Method for producing hydrocarbon mixtures

The present invention relates to a microbial method of producing hydrocarbon mixtures.
According to the present invention, there can be produced hydrocarbons, for example, a saturated hydrocarbon such as ethane, propane, n-butane, isobutane, n-pentane and isopentane etc., and an unsaturated hydrocarbon such as ethylene, propylene, 1-butene, isobutene, trans-2-butene and cis-2-butene etc. as a mixture containing at least two kinds of hydrocarbons by means of microorganisms. These hydrocarbons occur in petroleum cracking product gases and natural gases, and have been made available from various stages of their purification and fractionation. However, the terrestrial reserves of these materials are limited.
Regarding the formation of ethane by microorganisms, there are reports in relation to a culture employing bovine feces or digested sludge as well as microorganisms grown on the surface of an agar medium [J. B. Davis and R. M. Squires; Science, 119, 381-382 (1954)], settled sludge in San Francisco Bay [R. S. Oremland; Appl. Environment. Microbiol., 42, 122-129 (1981)], and mushrooms [E. M. Turner; J. Gen. Microbiol.; 91, 167-176 (1975)]. However, these reports are no more than exploratory in nature, and almost no definite mention has been made of the type of ethane-producing microorganisms involved.
Regarding the production of ethylene by microorganisms, there have been several reports, for example, an exploratory investigation of 228 fungi species [L, Ilag, and Roy W/.Curtis; Science, 159, 1357-1358 (1968)], studies on microorganisms of the genus Mucor and on Aspergillus clavatus [J. M. Lynch, and S. H. Harper; J. Gen. Microbiol. 80, 187-195 (1974)], exploratory studies on soil bacteria [S. B. Primrose; J. Gen. Microbiol. 97, 343-346 (1976)], studies on Escherichia coli and Pseudomanas species [S. B. Primrose; J. Gen. Microbiol. 95, 159-165 (1976); S. B. Primrose and Dilworth; J. Gen. Microbiol. H. T. Freebairn and I. W. Budenhagen; Nature, 202, 313-314 (1964)], a study on Saccharomyces cerevisiae [K. C. Thomas and M. Spencer; Can. J. Microbiol. 23, 1669-1674)], a study on mushrooms [E. M. Turner; j. Gen. Microbiol. 91, 167-176 (1975)], and a comprehensive review of such literatures [M. Lieberman; Ann. Rev. Plant Physiol. 30, 533-591 (1979)]. However, the majority of these reports are no more than exploratory in nature, and no definite mention has been made of the types of ethylene-producing microorganisms involved.
Regarding the production of propane, propylene, butane and butene by microorganisms, there is a report that methane as well as trace amount of ethane, propane, butane (chemical structures not established) and butene (chemical structures not established) were detected when a mixture of microorganisms in fermented bovine feces (strains not isolated or identified) was anaerobically cultivated [K. G. Gollakota and B. Jayalakshmi; Biochemical and Biophysical Research Communications, 110, 32-35 (1983)], a report that small amounts of ethane, ethylene, propane, propylene, and n-butane were formed by mushrooms [E. M. turner, M. Wright, T. Ward, and D. J. Osborne; J. Gen. Microbiol., 91, 167-176 (1975)], and a report that small amounts of ethane, ethylene, propane and propylene were detected in anaerobic methane fermentation with a mixture of microorganisms contained in bovine feces (strains not isolated or identified) and on agar plate culture of Penicillium digitatum ATCC 10030 [J. B. Davis and R. M. Squires; Science, 119, 381-382 (1954)]. However, according to these reports, the yields of hydrocarbons are invariably small, the processes are either anaerobic culture or solid surface culture, and either the microorganisms involved are indefinite or the chemical structure of product hydrocarbons are not identified.
In any of the above prior reports, the yield of hydrocarbons of not less than C.sub.2 is small and anaerobic culture or solid culture employed in the reports is not suitable for industrial large scale production.
Furthermore, because there is no clear description of the species of the microorganisms, the reports have insufficient reproduceability.
The present inventors have conducted research to find a method for producing mixtures of hydrocarbons having at least carbon number C.sub.2 by means of microorganisms with sufficient reproduceability and conceived the present invention.
The present invention is directed to a method for producing a hydrocarbon mixture which comprises cultivating aerobically a strain of microorganism capable of producing simultaneously at least two kinds of saturated or unsaturated C.sub.2 -C.sub.5 hydrocarbons in a water-containing medium to thereby cause the formation of said hydrocarbons in the liquid phase and/or the gaseous ambience of the medium, and recovering said hydrocarbons as a mixture from said liquid phase and/or gaseous ambience.
