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JP2582622B2 - Production of polyunsaturated fatty acids by filamentous fungi - Google Patents

Production of polyunsaturated fatty acids by filamentous fungi

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Publication number
JP2582622B2
JP2582622B2 JP63134354A JP13435488A JP2582622B2 JP 2582622 B2 JP2582622 B2 JP 2582622B2 JP 63134354 A JP63134354 A JP 63134354A JP 13435488 A JP13435488 A JP 13435488A JP 2582622 B2 JP2582622 B2 JP 2582622B2
Authority
JP
Japan
Prior art keywords
fatty acids
polyunsaturated fatty
genus
filamentous fungi
acid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP63134354A
Other languages
Japanese (ja)
Other versions
JPH01199588A (en
Inventor
不二夫 湯
貞彦 本吉
雄康 二階堂
元男 柳田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nitto Chemical Industry Co Ltd
Original Assignee
Nitto Chemical Industry Co Ltd
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Filing date
Publication date
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Priority to JP63134354A priority Critical patent/JP2582622B2/en
Publication of JPH01199588A publication Critical patent/JPH01199588A/en
Application granted granted Critical
Publication of JP2582622B2 publication Critical patent/JP2582622B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は糸状菌を栄養倍値に培養し、培養物より高度
不飽和脂肪酸含量の高い脂質を得ることによる高度不飽
和脂肪酸の製造法に関する。
The present invention relates to a method for producing polyunsaturated fatty acids by culturing filamentous fungi at a nutrient doubling value and obtaining a lipid having a higher content of polyunsaturated fatty acids from the culture. .

本発明において製造される高度不飽和脂肪酸は炭素数
18〜22、不飽和二重結合数3以上の脂肪酸であり、具体
的には、例えばγ−リノレン酸(9,12,15−オクタデカ
トリエン酸)、ジホモ−γ−リノレン酸(8,11,14−エ
イコサトリエン酸)、アラキドン酸(5,8,11,14−エイ
コサテトラエン酸)、EPA(5,8,11,14,17−エイコサペ
ンタエン酸)、DTA(7,10,13,16−ドコサテトラエン
酸)、DPA(4,7,10,13,16−または7,10,13,16,19−ドコ
サペンタエン酸)およびDHA(4,7,10,13,16,19−ドコサ
ヘキサエン酸)等を総称するものである。
The polyunsaturated fatty acid produced in the present invention has a carbon number
18-22, fatty acids having 3 or more unsaturated double bonds, specifically, for example, γ-linolenic acid (9,12,15-octadecatrienoic acid), dihomo-γ-linolenic acid (8,11 , 14-eicosatrienoic acid), arachidonic acid (5,8,11,14-eicosatetraenoic acid), EPA (5,8,11,14,17-eicosapentaenoic acid), DTA (7,10, 13,16-docosatetraenoic acid), DPA (4,7,10,13,16- or 7,10,13,16,19-docosapentaenoic acid) and DHA (4,7,10,13,16 , 19-docosahexaenoic acid) and the like.

これら高度不飽和脂肪酸は、哺乳動物では体内におい
て合成することのできない必須脂肪酸である。ジホモ−
γ−リノレン酸はプロスタグランジンE1、F1など、アラ
キドン酸はプロスタグランジンE2、F2、I2、トロンボキ
サンA2など、EPAはプロスタグランジンE3、F3、I3、ト
ロンボキサンA3などのそれぞれ前駆体として知られてお
り、重要であると同時に、高度不飽和脂肪酸自身、生体
内において多くの生理活性を示すことが知られている。
例えば、EPA、DHA等は抗血栓作用、心臓病、血清全コレ
ステロールの低下作用等に対する効果が注目されてい
る。
These highly unsaturated fatty acids are essential fatty acids that cannot be synthesized in the body in mammals. Dihomo
etc. γ- linolenic acid prostaglandin E 1, F 1, arachidonic acid is prostaglandin E 2, F 2, I 2 , such as thromboxane A 2, EPA is prostaglandin E 3, F 3, I 3 , known as the respective precursor such as thromboxane a 3, at the same time is important, polyunsaturated fatty acids themselves, are known to exhibit a number of physiological activity in vivo.
For example, EPA, DHA, and the like have been noted for their effects on antithrombotic effects, heart disease, serum total cholesterol lowering effects, and the like.

