WO2012077801A1 - ボトリオコッカス・ブラウニー(Botryococcus braunii)属の新規株 - Google Patents
ボトリオコッカス・ブラウニー(Botryococcus braunii)属の新規株 Download PDFInfo
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- WO2012077801A1 WO2012077801A1 PCT/JP2011/078606 JP2011078606W WO2012077801A1 WO 2012077801 A1 WO2012077801 A1 WO 2012077801A1 JP 2011078606 W JP2011078606 W JP 2011078606W WO 2012077801 A1 WO2012077801 A1 WO 2012077801A1
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P5/00—Preparation of hydrocarbons or halogenated hydrocarbons
- C12P5/02—Preparation of hydrocarbons or halogenated hydrocarbons acyclic
- C12P5/026—Unsaturated compounds, i.e. alkenes, alkynes or allenes
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/12—Unicellular algae; Culture media therefor
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/12—Unicellular algae; Culture media therefor
- C12N1/125—Unicellular algae isolates
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P5/00—Preparation of hydrocarbons or halogenated hydrocarbons
- C12P5/007—Preparation of hydrocarbons or halogenated hydrocarbons containing one or more isoprene units, i.e. terpenes
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
- C12R2001/89—Algae ; Processes using algae
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/30—Fuel from waste, e.g. synthetic alcohol or diesel
Definitions
- the present invention relates to a novel strain belonging to Botryococcus brownie that can grow under a wide range of culture conditions, has a high content of produced hydrocarbons, and has a high purity of the target hydrocarbon.
- Algae are listed as photosynthetic organisms that are attracting attention as energy resources, among which green algae and diatoms are attracting attention. Ordinary green algae are composed of 15-17% of lipids, and this lipid is largely free of neutral lipids (30%), glycolipids (37%), phospholipids (26%) and fatty acids. Divided into lipids (7%).
- Botryococcus braunii has recently attracted attention as an oil-producing green algae.
- the main component of the lipid produced by Botryococcus brownie is a hydrocarbon composed of carbon and hydrogen, and is known to accumulate hydrocarbons such as linear alkenes and triterpenes inside and outside the cell.
- Botryococcus brownies are classified into three categories: Race-A, Race-B, and Race-L.
- Race-A is a group that produces hydrocarbons having an odd number of carbon atoms of 25 to 31 and having a straight chain and having 2 or 3 double bonds in the molecule.
- Race-L produces a hydrocarbon having a tetraterpene lycopadiene (C 40 H 78 ) structure.
- Race-A varies depending on the strain and is reported to be in the range of 0.4 to 61.0% (weight of hydrocarbon relative to dry alga body weight) (Non-patent Document 1). Race-B often produces 30-40% hydrocarbons by weight, but strains producing only about 9% have also been reported (Non-patent Document 2). Race-L is reported to be 0.1% for Indian stocks and 8.0% for Thai stocks (Non-Patent Document 3), which is known to be less than Race-B.
- the composition of these hydrocarbons is a mixture of those having various carbon chain lengths and / or structures.
- hydrocarbons can be used for production of thermal energy as solid fuel or heavy oil without any treatment, but when they are further processed and used, the hydrocarbons that are used as raw materials to obtain uniform compounds Is preferably a uniform composition.
- a strain having a simple hydrocarbon synthesis route has been required as a physiological research model for the application and use of Botryococcus.
- the establishment of a low-cost mass culture method can be raised, but in order to reduce the cost, it is necessary to carry out the culture outdoors using sunlight.
- the most efficient method is to perform culture using a low water level pool or a thin bioreactor at a time or place where the amount of solar radiation is high. .
- the water temperature rises, so that the optimum temperature for growth is 15 ° C. to 30 ° C., and the existing Botryococcus that stops the growth above 35 ° C. has the highest solar radiation amount. Proliferation stops at many times.
- the present invention has been made in view of the above demands, and an object of the present invention is to provide a new strain of Botryococcus brownie that has high purity of produced hydrocarbons and can grow under a wide range of culture conditions.
- the present inventors collected Botryococcus brownie from nature, found a strain that solves the above problems from among a genus having a large number of systematically different subgroups, isolated this, and completed the present invention I came to let you.
- the present invention provides a strain belonging to Botryococcus brownie lace-B that produces 60% by mass or more of hydrocarbons having the molecular formula C 34 H 58 with respect to all the hydrocarbons produced.
