JPH01153020A - Artificial culture of mushroom - Google Patents
Artificial culture of mushroomInfo
- Publication number
- JPH01153020A JPH01153020A JP62310534A JP31053487A JPH01153020A JP H01153020 A JPH01153020 A JP H01153020A JP 62310534 A JP62310534 A JP 62310534A JP 31053487 A JP31053487 A JP 31053487A JP H01153020 A JPH01153020 A JP H01153020A
- Authority
- JP
- Japan
- Prior art keywords
- mushroom
- mushrooms
- substance
- culture
- pumpkin seeds
- 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.)
- Granted
Links
- 235000001674 Agaricus brunnescens Nutrition 0.000 title claims abstract description 30
- 241000408747 Lepomis gibbosus Species 0.000 claims abstract description 16
- 235000020236 pumpkin seed Nutrition 0.000 claims abstract description 16
- 239000000126 substance Substances 0.000 claims abstract description 8
- 230000001737 promoting effect Effects 0.000 claims abstract description 5
- 238000000034 method Methods 0.000 claims description 14
- 235000012054 meals Nutrition 0.000 claims description 11
- 229920001592 potato starch Polymers 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 4
- 230000033937 fruiting body development Effects 0.000 claims description 2
- 239000002245 particle Substances 0.000 claims description 2
- 229920002472 Starch Polymers 0.000 abstract description 9
- 235000019698 starch Nutrition 0.000 abstract description 9
- 239000008107 starch Substances 0.000 abstract description 9
- 240000006499 Flammulina velutipes Species 0.000 abstract description 7
- 235000016640 Flammulina velutipes Nutrition 0.000 abstract description 6
- 235000000832 Ayote Nutrition 0.000 abstract description 3
- 235000009854 Cucurbita moschata Nutrition 0.000 abstract description 3
- 240000001980 Cucurbita pepo Species 0.000 abstract description 3
- 235000009804 Cucurbita pepo subsp pepo Nutrition 0.000 abstract description 3
- 238000012258 culturing Methods 0.000 abstract description 3
- 239000003814 drug Substances 0.000 abstract description 3
- 235000013305 food Nutrition 0.000 abstract description 3
- 235000015136 pumpkin Nutrition 0.000 abstract description 3
- 239000004743 Polypropylene Substances 0.000 abstract description 2
- 235000013376 functional food Nutrition 0.000 abstract description 2
- -1 polypropylene Polymers 0.000 abstract description 2
- 229920001155 polypropylene Polymers 0.000 abstract description 2
- 235000013399 edible fruits Nutrition 0.000 abstract 2
- 239000001963 growth medium Substances 0.000 description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- 241000209094 Oryza Species 0.000 description 9
- 235000007164 Oryza sativa Nutrition 0.000 description 9
- 235000009566 rice Nutrition 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 6
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
- 241000894006 Bacteria Species 0.000 description 5
- 239000002609 medium Substances 0.000 description 5
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 4
- 235000011941 Tilia x europaea Nutrition 0.000 description 4
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 4
- 239000000920 calcium hydroxide Substances 0.000 description 4
- 235000011116 calcium hydroxide Nutrition 0.000 description 4
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 4
- 239000004571 lime Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229920001277 pectin Polymers 0.000 description 4
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 230000018044 dehydration Effects 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 235000019253 formic acid Nutrition 0.000 description 3
- 239000004310 lactic acid Substances 0.000 description 3
- 235000014655 lactic acid Nutrition 0.000 description 3
- 230000000813 microbial effect Effects 0.000 description 3
- 235000010987 pectin Nutrition 0.000 description 3
- 239000001814 pectin Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- 240000000599 Lentinula edodes Species 0.000 description 2
- 240000001462 Pleurotus ostreatus Species 0.000 description 2
- 235000001603 Pleurotus ostreatus Nutrition 0.000 description 2
