Trans., 4, (1976), pages 492 to 493.

A biotechnological process for the production of regiospecific hydroxylated pyrazine derivatives, starting from substituted pyrazine derivatives with microorganisms, which grow with pyrazine, is not known.

BROAD DESCRIPTION OF THE INVENTION

The main object of the invention is to provide new microorganisms, which regiospecifically hydroxylate pyrazine derivatives of general formula I economically in a biotechnological way and in a simple way, as well as to provide a biotechnological process for the production of hydroxylated pyrazine derivatives. Other objects and advantages of the invention are set out herein or are obvious herefrom to one skilled in the art.

The objects and advantages of the invention are achieved by the microorganisms of the invention and the processes of the invention. The microorganisms of the invention are capable or growing with pyrazine as the sole carbon, nitrogen and energy source and as substrate react pyrazine derivatives of the general formula: ##STR4## wherein R.sub.1 is a hydrogen atom or a halogen atom and R.sub.2 and R.sub.3 are the same or different and are each a hydrogen atom or a C.sub.1 -C.sub.4 alkyl group, but R.sub.1, R.sub.2 and R.sub.3 are not all simultaneously hydrogen, to a hydroxylated pyrazine derivative of the general formula: ##STR5## wherein R.sub.1, R.sub.2 and R.sub.3 have the above-mentioned meaning, and the latter is accumulated in the growth medium. The invention includes the microorganisms of the invention in the form of biologically pure or substantially biologically pure cultures thereof.

A preferred microorganism according to the invention is the microorganism with the designation Agrobacterium sp. deposited in the DSM with the number 6136. The invention includes its descendants and mutants.

The invention includes a process for the production of hydroxylated pyrazine derivatives using one of the invention microorganisms to convert a pyrazine derivative of the general formula: ##STR6## wherein R.sub.1 is a hydrogen atom or a halogen atom and R.sub.2 and R.sub.3 are the same or different and are each a hydrogen atom or a C.sub.1 -C.sub.4 alkyl group, but R.sub.1, R.sub.2 and R.sub.3 are not all simultaneously hydrogen, to a hydroxylated pyrazine derivative of the general formula: ##STR7## wherein R.sub.1 R.sub.2 and R.sub.3 have the above-mentioned meaning, and the concentrated product is isolated.

Preferably the active enzymes of the microorganism are induced with pyrazine. Preferably the reaction is performed with one-time or continuous addition of the substrate, so that the substrate concentration in the culture medium does not exceed 20 percent (w/v). Preferably the reaction is performed at a pH of 4 to 10. Also, preferably, the reaction is performed at temperatures of 0.degree. to 55.degree. C.

The invention also includes the compound 6-Ethyl-2-hydroxypyrazine.

DETAILED DESCRIPTION OF THE INVENTION

According to the invention, all microorganisms are suitable which use pyrazine as the sole carbon, nitrogen and energy sources and are selected according to usual microbiological techniques, e.g., from soil samples, sewage treatment plants, earth, anthills and compost piles. Suitably, all gram-positive and gram-negative microorganisms can be used which catabolize pyrazine and hydroxylate a pyrazine derivative of general formula I as a substrate in a hydroxylated pyrazine derivative of general formula II and accumulate the latter in the growth medium.

A preferred microorganism is Agrobacterium radiobacter DRS 3 with DSM (German Collection of Microorganisms) no. 6136, which is designated below, because of detailed identification data, as microorganism Agrobacterium sp. (DSM no. 6136). This strain was deposited on Sep. 7, 1990 in the German Collection of Microorganisms (DSM) and Zellkulturen [Cell Cultures] GmbH, Mascherodeweg 1b, 3300 Brunswick/FRG.

______________________________________Scientific description of Agrobacterium sp. (DSM no. 6136)______________________________________cell shape rods ADH -width micron 0.6-0.8 LDC -length micron 1.5-3.0 ODC -mobility + ONPG +gram-reaction - VP -lysis by 3% KOH + indole -aminopeptidase (Cerny) + NO.sub.2 from NO.sub.3 +spores - denitrification +oxidase + phenylalanine- -catalase W desaminasegrowth lecithinase -anaerobic - urease +37/41.degree. C. -/- Simmons citrate -pH 5.6 - malonate -Mac-Conkey-Agar + ketolactose -SS-Agar - hydrolysis ofcetrimide agar - starch -2% NaCl - gelatin -pigments - casein -nondiffusing - DNA -diffusing - Tween 80 -fluorescing - Aesculin +pyocyanin - tyrosine -acid from (OF test) catabolismaerobic glucose - alkalization of +anaerobic glucose - litmus milkgas from glucose - growth substance -acid from (ASS) requirementglucose + substrate utilizationfructose + acetate +xylose + adipate -ethanol + caprate -m-erylthritol + citrate -melezitose - glycolate +arabinoze + lactate +saccharose + laevulinat -cellobiose + malate +trehalose +rhamnose +dulcitol -sorbitol +glycerol +malonate -phenyl acetate -suberate -sebacinate -m-tartrate -L-arabinose +fructose +glucose +mannose +maltose +xylose +fucose -mannitol +2-ketogluconate -N-acetylglocosamine +L-asparate +L-serine +L-glutamate +L-histidine -hydroxybutyrate -betaine +methylamine -methanol -ethanol -______________________________________

