JPH0125558B2 - - Google Patents
Info
- Publication number
- JPH0125558B2 JPH0125558B2 JP20854682A JP20854682A JPH0125558B2 JP H0125558 B2 JPH0125558 B2 JP H0125558B2 JP 20854682 A JP20854682 A JP 20854682A JP 20854682 A JP20854682 A JP 20854682A JP H0125558 B2 JPH0125558 B2 JP H0125558B2
- Authority
- JP
- Japan
- Prior art keywords
- koji
- raw materials
- solid
- bottom plate
- raw material
- 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
Links
- 239000002994 raw material Substances 0.000 claims description 28
- 239000007787 solid Substances 0.000 claims description 23
- 150000001720 carbohydrates Chemical class 0.000 claims description 11
- 241000233866 Fungi Species 0.000 claims description 10
- 238000007796 conventional method Methods 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 241000894006 Bacteria Species 0.000 description 13
- 108091005804 Peptidases Proteins 0.000 description 9
- 239000004365 Protease Substances 0.000 description 9
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 9
- 241000209140 Triticum Species 0.000 description 8
- 235000021307 Triticum Nutrition 0.000 description 8
- 244000068988 Glycine max Species 0.000 description 7
- 235000010469 Glycine max Nutrition 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 230000014075 nitrogen utilization Effects 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000011109 contamination Methods 0.000 description 5
- 238000009423 ventilation Methods 0.000 description 5
- 240000006439 Aspergillus oryzae Species 0.000 description 4
- 235000002247 Aspergillus oryzae Nutrition 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 102000004190 Enzymes Human genes 0.000 description 4
- 108090000790 Enzymes Proteins 0.000 description 4
- 244000294411 Mirabilis expansa Species 0.000 description 4
- 235000015429 Mirabilis expansa Nutrition 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 235000013536 miso Nutrition 0.000 description 4
- 235000013555 soy sauce Nutrition 0.000 description 4
- 240000007594 Oryza sativa Species 0.000 description 3
- 235000007164 Oryza sativa Nutrition 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 3
- 238000011049 filling Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 235000009566 rice Nutrition 0.000 description 3
- 240000005979 Hordeum vulgare Species 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- 238000000855 fermentation Methods 0.000 description 2
- 230000004151 fermentation Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000011068 loading method Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 235000018102 proteins Nutrition 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 235000019992 sake Nutrition 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 229920001817 Agar Polymers 0.000 description 1
- 241000228212 Aspergillus Species 0.000 description 1
- 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 1
- 108010068370 Glutens Proteins 0.000 description 1
- 239000001888 Peptone Substances 0.000 description 1
- 108010080698 Peptones Proteins 0.000 description 1
- 240000005384 Rhizopus oryzae Species 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 235000021312 gluten Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 239000013028 medium composition Substances 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Landscapes
