JPS62275669A - Production of yeast extract - Google Patents
Production of yeast extractInfo
- Publication number
- JPS62275669A JPS62275669A JP61119086A JP11908686A JPS62275669A JP S62275669 A JPS62275669 A JP S62275669A JP 61119086 A JP61119086 A JP 61119086A JP 11908686 A JP11908686 A JP 11908686A JP S62275669 A JPS62275669 A JP S62275669A
- Authority
- JP
- Japan
- Prior art keywords
- yeast
- basidiomycetes
- extract
- yeast extract
- soft
- 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
Links
- 239000012138 yeast extract Substances 0.000 title claims abstract description 30
- 229940041514 candida albicans extract Drugs 0.000 title claims abstract description 29
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 13
- 241000221198 Basidiomycota Species 0.000 claims abstract description 24
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims abstract description 23
- 238000000034 method Methods 0.000 claims abstract description 12
- 239000000284 extract Substances 0.000 claims abstract description 10
- 240000001462 Pleurotus ostreatus Species 0.000 claims abstract description 5
- 235000001603 Pleurotus ostreatus Nutrition 0.000 claims abstract description 5
- 240000008397 Ganoderma lucidum Species 0.000 claims abstract description 4
- 235000001637 Ganoderma lucidum Nutrition 0.000 claims abstract description 4
- 239000000203 mixture Substances 0.000 claims abstract description 4
- 240000000599 Lentinula edodes Species 0.000 claims abstract description 3
- 235000001674 Agaricus brunnescens Nutrition 0.000 claims description 7
- 230000002538 fungal effect Effects 0.000 claims 2
- 238000004113 cell culture Methods 0.000 claims 1
- 239000012228 culture supernatant Substances 0.000 claims 1
- 239000012634 fragment Substances 0.000 claims 1
- 239000000796 flavoring agent Substances 0.000 abstract description 9
- 235000019634 flavors Nutrition 0.000 abstract description 9
- 239000007788 liquid Substances 0.000 abstract description 8
- 239000000725 suspension Substances 0.000 abstract description 4
- 235000011194 food seasoning agent Nutrition 0.000 abstract description 3
- 239000006228 supernatant Substances 0.000 abstract description 3
- 235000001715 Lentinula edodes Nutrition 0.000 abstract 1
- 235000007685 Pleurotus columbinus Nutrition 0.000 abstract 1
- 235000013399 edible fruits Nutrition 0.000 abstract 1
- 238000006911 enzymatic reaction Methods 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 108090000790 Enzymes Proteins 0.000 description 20
- 102000004190 Enzymes Human genes 0.000 description 20
- 229940088598 enzyme Drugs 0.000 description 20
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000000354 decomposition reaction Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 230000002255 enzymatic effect Effects 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 208000035404 Autolysis Diseases 0.000 description 4
- 206010057248 Cell death Diseases 0.000 description 4
- 239000002609 medium Substances 0.000 description 4
- 230000028043 self proteolysis Effects 0.000 description 4
- 101710130006 Beta-glucanase Proteins 0.000 description 3
- 241000233866 Fungi Species 0.000 description 3
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000008103 glucose Substances 0.000 description 3
- 235000013372 meat Nutrition 0.000 description 3
- 239000002773 nucleotide Substances 0.000 description 3
- 235000002639 sodium chloride Nutrition 0.000 description 3
- 229920002498 Beta-glucan Polymers 0.000 description 2
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 2
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 2
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 2
- 239000004472 Lysine Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 235000004279 alanine Nutrition 0.000 description 2
- 235000001014 amino acid Nutrition 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000012258 culturing Methods 0.000 description 2
- 235000013922 glutamic acid Nutrition 0.000 description 2
- 239000004220 glutamic acid Substances 0.000 description 2
- RQFCJASXJCIDSX-UUOKFMHZSA-N guanosine 5'-monophosphate Chemical compound C1=2NC(N)=NC(=O)C=2N=CN1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O RQFCJASXJCIDSX-UUOKFMHZSA-N 0.000 description 2