As the microorganisms which can be employed in accordance with the present invention, there may be exemplified fungi belonging to the genera Saprolegnia, Phytophthora, Mucor, Rhizopus, Absidia, Mortierella, Cunninghamella, Taphrina, Monascus, Nectria, Gibberella, Chaetomium, Neurospora, Geotrichum, Monilia, Trichoderma, Aspergillus, Penicillium, Paecilomyces, Gliocladium, Sporotrichum, Microsporum, Trichophyton, Cladosporium, Syncephalastrum, Phycomyces and Eupenicillium, inclusive of mutant strains thereof; yeast belonging to the genera Endomyces, Shizosaccharomyces, Pichia, Hansenula, Debaryomyces, Saccharomycopsis, Rhodotorula, Sporobolomyces, Cryptococcus, Candida, and Brettanomyces, inclusive of mutant strains thereof; bacteria belonging to the genera Bacillus, Brevibacterium, Corynebacterium, Flavobacterium, Klebsiella, Micrococcus, Mycoplana, Paracoccus, Proteus, Pseudomanas, Salmonella, Serratia, and Acetobacter, inclusive of mutant strains thereof; and actinomycetes belonging to the genera Streptomyces, Actinomyces and Intrasporangium, inclusive of mutant strains thereof.
Of these microorganisms, the following strains are representative of the organisms capable of producing C.sub.2 -C.sub.5 hydrocarbons in substantial quantities.
FUNGI: Saprolegnia parasitica IFO-8978, Phytophtora capsici IFO-8386, Mucor hiemalis f. corticolus IFO-9401, Mucor hiemalis f. luteus IFO-9411, Rhizopus delemar IFO-4801, Rhizopus formosaensis IFO-4732, Rhizopus javanicus IFO-5441, Rhizopus japonicus IFO-4758, IFO-4780, IFO-5318, IFO-5319, Rhizopus niveus IFO-4759, Rhizopus oryzae IFO-4705, Rhizopus stolonifer IFO-5411, Absidia cylindrospora IFO-4000, Mortierella isabellina IFO-8183, Mortierella elongata IFO-8570, Cunninghamella elegans IFO-4441, Taphrina Caerulescens IFO-9242, Taphrina wiesneri IFO-7776, Monascus anka IFO-6540, Monascus albidus IFO-4489, Nectria flammea IFO-9628, Gibberella fujikuroi IFO-5268, Chaetomium globosum IFO-6347, Neurospora crassa IFO-6067, Geotrichum candidum IFO-4597, Monilia geophila IFO-5425, Trichoderma viride IFO-4847, Aspergillus clavatus IFO-4045, IFO-8606, Penicillium digitatum IFO-7758, Paecilomyces carneus IFO-8292, Paecilomyces elegans IFO-6619, Gliocladium aureum IFO-9055, Gliocladium deliquescens IFO-7062, Gliocladium roseum IFO-7063, Sporotrichum aureum IFO-9381, Microsporum gypseum IFO-5948, Microsporum cookei IFO-7862, Trichophyton mentagrophytes IFO-5466, Cladosporium resinae IFO-8588, Syncephalastrum racemosum IFO-4816, Phycomyces nitens IFO-9422, Eupenicillium lapidosum IFO-6100, IFO-9700, IFO-9701 etc.,
YEASTS: Endomyces geotrichum IFO-9541, Endomyces reessii IFO-1112, Endomyces magnusii IFO-0110, Schizosaccharomyces octosporus IFO-0353, Schizosaccharomyces pombe IFO-0340, Saccharomyces bailii IFO-0468, Saccharomyces sp. IFO-2363, IFO-2266, IFO-2112, IFO-2115, IFO-2242, IFO-2343, IFO-2344, IFO-2345, IFO-2346, IFO-2347 and IFO-2376, Pichia membranaefaciens IFO-0181, Pichia acaciae IFO-1681, Pichia besseyi IFO-1707, Pichia farinosa IFO-0459, Hansenula capsulata IFO-0721, Debaryomyces nepalensis IFO-1428, Saccharomycopsis lipolytica IFO-1658, Saccharomycopsis crataegensis IFO-1708, Saccharomycopsis fibuligera IFO-1745, Rhodotorula glutinis IFO-0697, IFO-1501, Rhodotorula minuta IFO-0387, IFO-1435, Rhodotorula minuta var. texensis IFO-0879, IFO-0932, IFO-1006 and IFO-1102, Rhodotorula marina IFO-1421, Sporobolomyces salmonicolor IFO-0374, Sporobolomyces pararoseus IFO-0376, Cryptococcus albidus IFO-0378, IFO-0434, IFO-0939, IFO-1044 and IFO- 1320, Cryptococcus flavus IFO-0407, Cryptococcus laurentii var. flavescens IFO-0384, Cryptococcus luteolus IFO-0411, Candida albicans IFO-1060, Candida butyri IFO-1571, Cnadida guilliermondii IFO-0454, Brttanomyces bruxellensis IFO-0628, Brttanomyces intermedius IFO-1587 etc.,
BACTERIA: Bacillus circulans IFO-3329, Bacillus coagulans IFO-3557, Bacillus pumilus IFO-3813, Bacillus subtilis IFO-3023, Brevibacterium ammoniagenes ATCC-6872, Brevibacterium lactofermentum ATCC-13655, Corynebacterium aquaticum IFO-12154, Corynebacterium fascians IFO-12077, Corynebacterium paurometabolum IFO-12160, Flavobacterium capsulatum IFO-12533, Klebsiella pneumoniae IFO-3317, Micrococcus luteus IFO-3064, Mycrococcus roseus IFO-3764, Mycroplana dimorpha IFO-13291, Paracoccus denitrificans IFO-12422, Proteus mirabilis IFO-3849, Pseudomonas aeruginosa IFO-3445, Pseudomonas putida IFO-3738, Pseudomonas stutzeri IFO-3773, Salmonella typhimurium IFO-12529, Serratia marcescens IFO-12648, Acetobacter aceti IFO-3281 etc.,
ACTINOMYCETES: streptomyces flaveolus IFO-3408, Streptomyces fradiae IFO-3360, Streptomyces griseus IFO-3102, Streptomyces lavendulae IFO-3145, IFO-13709, Streptomyces viridochromogenus IFO-3113, Streptomyces regensis IFO-13448, Actinomyces vulgaris IFO-13109, Intrasporangium calvum IFO-12989 etc.
