JPH0775563A - Culture of mucor - Google Patents

Culture of mucor

Info

Publication number
JPH0775563A
JPH0775563A JP5248646A JP24864693A JPH0775563A JP H0775563 A JPH0775563 A JP H0775563A JP 5248646 A JP5248646 A JP 5248646A JP 24864693 A JP24864693 A JP 24864693A JP H0775563 A JPH0775563 A JP H0775563A
Authority
JP
Japan
Prior art keywords
mucor
beer
acid
cake
beer lees
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.)
Pending
Application number
JP5248646A
Other languages
Japanese (ja)
Inventor
Naganori Daihisa
長範 大久
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.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to JP5248646A priority Critical patent/JPH0775563A/en
Publication of JPH0775563A publication Critical patent/JPH0775563A/en
Pending legal-status Critical Current

Links

Classifications

    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P60/00Technologies relating to agriculture, livestock or agroalimentary industries
    • Y02P60/80Food processing, e.g. use of renewable energies or variable speed drives in handling, conveying or stacking
    • Y02P60/87Re-use of by-products of food processing for fodder production

Abstract

PURPOSE:To obtain a mucor malt having excellent storage stability and useful for feed, etc., in high efficiency by adding a fatty acid, etc., to moist beer cake, inoculating Mucor sarcineroides to the cake and culturing the microorganism. CONSTITUTION:The mucor malt is produced by adding one or more kinds of fatty acids such as acetic acid or a floating material in aquatic food processing to moist beer cake (the amount of the additive is preferably 1-20% based on the dehydrated beer cake), inoculating Mucor sarcineroides to the cake and culturing under aerobic condition.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】この発明は、脂肪酸を資化分解す
る能力の強いムコール・サーシネロイデスの培養方法に
関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for culturing mucor sarcyneloides which has a strong ability to assimilate and decompose fatty acids.

【0002】[0002]

【従来の技術】ビールの製造過程で多量に副産するビー
ル粕はサイロに詰めて醗酵し、酪農用の飼料として供給
し利用されていた(特公昭53−46749、実公昭5
7 −38999)。
2. Description of the Related Art Beer lees, which are produced as a by-product in a large amount in the process of beer production, are packed in silos and fermented, and then used as feed for dairy farming (Japanese Patent Publication No. 53-46749, Japanese Utility Model Publication No. 5).
7-38999).

【0003】[0003]

【考案が解決しようとする課題】多量に発生したビール
粕は水分が75から85%の高湿潤物である為に日持ち
がせず、短期間で腐敗することから、飼料価値が無くな
り廃棄処分となることが多かった。栄養物とラクトバチ
ルス・ブルガリカス、ストレプトコッカス・ファエカリ
ス等の醗酵促進菌を加え嫌気醗酵させ、牛用飼料を製造
する方法も開示されている(特開昭60−21095
3)。この方法によるとビール粕の腐敗を防止できる
が、湿潤状態の醗酵物が得られ為に保存には限界があっ
た。
[Problems to be solved by the invention] Beer meal produced in a large amount is a highly moist product with a water content of 75 to 85%, so it does not last long and decays in a short period of time. It was often A method for producing a cattle feed by adding a nutrient and a fermentation-promoting bacterium such as Lactobacillus bulgaricus, Streptococcus faecalis, etc. and anaerobically fermenting it has also been disclosed (JP-A-60-21095).
3). According to this method, spoilage of beer lees can be prevented, but there is a limit to storage because a fermented product in a wet state can be obtained.

【0004】[0004]

【課題を解決するための手段】本発明者らはムコール・
サーシネロイデス(Mucor circinelloides) を水産加工
廃液から得られる浮上物(スカム)に適用し肥料化する
方法を発明した(特開昭60−260489) 。この発
明はムコール・サーシネロイデスの強力な油分解能を利
用したものである。ムコール・サ−シネロイデスの特徴
を更に解析したところ、本菌の油分解能の本質はリパ−
ゼ活性によるのではなく、強力な脂肪酸資化能にあるこ
とを見出した。即ち、ツアペックドック無機培地に各種
の脂肪酸を加え、25°Cで培養することにり、ムコー
ル・サーシネロイデスNo.3の脂肪酸資化能(増殖程
度)を調べたところ1表に示す結果を得た。プロピオン
酸は資化できなかったが、短鎖から長鎖に至までの脂肪
酸を資化し増殖することが出来た。中でも不飽和脂肪酸
の代表的なリノ−ル酸により良好な増殖が観察された
(表1)。このムコール・サーシネロイデスNo.3を
サイレ−ジに保存したビ−ル粕に接種し、培養したとこ
ろ、良好な増殖が認められた。つぎに新鮮なビ−ル粕に
有機酸の混合物を添加した後にムコール・サーシネロイ
デスNo.3を接種し、培養したところ、良好な増殖が
られ、発明を完成させた。
Means for Solving the Problems The present inventors
A method has been invented for applying fertilizer by applying Mucor circinelloides to a float (scum) obtained from a marine processing waste liquor (Japanese Patent Laid-Open No. 60-260489). This invention utilizes the powerful oil-degrading ability of Mucor sircineroides. Further analysis of the characteristics of Mucor sirneroides revealed that the essential oil-degrading ability of this bacterium was lipase.
It was found that it has a strong ability to assimilate fatty acids, not due to its activity. That is, various fatty acids were added to the Tuapec Dock inorganic medium and cultured at 25 ° C. to obtain Mucor sircineloides No. When the fatty acid utilization ability (proliferation degree) of 3 was examined, the results shown in Table 1 were obtained. Although propionic acid could not be assimilated, it was able to assimilate and grow fatty acids ranging from short chains to long chains. Above all, good growth was observed with linoleic acid, which is a typical unsaturated fatty acid (Table 1). This Mucor Sir Cineroides No. When 3 was inoculated into beer lees stored in silage and cultured, good growth was observed. Next, after adding a mixture of organic acids to fresh beer meal, Mucor sircineloides No. When 3 was inoculated and cultured, good growth was obtained, and the invention was completed.