- 244000061456 Solanum tuberosum Species 0.000 description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000001580 bacterial effect Effects 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 210000000170 cell membrane Anatomy 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 235000019197 fats Nutrition 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 235000016709 nutrition Nutrition 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- ODHCTXKNWHHXJC-VKHMYHEASA-N 5-oxo-L-proline Chemical compound OC(=O)[C@@H]1CCC(=O)N1 ODHCTXKNWHHXJC-VKHMYHEASA-N 0.000 description 1
- 239000002028 Biomass Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- AEMOLEFTQBMNLQ-YMDCURPLSA-N D-galactopyranuronic acid Chemical compound OC1O[C@H](C(O)=O)[C@H](O)[C@H](O)[C@H]1O AEMOLEFTQBMNLQ-YMDCURPLSA-N 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 1
- 229920002488 Hemicellulose Polymers 0.000 description 1
- 235000001715 Lentinula edodes Nutrition 0.000 description 1
- 244000168667 Pholiota nameko Species 0.000 description 1
- 235000014528 Pholiota nameko Nutrition 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- ODHCTXKNWHHXJC-GSVOUGTGSA-N Pyroglutamic acid Natural products OC(=O)[C@H]1CCC(=O)N1 ODHCTXKNWHHXJC-GSVOUGTGSA-N 0.000 description 1
- 235000019774 Rice Bran oil Nutrition 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- ODHCTXKNWHHXJC-UHFFFAOYSA-N acide pyroglutamique Natural products OC(=O)C1CCC(=O)N1 ODHCTXKNWHHXJC-UHFFFAOYSA-N 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000001093 anti-cancer Effects 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 238000009264 composting Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000012364 cultivation method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 235000013402 health food Nutrition 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 235000008935 nutritious Nutrition 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 210000002826 placenta Anatomy 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000008165 rice bran oil Substances 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 241001148471 unidentified anaerobic bacterium Species 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
Landscapes
- Mushroom Cultivation (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
Description
【発明の詳細な説明】
(イ)産業上の利用分野
本発明は、かぼちゃの種子を子実体発生促進物質として
利用するきのこの人工栽培法に関するものである。DETAILED DESCRIPTION OF THE INVENTION (a) Field of Industrial Application The present invention relates to a method for artificially cultivating mushrooms using pumpkin seeds as a substance for promoting fruiting body development.
(ロ)従来の技術
従来、きのこの栽培は、主に鋸屑10部に対して米糠1
〜10部の乾物重量比で混合した培養基を用いた菌床人
工栽培法が実施されてきた。(b) Conventional technology Traditionally, mushroom cultivation was mainly done by using 1 part of rice bran for 10 parts of sawdust.
Artificial bacterial bed cultivation methods using culture media mixed at a dry weight ratio of ~10 parts have been practiced.
(ハ)発明が解決しようとする問題点
しかし、近年米糠の供給量が低下していること、また、
米糠油を回収した後の脱脂米糠は、特にエノキタケ(シ
イタケに次ぐ生産量がある)の発茸効果を消失させるこ
とを考えれば、米糠に代わる有効な発茸促進物質の探究
は極めて重要な課題となっている。(c) Problems that the invention aims to solve However, the supply of rice bran has been decreasing in recent years, and
Considering that defatted rice bran after rice bran oil is recovered will eliminate the mushroom-promoting effect of enokitake mushrooms (the second most produced after shiitake mushrooms), the search for an effective mushroom-promoting substance to replace rice bran is an extremely important issue. It becomes.
本発明は、こうした観点に立ち検討した結果発明に至っ
たものであり、皮付きかぼちゃの種子が、ヒラタケ、シ
メン、ナメコなとはもちろんのこと、従来、米[添加培
養基以外では栽培不可能とされてきたエノキタケに対し
ても極めて有効な方法であることが判明したものである
。The present invention was developed as a result of studies from these viewpoints, and the skinned pumpkin seeds can be used not only for oyster mushrooms, cymens, and nameko seeds, but also for rice [which cannot be cultivated except with an added culture medium]. This method has also been found to be extremely effective against enokitake mushrooms, which have been cultivated for a long time.
かぼちゃは、年間約27万トン生産されており、そのう
ち加工用に約2万トンが向けられている。Approximately 270,000 tons of pumpkin are produced annually, of which approximately 20,000 tons are destined for processing.