In addition to these strains, many strains of the genera mentioned above have been found to produce the hydrocarbon mixtures.
The culture of the strains in the present invention may be carried out employing a liquid or solid medium and, if desired, the liquid medium may be contacted with the strains fixed in a suitable carrier in the form of bioreactor.
The culture medium used for cultivation of such microorganisms may be a conventional medium for culture of fungi, yeasts, bacteria or actinomycetes, which contains carbon sources, nitrogen sources, inorganic salts, and other nutrients.
Thus, various carbohydrates such as glucose, sucrose, maltose, starch, xylose, sorbitol, etc., alcohols such as glycerol, ethanol, etc., organic acids such as acetic acid and other fatty acids, and crude materials containing them may be used as carbon sources. The main raw materials which are particularly useful for the purposes of present invention are reproducible biomass which are either naturally occurring or available artificially as by-products, such as materials from agricultural, forestal, fisheries and live-stock industry activities, industrial waste water, various industrial wastes, and active sludges from the biological treatment of public sewage, plant effluents, or excreta, etc. Though it depends on the strains of organisms used, these main materials are preliminarily dissolved, decomposed or otherwise pretreated, if necessary. As nitrogen sources, there can be advantageously used ammonia gas, aqueous ammonia and ammonium salts.
When a biomass is used as the main raw material, the addition of such nitrogen sources may not be essential. As inorganic salts, phosphates, potassium salts, magnesium salts, sodium salts, calcium salts, etc. can be routinely employed, although these may be dispensed with when a biomass is employed.
The addition of vitamins and amino acids or of materials containing them such as yeast extract, peptone, meat extract, corn steep liquor, etc. may contribute to accelerated growth of the strain used or improved yields of desired hydrocarbon mixtures.
In particular, the addition of some kinds of amino acids and benzene compounds increase the yield of isobutane, some kinds of amino acids increase the yield of ethylene and some kinds of amino acids increase the yield of saturated hydrocarbons. The facts are explained concretely by the following test examples:
Employing culture media and conditions for yeasts and fungi indicated in Tables 1 and 2, microorganisms belonging to genera Rhodotorula, Cryprococcus and Rhizopus were cultivated and the formation rate of hydrocarbons was determined by the method below-mentioned. The results are shown in Tables 3 and 4.