- the present invention provides a strain belonging to Botryococcus brownie lace-B according to (1), wherein the optimum culture temperature is 30 ° C. or higher.
- the present invention provides Botryococcus brownie tsukuba-1 stock (reception number: FERM ABP-11441, trustee: National Institute of Advanced Industrial Science and Technology (AIST)).
- the present invention provides a compound of formula (I) A strain belonging to Botryococcus brownie lace-B according to any one of (1) to (3), which produces a hydrocarbon having the molecular formula C 34 H 58 having the structure:
- the present invention provides a method for producing hydrocarbons from the strain belonging to Botryococcus brownie lace-B described in any one of (1) to (4).
- the new strain of Botryococcus brownie lace-B of the present invention can produce high-purity hydrocarbons and can grow under a wide range of culture conditions.
- the Botryococcus brownie lace-B strain of the present invention can be directly used in ships and agricultural vehicles as oil equivalent to heavy oil in order to produce hydrocarbons having 34 carbon atoms with high purity. Furthermore, it can be converted directly to light oil, naphtha, kerosene, and gasoline by an existing catalyst cracking system.
- the Botryococcus brownie lace-B strain of the present invention can be cultured at a culture temperature of about 10 ° C. to 45 ° C., preferably about 15 ° C. to 40 ° C., and particularly at about 39 ° C. .
- the Botryococcus brownie lace-B strain of the present invention is selected by, for example, setting the culture temperature generally above about 35 ° C. Has the advantage that it can be obtained in an automated manner. In addition, there is an advantage that culture is possible even in a situation where temperature control outdoors is difficult, for example, when the culture temperature becomes high during the day when the amount of sunlight is large.
- FIG. 1 shows a photomicrograph of squashed cells of Botryococcus brownie tsukuba-1 strain.
- FIG. 2 shows a photomicrograph of cells of Botryococcus brownie tsukuba-1 strain.
- FIG. 3 shows a comparison of the culture temperature of the Botryococcus brownie lace-B strain of the present invention and various algae (AG) of the genus Botryococcus.
- FIG. 4 shows the specific growth rate of the Botryococcus brownie race-B strain of the present invention with respect to the culture temperature.
- Novel strain of the present invention The new strain of Botryococcus brownie lace-B of the present invention has the following characteristics. Appearance features: Colonies that can be seen with the naked eye are spherical and yellow-green to green. When crushed under a microscope, it is observed as a tufted colony of grapes (FIG. 1). The average colony size is 30-100 ⁇ m, and the maximum reaches 500 ⁇ m.
- Cell shape characteristics Shape; usually in the shape of a club, with a cell wall, but an outer shell called a socket wall can be formed around the cell wall (FIG. 2). Hydrocarbons secreted from the cell can accumulate between the cell and the outer shell. Size: The short axis is about 8 ⁇ m and the long axis is about 14 ⁇ m, and the ratio is about 1.8.
- the Botryococcus brownie tsukuba-1 strain of the present invention is the National Institute of Advanced Industrial Science and Technology, Patent Biological Deposit Center (1st, 1st East, Tsukuba City, Ibaraki, Japan, 6th Central (postal code 305-8586). )) was deposited in Japan on December 9, 2010, and the accession number FERM P-22046 was obtained. Later, on November 25, 2011, the institute transferred to an international deposit under the Budapest Treaty, and was given the receipt number FERM ABP-11441.
- the microorganism used in the method for producing high-purity hydrocarbons of the present invention is not limited to the aforementioned Botryococcus brownie tsukuba-1 strain, but is substantially the same as the aforementioned strain of Botryococcus brownie lace-B. Any strain can be used as long as it has the same mycological properties.
- the new strain of Botryococcus brownie lace-B of the present invention is isolated from samples containing Botryococcus algae collected from lakes and ponds using the following method. be able to.
- the sample containing the algae belonging to the genus Botryococcus can be collected from a lake or pond using a plankton net having a mesh size of 30 to 100 ⁇ m.
- ⁇ Effective chlorine is allowed to act on the sample containing the algae belonging to the genus Botryococcus to sterilize microorganisms other than the genus Botryococcus.
- the sample to be treated may be cultured in advance in an appropriate medium to grow algae.
- the medium include CHU medium, JM medium, MDM medium, AF-6 medium, and the like.