〔従来の技術およびその問題点〕[Conventional technology and its problems]

これら高度不飽和脂肪酸中、アラキドン酸を含む微生
物としては、これまでに、原生動物のユウグレナのほか
に、糸状菌であるConidiobolus属、Tricnothecium属、E
ntomophthora属、Phytophthora属、Saprolegnia属、Pyt
hium属、Mortierella属およびBlastocladiella属が知ら
れている。これらの微生物は同時にジホモ−γ−リノレ
ン酸を含んでいる。また、EPAを含む微生物としても糸
状菌であるPhytophthora属、Saprolegnia属、Pythium
属、Mortierella属が報告されている〔H.B.WHITE and
S.S.PWELL Biochim.Biophys.Acta116:391(1966)、D.T
yrell Can.J.Microbiol.13:755(1967)等〕。その他、
培養の際に炭化水素を添加することにより、アラキドン
酸が得られる菌として、糸状菌のAspergillus属、Fusar
ium属、Penicillium属、Porphyridium属、Mucor属およ
びRhizopus属が知られている〔特開昭56−19231号公
報〕。
Among these polyunsaturated fatty acids, microorganisms containing arachidonic acid include, in addition to protozoa Euglena, fungi such as Conidiobolus, Tricnothecium, and E.
Genus ntomophthora, Phytophthora, Saprolegnia, Pyt
The genus hium, the genus Mortierella and the genus Blastocladiella are known. These microorganisms simultaneously contain dihomo-γ-linolenic acid. Microorganisms containing EPA include filamentous fungi such as Phytophthora, Saprolegnia, and Pythium.
The genus Mortierella has been reported (HBWHITE and
SSPWELL Biochim. Biophys. Acta116: 391 (1966), DT
yrell Can. J. Microbiol. 13: 755 (1967) and the like]. Others
Arachidonic acid can be obtained by adding hydrocarbons during culturing, as filamentous fungi Aspergillus, Fusar
The genera genus Penicillium, Porphyridium, Mucor and Rhizopus are known (Japanese Patent Application Laid-Open No. 56-19231).

また、DHAなどの高度不飽和脂肪酸は魚油から抽出さ
れているが、魚油(鯨油、鰯油)中の該脂肪酸の含有量
が低いことや、高度不飽和脂肪酸はそれ自身酸化分解さ
れ易い等により、高純度に目的とする高度不飽和脂肪酸
を得ることは困難である。
In addition, polyunsaturated fatty acids such as DHA are extracted from fish oil. However, the content of the fatty acids in fish oil (whale oil, sardine oil) is low, and polyunsaturated fatty acids themselves are easily oxidatively decomposed. It is difficult to obtain the desired highly unsaturated fatty acid with high purity.

〔問題点を解決するための手段〕[Means for solving the problem]

このような状況下、本発明者らは、高度不飽和脂肪酸
を微生物を用い製造することが最も有利と考え、高度不
飽和脂肪酸含量の高い脂質を生産する能力を有する糸状
菌について鋭意検討した結果American Type Culture Co
llection(ATCC)に保存され、カタログに記載されてい
る糸状菌であるThraustotheca clavata ATCC 34112、Ac
hlya bisexualis ATCC 14524、Haliphthorous philippi
nensis ATCC 58303、Rizophydium littoreum ATCC 3610
0およびJaponochytrium sp.ATCC 28207が、高度不飽和
脂肪酸を生産することを見出し、本発明はこの知見によ
りなされたものである。
Under such circumstances, the present inventors considered that it is most advantageous to produce polyunsaturated fatty acids using microorganisms, and as a result of intensive studies on filamentous fungi having the ability to produce lipids having a high content of polyunsaturated fatty acids. American Type Culture Co
thraustotheca clavata ATCC 34112, Ac, stored in the LLection (ATCC) and listed in the catalog
hlya bisexualis ATCC 14524, Haliphthorous philippi
nensis ATCC 58303, Rizophydium littoreum ATCC 3610
0 and Japonochytrium sp. ATCC 28207 produce polyunsaturated fatty acids, and the present invention has been made based on this finding.