TABLE 1______________________________________Composition of media for each type of strain(Numerals in the Table show g/l) Type of strain Actino-Medium Fungi Yeasts Bacteria mycetesingre- Kind of mediadients NB C.D.* NB C.D.* NB NB______________________________________Glucose 20 20 20 20 20 20Polypeptone 5 -- 5 -- 5 5Meat extract 3 -- 3 -- 3 --Ammonium -- 3.0 -- 5.0 -- 2sulfatePotassium -- -- -- 1.0 -- --primaryphosphatePotassium -- 1.0 -- -- -- --secondaryphosphateMagnesium -- 0.5 -- 0.5 -- --sulfate(7H.sub.2 O)Ferrous -- 0.01 -- -- -- --sulfate(7H.sub.2 O)Zinc sulfate -- 0.22 -- -- -- --(7H.sub.2 O)Calcium -- 0.1 -- 0.1 -- --chloride(2H.sub.2 O)Calcium -- -- -- 3.0 -- --carbonatePotassium -- 0.25 -- -- -- --chlorideSodium 2 0.1 2 0.1 2 2chlorideSolution of -- -- -- 10 ml -- --inorganicsaltsMixed -- -- -- 10 ml -- --vitaminsolutionInitial pH 6.0 6.0 6.0 5.0- 7.0 7.0 6.0______________________________________ *Chemically defined media
TABLE 2__________________________________________________________________________Culture conditions for each type of strainCulture Type of strainconditions Fungi Yeasts Bacteria Actinomycetes__________________________________________________________________________Provisional Temperature (.degree.C.) 25 -- -- --culture Period (day) 2 -- -- --Main Liquid quantity 50/300 50/300 50/300 50/300culture [ml/ml (flask)] (Erlenmeyer) (Erlenmeyer) (Sakaguchi) (Erlenmeyer) Temperature (.degree.C.) 25 25 30 25 Shaking Rotary Rotary Recipro.* Rotary conditions (dia. 7 cm, (dia. 7 cm (amp.** 7 cm, (dia. 7 cm, 180 rpm) 180 rpm) 120 cpm) 180 rpm) Period (day) 4-7 2-3 1-2 3-7Sealed Liquid quantity 1-2/34 1-2/34 1-2/34 1-2/34culture [ml/ml (tube)] Temperature (.degree.C.) 25 25 30 25 Shaking Recipro. Recipro. Recipro. Recipro. conditions (amp. 3.5 cm, (amp. 3.5 cm, (amp. 3.5 cm (amp. 3.5 cm, 130 cpm) 130 cpm) 130 cpm) 130 cpm) Period (hour) 5-10 5-10 5-10 5-10__________________________________________________________________________ *Reciprocatory **amplitude
TABLE 3__________________________________________________________________________Effects of additives on mixed gas formation (1)* C.sub.4 C.sub.5 C.sub.2 C.sub.3 iso- 1- iso-Strain Kind of Additives eth- ethyl- pro- propyl- bu- n- bu- iso- trans-2 cis-2- pen- n-name medium (1) (2) ane ene pane ene tane butane tene butene butene butene tane pentane__________________________________________________________________________Rhodo- NB -- -- 0.2 0.2 0.1 4.3 0.1 0.7torula C.D.** -- --minuta C.D. Leu -- trace 0.1 3.0IFO 1102 C.D. Leu Trp 0.1 5.5 C.D. Leu Trp 0.1 15.5 C.D. Leu Phe trace 0.1 58.0 C.D. Leu Benzoic 0.1 25.0 acid C.D. Leu L-Phenyl- 0.1 20.0 C.D. Leu glycine L-Phenyl- 0.1 32.0 piruvic acid C.D. Ile -- 0.1 0.6 0.1 C.D. Ile Phe 0.1 1.7 0.2 C.D. Met -- 6.0 0.3 0.1 C.D. Cys -- trace 0.1 trace 0.1 0.2Rhodo- NB -- -- 0.1 0.2 0.1 2.7 0.1torula C.D. -- --marina C.D. Leu -- 0.3IFO 1421Crypto- NB -- -- 0.2 6.5 0.1 0.1 0.1 0.1coccus C.D. -- --albidus C.D. Leu -- 0.1 0.1IFO 0378Crypto- NB -- -- 0.2 0.1 4.4coccus C.D. -- --albidus C.D. Leu -- 2.5 0.2IFO 1044__________________________________________________________________________ *Numerals in the Table show gas formation rate (nl/ml. hr), **Chemically defined media
TABLE 4__________________________________________________________________________Effects of additives on mixed gas formation (2)* C.sub.2 C.sub.3 C.sub.4 C.sub.5Strain Kind of Additives eth- ethyl- pro- propyl- iso- n- 1- iso- trans-2 cis-2- iso- n-name medium (1) (2) ane ene pane ene butane butane butene butene butene butene pentane pentane__________________________________________________________________________Rhizopus NB -- -- trace trace tracechinens- C.D.** -- --is C.D.** Cys -- trace 0.2 trace 0.1IFO 4768Rhizopus NB -- -- trace 0.6 tracedelmar C.D. -- --IFO 4697 -- Cys " trace 0.2 0.1 trace 0.1 0.2Rhizopus NB -- -- 0.1 0.1 0.3 0.1 0.2 0.1 0.6 1.5formosa- C.D. -- --ensis C.D. Cys -- 0.1 0.1 trace 0.1 0.1IFO 4732Rhizopus NB -- -- 0.1 0.6 0.7 0.1 0.3 0.2 0.7 1.7japon- C.D. -- -- trace 0.1 0.2 trace trace 0.1 0.4icus C.D. Cys -- trace 0.1 2.5 0.1 0.6 2.8 5.8IFO 4758Rhizopus NB -- -- 0.1 0.2 0.1 0.1 0.2 0.2 0.4niveus C.D. -- --IFO 4759 C.D. Cys -- trace 0.2 0.1 0.1 0.2 0.5Rhizopus NB -- --oligo- C.D. -- --sporus C.D. Cys -- trace 0.2 0.1 0.1IFO 8631__________________________________________________________________________ *Numerals in the Table show gas formation rate (nl/ml. hr), **Chemically defined media
The test example of Table 3 shows the following facts;
(1) The addition of 1 g/l of L-leucine (abbreviated as Leu in the Table) increases the formation rate of isobutene, and further addition of an aromatic amino acid such as L-tryptophane (Trp in the Table), L-tyrosine (Tyr in the Table), L-phenylalanine (Phe in the Table ), etc. increases more remarkably the formation rate of isobutene. The addition of a benzene compound such as benzoic acid, L-phenylglycine, L-phenylpyruvic acid, etc. in place of the above aromatic amino acid increases the formation rate of isobutene similarly to the aromatic amino acid.
