JPS6240980B2 - - Google Patents
Info
- Publication number
- JPS6240980B2 JPS6240980B2 JP57166794A JP16679482A JPS6240980B2 JP S6240980 B2 JPS6240980 B2 JP S6240980B2 JP 57166794 A JP57166794 A JP 57166794A JP 16679482 A JP16679482 A JP 16679482A JP S6240980 B2 JPS6240980 B2 JP S6240980B2
- Authority
- JP
- Japan
- Prior art keywords
- starch
- instant noodles
- reference example
- fried
- parts
- 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
- 229920002472 Starch Polymers 0.000 claims description 57
- 235000019698 starch Nutrition 0.000 claims description 55
- 239000008107 starch Substances 0.000 claims description 49
- 235000008446 instant noodles Nutrition 0.000 claims description 33
- 238000006467 substitution reaction Methods 0.000 claims description 16
- 108010068370 Glutens Proteins 0.000 claims description 9
- 235000021312 gluten Nutrition 0.000 claims description 9
- 239000001341 hydroxy propyl starch Substances 0.000 claims description 9
- 235000013828 hydroxypropyl starch Nutrition 0.000 claims description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 claims description 4
- 229920001612 Hydroxyethyl starch Polymers 0.000 claims description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 3
- KCYQMQGPYWZZNJ-BQYQJAHWSA-N hydron;2-[(e)-oct-1-enyl]butanedioate Chemical compound CCCCCC\C=C\C(C(O)=O)CC(O)=O KCYQMQGPYWZZNJ-BQYQJAHWSA-N 0.000 claims description 2
- 229940050526 hydroxyethylstarch Drugs 0.000 claims description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 1
- 239000011976 maleic acid Substances 0.000 claims 1
- 239000001384 succinic acid Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 235000012149 noodles Nutrition 0.000 description 16
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 230000000052 comparative effect Effects 0.000 description 11
- 229920002261 Corn starch Polymers 0.000 description 8
- 239000008120 corn starch Substances 0.000 description 8
- 229940099112 cornstarch Drugs 0.000 description 8
- 235000013312 flour Nutrition 0.000 description 8
- 241000209140 Triticum Species 0.000 description 6
- 235000021307 Triticum Nutrition 0.000 description 6
- 239000000796 flavoring agent Substances 0.000 description 6
- 235000019634 flavors Nutrition 0.000 description 6
- 229920001592 potato starch Polymers 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000007774 longterm Effects 0.000 description 4
- 238000010025 steaming Methods 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 102000013142 Amylases Human genes 0.000 description 3
- 108010065511 Amylases Proteins 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 229940111205 diastase Drugs 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 230000001953 sensory effect Effects 0.000 description 3
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 2
- GUOCOOQWZHQBJI-UHFFFAOYSA-N 4-oct-7-enoxy-4-oxobutanoic acid Chemical compound OC(=O)CCC(=O)OCCCCCCC=C GUOCOOQWZHQBJI-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 244000017020 Ipomoea batatas Species 0.000 description 2
- 235000002678 Ipomoea batatas Nutrition 0.000 description 2
- 240000003183 Manihot esculenta Species 0.000 description 2
- 235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- FLISWPFVWWWNNP-BQYQJAHWSA-N dihydro-3-(1-octenyl)-2,5-furandione Chemical compound CCCCCC\C=C\C1CC(=O)OC1=O FLISWPFVWWWNNP-BQYQJAHWSA-N 0.000 description 2
- 239000012374 esterification agent Substances 0.000 description 2
- 238000006266 etherification reaction Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 230000000977 initiatory effect Effects 0.000 description 2
- 239000002075 main ingredient Substances 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 235000015067 sauces Nutrition 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 2