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Description
本発明は固体麹の製造法に関し、その目的とす
るところは細菌汚染が少なくしかもプロテアーゼ
等の酵素力価の高い固体麹を得ることにある。
従来醤油、味噌、清酒、味淋等の醸造食品を製
造する際に使用される固体麹を製造する場合に
は、例えば必要とする麹の製造に用いられる全量
の大豆、麦、米等の原料に直接麹菌等糸状菌を接
種したものを盛込み製麹している。
しかしながらこのような製麹方法においては、
麹原料の水分が多いために、この麹原料が製麹装
置の盛込底板と接する部分に凝縮水などが生じ、
麹原料の細菌汚染を受け易く、そのため以後の手
入操作等によつてこの汚染が麹原料全体に広が
り、その結果麹品質を著しく低下させている。
そこで本発明者等は製麹装置の盛込底板からの
細菌汚染を出来るだけ受けない固体麹の製造法に
つき種々検討した結果、炭水化物原料の一部をあ
らかじめ製麹装置の盛込底板上に撒布し、その上
に糸状菌を接種した固体麹原料を盛込み製麹すれ
ば、盛込底板と水分の多い盛込物料が直接接触す
る事がなく、従つて盛込底板に起因する雑細菌の
汚染を防止することができ、その結果以後の製麹
経過中の雑細菌の増殖を抑制し、しかも糸状菌の
生育を旺盛にすることができるのでプロテアーゼ
力価の高い高品質の固体麹を得ることが出来ると
いう知見を得て本発明を完成した。
すなわち、本発明は固体麹を製造するに際し、
あらかじめ炭水化物原料を製麹装置の盛込底板上
に撒布し、その上に糸状菌を接種した固体麹原料
を盛込んだのち、常法により製麹することを特徴
とする固体麹の製造法である。
以下本発明を詳細に説明する。
本発明に用いられる固体麹原料としては、通常
用いられる固体麹原料であるならば如何なるもの
でも良く、例えば大豆、脱脂大豆、グルテン等の
蛋白質原料、米、麦、トウモロコシ等の炭水化物
原料並びに醤油粕、味淋粕、酒粕、〓、糠、フイ
ツシユミール等の醸造食品の製造工程中で生成す
る副産物等が挙げられる。これらは、単独でも併
用して用いても良い。
そして、これらの固体麹原料をそのままもしく
は加水したものを、常法により加圧加熱等して変
性もしくはα化し、必要により割砕する。
次いで、このようにして得られた固体麹原料の
うち炭水化物原料の所定量をあらかじめ製麹装置
の盛込底板上に撒布する。上記製麹装置の盛込底
板とは、例えば通風製麹装置における多孔板、網
蓋における網及び板蓋における板等固体麹原料を
盛込む際に盛込物料が接触する面をいい、上記以
外にも固体麹を製造する場合に原料を盛込むもの
ならすべて含まれる。
この盛込底板上に撒布する炭水化物原料の量
は、使用する炭水化物総原料の0.1〜25%(W/
W)、好ましくは2〜10%(W/W)程度である。
そして上記した炭水化物原料を製麹装置の盛込底
板の上に均一に撒布する。
次いで炭水化物原料の残部及び蛋白質原料から
なる固体麹原料に糸状菌を接種混合したものを、
上述した盛込底板上に撒布した炭水化物原料の上
に盛込み、以後常法により通風製麹もしくは静置
製麹を行ない30〜70時間程度製麹する。
本発明に用いられる糸状菌は、醤油、味噌、清
酒、味淋等の醸造工業、酵素製造等の発酵工業等
糸状菌利用工業、試験研究に用いられる市販の醸
造用種麹を含め如何なる種別のものでも良い。そ
して、その具体例としては、アスペルギルス・オ
リーゼ(ATCC14895)、アスペルギルス・フオエ
ニシス(ATCC14332)、リゾープス・ヤポニカス
(IAM6002)等である。
以上の如く、本発明によれば、雑細菌の繁殖し
易い盛込物料が製麹装置の盛込底板と直接接触す
ることを防止することにより、製麹中の雑細菌の
増殖を大巾に抑制し、しかも糸状菌の生育を著し
く促進することが出来、プロテアーゼ等の酵素力
価の高い高品質の固体麹が得られるので産業上極
めて有用である。
以下本発明を実施例により具体的に説明する。
実施例 1
通常の通風製麹装置のカステン多孔板上に、常
法により炒熬割砕した小麦30Kg(使用する炭水化
物総原料の10%・W/W)を均一に撒布した。次
い、脱脂大豆300Kgに水420を撒水し、圧力2
Kg/cm2(ゲージ圧力)で温度133℃の飽和水蒸気
を用いて10分間加圧加熱蒸煮処理したものに炒熬
割砕小麦270Kgを混和し、これにアスペルギル
ス・オリーゼ(ATCC14895)の〓種麹1Kgを接
種したものを上記炒熬割砕小麦の上に盛込んだの
ち、常法により温度30℃、通風量7cm/secで通
風し42時間製麹して固体麹を得た(本発明)。
なお、対照は炒熬割砕した小麦及び脱脂大豆の
全量を盛込時に使用する他は、本発明の製麹方法
と全く同様に通風製麹して得たものである。
このようにして得た両者の麹について、1手入
時の生細菌数、出麹のプロテアーゼ力価、生細菌
数及び窒素利用率を夫々第1表に示した。
プロテアーゼ力価及び生細菌数の測定は下記の
方法により行つた。
◎プロテアーゼ力価の測定
麹を20倍量の水で3時間浸出したのち、常法に
より濾過して得た濾液1mlを、酵素液とした。
そして、力価の測定は、ミルクカゼインを基質
とし、PH7.0のアンソン−萩原氏変法により測定
し、波長660nmのO.D.値で示した。
◎生細菌数の測定
麹10gを生理食塩水100mlに懸濁し、このうち
1mlを下記組成の培地7mlに平板し、これを温度
35℃にて48時間培養したのち、出現したコロニー
数を測定して求めた。
<生細菌数測定用培地組成>
グルコース1%(W/V)、肉エキス1%
(W/V)、ペプトン1%(W/V)、食塩0.5%
(W/V)、寒天1.5%、PH:7.2
なお、窒素利用率は、前記2区分の麹を、夫々
25%(W/V)食塩水1100と共に仕込み、温度
20〜30℃にて200日間常法により諸味管理を行つ
たものを濾過して得た液汁の窒素利用率であり、
醤油原料中の全窒素に対する溶解窒素の割合を%
で表したものである。
The present invention relates to a method for producing solid koji, and its purpose is to obtain solid koji with less bacterial contamination and high enzyme titer such as protease. When producing solid koji, which is conventionally used to produce brewed foods such as soy sauce, miso, sake, and miso, for example, the entire amount of raw materials such as soybeans, barley, and rice used to produce the required koji is used. Koji is made by directly inoculating filamentous fungi such as Aspergillus oryzae into koji. However, in this type of koji making method,