(2) The addition of 1 g/l of L-isoleucine (Ile in the Table) increases the formation rate of trans-2-butene and cis-2-butene and further addition of 1 g/l of L-phenylalanine remarkably increases the formation rate of these hydrocarbons.
(3) The addition of 1 g/l of L-methionine (Met in the Table) increases the formation rate of ethylene.
(4) The addition of 1 g/l of L-cysteine (Cys in the Table) increases the formation rate of saturated hydrocarbons such as ethane, propane, n-butane, isobutane, n-pentane, etc. The same facts are shown by the test examples in Table 4.
Accordingly, it is shown that hydrocarbons can be converted or fermentatively converted to an ingredient of the hydrocarbons by the addition of an amino acid or other compound.
In the NB medium in Tables 3 and 4, there are contained some amounts of the above-mentioned effective additives originated from the natural ingredients of the medium such as peptone, meat extract, yeast extract etc. However, depending on the purpose, it will be necessary to supply these effective additives which may be insufficient in the medium by the addition of some other cheap natural products. As already shown in Table 2, the cultivation of the mixed hydrocarbon-producing microorganisms is carried out under aerobic conditions, for example, by aerated stirring or stationary culture, with the pH and temperature being controlled at pH 2 to 9, preferably 3.0 to 8.0, and 20.degree. to 45.degree. C., preferably 25.degree. to 30.degree. C., respectively. Thus, for each strain, he optimum pH and temperature are selected. As the cultivation is conducted for 1 to 7 days, a significant amount of mixed hydrocarbons is produced.
The content of each hydrocarbon in the mixed gases produced is assayed as follows;
A x=1 to 5 ml portion of the broth in the course of cultivation or at the end of cultivation is taken into a test tube with a total volume of V=10 to 50 ml and after closure with a sterile rubber stopper, the broth is incubated on a reciprocating shaker at 20.degree. to 45.degree. C. for t=1 to 7 hours. Since the respiration rate varies with different strains, it is preferable to vary the parameters V, x and t so as to prevent oxygen deficiency during shaking.
After the reciprocal shaking, y=0.1 to 2 ml of the gas is taken from the top plenum of the tube using a gas syringe and subjected to the conventional FID gas chromatography using nitrogen gas as the carrier gas, (The optimum column temperature is used according to the type of the column packing. The injection temperature is also varied accordingly.)
Preferred examples of the column packing material are Porapak Q, X-28, Bond-GC/PIC, and activated alumina, and a packing material is selected according to the type of hydrocarbon. Separately, standards of various hydrocarbons are prepared and subjected to gas chromatography under the above conditions by the same procedure to measure the retention times of the hydrocarbons on the recording paper. The calibration curves of hydrocarbons are also constructed using the standards.
Referring to the gas chromatogram of the above test gas, the retention times of the peaks on the recording paper are measured and compared with, those of said standards to identify the corresponding hydrocarbons. Then, the area of the fraction corresponding to each hydrocarbon is measured and the amount Ei.sup.n1 of the hydrocarbon is calculated by reference to the calibration curve of the standard gas.
The rate of production pi.sup.n1 /ml.hr of each hydrocarbon in the test gas can be calculated by means of the following equation. The subscript i means that it varies depending on the kind of hydrocarbon in the test gas. ##EQU1##
The present invention has one of its characteristics in that hydrocarbons formed in the form of gaseous material can be collected, concentrated and recovered as mixed gases. For example, the mixed hydrocarbons can be obtained by absorbing the mixture onto an adsorbent having a wide range of adsorbability suitable for the purpose to remove unadsorbable impurity gases and desorbing the mixture; or by separating impurity gases by liquefaction of the gaseous material under low temperature. Or the mixed hydrocarbons can be obtained by contacting the gaseous material with aqueous strong alkali such as caustic soda to remove the carbon dioxide contained in the material as a by-product, followed by adsorption unto and desorption from the above-mentioned adsorbent.