それから発生する胎座(ねた)を含めた皮付き種子はそ
の12〜15%、皮付き種子だけでは4〜7%である。The skinned seeds including the placenta that develop from this amount account for 12 to 15% of the total, and the skinned seeds alone account for 4 to 7%.
しかし、この種子は、これまでかぼちゃ加工工場などに
おいては利用したくともこれといった方法がなく、当初
は土中に埋め立てられ処理されてきたが、いつまでも腐
敗しないことから、最近では地表にまき、発芽を待って
土中にすき込んでいるのが実状である。However, until now, there has been no suitable method for using these seeds in pumpkin processing factories, etc., and they were initially disposed of by being buried in the ground, but since they do not rot forever, recently they have been sown on the ground and germinated. The reality is that they are being dug into the soil, waiting for the next step.
一方、培養基の基を才となる鋸屑あるいは馬鈴薯澱粉粕
のうち、前者はともかくも、後者については未だ確固た
る利用がなされているとは言い難い。On the other hand, among the sawdust and potato starch meal that can be used as a base for a culture medium, it is difficult to say that the latter has yet been firmly used, although the former may be the case.
表1 馬鈴薯澱粉粕の各種処理法による生産量(トン)
表1は馬鈴薯澱粉生産19工場についての澱粉粕の処理
生産状況であるが、イニシャルコスト的にみて堆肥化も
かなわず、飼料化を目的に各種の形に処理されている。Table 1 Production volume of potato starch meal by various processing methods (tons) Table 1 shows the processing and production status of starch meal at 19 potato starch production factories, but from the initial cost perspective, composting is not possible and the purpose is to make it into feed. It is processed into various shapes.
これらは、円高以前の状況下においては輸入ものの価格
高から生餌としての引き合いもあったが、最近の円高下
においては600〜800円/トンが限界であり、飼料
に代わる有効利用法の開発が待たれているものである。Before the appreciation of the yen, there were inquiries as raw feed due to the high price of imported products, but with the recent appreciation of the yen, the price has been reduced to 600 to 800 yen/ton, making it an effective alternative to feed. The development of this technology is awaited.
(ニ)問題点を解決するための手段
かぼちゃの種子は表2に示すとおり、高品質の蛋白質や
脂肪が多く含まれ、しかもその脂肪中には表3に示すと
おり、リノール酸、いわゆるビタミンFと称され、きの
この発生促進作用があるといわれる成分を60.7%も
の高率で含有するなと極めて栄養価の高いものとして、
中国では古くより健康食品として常食されてきたもので
もある。(d) Measures to solve the problem As shown in Table 2, pumpkin seeds contain a large amount of high-quality protein and fat, and as shown in Table 3, the fat contains linoleic acid, the so-called vitamin F. It is said to be extremely nutritious, containing as high as 60.7% of ingredients that are said to have the effect of promoting the growth of mushrooms.
In China, it has been eaten regularly as a health food since ancient times.
また、米糠配合法に対する優位性としては、米糠は時間
とともに脂質の酸化が進行し、きのこの素材としても好
ましくなくなるのに対し、かぼちゃの種子は皮付きであ
ることから使用に応じて粉砕利用が可能であり、腐敗は
もちろんのこと酸化表2 風乾した皮付きかぼちや
種子の一般成分(%)
表3 かぼちや種子の脂肪酸組成(%)なとの変質の心
配もない。そのうえ、種子を包む皮を6〜1δO(好ま
しくは6〜60)メツシュに粉砕することによフて、培
養基に適度の空隙をつくる効果があり、菌糸の発育に極
めて良好な結果をもたらす。特にR扮拍単体の場合は、
粕中のペクチン質が吸水して培養容器に充填する際に、
ややもすると圧密化しやすく通気性を欠くきらいがある
が、かぼちゃ種子を混合することは、それを緩和するの
に十分な効果がある。実際、菌まわりは米I!使用に比
べて速く、その菌叢密度は極めて高い。In addition, its advantage over the rice bran blending method is that rice bran's lipid oxidation progresses over time, making it undesirable as a material for mushrooms, whereas pumpkin seeds have skins and can be crushed depending on the use. It is possible, and there is no need to worry about deterioration, not only from spoilage but also from oxidation. Furthermore, by crushing the skin surrounding the seeds into a mesh of 6 to 1 δO (preferably 6 to 60), it has the effect of creating appropriate voids in the culture medium, resulting in extremely good results for the growth of mycelia. Especially in the case of a single R beat,
When the pectin in the lees absorbs water and fills the culture container,
Although it tends to become compacted and lack air permeability, mixing pumpkin seeds has a sufficient effect to alleviate this problem. In fact, around bacteria is rice I! It is fast compared to the usage, and the bacterial flora density is extremely high.