- 235000013928 guanylic acid Nutrition 0.000 description 2
- 238000009630 liquid culture Methods 0.000 description 2
- 230000001293 nucleolytic effect Effects 0.000 description 2
- -1 sawdust Substances 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 210000005253 yeast cell Anatomy 0.000 description 2
- FYGDTMLNYKFZSV-URKRLVJHSA-N (2s,3r,4s,5s,6r)-2-[(2r,4r,5r,6s)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2r,4r,5r,6s)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1[C@@H](CO)O[C@@H](OC2[C@H](O[C@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-URKRLVJHSA-N 0.000 description 1
- RQFCJASXJCIDSX-UHFFFAOYSA-N 14C-Guanosin-5'-monophosphat Natural products C1=2NC(N)=NC(=O)C=2N=CN1C1OC(COP(O)(O)=O)C(O)C1O RQFCJASXJCIDSX-UHFFFAOYSA-N 0.000 description 1
- 239000004278 EU approved seasoning Substances 0.000 description 1
- 101710121765 Endo-1,4-beta-xylanase Proteins 0.000 description 1
- 229920002488 Hemicellulose Polymers 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
- 102000035195 Peptidases Human genes 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- 239000001888 Peptone Substances 0.000 description 1
- 108010080698 Peptones Proteins 0.000 description 1
- 241001417495 Serranidae Species 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000002358 autolytic effect Effects 0.000 description 1
- 235000013405 beer Nutrition 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000002361 compost Substances 0.000 description 1
- 239000012531 culture fluid Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 239000004226 guanylic acid Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 235000018977 lysine Nutrition 0.000 description 1
- 230000002101 lytic effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000014102 seafood Nutrition 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Coloring Foods And Improving Nutritive Qualities (AREA)
Abstract
Description
【発明の詳細な説明】
3、発明の詳細な説明
〔産業上の利用分野〕
本発明は酵母エキスの製造法に関し、詳しくは香味の改
良された酵母エキスを効率的に製造する方法に関する。Detailed Description of the Invention 3. Detailed Description of the Invention [Field of Industrial Application] The present invention relates to a method for producing a yeast extract, and more particularly to a method for efficiently producing a yeast extract with improved flavor.
酵母エキスは天然調味料として肉エキス、野菜エキス、
魚介類エキス等と共に化学調味料にはない複雑な呈味性
を有しているため、近年広く利用されてきている。Yeast extract is used as a natural seasoning for meat extract, vegetable extract,
It has been widely used in recent years because, along with seafood extracts, it has a complex taste that is not found in chemical seasonings.
しかしながら、酵母エキスは特有の香味を有するため、
その使用量や用途などに制約を受けるなどの問題点があ
った。However, since yeast extract has a unique flavor,
There were problems such as restrictions on the amount of use and applications.
一般に、酵母エキスは自己消化法、酸分解法。Generally, yeast extract is produced by autolysis or acid decomposition.
酸素分解法などによって製造されているが、自己消化法
では酵母の持つ酵素力を利用するため、その作用が緩慢
であり、かつ強固な酵母細胞壁が残留する。また、酸分
解法では酸により強制的に加熱加水分解するため、その
香味は好ましいものではない。さらに、酵素分解法では
各種の酵素を用いているけれども、これら酵素はカビや
ハタテリア等から得られたものが多く、食品添加物とし
てあまり好ましいものではなかった。It is produced using oxygen decomposition methods, etc., but since the autolysis method uses the enzymatic power of yeast, its action is slow and strong yeast cell walls remain. In addition, in the acid decomposition method, the flavor is not desirable because the acid is used to forcibly heat and hydrolyze the product. Furthermore, although various enzymes are used in the enzymatic decomposition method, many of these enzymes are obtained from molds, groupers, etc., and are not very desirable as food additives.
本発明者らは、これら酵母エキスの香味の改良、製造条
件の改善、収率の向上等を目指して研究を重ねた結果、
本発明を完成するに至ったのである。As a result of repeated research aimed at improving the flavor, manufacturing conditions, and yield of these yeast extracts, the present inventors found that
This led to the completion of the present invention.
すなわち本発明は、酵母エキスを製造するにあたり、酵
母に軟質を旦子菌類を作用させることを特徴とする酵母
エキスの製造法である。That is, the present invention is a method for producing a yeast extract, which is characterized in that, in producing the yeast extract, a yeast fungus is applied to soften the yeast.