すなわち、本発明はThraustotheca属、Achlya属、Hal
iphthorous属、Rizophydium属またはJaponochytrium属
に属し、高度不飽和脂肪酸含量の高い脂質生産能を有す
る糸状菌を培養し、培養物より高度不飽和脂肪酸含量の
高い脂質を採取することを特徴とする糸状菌による高度
不飽和脂肪酸の製造法である。
That is, the present invention relates to the genera Thraustotheca, Achlya, Hal
A filamentous fungus belonging to the genus iphthorous, Rizophydium or Japonochytrium, culturing a filamentous fungus having a high unsaturated fatty acid content and having a high lipid-producing ability, and collecting a lipid having a high unsaturated fatty acid content from the culture. Is a method for producing polyunsaturated fatty acids.

上記糸状菌を培養する培地組成については特に規定す
るものではないが、炭素源ととしては、グルコース、エ
タノール、グリセロールなどが好ましく、その使用量は
通常0.5〜20重量%の範囲である。また、窒素源として
はイースト・エキス、マルツ・エキス、ペプトンなどの
有機窒素源の使用が好ましいが、ほかに硝酸塩などの無
機窒素も使用でき、その使用量は通常0.1〜10重量%の
範囲である。また、これらの成分のほかにアミノ酸、ビ
タミン類などの微量要素や無機塩類の添加は菌の生育を
促進させるのに効果的である。
The composition of the medium for culturing the filamentous fungus is not particularly limited. However, as the carbon source, glucose, ethanol, glycerol and the like are preferable, and the amount used is usually in the range of 0.5 to 20% by weight. As the nitrogen source, it is preferable to use an organic nitrogen source such as yeast extract, malt extract, peptone, etc. In addition, inorganic nitrogen such as nitrate can also be used, and the amount used is usually in the range of 0.1 to 10% by weight. is there. Further, in addition to these components, the addition of trace elements such as amino acids and vitamins and inorganic salts are effective in promoting the growth of bacteria.

培地のpHは4〜10、好ましくは5〜8、培養温度は10
〜35℃の範囲が良く、培養時間は2〜15日間程度必要で
ある。
The pH of the medium is 4-10, preferably 5-8, and the culture temperature is 10
The temperature is preferably in the range of ~ 35 ° C, and the culturing time is required about 2 to 15 days.

培養は、通常液体培養培地で、静置培養、振とう培
養、通気攪拌培養などの方法により行う。
The cultivation is usually performed in a liquid culture medium by a method such as stationary culture, shaking culture, or aeration and stirring culture.

このようにして得られた培養物より、濾過、遠心分離
などの方法で菌体を集め、その菌体より脂質抽出を行
う。脂質の抽出は常法に従い、例えば溶媒抽出などによ
って行われる。
Cells are collected from the thus obtained culture by filtration, centrifugation, or the like, and lipids are extracted from the cells. Extraction of lipids is performed by a conventional method, for example, by solvent extraction.

〔実施例〕〔Example〕

実施例1. 下記の有機栄養培地1にThraustotheca clavata AT
CC 34112を接種し、25℃で7日間振とう培養後、濾過に
て菌体を回収し凍結乾燥した。これにより、5.8gの乾燥
菌体を得た。この乾燥菌体を粉砕してFolch法により抽
出精製した後、溶媒を減圧留去し、重量法により全脂質
を測定した。その結果、0.5gの粗脂質が得られた。
Example 1. Thraustotheca clavata AT in the following organic nutrient medium 1
After inoculating CC 34112 and culturing with shaking at 25 ° C. for 7 days, the cells were collected by filtration and freeze-dried. As a result, 5.8 g of dried cells were obtained. After the dried cells were pulverized and extracted and purified by the Folch method, the solvent was distilled off under reduced pressure, and the total lipid was measured by a gravimetric method. As a result, 0.5 g of crude lipid was obtained.