本発明で培養基の基材となる未乾燥馬鈴薯澱粉粕の原料
である澱粉用馬鈴薯は年間160万トン(馬鈴薯総生産
額の約56%)が消費され、そこから澱粉粕は12〜1
5%産出される。その水分は当初91〜92%であり、
現在、それは表1に示すとおり、生のものから乾燥のも
の(水分約13%)まで種々の形に処理されている。し
かし、オイルショック当時、コスト高のミール工場が4
か所から1か所に減少した事情からも明かなように、今
後世界情勢によっては、また乾燥コストがネックになら
ないとも限らない。したがって、乾燥しないで脱水処理
程度で有効利用できれば、現在その処置に頭を1とえて
いる。n粉工業界にとってもまたとない朗報となる。In the present invention, 1.6 million tons (approximately 56% of total potato production) of potatoes for starch, which is the raw material for the undried potato starch meal that is the base material for the culture medium, are consumed annually, from which 12 to 1
5% is produced. Its moisture content was initially 91-92%,
Currently, it is processed into various forms, from fresh to dried (approximately 13% moisture), as shown in Table 1. However, at the time of the oil crisis, four high-cost meal factories
As is clear from the reduction from one location to one location, depending on the world situation, there is no guarantee that drying costs will not become a bottleneck in the future. Therefore, if it can be used effectively by dehydrating it without drying it, we are currently considering that method. This is great news for the powder industry.
一方、かぼちゃの皮付き種子の水分は、風乾によって簡
単に6%近くに引き下げることができ、仮にこれを澱粉
粕に乾物重量比で20〜30%配合して、培養基の水分
を65%に調整するとすれば、1わ松柏の水分は大体7
0〜72%程度であればよく、この値は現在澱粉工場で
使用されているベルトプレスの脱水能力の範囲内にあり
、たとえ80%以上であっても、やはり水分の少ない鋸
屑な混合使用することで容易に調整可能である。つまり
、92%水分の生拍を脱水処理するのみて目的が果たせ
るわけである。これは6%という低水分であるかぼちゃ
の種子あるいは鋸屑との組み合わせにおいて始めて可能
となる。On the other hand, the moisture content of pumpkin seeds with skin can be easily reduced to nearly 6% by air drying, and if this is mixed with starch meal at a dry weight ratio of 20 to 30%, the moisture content of the culture medium can be adjusted to 65%. If so, the water content of 1 pine oak is approximately 7
It is sufficient if it is about 0 to 72%, and this value is within the dewatering capacity of belt presses currently used in starch factories, and even if it is 80% or more, it is still necessary to use a mixture of sawdust with low moisture content. This makes it easy to adjust. In other words, the purpose can be achieved only by dehydrating the raw heart, which is 92% water. This is only possible in combination with pumpkin seeds or sawdust, which have a moisture content as low as 6%.
なお、新鮮なうちに使いきれない場合の脱水粕の保存法
については、次の2つの方法が採用できる。The following two methods can be used to preserve the dehydrated lees if it cannot be used up while it is still fresh.