本発明は酵素分解法による酵母エキスの製造法に分類さ
れるものであるが、まんねんたけ、ひらたけ、しいたけ
、なめたけ等の軟質担子菌類、好ましくは食用、薬用担
子菌類の1種もしくは2種以上の培養によって得られる
酵素を利用して酵母エキスを製造するものである。The present invention is classified as a method for producing yeast extract by enzymatic decomposition method, and the method uses soft basidiomycetes such as Mannentake mushroom, Hiratake mushroom, Shiitake mushroom, Nametake mushroom, etc., preferably one or two types of edible and medicinal basidiomycete fungi. Yeast extract is produced using the enzyme obtained by the above culture.
本発明は、主にこれら菌類を培養する工程と、その培養
物を利用して酵母エキスを得る工程から成っている。The present invention mainly consists of a step of culturing these fungi and a step of obtaining yeast extract using the culture.
軟質担子菌類は通常、ホダ木やオガ屑、堆肥等に固体培
養され、その子実体は好んで食用とされるが、これら菌
類はセルロース、ヘミセルロース。Soft basidiomycetes are usually cultivated on solid wood, sawdust, compost, etc., and their fruiting bodies are often eaten, but these fungi produce cellulose and hemicellulose.
リグニン等を分解する酵素力を有しており、さらに種々
の核酸分解酵素をも含有している。本発明はこれら担子
菌類の酵素力をそのままあるいは部分的に利用して酵母
エキスを製造するものであり、担子菌類の利用法はそれ
が子実体であるか菌糸であるかを問わない。また、担子
菌体の破砕物や抽出物などであってもよい。さらには、
担子菌類を液体培養した培養液そのものや該培養液から
固液分離して得られる上清であってもよい。また、これ
らを精製処理したものであってもよい。担子菌類を液体
培養すると、菌糸の生育と共に菌糸は勿論のこと培養液
中にも強力な酵素を蓄積する。したがって、担子菌体破
砕物あるいは抽出物等の利用も可能であるが、培養液(
担子菌体の有無に拘らず)の利用の方が容易であり、実
用性に富むものである。なお、これら菌類は混合物とし
て用いることが出来ることは勿論である。It has enzymatic power to decompose lignin, etc., and also contains various nucleolytic enzymes. The present invention uses the enzymatic power of these basidiomycetes directly or partially to produce a yeast extract, and the basidiomycetes can be used regardless of whether they are fruiting bodies or hyphae. It may also be a crushed product or extract of basidiomycete cells. Furthermore,
The culture solution itself obtained by liquid culturing Basidiomycetes or the supernatant obtained by solid-liquid separation from the culture solution may be used. Moreover, these may be purified. When basidiomycetes are cultured in liquid, strong enzymes accumulate not only in the hyphae but also in the culture solution as the hyphae grow. Therefore, it is possible to use crushed basidiomycete cells or extracts, but culture fluid (
It is easier to use basidiomycetes (with or without basidiomycetes) and is more practical. It goes without saying that these fungi can be used as a mixture.
担子菌類を液体培養するために用いる培地としては通常
の栄養培地でよく、特殊な成分を加えたりする必要はな
い。具体的には、一般に用いられる培地素材、たとえば
ペプトン、肉エキス、麦芽エキス、酵母エキス、ブドウ
糖、無機塩類等を適宜組合わせ、水に希釈して用いれば
よく、各成分の濃度は1〜5%程度で十分である。The medium used for liquid culture of basidiomycetes may be a normal nutrient medium, and there is no need to add special ingredients. Specifically, commonly used culture medium materials such as peptone, meat extract, malt extract, yeast extract, glucose, inorganic salts, etc. may be appropriately combined and used after being diluted with water, and the concentration of each component may be 1 to 5. % is sufficient.