The present invention is further characterized in that readily-available, reproducible biomass, particularly the waste resources from agricultural, forestal, fisheries and livestock industry, industrial wastes, sludges available from the biological treatment of public sewage, factory waste, or excreta can be advantageously utilized as main raw materials and that practicing the present invention is tantamount to carrying out a microbiological disposal of wastes and effluents with regard to the above-mentioned biomass employed as the main raw materials. Furthermore, the method of present invention is advantageous over the conventional methods in that the main raw material is a reproducible biomass which will never be depleted, the production is accomplished under mild conditions such as relatively low temperature and low pressure because of its being a microbiological process, and the impurity gases are mostly carbon dioxide. A result, it is easy to collect, concentrate and recover the product of hydrocarbon mixtures.
The following examples are further illustrative of present invention.

EXAMPLE 1
Fifty ml of the NB medium in Table 1 was added to a conical flask of 300 ml capacity and after steam sterilization by autoclaving at 120.degree. C. for 15 minutes, a loopful of one of precultured strains in the case of fungi or of strains from slant culture in the other cases was inoculated to the flask which was incubated in accordance with the culture conditions indicated in Table 2.
The strains employed in the cultivation are shown in Table 5.
A 1 to 2 ml of the culture thus prepared was taken into a sterile test tube of 34 ml capacity and after hermetic closure, subjected to seal-cultivation under conditions described in Table 2 to form and accumulate mixed hydrocarbons. After the completion of the seal-cultivation, a 1 ml portion of the plenum gas was taken from each test tube with a gas syringe and subjected to gas chromatography and the formation rate of each ingredient in the gas was calculated as set forth in the foregoing. The results are shown in Table 5.
TABLE 5 Formation of hydrocarbon mixtures by each strain [Numerals in the Table show formation rates (nl/ml/hour)] C.sub.4 C.sub.5 C.sub.1 C.sub.2 C.sub.3 iso- n- 1- iso- trans-2- cis-2- iso- n- Genera Species Strains methane ethane ethylene acetylene propane propylene butane butane butene b utene butene butene pentane pentane remarks Fungi (1) Saprolegnia parasitica IFO 0.4 4.5 8978 Phytophthora capsici 8386 7.1 0.1 0.1 0.2 Mucor hiemalis 9401 1.9 0.1 0.1 f. corticolus Mucor hiemalis 9411 1.1 0.1 f. luteus Rhizopus delemar 4801 0.1 0.2 0.1 0.1 0.1 0.3 0.3 Rhizopus f ormosaensis 4732 0.1 0.1 0.3 0.1 0.2 0.1 0.6 1.5 Rhizopus javanicus 5441 0.7 0.1 0.2 0.1 0.2 0.5 0.1 0.1 Rhizopus japonicus 4758 0.1 0.6 0.7 0.1 0.3 0.2 0.7 1.7 Rhizopus japonicus 4780 0.2 0.1 0.1 0.3 0.2 0.3 Rhizopus japonicus 5318 0.2 0.1 0.1 0.2 0.4 0.4 Rhizopus japonicus 5319 0.1 0.1 0.1 0.1 0.2 0.1 0.2 Rhizopus niveus 4759 0.1 0.2 0.1 0.1 0.2 0.2 0.4 Rhizopus oryzae 4705 0.1 0.1 0.1 0.2 0.2 0.2 Rhizopus stolonifer 5411 0.2 0.1 0.1 0.4 0.4 Absidia cylindrospora 4000 0.9 7.1 0.8 Mortierella isabellina 8183 4.5 0.1 0.1 0.2 Mortierella eleongata 8570 0.6 0.1 0.1 0.1 Cunninghamella elegans 4441 7.1 0.6 0.1 Taphrina caerulescens 9242 0.3 0.6 Taphrina wiesneri 7776 1.1 11.6 0.2 0.2 0.5 0.5 Monascus anka 6540 0.5 0.4 Monascus albidus 4489 1.1 24.9 0.4 Nectria flammea 9628 2.6 44.1 1.2 