(1)まず、消石灰無添加で処理され70〜80%前後
の水分状態で野積みあるいは放置されている場合は、常
時10°C以下の環境であれば、当初のpHも 5.4
位で極めてパサパサして分散度もよく、他の栄養素材を
容易に均一混合することができ、きのこ培地として極め
て良好な状態にあるが、10℃以上の外気にさらされる
うちに徐々に外層部はりゾーブス属なとのカビに、内層
部は酵母やバクテリアの繁殖によって、ペクチン質の微
生物分解を受はガラクチュロン酸なとのウロン酸の生成
に伴って、pH4弱までの低下とバルブの粘性増大によ
り、ダンゴ状をなして極めて分散度の悪いものとなる。(1) First of all, if it is treated without the addition of slaked lime and is piled up or left in the open with a moisture content of around 70-80%, the initial pH will be 5.4 if the environment is always below 10°C.
It is extremely dry and has a good dispersion degree, and other nutritional materials can be mixed easily and uniformly, making it an excellent mushroom culture medium. The inner layer undergoes microbial decomposition of pectin due to the growth of yeast and bacteria, and the production of uronic acids such as galacturonic acid causes the pH to drop to just under 4 and increase the viscosity of the valve. As a result, the particles form a lump-like shape and have an extremely poor degree of dispersion.
したがって、他の基質を均一混合し、きのこ培養におけ
る適正p)(値範囲6〜5(許容範囲は8〜4.5)ま
でにアルカリを添加するにしても容易ではない。Therefore, it is not easy to uniformly mix other substrates and add alkali to the appropriate p value for mushroom culture (value range 6 to 5 (acceptable range is 8 to 4.5)).
この現象を防止する長期保存法は、脱水前の91〜92
%水分の生の状態のまま放置しておき、使用時にpl(
調整を兼ねて消石灰を添加し脱水処理すれば、他の基質
を均一混合することも容易で、容積量の多いこと以外極
めて良好な培地となる。A long-term storage method to prevent this phenomenon is to store 91-92 before dehydration.
Leave it in the raw state of % moisture, and when using it, pl (
If slaked lime is added and dehydrated for adjustment, it is easy to mix other substrates uniformly, and it becomes an extremely good medium except for its large volume.
この場合、時に酢酸生成の可能性もあるが、バクテリア
の場合とは全く異なり、きのこ栽培には何ら支障はない
、一般にきのこ菌糸と子実体中に含まれる有機酸は同一
種で、ピログルタミン酸、リンゴ酸、フマール酸、クエ
ン酸が主であり、酢酸は中程度、乳酸、ギ酸、シュウ酸
がわずかを占める。したがって、培地に多量の乳酸やギ
酸があれば発育は阻害されるが、酢酸は影響がない。In this case, there is a possibility of acetic acid production, but this is completely different from the case of bacteria, and does not pose any problem for mushroom cultivation.Generally, the organic acids contained in mushroom mycelia and fruiting bodies are the same type, such as pyroglutamic acid, Malic acid, fumaric acid, and citric acid predominate, acetic acid accounts for a moderate amount, and lactic acid, formic acid, and oxalic acid account for a small amount. Therefore, if there is a large amount of lactic acid or formic acid in the medium, growth will be inhibited, but acetic acid will have no effect.
(2)次に、消石灰添加によって脱水処理する場合は、
これまでの単に脱水効率を上げるための石灰添加(粕乾
物に対して11〜12%)では、先の石灰無添加法とは
全く異なった微生物分解を受け、上層のカビ繁殖部はき
のこ菌糸生育阻害物質の生成もほとんど見られないが、
内層部は嫌気性バクテリアによって酢酸だけでなくかな
りの乳酸と若干のギ酸が生成されるため、当初のp H
10,5前後の値を中性付近に低下させることはきのこ
の培養にとって好都合であるが、他の栄養素材を混合し
滅菌処理しても順調な菌糸の伸長は阻害される。(2) Next, when dehydrating by adding slaked lime,
The conventional method of simply adding lime (11-12% to the dry matter of lees) to increase dewatering efficiency resulted in microbial decomposition that was completely different from the previous method without adding lime, and the mold breeding area in the upper layer grew mushroom hyphae. Although almost no inhibitory substance production is observed,
In the inner layer, anaerobic bacteria produce not only acetic acid but also a considerable amount of lactic acid and some formic acid, so the initial pH
Lowering the value of around 10.5 to near neutrality is convenient for culturing mushrooms, but even if other nutritional materials are mixed and sterilized, the smooth growth of mycelia is inhibited.