担子菌類培養物は強力なβ−グルカナーゼ活性を有して
おり、これはβ−グルカンから還元垢を生成することか
ら確認できる(第1図参照)。この酵素は酵母細胞壁に
も作用して、これを溶解することが検鏡により観察され
た。さらに、この培養物はキシラナーゼ活性を有してい
ることが認められた。Basidiomycete cultures have strong β-glucanase activity, which is confirmed by the production of reduced plaque from β-glucans (see Figure 1). Using a microscope, it was observed that this enzyme also acts on yeast cell walls and dissolves them. Furthermore, this culture was found to have xylanase activity.
酵母に担子菌類に作用させるには、酵母エキス製造過程
の適宜時期に行なえばよいが、通常は酵母懸濁液に該担
子菌類を加え、pH,温度などを酵素作用が発現しやす
い条件として所定時間(通常1〜20時間)接触させれ
ばよい。この場合、酵母懸濁液の濃度は圧搾酵母濃度を
5〜45%、好ましくは15〜35%として用いるとよ
く、担子菌類として液体培養物を用いるときは、培養開
始後約1ケ月経過したものを0.3〜10%程度、好ま
しくは1〜5%程度の割合で添加するのがよい。さらに
、酵素の作用温度、 pHについては、β−グルカナー
ゼ活性が発現し、かつ良好な呈味を持つ酵母エキスを得
るための条件として、pHが4.5〜9.0、好ましく
は6.5〜8.5、温度が30〜60℃、好ましくは4
0〜55℃で作用させるのがよい。また、酵母は生酵母
を用いて自己消化法による酵母エキスの製造法と併用す
る形式としてもよく、乾燥酵母や熱変性処理した酵母な
どを用いてもよく、特に制約されることはない。To make yeast act on the basidiomycetes, it can be done at an appropriate time during the yeast extract production process, but usually the basidiomycetes are added to the yeast suspension and the pH, temperature, etc. are adjusted to certain conditions that facilitate the expression of enzyme action. The contact may be made for a period of time (usually 1 to 20 hours). In this case, the concentration of the yeast suspension should be 5 to 45%, preferably 15 to 35%, of the compressed yeast concentration, and when using a liquid culture as the basidiomycete, the yeast suspension should be used after about 1 month has passed after the start of culture. It is preferable to add about 0.3 to 10%, preferably about 1 to 5%. Furthermore, regarding the action temperature and pH of the enzyme, the pH is 4.5 to 9.0, preferably 6.5, as conditions for expressing β-glucanase activity and obtaining a yeast extract with good taste. ~8.5, temperature is 30-60℃, preferably 4
It is preferable to act at a temperature of 0 to 55°C. Further, the yeast may be used in combination with the method for producing yeast extract by autolysis using fresh yeast, or dried yeast or heat-denatured yeast may be used, and there are no particular restrictions.
本発明によれば、酵母臭がなく香味の改善された呈味力
のある酵母エキスが得られる。たとえば、実施例2にお
いて得られた酵母エキスの分析を行なったところ、グル
タミン酸、アラニン、リジンなどのアミノ酸類を多く含
み、かつ種々の5′−ヌクレオチド類、とりわけ5゛−
グアニル酸を多量に含んでいることが判明した。したが
って、本発明による酵母エキスが呈味性に優れている理
由は、これらアミノ酸類と5′−ヌクレオチド類の相互
作用によるものであると認められる。このことは、本発
明に用いる担子菌類に含まれる酵素が単に細胞壁溶解酵
素としてだけでなく、蛋白質分解酵素、核酸分解酵素な
どをも含む複合酵素として作用していると考えられるば
かりでなく、酵母エキス製造時の自己消化酵素系とも連
動して作用し、その呈味性を増幅しているものと思われ
る。According to the present invention, a yeast extract with no yeast odor, improved flavor, and strong taste can be obtained. For example, analysis of the yeast extract obtained in Example 2 revealed that it contained a large amount of amino acids such as glutamic acid, alanine, and lysine, as well as various 5'-nucleotides, especially 5'-nucleotides.
It was found that it contains a large amount of guanylic acid. Therefore, it is recognized that the reason why the yeast extract according to the present invention has excellent taste is due to the interaction between these amino acids and 5'-nucleotides. This suggests that the enzymes contained in the basidiomycetes used in the present invention not only act as cell wall lytic enzymes but also as complex enzymes that include proteolytic enzymes, nucleolytic enzymes, etc. It is thought that it acts in conjunction with the autolytic enzyme system during extract production to amplify its taste.