培地 グルコース 10g/ イースト・エキス 3g/ マルツ・エキス 3g/ トリプトン 5g/ 蒸留水 1 pH 7.0 菌体から抽出精製した脂質は一部をメチルエステル化
した後、ガスクロマトグラフィーにより脂肪酸組成の分
析を行った。その結果を表−1に示した。
Medium Glucose 10g / Yeast extract 3g / Malt's extract 3g / Tryptone 5g / Distilled water 1 pH 7.0 Lipids extracted and purified from cells were partially methylesterified, and fatty acid composition was analyzed by gas chromatography. . The results are shown in Table 1.

尚、ガスクロマトグラフィーにより得られた各ピーク
は、マススペクトロメトリーにより同定を行った。ガスクロマトフラフィー分析条件 カラム充填剤 Diasolid ZF カラム温度200℃ キャリアーガス N2 検出器温度250℃ 検出器 FID 注入温度 250℃ カラム 1.5m×3φ 乾燥菌体当りのアラキドン酸含量は21.6mg/gである。
In addition, each peak obtained by gas chromatography was identified by mass spectrometry. Gas chromatographic analysis conditions Column packing Diasolid ZF Column temperature 200 ° C Carrier gas N 2 Detector temperature 250 ° C Detector FID injection temperature 250 ° C Column 1.5m × 3φ The arachidonic acid content per dry cell is 21.6 mg / g.

乾燥菌体当りのEPA含量は4.6mg/gである。 The EPA content per dry cell is 4.6 mg / g.

実施例2. 下記の有機栄養培地1にAchlya bisexualis ATCC 1
4524を接種し、以後、実施例1と同様の操作を行い、脂
肪酸組成を分析した。
Example 2. Achlya bisexualis ATCC 1 in the following organic nutrient medium 1
After inoculating 4524, the same operation as in Example 1 was performed, and the fatty acid composition was analyzed.

結果を表−2に示した。 The results are shown in Table-2.

培地 グルコース 10g/ イースト・エキス 3g/ マルツ・エキス 3g/ ポリペプトン 5g/ 蒸留水 1 pH 6.5 実施例3. 下記の有機栄養培地1にHaliphthorous philippine
nsis ATCC 58303を接種し、以後、実施例1と同様の操
作を行い、脂肪酸組成を分析し、結果を表−3に示し
た。
Medium Glucose 10g / Yeast extract 3g / Malt's extract 3g / Polypeptone 5g / Distilled water 1 pH 6.5 Example 3. Haliphthorous philippine was added to the following organic nutrient medium 1.
nsis ATCC 58303 was inoculated, and thereafter the same operation as in Example 1 was performed to analyze the fatty acid composition. The results are shown in Table-3.

培地 グルコース 5g/ イースト・エキス 1g/ ポリペプトン 1g/ 人工海水 1 pH 6.5 実施例4. 下記の有機栄養培地1にRizophydium littoreum AT
CC 36100を接種し、以後、実施例1と同様の操作を行
い、脂肪酸組成を分析し、結果を表−4に示した。
Medium Glucose 5g / Yeast extract 1g / Polypeptone 1g / Artificial seawater 1 pH 6.5 Example 4. Rizophydium littoreum AT in the following organic nutrient medium 1
After inoculating CC 36100, the same operation as in Example 1 was performed, and the fatty acid composition was analyzed. The results are shown in Table-4.