0.6 Giberella fujikuroi 5268 7.1 0.1 0.1 0.2 Chaetomium globosum 6347 0.1 0.1 0.2 Neurospora c rassa 6067 0.3 0.4 Geotrichum candidum 4597 7.1 0.1 0.1 Monilia g eophila 5425 0.7 31.2 0.8 Trichoderma viride 4847 1.2 16,0 1.0 0.1 0.1 Aspergillus clavatus 4045 0.7 0.1 Aspergillus clavatus 8606 22.4 0.6 Fungi (2) Penicillium digitatum IFO 1.0 0.1 0.1 0.1 7758 Penicillium digitatum 9372 trace 1394 Paecilomyces careus 8292 1.1 0.2 0.2 0.4 Paecilomyces elegans 6619 16.0 1.0 0.1 0.1 Gliocladium aureum 9055 2.1 0.9 0.1 0.7 0.1 0.1 Gliocladium d iligenscens 7062 0.1 9.8 0.1 0.1 0.6 Gliocladium roseum 7063 8.9 3.0 0.3 Sporotrichum aureum 9381 2.4 0.5 0.5 0.5 Microsporum gypseum 5948 7.1 0.2 0.1 0.1 0.2 Microsporum cookei 7862 1.4 0.1 Tricophyton mentagrophytes 5466 1.9 29.4 0.1 Cladosporium resinae 8588 11.6 0.2 0.1 0.5 Syncephalastrum racemosum 4816 1.3 38.2 0.1 0.2 0.1 0.1 0.2 Phycomyces nitens 9422 0.1 0.1 0.3 Eupenicill ium lapidosum 6100 0.1 0.1 0.1 0.1 Eupenicillium lapidosum 9700 0.1 0.1 0.1 0.1 Eupenicillium lapidosum 9701 0.1 0.1 0.1 0.1 Yeasts (1) Endomyces geotrichum IFO 0.2 1.0 0.1 0.2 9541 Endomyces reessii 1112 0.1 1.0 0.1 0.6 Endomyces magnusii 0110 0.3 0.3 0.5 0.1 0.1 Schizosaccharomyces octosporus 0353 12.1 204.4 0.1 1.2 0.1 0.5 Schizosaccharomyces pombe 0340 11.4 0.1 0.1 S accharoyces bailii 0468 0.6 0.2 0.1 Pichia membranaefaciens 0181 0.2 0.7 Pichia acaciae 1681 0.2 0.7 0.1 0.1 0.1 Pichia besseyi 1707 0.9 0.1 0.1 0.1 0.1 Pichia farinosa 0459 0.1 0.9 0.1 0.2 0.1 0.1 Hansenula capsulata 0721 0.2 0.1 0.1 Debaryomyces nepalensis 1428 0.4 0.2 0.1 0.1 Saccaromycopsis lipolytica 1658 0.1 0.6 0.5 0.1 Saccaromycopsis crataegensis 1708 0.3 0.4 0.1 0.1 0.1 0.1 Saccaromycopsis fiburigera 1745 1.1 0.2 0.1 0.1 Rhodotorula glutinis 0697 0.2 3.6 0.7 0.1 0.3 Rhodotorula glutinis 1501 0.7 0.1 Rhodotorula minuta 0387 0.2 0.2 1.7 Rhodotorula minuta 1435 0.1 1.0 Rhodotorula minuta var. 0879 0.1 0.9 texensis Rhodotorula minuta var. 0932 0.2 0.2 1.6 0.1 texensis Rhodotorul a minuta var. 1006 0.1 0.1 1.1 texensis Rhodotorula minuta var. 1102 0.2 0.2 0.1 4.3 0.1 0.7 texensis Rhodotorula marina 1421 0.1 0.2 0.1 2.7 0.1 Sporobolomyces salmonicolor 0374 0.9 0.4 0.1 0.1 0.1 0.2 Sporobolomyces pararoseus 0376 0.5 12.2 0.3 0.1 0.3 Candida albicans 1060 1.4 5.3 0.3 0.2 Candida butyri 1571 1.2 0.1 0.2 Candida guilliermodii 0454 0.2 0.5 0.1 Brettanomyces bruxellensis 0628 15.8 10.8 0.2 0.1 Brettanomyces intermedius 1587 0.6 0.1 0.1 Yeasts (2) Cryptococcus albidus IFO 0.2 6.5 0.1 0.1 0.1 0.1 0378 Cryptococcus albidus 0434 0.1 0.6 0.3 0.3 0.3 Cryptococcus albidus 0939 0.3 4.2 0.1 0.1 0.1 Cryptococcus albidus 1044 0.2 0.1 4.4 Cryptococcus albidus 1320 0.1 1.3 1.4 0.4 0.4 1.9 0.3 Cryptococcus flavus 0407 1.0 1.0 0.1 0.8 0.1 0.2 0.7 Cryptococcus laurentii 0384 3.1 54.6 0.9 0.1 0.1 0.1 var. flavescens Cryptococcus luteolus 0441 0.1 0.6 0.3 0.2 0.1 0.2 0.1 Saccharomyces sp. 2363 0.3 0.2 0.2 Saccharomyces sp. 2226 0.1 0.5 Saccharomyc es sp. 2112 0.5 0.1 Saccharomyces sp. 2115 0.2 0.5 0.1 0.1 0.1 Saccharomyces sp. 2342 1.3 0.1 Saccharomyces sp. 2343 0.1 0.1 Saccharomyces sp. 2344 0.1 0.2 0.1 0.1 0.2 Saccharomyces sp. 2345 0.4 0.1 Saccharomyces sp. 2346 0.4 1.1 0.1 Saccharomyces sp. 2347 0.2 0.1 0.1 Saccharomyces sp. 2376 0.1 0.2 Bacteria Acetobacter aceti IFO 0.1 0.2 0.2 3281 Bacillus circulans 3329 0.4 0.1 0.1 0.1 0.2 0.2 Bacillus coagulans 3557 0.3 0.2 0.2 Bacillus pumilus 3813 0.1 0.1 0.4 Bacillus subtilis 3023 0.2 0.1 0.1 0.1 