【0005】先ず新鮮なビ−ル粕を機械的に脱水した後
に、有機酸の混合物を脱水ビ−ル粕に対して1か20%
になるように添加する。次にムコール・サーシネロイデ
スを接種し通気培養する。水分含量は40から75%、
pHは4.4から6.5の範囲になるよう調整すること
が望ましい。有機酸の混合物として酢酸や1表の各種の
有機酸を混合し、調整してもよいが、水産加工排液から
得られる浮上物(スカム)を用いてもよい。ムコールは
醗酵研究所の Mucor circinelloides IFO 6746, Mucor
circinellides IFO 3318, あるいは Mucor circinelloi
des No.3(特開昭60−260489)等の Mucor
circinelloides に属する菌株であれば可能である。
After mechanically dehydrating fresh beer meal, a mixture of organic acids is added to the dehydrated beer meal in an amount of 1 or 20%.
To be added. Then, Mucor sircineloides is inoculated and aerobically cultured. Water content is 40 to 75%,
It is desirable to adjust the pH to be in the range of 4.4 to 6.5. Although acetic acid and various organic acids shown in Table 1 may be mixed and adjusted as a mixture of organic acids, a float (scum) obtained from a marine product processing effluent may be used. Mucor is a fermentation laboratory Mucor circinelloides IFO 6746, Mucor
circinellides IFO 3318, or Mucor circinelloi
des No. 3 (Japanese Patent Laid-Open No. 60-260489), etc.
It can be any strain belonging to circinelloides.

【0006】ビール粕に油あるいは脂肪酸の混合物を添
加しムコールを接種し培養することにより、ムコール麹
を製造することが出来る。出来たムコール麹はそのまま
牛等の飼料として活用でき、また醤油等の原料としても
利用できる。
[0006] Mucole koji can be produced by adding a mixture of oil or fatty acid to beer lees and inoculating mucoles and culturing. The resulting mucor koji can be used as it is as feed for cattle and the like, and also as a raw material for soy sauce and the like.

【0007】[0007]

【表1】 ムコール・サーシネロイデスNo.3の脂肪酸資化能 ────────────────────────── 増殖程度 脂肪酸の種類 ─────────────── 脂肪酸濃度(%) 0.01 0.1 1.0 ────────────────────────── 酢酸 + + + プロピオン酸 − − − n−酪酸 ± + − カプロン酸 ± + − カプリン酸 − + + パルミチン酸 ± + + ステアリン酸 ± ± ± オレイン酸 + + + リノ−ル酸 + ++ ++ リノレン酸 + + + ミリスチン酸 + + + ────────────────────────── −:増殖せず、 ±、+、++:増殖程度の増加を示す[Table 1] Mucor Sir Cineroides No. Fatty acid utilization capacity of 3 ────────────────────────── Proliferation degree Type of fatty acid ────────────── ── Fatty acid concentration (%) 0.01 0.1 1.0 ─────────────────────────── Acetic acid + + + Propionic acid − − -N-butyric acid ± + -caproic acid ± + -capric acid- + + palmitic acid ± + + stearic acid ± ± ± oleic acid + + + linoleic acid + + + + + linolenic acid + + + myristic acid + + + + ─ ───────────────────────── −: No proliferation, ±, +, ++: Increase in proliferation degree

【0008】[0008]

【作用】ムコール・サーシネロイデスは有機酸や水産加
工排液から得られる浮上物(スカム)を資化し醗酵する
ことにより、粗脂肪含量が減少し粗蛋白質含量が上昇す
る。ビール粕は醗酵熱により乾燥する。
[Function] Mucor sircineloides reduces the crude fat content and increases the crude protein content by assimilating and fermenting the floated material (scum) obtained from the organic acid and the marine product processing effluent. Beer lees are dried by the heat of fermentation.