培地 グルコース 5g/ イースト・エキス 1g/ ポリペプトン 1g/ 人工海水 1 pH 6.5 実施例5. 下記の有機栄養培地1にJaponochytrium sp.ATCC 2
8207を接種し、以後、実施例1と同様の操作を行い、1.
7gの乾燥菌体、次いで0.14gの粗脂質が得られた。さら
に、実施例1と同様にして、この脂質の脂肪酸組成を分
析した。
Medium Glucose 5g / Yeast extract 1g / Polypeptone 1g / Artificial seawater 1 pH 6.5 Example 5. Japonochytrium sp. ATCC 2 was added to the following organic nutrient medium 1.
8207, and the same operation as in Example 1 was carried out.
7 g of dried cells were obtained, followed by 0.14 g of crude lipid. Further, the fatty acid composition of this lipid was analyzed in the same manner as in Example 1.

結果を表−5に示した。 The results are shown in Table-5.

培地 グルコース 10g/ イースト・エキス 3g/ マルツ・エキス 3g/ ペプトン 1g/ 人工海水 1 pH 7.0 Medium Glucose 10g / Yeast extract 3g / Malt's extract 3g / Peptone 1g / Artificial seawater 1 pH 7.0

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】Thraustotheca属、Achlya属、Haliphthoro
us属Rizophydium属またはJaponochytrium属に属し、高
度不飽和脂肪酸含量の高い脂質生産能を有する糸状菌を
培養し、培養物より高度不飽和脂肪酸含量の高い脂質を
採取することを特徴とする糸状菌による高度不飽和脂肪
酸の製造法。
1. The genus Thraustotheca, the genus Achlya, the Haliphthoro
By culturing a filamentous fungus belonging to the genus Rizophydium or Japonochytrium and having a lipid-producing ability with a high content of highly unsaturated fatty acids, and collecting a lipid with a high content of a highly unsaturated fatty acid from the culture, a filamentous fungus characterized by A method for producing polyunsaturated fatty acids.
JP63134354A 1987-10-27 1988-06-02 Production of polyunsaturated fatty acids by filamentous fungi Expired - Fee Related JP2582622B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63134354A JP2582622B2 (en) 1987-10-27 1988-06-02 Production of polyunsaturated fatty acids by filamentous fungi

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP27062487 1987-10-27
JP62-270624 1987-10-27
JP63134354A JP2582622B2 (en) 1987-10-27 1988-06-02 Production of polyunsaturated fatty acids by filamentous fungi

Publications (2)

Publication Number Publication Date
JPH01199588A JPH01199588A (en) 1989-08-10
JP2582622B2 true JP2582622B2 (en) 1997-02-19

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Country Link
JP (1) JP2582622B2 (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE200619T1 (en) * 1991-01-24 2001-05-15 Martek Corp MICROBIAL OILS AND THEIR USES
PT1785492E (en) 1996-07-23 2010-07-06 Nagase Chemtex Corp Process for preparing docosahexaenoic acid and docosapentaenoic acid
EP2308988A1 (en) 1996-12-27 2011-04-13 Suntory Holdings Limited Media for culturing microorganisms and process for producing unsaturated fatty acids or lipids containing the same
JP4088097B2 (en) 2002-04-26 2008-05-21 サントリー株式会社 Method for producing highly unsaturated fatty acid-containing lipid
JP3840459B2 (en) * 2003-03-20 2006-11-01 裕司 島田 Glyceride and method for producing the same
US7550286B2 (en) 2004-11-04 2009-06-23 E. I. Du Pont De Nemours And Company Docosahexaenoic acid producing strains of Yarrowia lipolytica
JP2013525549A (en) 2010-04-22 2013-06-20 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー Method for obtaining a polyunsaturated fatty acid-containing composition from microbial biomass
EP2603092A1 (en) 2010-08-11 2013-06-19 E.I. Du Pont De Nemours And Company Improved aquaculture meat products
US20120040076A1 (en) 2010-08-11 2012-02-16 E. I. Du Pont De Nemours And Company Aquaculture feed compositions

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