この場合、バルブ全体を好気的状態に保持する方法は難
しいことから考えて、石灰添加量をこれまで以上の約1
4%(対粕乾物比16%以上を添加することは生育上好
ましくない。)添加することにより、p)lを11以上
に保持して嫌電性細菌の繁殖を抑制し、使用時に鉱酸を
用いてpi(調整してから、他の基質を均一混合し、水
分調整後滅菌処理すれば良好なきのこ栽培用培地となる
。In this case, since it is difficult to maintain the entire valve in an aerobic state, the amount of lime added should be increased to about 1
By adding 4% (Adding more than 16% of dry matter ratio to lees is unfavorable for growth.) By adding p)l to 11 or more, the growth of electrophobic bacteria is suppressed, and mineral acid is removed during use. A good mushroom cultivation medium can be obtained by uniformly mixing other substrates, adjusting the moisture content, and sterilizing the medium.
この場合の石灰添加は2つのメリットを伴う。Adding lime in this case has two benefits.
1つは、約14%の消石灰添加によって、スクリュープ
レスなどによる脱水だけで、バルブ水分を60%以下に
低下させるのに十分であり、それは後にpH調整に鉱酸
を添加するのに好都合であること。また、前述の化1呆
存法とは異なり、微生物分解によるペクチン質の可溶化
成分の損失も少なく、カルシウムによって十分に固定化
されて、極めてパサパサした分散度の良いものとなるこ
と。One is that with the addition of about 14% slaked lime, dehydration alone such as by screw press is sufficient to reduce the bulb moisture to below 60%, which is convenient for later addition of mineral acids for pH adjustment. thing. In addition, unlike the above-mentioned chemical 1 retention method, there is little loss of pectic solubilized components due to microbial decomposition, and they are sufficiently fixed by calcium, resulting in extremely dry and well-dispersed products.
2つめは、先の生保存法についても言えるが、特許公告
昭和57年第14831号にもあるとおり、培地へのカ
ルシウム塩の添加はきのこのカルシウム強化法として有
効となることである。The second point, which can also be said about the fresh preservation method mentioned above, is that the addition of calcium salts to the medium is effective as a method for enriching mushrooms with calcium, as stated in Patent Publication No. 14831 of 1982.
現在、実際に生産されている脱水バルブの一般成分分析
結果は表4に示したとおりであるが、澱粉製造時に81
械的破砕を逃れた細胞膜に包まれた澱粉を主体として、
その他細胞膜を構成するヘミセルロースとペクチンから
成ることから、きのこ栽培にはこの上ない鋸屑に優る優
秀な炭素源である。The general component analysis results of dehydration valves currently being produced are shown in Table 4.
Mainly composed of starch wrapped in cell membranes that escaped mechanical crushing,
In addition, since it is composed of hemicellulose and pectin that make up cell membranes, it is an excellent carbon source for mushroom cultivation, superior to sawdust.
表4 脱水馬鈴薯澱粉粕の一般成分(%)(本)実施例
以下に3つの実施ηりと対照例を記し、その結果を表5
にまとめて示した。Table 4 General components (%) of dehydrated potato starch meal
are summarized in the following.
実施例1
容It 800 m lのポリプロピレン製培養ビンに
、澱粉粕(含水率72%)658gと皮付きかぼちゃ種
子の粉砕物(6〜150メツシュ)66gを十分に混合
した培養基を適当に充填し、120℃、30分間滅菌後
、冷却してからエノキタケ菌を接挿し、25°Cで1次
培養し、菌糸が全体に蔓延後、菌掻きし、13℃で芽出
し培養を行った後、5℃において生育培養を実施した。Example 1 A polypropylene culture bottle with a volume of 800 ml was filled with a culture medium in which 658 g of starch meal (moisture content 72%) and 66 g of crushed pumpkin seeds with skin (6 to 150 mesh) were thoroughly mixed. After sterilizing at 120°C for 30 minutes, cooling, injecting the enokitake fungus and culturing at 25°C for the first time.After the mycelium spreads throughout, the fungi were scraped, and the cells were sprouted and cultured at 13°C. Growth cultures were carried out at °C.