また、本発明の方法によれば、酵母エキスの製造時間を
短縮することが出来る上に、その収率も向上する。Moreover, according to the method of the present invention, not only can the manufacturing time of yeast extract be shortened, but also its yield can be improved.
次に、本発明を実施例により説明するが、本発明はこれ
らによって制限されるものではない。Next, the present invention will be explained by examples, but the present invention is not limited thereto.
実施例1
麦汁(温度約1.5%)1)に粉末酵母エキス2.5g
(0,25%)およびグルコース20g(2,0%)を
添加し、オートクレーブで120℃、15分の殺菌を行
なった。冷却後、この培地にまんねんたけを接種し、2
0℃で静置培養を行なった。Example 1 2.5 g of powdered yeast extract in wort (temperature approximately 1.5%) 1)
(0.25%) and 20 g (2.0%) of glucose were added and sterilized in an autoclave at 120° C. for 15 minutes. After cooling, this medium was inoculated with Mannentake mushrooms, and 2
Static culture was performed at 0°C.
約1週間後には培養液表面に白色の菌糸が観察され、さ
らに培養を続けると、約1ケ月後には厚い菌糸蓋となり
、β−グルカナーゼ活性が最大となる。この培養液を濾
過して得た濾液を粗酵素とした。After about one week, white hyphae are observed on the surface of the culture solution, and if the culture is continued further, after about one month a thick hyphae is formed and the β-glucanase activity reaches its maximum. The filtrate obtained by filtering this culture solution was used as a crude enzyme.
ビール酵母を洗浄して得た圧搾酵母200g(酵母乾物
21%)を水に分散し、これに上記まんねんたけ粗酵素
20m1を加え、加水して1)とした。次に、pH6,
5、温度45℃で保持し、20時間後に遠心分離を行な
い、液部と粕部に分けた。液部に一定量の食塩を添加し
たのち濃縮し温度約55%として殺菌した。このときの
酵母エキス収率は52%であった。一方、対照として粗
酵素を加えることなく自己消化法としたこと以外は同様
にして得た酵母エキスは収率が約10%も低いものであ
った。また、官能検査(パネル4名による2%溶液の試
飲による比較)により酵母エキスの香味について検討し
たところ、第1表に示した如く、本発明による製品は香
味も優れていることが判明した。200 g of compressed yeast (21% yeast dry matter) obtained by washing beer yeast was dispersed in water, and 20 ml of the above-mentioned Mannake mushroom crude enzyme was added thereto and water was added to obtain 1). Next, pH 6,
5. The temperature was maintained at 45°C, and after 20 hours, centrifugation was performed to separate the liquid part and the lees part. After adding a certain amount of common salt to the liquid part, it was concentrated and sterilized at a temperature of about 55%. The yeast extract yield at this time was 52%. On the other hand, as a control, the yield of yeast extract obtained in the same manner except that the autolysis method was used without adding crude enzyme was about 10% lower. Furthermore, when the flavor of the yeast extract was investigated through a sensory test (comparison by tasting 2% solutions by four panelists), it was found that the product according to the present invention also had an excellent flavor, as shown in Table 1.
第 1 表
1♂L−評 価
対照品 酵母臭あり、呈味力やや乏しい本発明品
酵母臭なし、呈味力あり実施例2
麦汁(温度約1.5%)1)に肉エキス2.0g(0,
2%)およびグルコース20g(2,0%)を添加し、
オートクレーブで120℃、15分の殺菌を行なった。Table 1 ♂L-Evaluation control product Inventive product with yeast odor and slightly poor taste power Example 2: Wort (temperature approx. 1.5%) 1) with meat extract 2 .0g(0,
2%) and glucose 20g (2,0%),
Sterilization was performed in an autoclave at 120°C for 15 minutes.
冷却後、この培地にひらたけを接種し、20℃で静置培
養を行なった。After cooling, this medium was inoculated with oyster mushrooms and statically cultured at 20°C.