- the medium is not particularly limited as long as it is suitable as a medium for Botryococcus algae.
- colonies of the genus Botryococcus may be separated by means such as centrifugation, filtration, or using a micropipette under a microscope.
- the sample After treating the sample with available chlorine as described above, the sample may be used as it is, but it is washed by repeating the operation of separating the algal bodies by filtration or centrifugation, etc., and suspending them in the culture solution. Is preferred.
- the sample treated with the effective chlorine is applied to a medium suitable for culturing Botryococcus algae, for example, a plate medium such as CHU medium, JM medium, MDM medium, AF-6 medium, and the like.
- a medium suitable for culturing Botryococcus algae for example, a plate medium such as CHU medium, JM medium, MDM medium, AF-6 medium, and the like.
- the pH of the medium can be adjusted to pH 1 to 14, preferably pH 2 to 13, more preferably pH 3 to 11, and still more preferably pH 4 to 10.
- the culture temperature can be generally 0 to 50 ° C., preferably 5 to 40 ° C., more preferably 10 to 30 ° C.
- the culture is performed under light irradiation using a fluorescent lamp or the like. This light irradiation may be performed continuously or may be performed for a certain period of time at intervals.
- the time interval can be selected from 1 to 72 hours, preferably 1 to 24 hours, more preferably 1 to 12 hours.
- the illuminance is usually 0 to 300 ⁇ E / m 2 / s, preferably 5 to 100 ⁇ E / m 2 / s.
- the culture period is usually 1 to 60 days, preferably 1 to 30 days.
- a single colony of Botryococcus algae is obtained by collecting a single colony of Botryococcus algae generated on the plate medium.
- it may be performed under a microscope.
- the strain isolated as described above is cultured in a liquid medium.
- a liquid medium for example, CHU medium, JM medium, MDM medium, AF-6 medium, or a modified medium thereof can be used.
- the pH of the medium can be adjusted to pH 1 to 14, preferably pH 2 to 13, more preferably pH 3 to 11, and still more preferably pH 4 to 10.
- the culture temperature can be generally 0 to 60 ° C., preferably 5 to 50 ° C., more preferably 10 to 40 ° C.
- the culture is performed under light irradiation using a fluorescent lamp or the like. This light irradiation may be performed continuously or may be performed for a certain period of time at intervals.
- the time interval can be selected from 1 to 72 hours, preferably 1 to 24 hours, more preferably 1 to 12 hours.
- the illuminance is usually 0 to 300 ⁇ E / m 2 / s, preferably 5 to 100 ⁇ E / m 2 / s.
- the culture period is usually 1 to 5 months, preferably 1 to 3 months. Further, during culturing, it may be left aerated or not aerated, but it is preferable to leave without aeration.
- the optimum temperature for growth can be examined by changing the temperature and measuring the amount of chlorophyll.
- the culture can be performed on a 48-well microplate or the like, and the amount of chlorophyll can be measured with a microplate reader.
- hydrocarbons produced by Botryococcus algae can be extracted and analyzed by methods known to those skilled in the art.
- algae of the genus Botryococcus is cultured and grown, and wet algal bodies recovered from the obtained culture solution by filtration or the like are dried by freeze drying or drying by heating. Thereafter, hydrocarbons can be extracted from the dried alga using an organic solvent. The extraction may be performed twice or more using different organic solvents.
- the organic solvent n-hexane, chloroform: methanol mixture (for example, 1: 1, 1: 2) or the like can be used.
- methanol mixture for example, it is concentrated to dryness under a stream of nitrogen and extracted again with n-hexane.
- the obtained extract is analyzed by NMR, IR, gas chromatography, GC / MS and the like.
- the hydrocarbons produced from Botryococcus obtained by the above procedure are analyzed by the above procedure, and 80% or more of hydrocarbons having the molecular formula C 34 H 58 (molecular weight 466) are produced with respect to all hydrocarbons.
- the Botryococcus brownie lace-B strain of the present invention can be obtained by screening for Botryococcus.
- the Botryococcus brownie lace-B strain of the present invention can be obtained by screening for Botryococcus having an optimum culture temperature of 30 ° C. or higher.
- the culture temperature refers to the temperature of the liquid medium in liquid culture.
- the optimum culture temperature means a culture temperature at which the specific growth rate is maximized when the specific growth rate is plotted against the culture temperature.