実施例2
実施例1と同じ容器に、澱粉粕(含水率80%)526
gと皮付きかぼちゃ種子(6〜150メツシュ)66g
及び鋸屑(含水$34%)133gを十分に混合した培
養基を適当に充填し、以下実施例1と同様にしてエノキ
タケの培養を行った。Example 2 In the same container as in Example 1, starch meal (80% moisture content) 526
g and 66 g of pumpkin seeds with skin (6-150 mesh)
A culture medium in which 133 g of sawdust and sawdust (water content: $34%) were sufficiently mixed was filled appropriately, and enoki mushrooms were cultured in the same manner as in Example 1.
実施例3
実施例1と同じ容器に、皮付きかぼちゃ種子の粉砕物(
6〜150メツシュ)66gに鋸屑(含水率34%)2
77gと水356gを混合した培養基を適当に充填し、
以下実施例1と同様にしてエノキタケの培養を行った。Example 3 In the same container as in Example 1, crushed pumpkin seeds with skin (
66g of sawdust (water content 34%) 2
Appropriately fill the culture medium with a mixture of 77 g and 356 g of water.
Thereafter, enokitake mushrooms were cultured in the same manner as in Example 1.
対照例
実施例1と同じ容器に、鋸屑(含水率34%)277g
に米糠66g及び水350gを添加混合表5 実施例に
おける各工程の培養日数及び子実体収量
(菌掻きを境に1次及び2次培養とした。)して水分を
約65%に調整した培養基を充填し、実施例1と同様に
してエノキタケの培養を行った。Control Example In the same container as Example 1, 277 g of sawdust (water content 34%)
66 g of rice bran and 350 g of water were added to the mixture Table 5 Culture medium with moisture content adjusted to approximately 65% based on culture days and fruiting body yields for each step in the example (primary and secondary culture was determined by scraping the bacteria) was filled, and enokitake was cultured in the same manner as in Example 1.
なお、実施例1〜3において収穫された子実体はいずれ
も茎の太い良質なエノキタケであった。The fruiting bodies harvested in Examples 1 to 3 were all high-quality enoki mushrooms with thick stems.
また、エノキタケ以外のシイタケ、ヒラタケなどについ
ても良好な発茸効果を確認した。In addition, we have confirmed that mushrooms other than enokitake, such as shiitake and oyster mushrooms, have good mushroom-starting effects.
(ネ)発明の効果
本発明によって、抗カン活性などが判明していて医食同
源的付加価値の高い機能性食品であるきのこの生産にお
いて、これまで利用価値のほとんとなかったかぼちゃの
種子や年々付加価値が低下していく澱粉粕を未乾燥のま
ま脱水処理のみで、培地として用いることが可能となる
。また、きのこの収穫後の培養基は、肥料としての効果
も実証済みであり、生餌としての価値も十分に考えられ
る極めて有用なバイオマスとなる。(n) Effects of the invention The present invention enables the production of mushrooms, which have been shown to have anti-cancer activity and are functional foods with high added value in medicine and food. It becomes possible to use starch meal, whose added value decreases year by year, as a culture medium by simply dehydrating it without drying it. In addition, the culture medium after harvesting mushrooms has been proven to be effective as a fertilizer, and is an extremely useful biomass that can also be considered valuable as live feed.
特許出願人 岩 崎 達 也 1) 中 常 雄Patent applicant: Tatsuya Iwasaki 1) Middle male
Claims (3)
種子(皮付き)を子実体発生促進物質として使用するこ
とを特徴とする、きのこの人工栽培法。(1) A method for artificially cultivating mushrooms using pumpkin seeds (with skin) as a substance for promoting fruiting body development in the artificial bed cultivation of edible mushrooms.