For the process for the production of hydroxylated pyrazine derivatives a pyrazine derivate of the general formula I as substrate: ##STR8## where R.sub.1 is a hydrogen atom or a halogen atom and R.sub.2 and R.sub.3 are the same or different and are a hydrogen atom or a C.sub.1 -C.sub.4 alkyl group, but R.sub.1, R.sub.2 and R.sub.3 are not all simultaneously hydrogen is converted with the microorganisms set out above to a hudroxylated pyrazine derivative of general formula II: ##STR9## in which R.sub.1, R.sub.2 and R.sub.3 have the above-mentioned meaning, and the concentrated product is isolated. Preferably, hydroxylated pyrazine derivatives are produced by these microorganisms, wherein R.sub.1 means a hydrogen atom or a chlorine atom and R.sub.2 and R.sub.3 are the same or different and are a hydrogen atom, a methyl group or ethyl group, but R.sub.1, R.sub.2 and R.sub.3 are not all simultaneously hydrogen.

Also, a new hydroxylated pyrazine derivative, 6-ethyl-2-hydroxypyrazine, was produced by these microorganisms.

Usually, the microorganisms are cultivated before the actual process (substrate reaction) in a medium containing a growth substrate. The growth substrate pyrazine is used in an amount of 0.001 to 10 percent by weight, relative to the culture medium, preferably in an amount of 0.001 to 5 percent by weight, relative to the culture medium.

The enzymes of the microorganism responsible for hydroxylation are suitably induced by pyrazine. The compound used for induction either can be present during the reaction of the pyrazine derivative (substrate) or the feed of this induction compound can be stopped during the reaction. Preferably, the feed of the compounds used for induction is stopped during the reaction of the pyrazine derivative either by stopping the feed or by centrifuging the cells.

Before adding the substrate, the cells are cultivated up to an optical density of 100 at 650 nm, preferably up to an optical density of 10 to 60 at 650 nm.

As a nutrient medium for the microorganisms, both for the cultivation and for the actual process, the media usual among experts can be used. Preferably, the medium is used whose composition is indicated in Table 1 below.

Usually, the actual process is then performed with dormant cells.

The pyrazine derivative of general formula I can be fed as a substrate one-time or continuously to the cell suspension, preferably so that the substrate concentration in the culture medium does not exceed 20 percent (w/v). In particular, the substrate concentration does not exceed 5 percent (w/v) in the culture medium.

The reaction is suitably performed in a pH range of 4 to 10, preferably 6 to 8. Usually the reaction is performed at a temperature of 0.degree. to 55.degree. C., preferably at 20.degree. to 40.degree. C.

After a usual reaction time of 5 to 100 hours, the hydroxylated pyrazine derivatives can be isolated in the known way, for example, by extraction with a suitable organic solvent. Suitably, the hydroxylated pyrazine derivatives are isolated by extraction with chlorinated organic solvents, such as, chlorinated hydrocarbons or ethyl acetate.

EXAMPLE 1

Isolation of pyrazine-metabolizing microorganisms

Aerobic pyrazine-metabolizing microorganisms were concentrated in the A+N medium (Table 1) with the adding of 0.1 percent (w/v) of pyrazine as the sole carbon and energy source. The general techniques for isolating microorganisms are described, for example, in G. Drews, Mikrobiologisches Praktikum [Microbiological Workshop], 4th ed., Springer Verlag, (1983).

As an inoculum, samples from the earth, sewage treatment plants, compost and anthills were used. The concentrations were cultivated in shaking flasks at 30.degree. C. After inoculating three times in fresh medium, the concentrations of the same medium were streaked by adding 16 g of agar per liter and were incubated at 30.degree. C. After repeated streaking on agar medium, pure cultures were able to be isolated.