- the specific growth rate is defined as an increase in the amount of cells per unit time, and can be determined by the following equation.
- N 2 and N 1 are biomass at times t 2 and t 1 , respectively.
- the hydrocarbon obtained from the Botryococcus brownie race-B strain of the present invention has the following characteristics.
- the produced hydrocarbon is 20 to 70% by mass, preferably 25 to 65% by mass, more preferably 30 to 60% by mass, and even more preferably 30 to 50% by mass in dry weight with respect to algal cells. possible.
- the proportion of the hydrocarbon with the highest content in the total hydrocarbons produced is 60% by mass or more, preferably 70% by mass or more, more preferably 80% by mass or more, further preferably 90% by mass or more, further preferably It is present at 95% by weight or more, most preferably at 100% by weight.
- the hydrocarbon other than the hydrocarbon having the highest content may include isomers thereof, for example, geometric isomers.
- the hydrocarbon with the highest content is a hydrocarbon of molecular formula C 34 H 58 (molecular weight 466).
- the hydrocarbon may have a double bond at an arbitrary position, or may be cyclohexene.
- the hydrocarbon has the following structural formula (I):
- hydrocarbons obtained in the present invention can be used directly as fuel.
- treatment such as thermal decomposition or cracking using a catalyst is required.
- a method for producing an aromatic hydrocarbon by cyclization by catalytic cracking is known (Banerjee A., et al., Critical Reviews in Biotechnology (CRC Presss), 22).
- a method in which the terminal vinyl group of the resulting hydrocarbon is selectively oxidized to be used as a methyl ketone derivative (C 34 H 56 O) is also known (Chisti, YJ Ramasay Society, 27-28, 24-26, 1980).
- the obtained hydrocarbon may be polymerized by cationic polymerization, radical polymerization or ultraviolet light and used as a polymer material.
- MS gravimetric analysis
- ion source EI and CI, positive in the case of CI, gas: isobutene
- ionization current 200 microA
- ion source vacuum 4 ⁇ 10 ⁇ 4 Pa
- ionization Energy 38 eV
- analysis tube vacuum 1.0 ⁇ 10 ⁇ 5 Pa
- acceleration voltage 8.0 kV
- chamber temperature 200 ° C.
- ion Multi The test was performed under the conditions of 1.0 kV and magnetic field: HS. Further, the exact m / z was measured by high resolution GC / EI-MS.
- the characteristics of the Botryococcus brownie tsukuba-1 strain are as follows. -Optimum culture temperature is 30-36 ° C, and culture is possible at 15-40 ° C (Fig. 4). -It can be cultured in a wide pH range of pH 4-10. -Easy to adhere to stainless steel and ceramics. The cells are in the shape of clubs, the average length is about 14 ⁇ m, the average width is about 7.6 ⁇ m, and the ratio is about 1.8; -The colony is yellow-green to green and shows a shape in which the tip of the rod-shaped cell protrudes from the colony, and the size is usually 30 to 100 ⁇ m, and the maximum reaches 500 ⁇ m.