約1ケ月後に培養液表面に生育した菌糸を採取し、これ
に水を加えて磨砕し、次いぞ遠心分離して得た上清を粗
酵素とした。After about one month, the mycelium grown on the surface of the culture solution was collected, ground by adding water, and then centrifuged to obtain a supernatant, which was used as crude enzyme.
ビール乾燥酵母45gを水に分散し、上記ひらたけ粗酵
素20mlを加え、加水して1)とした。45 g of beer dry yeast was dispersed in water, 20 ml of the above-mentioned Hiratake crude enzyme was added, and water was added to prepare 1).
次に、pH8,0,温度45℃で保持し、10時間後に
遠心分離を行ない、液部と粗部に分けた。液部に一定量
の食塩を添加したのち濃縮し温度約55%として殺菌し
た。Next, the mixture was maintained at a pH of 8.0 and a temperature of 45° C., and centrifuged after 10 hours to separate a liquid portion and a coarse portion. After adding a certain amount of common salt to the liquid part, it was concentrated and sterilized at a temperature of about 55%.
この酵母エキスについて分析を行なったところ、グルタ
ミン酸4.5%、アラニン3.1%、リジン2.0%、
5゛−グアニル酸0.6%を含有しており、対照の酵素
無添加で調製した酵母エキスよりも香味が優れていた。Analysis of this yeast extract revealed that glutamic acid 4.5%, alanine 3.1%, lysine 2.0%,
It contained 0.6% of 5'-guanylic acid, and had a better flavor than the control yeast extract prepared without the addition of enzyme.
第1図は実施例1で得た粗酵素をpH6,0,温度45
℃の条件でβ−グルカンに作用させたときの還元糖の経
時的生成率を示すグラフである。Figure 1 shows the crude enzyme obtained in Example 1 at pH 6.0 and temperature 45.
It is a graph showing the production rate of reducing sugar over time when it is made to act on β-glucan under conditions of °C.
Claims (3)
菌類を作用させることを特徴とする酵母エキスの製造法
。(1) A method for producing a yeast extract, which comprises reacting yeast with a soft basidiomycete.
け、なめたけ等の中から選ばれたものである特許請求の
範囲第1項記載の方法。(2) The method according to claim 1, wherein the soft basidiomycete is selected from Mannentake mushroom, Oyster mushroom, Shiitake mushroom, Nametake mushroom, etc.
は抽出物、菌体培養液もしくはその培養上清またはこれ
らの混合物である特許請求の範囲第1項記載の方法。(3) The method according to claim 1, wherein the soft basidiomycete is a fruiting body, mycelium, a fungal cell fragment or extract, a fungal cell culture solution, a culture supernatant thereof, or a mixture thereof.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61119086A JPS62275669A (en) | 1986-05-26 | 1986-05-26 | Production of yeast extract |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61119086A JPS62275669A (en) | 1986-05-26 | 1986-05-26 | Production of yeast extract |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62275669A true JPS62275669A (en) | 1987-11-30 |
Family
ID=14752543
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61119086A Pending JPS62275669A (en) | 1986-05-26 | 1986-05-26 | Production of yeast extract |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62275669A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1078452C (en) * | 1992-12-02 | 2002-01-30 | Cpc国际有限公司 | Flavored yeast extracts |
JP2006129835A (en) * | 2004-11-09 | 2006-05-25 | Takeda-Kirin Foods Corp | Yeast essence highly containing glutamic acid and method for producing the same |
JP2019129795A (en) * | 2018-02-02 | 2019-08-08 | 三菱商事ライフサイエンス株式会社 | Flavor improver |
-
1986
- 1986-05-26 JP JP61119086A patent/JPS62275669A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1078452C (en) * | 1992-12-02 | 2002-01-30 | Cpc国际有限公司 | Flavored yeast extracts |
JP2006129835A (en) * | 2004-11-09 | 2006-05-25 | Takeda-Kirin Foods Corp | Yeast essence highly containing glutamic acid and method for producing the same |
JP4651361B2 (en) * | 2004-11-09 | 2011-03-16 | キリンフードテック株式会社 | Glutamic acid-rich yeast extract and method for producing the same |
JP2019129795A (en) * | 2018-02-02 | 2019-08-08 | 三菱商事ライフサイエンス株式会社 | Flavor improver |
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