Because the koji raw material has a high moisture content, condensed water is generated at the part where the koji raw material contacts the bottom plate of the koji making equipment.
The koji raw material is susceptible to bacterial contamination, and this contamination spreads throughout the koji raw material through subsequent handling operations, resulting in a significant deterioration in the quality of the koji. Therefore, the present inventors investigated various ways to produce solid koji that would minimize bacterial contamination from the bottom plate of the koji making equipment, and found that a portion of the carbohydrate raw material was sprinkled in advance onto the bottom plate of the koji making equipment. However, if the solid koji raw material inoculated with filamentous fungi is added onto the solid koji material and the koji is made, there is no direct contact between the bottom plate and the moisture-rich ingredients, which prevents the contamination of bacteria from the bottom plate. As a result, it is possible to suppress the growth of miscellaneous bacteria during the subsequent process of making koji, and also to encourage the growth of filamentous fungi, thereby obtaining high-quality solid koji with a high protease titer. The present invention was completed based on the knowledge that this can be done. That is, when producing solid koji according to the present invention,
A method for producing solid koji, which is characterized in that carbohydrate raw materials are spread on the bottom plate of a koji making device in advance, solid koji raw materials inoculated with filamentous fungi are poured thereon, and then koji is made by a conventional method. be. The present invention will be explained in detail below. The solid koji raw material used in the present invention may be any commonly used solid koji raw material, such as soybeans, defatted soybeans, protein raw materials such as gluten, carbohydrate raw materials such as rice, barley, and corn, and soy sauce lees. Examples include by-products generated during the manufacturing process of brewed foods such as ajirin lees, sake lees, rice bran, and fatsiyu meal. These may be used alone or in combination. Then, these solid koji raw materials as they are or with water added are denatured or pregelatinized by pressurizing and heating in a conventional manner, and are crushed if necessary. Next, a predetermined amount of the carbohydrate raw material among the solid koji raw materials obtained in this way is spread in advance on the filling bottom plate of the koji making apparatus. The loading bottom plate of the above-mentioned koji making equipment refers to the surface that comes into contact with the filling material when loading solid koji raw materials, such as the perforated plate in the ventilation koji making equipment, the net in the mesh lid, and the plate in the plate lid, and other than the above. It also includes all materials that are used to produce solid koji. The amount of carbohydrate raw materials to be sprinkled on this filled bottom plate is 0.1 to 25% (W/
W), preferably about 2 to 10% (W/W).