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Abstract
Description
本発明のボトリオコッカス・ブラウニー・レース-Bの新規株は、以下の特徴を有する。
外観的特徴:
肉眼で見えるコロニーは球形で、黄緑色~緑色である。顕微鏡下で押し潰すとブドウの房状のコロニーとして観察される(図1)。コロニーのサイズは平均的には30-100μm、最大で500μmに達する。
形状;通常はこん棒状で、細胞壁をもつが、細胞壁の周りにさらにソケットウオールと呼ばれる外殻を形成し得る(図2)。細胞から分泌された炭化水素は細胞と外殻に間に蓄積し得る。
大きさ;短径約8μm、長径約14μm、でその比は1.8程度である。
2.ボトリオコッカス属藻類の分離
本発明のボトリオコッカス・ブラウニー・レース-Bの新規株は、湖沼や池から採取した、ボトリオコッカス属の藻類を含むサンプルから、以下の方法を用いて分離することができる。
上記の液体培地での培養の際に、温度を変化させ、クロロフィル量を測定することにより、増殖至適温度を調べることができる。この場合、例えば、48穴マイクロプレート等で培養を行い、マイクロプレートリーダーでクロロフィル量を測定することができる。
ボトリオコッカス属の藻類が産生する炭化水素は、当業者に既知の方法で抽出及び分析することができる。例えば、ボトリオコッカス属の藻類を培養して増殖させ、得られた培養液から濾過等により回収した湿藻体を、凍結乾燥又は加温による乾燥等により乾燥させる。その後、この藻体乾燥物から有機溶媒を用いて炭化水素を抽出することができる。抽出は、異なる有機溶媒を用いて2度以上行ってもよい。有機溶媒としては、n-ヘキサン、クロロホルム:メタノール混合物(例えば、1:1、1:2)等を用いることができる。好ましくは、クロロホルム:メタノール混合物で抽出後、例えば、窒素気流下で濃縮乾固し、再びn-ヘキサンで抽出する。得られた抽出液を、NMR,IR、ガスクロマトグラフィー、GC/MS等により分析する。
ここで、培養温度とは液体培養における、液体培地の温度のことを言う。また、至適培養温度とは、培養温度に対する比増殖速度をプロットした場合、比増殖速度が極大となる培養温度のことを言う。ここで、比増殖速度とは、単位時間当たりの細胞量の増加と定義され、以下の式により求めることができる。
ここでN2、N1はそれぞれ時間t2およびt1の時のバイオマスである。
本願発明のボトリオコッカス・ブラウニー・レース-B株から得られる炭化水素は以下の特徴を有する。
産生される炭化水素は、藻体に対して、乾燥重量で、20~70質量%、好ましくは25~65質量%、より好ましくは30~60質量%、さらにより好ましくは30~50質量%があり得る。
産生される全炭化水素中、最も含有量が高い炭化水素の割合は、60質量%以上、好ましくは70質量%以上、より好ましくは80質量%以上、さらに好ましくは90質量%以上、さらに好ましくは95質量%以上、最も好ましくは100質量%で存在する。
前記最も含有量が高い炭化水素以外の炭化水素としては、その異性体、例えば、幾何異性体が含まれてもよい。
前記最も含有量が高い炭化水素は、分子式C34H58(分子量466)の炭化水素である。当該炭化水素は、任意の位置に二重結合を有してよく、あるいはシクロヘキセンであってもよい。好ましくは、当該炭化水素は、以下の式(I)の構造式を有する。
本発明で得られる炭化水素は、直接燃料として使用することができる。一方、内燃機関の燃料として使用する場合は、熱分解や触媒を用いるクラッキング等の処理が必要になる。一例として、触媒クラッキングにより環化させ、芳香族炭化水素を生成する方法が知られている(Banerjee A., et al., Critical Reviews in Biotechnology (CRC Presss), 22)。得られる炭化水素の末端ビニル基を選択的に酸化して、メエチルケトン誘導体(C34H56O)にして利用する方法も知られている(Chisti, Y. J. Ramasay Society, 27-28, 24-26, 1980)。また、得られる炭化水素をカチオン重合、ラジカル重合や紫外線によって重合させ、高分子材料として利用してもよい。
日本各地の湖沼や池から網目30~100μmのプランクトンネットを用いてボトリオコッカスを含むサンプルを採取した。このサンプルからボトリオコッカスのコロニーを顕微鏡下でマイクロピペットを用いて分離し、これを有効塩素濃度約0.1%になるように添加したAF-6培地に浸けてボトリオコッカス以外の微生物を殺菌した後、AF-6培地(表1)で3回洗浄し、22℃、12時間毎光照射下で培養を行った。その後、三角フラスコに200mlのChu改変培地(表2)と培養した株を加え、25℃、12時間毎光照射下で1~3ヶ月培養を行った。
得られたボトリオコッカスの培養液を、5μm孔のフィルターで濃縮し、凍結乾燥し、クロロホルム・メタノール(2:1,V/V)を用いて総脂質を抽出し、濃縮乾固後、n-ヘキサンで再抽出した。この試料を以下に示す手順でGC/MSにより解析した。
得られたボトリオコッカス株を、Chu改変培地をあらかじめ添加した48穴マイクロプレートに播種し、10~40℃の培養庫で培養し、クロロフィル量の増加速度をマイクロプレートリーダーで測定した。
以上の方法で多数の株について炭化水素構成成分と至適培養温度を調べたところ、沖縄本島漢那ダムから得られた株は単一の分子量の炭化水素のみ(92%が単一物質、8%はその幾何異性体)を生産するものであり、他の株は生育しない35℃付近で増殖が可能であることがわかった(図3)。