【0009】[0009]

【実施例】以下、実施例にもとずき本発明の詳細を説明
する。実施例1 Mucor circinelloides IFO 6746をポテトデキストロー
ス寒天培地(PDA)で5日間培養(30°C)したも
のに、滅菌水10mlを加え胞子懸濁液を調整した。オ
ートクレブで滅菌したビール粕(pH5,水分率70
%)20gに酢酸、リノール酸を0.1%になるように
添加し、よく混合した。このビール粕に前記胞子懸濁液
1.0mlを接種し、25°Cで3日間培養した後にム
コール菌数を測定した。表2に培養ビール粕1g当たり
のムコール菌数を示す。1表の結果と同様にリノール酸
の添加により Mucor circinelloides の増殖が促進し
た。菌数はPDA寒天平板にローズベンガルを2ppm
になるように添加し、25度Cで3日間培養し発生した
コロニー数から算出した。
EXAMPLES The present invention will be described in detail below based on examples. Example 1 Mucor circinelloides IFO 6746 was cultured in potato dextrose agar medium (PDA) for 5 days (30 ° C.), and 10 ml of sterilized water was added to prepare a spore suspension. Beer lees sterilized by autoclave (pH 5, moisture content 70
%), Acetic acid and linoleic acid were added to 0.1%, and mixed well. The beer lees were inoculated with 1.0 ml of the spore suspension and cultured at 25 ° C for 3 days, and then the number of mucor bacteria was measured. Table 2 shows the number of Mucor bacteria per 1 g of the cultured beer lees. Similar to the results shown in Table 1, addition of linoleic acid promoted the growth of Mucor circinelloides. The number of bacteria is 2ppm of rose bengal on PDA agar plate
And the number of colonies generated by culturing at 25 ° C for 3 days.

【0008】[0008]

【表2】 ビール粕によるムコールの培養 ─────────────────────── 培養条件 ムコール菌数(x1000) ─────────────────────── ビール粕のみ 6.3 +酢酸 100 +リノール酸 250 +酢酸+リノール酸 460 ─────────────────────── [Table 2] Culture of mucor with beer lees ─────────────────────── Culture conditions Mucor strain (x1000) ───────── ─────────────── Beer meal only 6.3 + Acetic acid 100 + Linoleic acid 250 + Acetic acid + Linoleic acid 460 ────────────────── ──────

【00010】実施例2 Mucor circinelloides IFO 6746 をポテトデキストロ
ース寒天培地(PDA)で5日間培養(30°C)した
ものに、滅菌水10mlを加え胞子懸濁液を調整した。
オートクレブで滅菌したビール粕(pH5,水分率70
%)20gにスカム(水分52.7%,粗蛋白質21.
9%,油脂分25.4%,pH5.9)2gを添加しよ
く混合した。このビール粕に前記胞子懸濁液1.0ml
を接種し、25°Cで4日間培養した後にムコール菌数
を測定した。表3に培養ビール粕1g当たりのムコール
菌数を示す。リノール酸の添加と同様にスカムを添加す
ることにより Mucor circinelloides の増殖が促進し、
良好なムコール麹が得られた。
Example 2 Mucor circinelloides IFO 6746 was cultivated in potato dextrose agar medium (PDA) for 5 days (30 ° C.), and 10 ml of sterilized water was added to prepare a spore suspension.
Beer lees sterilized by autoclave (pH 5, moisture content 70
%) Scum (water content 52.7%, crude protein 21.
2 g of 9%, fat and oil 25.4%, pH 5.9) was added and mixed well. 1.0 ml of the spore suspension in this beer meal
Was inoculated and cultured at 25 ° C for 4 days, and then the number of Mucor bacteria was measured. Table 3 shows the number of Mucor bacteria per 1 g of the cultured beer lees. As with the addition of linoleic acid, the addition of scum promotes the growth of Mucor circinelloides,
Good mucor koji was obtained.

【0011】[0011]

【表3】 ビール粕による糸状菌の培養 ──────────────────────── 培養条件 ムコール菌数(x1000) ──────────────────────── ビール粕のみ 6.5 ビール粕+スカム 330 ────────────────────────[Table 3] Culture of filamentous fungus with beer lees ──────────────────────── Culture conditions Mucor strain (x1000) ─────── ────────────────── Beer meal only 6.5 Beer meal + scum 330 ────────────────────── ──

【0012】試験例 実施例2で得られたビール粕を80°Cで6時間乾燥し
た後に、成分を分析した。表4には培養前のビール粕の
みの成分も併記しているが、この表から分かるようにム
コール処理により粗繊維含量と粗蛋白質含量が高まっ
た。
Test Example The beer lees obtained in Example 2 were dried at 80 ° C. for 6 hours, and then the components were analyzed. Table 4 also shows the components of beer lees only before culturing. As can be seen from this table, the mucole treatment increased the crude fiber content and crude protein content.