Then, the above-mentioned carbohydrate raw material is evenly spread on the bottom plate of the koji making apparatus. Next, the solid koji raw material consisting of the remainder of the carbohydrate raw material and the protein raw material was inoculated with filamentous fungi and mixed.
The mixture is placed on top of the carbohydrate raw material that has been spread on the above-mentioned filling bottom plate, and then koji is made by ventilation or static koji in a conventional manner for about 30 to 70 hours. The filamentous fungi used in the present invention can be used in any type of fermentation industry such as soy sauce, miso, sake, and miso, fermentation industries such as enzyme production, and filamentous fungi utilization industries, including commercially available brewing seed koji used for testing and research. Anything is fine. Specific examples thereof include Aspergillus oryzae (ATCC14895), Aspergillus phoensis (ATCC14332), and Rhizopus japonicus (IAM6002). As described above, according to the present invention, the growth of miscellaneous bacteria during koji making can be greatly reduced by preventing the ingredients on which bacteria can easily propagate from coming into direct contact with the bottom plate of the koji making device. It is extremely useful industrially because it can suppress the growth of filamentous fungi and significantly promote the growth of filamentous fungi, yielding high-quality solid koji with a high titer of enzymes such as protease. The present invention will be specifically explained below using examples. Example 1 30 kg of roasted and crushed wheat (10% W/W of the total carbohydrate raw materials used) was uniformly spread on a Kasten perforated plate of a conventional ventilation koji making apparatus. Next, 420 kg of water was sprinkled on 300 kg of defatted soybeans, and the pressure was 2
Kg/cm 2 (gauge pressure) using saturated steam at a temperature of 133°C for 10 minutes, and then 270 kg of roasted cracked wheat was mixed with this, followed by seed koji of Aspergillus oryzae (ATCC14895). After 1 kg of the inoculated material was placed on top of the above-mentioned roasted cracked wheat, koji was made using a conventional method at a temperature of 30°C and ventilation at an airflow rate of 7 cm/sec for 42 hours to obtain solid koji (the present invention). . The control was obtained by making koji through ventilation in exactly the same manner as the koji making method of the present invention, except that the whole amount of roasted and crushed wheat and defatted soybeans was used at the time of mixing. Table 1 shows the number of viable bacteria, the protease titer of the koji, the number of viable bacteria, and the nitrogen utilization rate for both types of koji thus obtained. The protease titer and the number of viable bacteria were measured by the following method. ◎Measurement of protease titer After leaching the koji with 20 times the amount of water for 3 hours, 1 ml of the filtrate obtained by filtration by a conventional method was used as an enzyme solution. The titer was measured by a modified Anson-Hagiwara method at pH 7.0 using milk casein as a substrate, and was expressed as an OD value at a wavelength of 660 nm. ◎Measurement of the number of viable bacteria: Suspend 10 g of koji in 100 ml of physiological saline, plate 1 ml of this on 7 ml of medium with the following composition, and
After culturing at 35°C for 48 hours, the number of colonies that appeared was determined. <Medium composition for measuring the number of viable bacteria> Glucose 1% (W/V), meat extract 1%
(W/V), peptone 1% (W/V), salt 0.5%
(W/V), agar 1.5%, PH: 7.2 The nitrogen utilization rate is for each of the above two categories of koji.
Prepared with 25% (W/V) saline solution at 1100 °C, temperature
It is the nitrogen utilization rate of the liquid juice obtained by filtering the moromi control using the conventional method at 20-30℃ for 200 days.