-培養至適温度が30~36℃であり、15~40℃で培養可能である(図4)。
-pH4~10の幅広いpH範囲で培養可能である。
-ステンレス、セラミック等に付着しやすい。
-細胞はこん棒状の形状であり、長さは平均で約14μm、幅は平均で約7.6μmで、その比は1.8程度である。
-コロニーは黄緑色~緑色で、こん棒状の細胞の先端がコロニーから突出している形状を示し、サイズは通常は30~100μm、最高で500μmに達する。
-産生した炭化水素を細胞外に分泌し、細胞と細胞を囲むソケットウォールと呼ばれる外殻の間に蓄積し、コロニー内に保持する。
-コロニー内に蓄積された炭化水素はガラスカバーを載せると簡単に外部に流出してくる。
-細胞内にも多数の炭化水素を含む顆粒状構造が観察される。
Claims (5)
- 産生される全炭化水素に対して分子式C34H58を有する炭化水素を60質量%以上産生する、ボトリオコッカス・ブラウニー・レース-Bに属する株。
- 培養至適温度が30℃以上である、請求項1に記載のボトリオコッカス・ブラウニー・レース-Bに属する株。
- 前記ボトリオコッカス・ブラウニー・レース-Bに属する株が、ボトリオコッカス・ブラウニー・tsukuba-1株(受領番号:FERM ABP-11441)である、請求項1又は2に記載の株。
- 請求項1~4のいずれか1項に記載のボトリオコッカス・ブラウニー・レース-Bに属する株を用いる、炭化水素の製造方法。
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JP2012547930A JP5534267B2 (ja) | 2010-12-09 | 2011-12-09 | ボトリオコッカス・ブラウニー(Botryococcusbraunii)属の新規株 |
EP11846393.4A EP2660312B1 (en) | 2010-12-09 | 2011-12-09 | Novel strain classified under botryococcus braunii |
US13/992,590 US9284577B2 (en) | 2010-12-09 | 2011-12-09 | Strain classified under Botryococcus braunii |
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Cited By (4)
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JP2013035791A (ja) * | 2011-08-09 | 2013-02-21 | Denso Corp | 保湿剤 |
JP2013170230A (ja) * | 2012-02-21 | 2013-09-02 | Kyodo Yushi Co Ltd | 潤滑グリース組成物 |
CN103571753A (zh) * | 2012-07-30 | 2014-02-12 | 新奥科技发展有限公司 | 布朗葡萄藻及其应用 |
CN103571752A (zh) * | 2012-07-30 | 2014-02-12 | 新奥科技发展有限公司 | 布朗葡萄藻及其应用 |
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JPH099953A (ja) | 1995-06-29 | 1997-01-14 | Chikyu Kankyo Sangyo Gijutsu Kenkyu Kiko | 新規なボツリオコッカス属に属する微細藻類 |
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JPH09173050A (ja) | 1995-12-22 | 1997-07-08 | Chikyu Kankyo Sangyo Gijutsu Kenkyu Kiko | 緑藻類に属する微細藻類の培養方法 |
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JPH099953A (ja) | 1995-06-29 | 1997-01-14 | Chikyu Kankyo Sangyo Gijutsu Kenkyu Kiko | 新規なボツリオコッカス属に属する微細藻類 |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2013035791A (ja) * | 2011-08-09 | 2013-02-21 | Denso Corp | 保湿剤 |
JP2013170230A (ja) * | 2012-02-21 | 2013-09-02 | Kyodo Yushi Co Ltd | 潤滑グリース組成物 |
CN103571753A (zh) * | 2012-07-30 | 2014-02-12 | 新奥科技发展有限公司 | 布朗葡萄藻及其应用 |
CN103571752A (zh) * | 2012-07-30 | 2014-02-12 | 新奥科技发展有限公司 | 布朗葡萄藻及其应用 |
CN103571752B (zh) * | 2012-07-30 | 2016-01-13 | 新奥科技发展有限公司 | 布朗葡萄藻及其应用 |
Also Published As
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EP2660312A1 (en) | 2013-11-06 |
US9284577B2 (en) | 2016-03-15 |
US20130252304A1 (en) | 2013-09-26 |
JP5534267B2 (ja) | 2014-06-25 |
EP2660312A4 (en) | 2014-06-18 |
EP2660312B1 (en) | 2017-02-22 |
JPWO2012077801A1 (ja) | 2014-05-22 |
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