0.1 0.2 Brevibacterium ammoniagenes ATCC 0.9 8.6 0.2 0.1 0.2 6872 Brevibacterium lactofermentum ATCC 0.6 0.2 0.2 0.1 0.2 0.1 0.2 13655 Corynebacterium aquaticum IFO 0.1 1.8 0.3 0.2 0.2 12154 Corynebacterium fascians 12077 1.5 0.1 0.7 Corynebacterium paurometabolum 12160 3.0 0.7 0.2 0.2 Flovobacterium capsulatum 12533 1.0 2.0 Klebsiella pneumoniae 3317 0.7 0.2 Micrococcus luteus 3064 2.3 0.2 0.1 0.1 Micrococcus roseus 3764 0.1 0.1 Mycoplana dimorpha 13291 1.5 9.0 Paracoccus denitrificans 12442 0.1 0.2 0.2 0.1 Proteus mirabilis 3849 0.2 2.2 0.3 0.1 0.1 0.2 0.2 Pseudomonas aeruginosa 3445 0.1 0.8 0.4 0.1 0.1 0.1 0.1 Pseudomonas putida 3738 3.1 0.5 0.2 0.1 0.2 Pseudomona s stutzeri 3773 0.1 2.3 0.2 Salmonella typhimurim 12529 2.3 0.2 0.1 0.1 Serratia marcescens 12648 0.4 0.1 0.1 0.1 0.2 Actinomycetes Streptomyces flaveolus IFO 0.4 0.2 3408 Streptomyces fradiae 3360 0.1 0.2 0.2 0.3 Streptomyces griseus 3102 0.2 0.3 Streptomyces lavendulae 3145 0.5 0.2 1.2 0.1 0.2 0.2 0.2 Streptomyces lavendulae 13709 0.2 1.2 0.1 0.2 0.4 Streptomyces viridochromogenes 3113 0.2 0.2 0.3 0.1 Streptomyces regensis 13448 0.2 0.1 0.1 Actinomyces vulgaris 13107 0.3 0.2 0.1 Intrasporangium calvum 12989 0.3 0.2 0.1
EXAMPLE 2
The two strains of Rhodotorula minuta var. texensis IFO-1102 and Rhizopus japanicus IFO-4758 were cultivated on the slants of agar (1.5 w/v %)-NB medium indicated in Table 1, and sterile distilled water was aseptically added to the cultures to give cell suspensions.
Five hundred ml of the media for yeasts and the chemically defined media for fungi indicated in Table 1 was added to 3 liter capacity Sakaguchi flask, respectively and after steam sterilization by autoclaving at 120.degree. C. for 15 minutes and cooling, the above cell suspensions were inoculated to each flask. The preculture of the yeast was conducted at 25.degree. C. for 2 days and that of the fungus at 25.degree. C. for 3 days, using a reciprocating shaker.
Jar fermentors of 14 liter capacity were charged with 10 liters of the NB media for yeasts or the chemically defined media (provided that 1 g/l of L-cystine was added) for fungi indicated in Table 1, respectively. After steam sterilization under pressure at 120.degree. C. for 20 minutes and cooling, the above pre-cultures were inoculated to each jar fermentor. The fermentation of the yeast was conducted at 25.degree. C. for 3 days and that of the fungus at 25.degree. C. for 4 days, under aeration with sterile air at 0.1.sup.VVM and at 200 to 300 r.p.m. (the r.p.m. was adjusted according to the degree of foaming).
Throughout the fermentation period, the gases discharged from each jar fermentor were independently passed through a 10% NaOH vessel, a washing vessel and a moisture separating vessel; followed by serial passage through Jeoram.RTM. A-3 and Jeoram.RTM. F-9 (geolite products of Toyo Soda Manufacturing Co., Ltd., Japan) columns and the hydrocarbons adsorbed on Jeoram F-9 were desorbed and recovered under vaccum saction.
The amounts of hydrocarbon mixtures thus obtained were 0.1 mg of ethylene, 0.1 mg of propane, 0.1 mg of n-butane, 3.8 mg of isobutene, 0.1 mg of isopentane and 0.1 mg of n-pentane with Rhodotorula minuta; and 2.3 mg of propane, 0.7 mg of n-butane, 4.3 mg of isopentane and 8.8 mg of n-pentane with Rhizopus japonicus.

Number	Date	Country
133597	Feb 1985	EPX
198983	Nov 1984	JPX

Method for producing hydrocarbon mixtures

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