Ratio of dissolved nitrogen to total nitrogen in soy sauce raw materials %
It is expressed as
【表】
第1表より明らかな如く、本発明の生細菌数は
対照のそれに比較して著しく低く、しかも出麹で
のプロテアーゼ力価も対照に比べ著しく高力価の
ものが得られ、また窒素利用率も格段に優れたも
のであつた。
実施例 2
通常の板蓋5枚の各々に常法により炒熬割砕し
た小麦15g(使用する炭水化物総原料の5%・
W/W)を均一に撒布した。別に、脱脂大豆1500
gに水2100mlを撒水し圧力2Kg/cm2(ゲージ圧
力)、温度133℃の飽和水蒸気を用いて10分間加圧
加熱蒸煮し、炒熬割砕小麦1425gを加え、アスペ
ルギルス・オリーゼ(ATCC14895)の〓種麹5
gを接種、混合したものを5等分し、上記炒熬割
砕小麦を撒布した板蓋にそれぞれ盛込んだ。そし
て恒温恒湿室にて30℃で48時間培養して固体麹を
得た(本発明)。
なお、対照は炒熬割砕した小麦及び脱脂大豆の
全量を盛込時に使用する他は、本発明の製麹方法
と全く同様にして得たものである。
このようにして得た両者の麹について、1手入
時生細菌数、出麹のプロテアーゼ力価、生細菌数
及び窒素利用率を夫々第2表に示した。[Table] As is clear from Table 1, the number of viable bacteria of the present invention is significantly lower than that of the control, and the protease titer in the koji produced is also significantly higher than that of the control. The nitrogen utilization rate was also extremely excellent. Example 2 15g of roasted and crushed wheat (5% of the total carbohydrate raw materials used) was placed on each of 5 ordinary plate lids.
W/W) was evenly spread. Separately, 1500 defatted soybeans
2,100 ml of water was sprinkled on 2,100 ml of water, and steamed under pressure for 10 minutes using saturated steam at a pressure of 2 Kg/cm 2 (gauge pressure) and a temperature of 133°C. 1,425 g of roasted cracked wheat was added, and Aspergillus oryzae (ATCC14895) was added. 〓 Seed koji 5
The mixture was divided into 5 equal parts, and each was placed on a plate lid on which the above-mentioned roasted cracked wheat had been sprinkled. Then, it was cultured at 30°C for 48 hours in a constant temperature and humidity room to obtain solid koji (the present invention). In addition, the control was obtained in exactly the same manner as the koji making method of the present invention, except that the whole amount of roasted and crushed wheat and defatted soybeans was used at the time of mixing. Table 2 shows the number of viable bacteria, the protease titer of the koji, the number of viable bacteria, and the nitrogen utilization rate for both types of koji thus obtained.
【表】
の測定法と同様にして行つた。
第2表の如く、本発明の生細菌数は対照に比べ
著しく低いものとなり、しかも出麹のプロテアー
ゼ力価も高く、また窒素利用率も著しく高いもの
であつた。It was carried out in the same manner as the measurement method in [Table].
As shown in Table 2, the number of viable bacteria of the present invention was significantly lower than that of the control, and the protease titer of the released koji was also high, and the nitrogen utilization rate was also significantly high.
Claims (1)
物原料を製麹装置の盛込底板上に撒布し、その上
に糸状菌を接種した固体麹原料を盛込んだのち、
常法により製麹することを特徴とする固体麹の製
造法。1. When producing solid koji, carbohydrate raw materials are spread on the bottom plate of the koji making equipment in advance, and after the solid koji raw materials inoculated with filamentous fungi are poured onto it,
A method for producing solid koji, which is characterized by making koji using a conventional method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20854682A JPS5998684A (en) | 1982-11-30 | 1982-11-30 | Preparation of solid koji |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20854682A JPS5998684A (en) | 1982-11-30 | 1982-11-30 | Preparation of solid koji |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5998684A JPS5998684A (en) | 1984-06-07 |
JPH0125558B2 true JPH0125558B2 (en) | 1989-05-18 |
Family
ID=16557971
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP20854682A Granted JPS5998684A (en) | 1982-11-30 | 1982-11-30 | Preparation of solid koji |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5998684A (en) |
-
1982
- 1982-11-30 JP JP20854682A patent/JPS5998684A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5998684A (en) | 1984-06-07 |
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