【表4】 ムコール処理ビール粕の成分 ───────────────────────────── 分析項目 ビール粕 ビール粕+スカム ───────────────────────────── ビタミンB1 (μg/g) 0.87 0.16 ビタミンB2 (μg/g) 0.74 9.46 粗繊維(%) 13.2 17.5 粗脂肪(%) 9.9 8.0 粗蛋白質(%) 25.5 28.1 灰分(%) 3.9 4.3 ───────────────────────────── ビタミンB1 :チオクロール蛍光法、 ビタミンB2 :ルミフラビン蛍光法、 粗繊維及び灰分:重量分析法(%)、 粗脂肪:ソックスレー法(%)、 粗蛋白質:ケルダール法(%)。[Table 4] Components of Mucor-treated beer lees ───────────────────────────── Analysis items Beer lees Beer lees + scum ─── ────────────────────────── Vitamin B 1 (μg / g) 0.87 0.16 Vitamin B 2 (μg / g) 0. 74 9.46 Crude fiber (%) 13.2 17.5 Crude fat (%) 9.9 8.0 Crude protein (%) 25.5 28.1 Ash (%) 3.9 4.3 ─── ────────────────────────── Vitamin B 1 : Thiochlor fluorescence method, Vitamin B 2 : Lumiflavin fluorescence method, Crude fiber and ash: Gravimetric method (%), Crude fat: Soxhlet method (%), crude protein: Kjeldahl method (%).

【0013】[0013]

【発明の効果】ビール粕は水分含量が高いために短時間
で細菌が繁殖し飼料として利用することが困難であった
が、ビール粕に油あるいは脂肪酸の混合物を添加しムコ
ールを接種し培養することにより、ムコール麹を製造す
ることが出来る。ムコール処理により粗繊維含量と粗蛋
白質含量が高まることから、飼料としての価値も向上す
る。
EFFECTS OF THE INVENTION Beer lees have a high water content, which makes it difficult for bacteria to grow in a short time and to be used as a feed. However, a mixture of oil or fatty acid is added to beer lees and mucoles are inoculated and cultured. As a result, mucor koji can be produced. The mucole treatment also increases the crude fiber content and crude protein content, thus improving the value of the feed.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】湿潤なビール粕を用いムコール・サーシネ
ロイデスを培養する方法において、脂肪酸を1種以上又
は水産加工浮上物を添加することを特徴とするムコール
麹の製造方法。
1. A method for producing mucor koji mold, wherein in the method of culturing mucor sarcyneloides using moist beer lees, at least one fatty acid or a processed marine product float is added.
JP5248646A 1993-09-09 1993-09-09 Culture of mucor Pending JPH0775563A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5248646A JPH0775563A (en) 1993-09-09 1993-09-09 Culture of mucor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5248646A JPH0775563A (en) 1993-09-09 1993-09-09 Culture of mucor

Publications (1)

Publication Number Publication Date
JPH0775563A true JPH0775563A (en) 1995-03-20

Family

ID=17181220

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5248646A Pending JPH0775563A (en) 1993-09-09 1993-09-09 Culture of mucor

Country Status (1)

Country Link
JP (1) JPH0775563A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000067588A1 (en) * 1999-05-06 2000-11-16 Masahiro Yamamoto Animal feed and production method thereof
EP1256282A1 (en) * 2001-05-11 2002-11-13 Masahiro Yamamoto Method for treating organic waste
EP1338208A1 (en) * 2002-02-21 2003-08-27 Masahiro Yamamoto Method for producing KOJI feed composition using oils
US6623771B2 (en) 2000-07-18 2003-09-23 Masahiro Yamamoto Livestock feed composition and its production method

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000067588A1 (en) * 1999-05-06 2000-11-16 Masahiro Yamamoto Animal feed and production method thereof
US6613365B1 (en) 1999-05-06 2003-09-02 Masahiro Yamamoto Animal feed and production method thereof
US6623771B2 (en) 2000-07-18 2003-09-23 Masahiro Yamamoto Livestock feed composition and its production method
EP1256282A1 (en) * 2001-05-11 2002-11-13 Masahiro Yamamoto Method for treating organic waste
US6703054B2 (en) 2001-05-11 2004-03-09 Masahiro Yamamoto Method for treating organic waste
EP1338208A1 (en) * 2002-02-21 2003-08-27 Masahiro Yamamoto Method for producing KOJI feed composition using oils
US7067164B2 (en) 2002-02-21 2006-06-27 Noriko Yamamoto Method for producing koji feed composition using oils

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