TABLE 1______________________________________A + N Medium ConcentrationComposition: (m/l)______________________________________(NH).sub.2 SO.sub.4 2000Na.sub.2 HPO.sub.4 2000KH.sub.2 PO.sub.4 1000NaCl 3000MgCl.sub.2.6H.sub.2 O 400CaCl.sub.2.2H.sub.2 O 14.5FeCl.sub.3.6H.sub.2 O 0.8pyridoxal-hydrochloride 10 .multidot. 10.sup.-3riboflavin 5 .multidot. 10.sup.-3nicotinic acid amide 5 .multidot. 10.sup.-3thiamin hydrochloride 2 .multidot. 10.sup.-3biotin 2 .multidot. 10.sup.-3pantothenic acid 5 .multidot. 10.sup.-3p-aminobenzoate 5 .multidot. 10.sup.-3folic acid 2 .multidot. 10.sup.-3vitamin B12 5 .multidot. 10.sup.-3ZnSO.sub.4.7H.sub.2 O 100 .multidot. 10.sup.-3MnCl.sub.2.4H.sub.2 O 90 .multidot. 10.sup.-3H.sub.3 BO.sub.3 300 .multidot. 10.sup.-3CoCl.sub.2.6H.sub.2 O 200 .multidot. 10.sup.-3CuCl.sub.2.2H.sub.2 O 10 .multidot. 10.sup.-3NiCl.sub.2.6H.sub.2 O 20 .multidot. 10.sup.-3Na.sub.2 MoO.sub.4. 2H.sub.2 O 30 .multidot. 10.sup.-3EDTANa.sub.2.2H.sub.2 O 5 .multidot. 10.sup.-3FeSO.sub.4.7H.sub.2 O 2 .multidot. 10.sup.-3______________________________________ (pH of the solution was adjusted to 7.0)

EXAMPLE 2

Reaction of 3-chloropyrazine to 3-chloro-2-hydroxypyrazine Agrobacterium sp.

Agrobacterium sp. DSM no. 6136 was cultivated in the A+N medium with 0.1 percent (w/v) of pyrazine in a fermenter at pH 7 and a temperature of 30.degree. C. Then, the cells were centrifuged, resuspended again in the A+N medium and adjusted to an optical density of 10 at 650 nm. This cell suspension was added in a shaking flask and mixed with 26 mmol of 3-chloropyrazine per liter (0.3 percent w/v).

After an incubation of 8 hours at 30.degree. C. in a shaking machine, 20 mmol of 3-chloro-2-hydroxypyrazine per liter, corresponding to a yield of 77 percent, was detected.

EXAMPLES 3 to 5

Examples 3 to 5 were performed corresponding to Example 2 and are summarized in Table 2. The position of the hydroxyl group was determined according to the data of MacDonald, J. C., Bishop, G. C., Mazurek, Tetrahedron, 32, (1976), p. 655 ff.

TABLE 2__________________________________________________________________________ Conc. of the heterocycle in % Reaction time YieldEx. Substrate (w/v) in the medium in hours End product in %__________________________________________________________________________3 2-methylpyrazine 0.2 1 2-hydroxy-6- 50 methylpyrazine4 2-ethylpyrazine 0.2 24 6-ethyl-2- 20 hydroxypyrazine5 2,3-dimethyl- 0.2 10 2-hydroxy-5,6- 20 pyrazine dimethylpyrazine__________________________________________________________________________

Claims

1. Process for the production of a hydroxylated pyrazine derivative, characterized in that pyrazine derivative of the formula I as substrate: ##STR10## wherein R.sub.1 is a hydrogen atom or a halogen atom and R.sub.2 and R.sub.3 are the same or different and are a hydrogen atom or a C.sub.1 -C.sub.4 alkyl group, but R.sub.1, R.sub.2 and R.sub.3 are not all simultaneously hydrogen, is converted with the microorganism Agrobacterium sp. DSM 6136, a descendant thereof or a mutant thereof, in a culture medium to a hydroxylated pyrazine derivative of the formula II: ##STR11## wherein R.sub.1, R.sub.2 and R.sub.3 have the above-mentioned meaning, and the hydroxylated pyrazine derivative of the formula II is isolated.

2. Process according to claim 1 wherein the active enzymes of the microorganism are induced with pyrazine.

3. Process according to claim 1 wherein the reaction is performed with one-time or continuous addition or substrate, so that the substrate concentration in the culture medium does not exceed 20 percent (w/v).

4. Process according to claim 3 wherein the reaction is performed at a pH of 4 to 10.

5. Process according to claim 4 wherein the reaction is performed at a temperatures of 0.degree. to 55.degree. C.

6. Process according to claim 1 wherein the reaction is performed at a pH of 4 to 10.

7. Process according to claim 6 wherein the reaction is performed at a temperature of 0.degree. to 55.degree. C.