50メッシュである、特許請求の範囲第1項記載のきの
この人工栽培法。(2) Particle size of crushed pumpkin seeds (with skin) is 6 to 1
50 mesh, the method for artificially cultivating mushrooms according to claim 1.
対して、未乾燥馬鈴薯澱粉粕と鋸屑を任意の比率で配合
した素材10部を、乾物重量比で混合する、特許請求の
範囲第1項または第2項記載のきのこの人工栽培法。(3) 1 to 10 parts of pulverized pumpkin seeds (with skin) are mixed with 10 parts of a material prepared by blending undried potato starch meal and sawdust in any ratio by dry weight. A method for artificially cultivating mushrooms according to item 1 or 2.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62310534A JPH01153020A (en) | 1987-12-08 | 1987-12-08 | Artificial culture of mushroom |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62310534A JPH01153020A (en) | 1987-12-08 | 1987-12-08 | Artificial culture of mushroom |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01153020A true JPH01153020A (en) | 1989-06-15 |
JPH0430803B2 JPH0430803B2 (en) | 1992-05-22 |
Family
ID=18006391
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62310534A Granted JPH01153020A (en) | 1987-12-08 | 1987-12-08 | Artificial culture of mushroom |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01153020A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1460245B1 (en) * | 2001-02-21 | 2007-04-11 | Isuzu Motors Limited | Diesel particulate filter unit and regeneration control method of the same |
-
1987
- 1987-12-08 JP JP62310534A patent/JPH01153020A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1460245B1 (en) * | 2001-02-21 | 2007-04-11 | Isuzu Motors Limited | Diesel particulate filter unit and regeneration control method of the same |
Also Published As
Publication number | Publication date |
---|---|
JPH0430803B2 (en) | 1992-05-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101948355B (en) | Preparation method of culture medium of edible fungi | |
CA1336749C (en) | Obtaining edible material from fungus-digested medium | |
CN104488545A (en) | Method for cultivating pleurotus nebrodensis, fresh edible fungi and coprinus comatus by virtue of cyclic utilization of straws | |
CN109463200A (en) | A kind of oil tea mushroom cultivation method | |
CN103621941A (en) | Edible fungi cake and baking method thereof | |
CN113748924A (en) | High-yield flower mushroom culture medium and preparation method and application thereof | |
KR101365273B1 (en) | Fermentation fertilizer | |
CN101337839A (en) | Edible fungus culture medium of citrus skin slag and method for preparing same | |
Yusminan et al. | Comparison of Jakaba growth with the addition of organic matter in rice washing water | |
Nikšić et al. | Farming of medicinal mushrooms | |
CN107637396A (en) | A kind of inoculation method of edible mushroom bacterium bag | |
CN109275500A (en) | Culture medium of edible fungus processing method | |
CN106747776B (en) | Method for preparing straw mushroom cultivation material by using waste tremella fungus chaff | |
CN104817366A (en) | Preparation method of biological organic fertilizer for improving storage quality of Fuji apples | |
CN105110985B (en) | A kind of crab flavour mushroom compost and preparation method | |
CN103387462B (en) | Pleurotus cornucopiae stock culture compatible product and preparation method of culture | |
JPH01153020A (en) | Artificial culture of mushroom | |
CN106615676A (en) | Method for processing silage | |
KR20090107177A (en) | Feed-stuff containing used-mushroom-media and eggs as main raw materials | |
CN104311312A (en) | Agrocybe cylindracea culture medium and preparation method thereof | |
CN109874600A (en) | A kind of seafood mushroom culture substrate and preparation method thereof | |
JPH03297325A (en) | Culture medium food proliferation and aging of edible mushroom mycelia | |
KR20150000107A (en) | Compost type nutritional supplements for apple cultivation and process for preparing the same | |
CN114208589B (en) | Lentinus edodes cultivation material and preparation method thereof | |
CN108271618A (en) | A kind of white squama mushroom new strains cover white tone 2 and its acclimation method |