- 229940014800 succinic anhydride Drugs 0.000 description 2
- 238000004448 titration Methods 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 229940100445 wheat starch Drugs 0.000 description 2
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229920000856 Amylose Polymers 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- 239000004368 Modified starch Substances 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- MKRNVBXERAPZOP-UHFFFAOYSA-N Starch acetate Chemical compound O1C(CO)C(OC)C(O)C(O)C1OCC1C(OC2C(C(O)C(OC)C(CO)O2)OC(C)=O)C(O)C(O)C(OC2C(OC(C)C(O)C2O)CO)O1 MKRNVBXERAPZOP-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical group CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 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
- 238000010306 acid treatment Methods 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 229940088598 enzyme Drugs 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000007602 hot air drying Methods 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- TWNIBLMWSKIRAT-VFUOTHLCSA-N levoglucosan Chemical group O[C@@H]1[C@@H](O)[C@H](O)[C@H]2CO[C@@H]1O2 TWNIBLMWSKIRAT-VFUOTHLCSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229940116317 potato starch Drugs 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 229940100486 rice starch Drugs 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- FDRCDNZGSXJAFP-UHFFFAOYSA-M sodium chloroacetate Chemical compound [Na+].[O-]C(=O)CCl FDRCDNZGSXJAFP-UHFFFAOYSA-M 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003900 succinic acid esters Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
Landscapes
- Noodles (AREA)
Description
本発明は、長期保存性および熱水復元性に優れ
滑らかで良好な食感、風味を有するノンフライ即
席麺の製造方法に関する。
従来、即席麺においては生麺線を蒸煮した後、
油で揚げることにより得られるフライ(油揚げ)
麺および蒸煮後、熱風乾燥して得られるノンフラ
イ麺が知られている。
フライ麺は熱水復元性が比較的良い反面、長期
間の保存により麺線内に含まれる油分が劣化変質
して著しく食感、風味を低下させてしまう。
一方、ノンフライ麺は油で揚げないため、フラ
イ麺の欠点はないが、長時間の乾燥が必要であり
作業性が悪く、しかも麺線のα化が不充分、不均
一になる危険性がある。このため熱水による復元
が不充分となり、食感、風味の低下を生じるとい
う問題を有する。
本発明者らはこのような問題点を解決すべく、
鋭意研究を重ねた結果、一定の置換度を有するエ
ーテル化澱粉およびエステル化澱粉を使用するこ
とにより、前述のノンフライ麺における問題点を
解決することを見出し本発明を完成するに至つ
た。
本発明に使用するエーテル化澱粉およびエステ
ル化澱粉は置換度(無水グルコース残基1モル当
りの置換度D.S.モル)D.S.=0.005〜0.3、好まし
くは0.01〜0.2のものである。これらは通常、未
変性澱粉に比べ糊化開始温度が約1〜30℃低下
し、糊化(α化)が容易になつている。
従つて、該エーテル化澱粉またはエステル化澱
粉をノンフライ即席麺の麺線として使用すれば、
蒸煮工程において、麺線の糊化が充分になされ高
いα化度が得られる。
また、短時間で高いα化度が得られるので、蒸
煮工程にかける時間を短縮することができる。
さらに、これを熱風乾燥して得られたノンフラ
イ即席麺は、熱透過性が優れているので、熱水に
よる復元が従来のノンフライ即席麺に比べはるか
に短時間になされ、また、比較的低温(例えば80
℃程度)の湯によつても充分復元され、優れた食
感、風味を有するものとなる。
本発明のエーテル化澱粉およびエステル化澱粉
は、未変性澱粉あるいは他の化工澱粉(例えば、
酸処理化、酸化、湿熱処理化などによるもの)に
比べ、糊化された後の安定性が良い(老化しにく
い。)そのため再加熱されると、熱透過性が良
く、短時間で充分に復元される。従つて、良好な
食感、風味を有するものが得られると考えられ
る。
本発明の要旨は、ノンフライ麺の製造工程にお
いて、置換度(D.S.)が0.00.5〜0.3のエーテル化
澱粉またはエステル化澱粉の少なくとも1種を使
用することを特徴とするノンフライ麺の製造法に
存する。
ここに言うエーテル化澱粉およびエステル化澱
粉は、小麦澱粉、馬鈴薯澱粉、米澱粉、タピオカ
澱粉、サゴ澱粉、甘藷澱粉、コーンスターチ、ワ
キシコーンスターチ、ハイアミロースコーンスタ
ーチなどの澱粉および小麦粉、コーンフラワー、
米粉などの澱粉含有物質を原料とし、エーテル化
剤またはエステル化剤を常法に従つて作用させる
ことによつて粒状またはα化状にて得られる。
エーテル化剤、エステル化剤はいずれも常套の
ものがすべて使用される。例えば、エーテル化剤
としては、エチレンオキシド、プロピレンオキシ
ド、モノクロル酢酸など、エステル化剤としては
無水酢酸、酢酸ビニルモノマー、無水マレイン
酸、無水コハク酸、1―オクテニル無水コハク
酸、などが挙げられる。
従来、即席麺に対してあまり適性を有しないと
されていた安価なコーンスターチ、タピオカ澱粉
も本発明明によるエーテル化またはエステル化を
施し、活性グルテンを適量添加すれば、充分使用
が可能となることが見出された。更に、本発明の
エーテル化澱粉またはエステル化澱粉を主原料と
し適量の活性グルテンを添加して得られるノンフ
ライ即席麺は、従来の小麦粉を主原料とするもの
と比較して大巾に復元時間を短縮することができ
ることを見出した。
また、本発明におけるノンフライ即席麺の製造
に際して、エーテル化澱粉またはエステル化澱粉
の少なくとも1種のみの使用だけでなく、小麦澱
粉、馬鈴薯澱粉、甘藷澱粉などの未変性澱粉との
併用が可能であり、活性グルテンを適量添加する
ことにより常法に従つて製造することができる。
次に、参考例、実施例および比較例を挙げて本
発明を更に詳述する。
参考例 1
水120重量部(以下部と略す)に水酸化ナトリ
ウム1部および硫酸ナトリウム、30部を溶解し、
これにコーンスターチ100部を撹拌下に分散さ
せ、さらにプロピレンオキシド2〜20部を添加
し、40℃で20時間反応させる。反応終了後、希塩
酸で中和し、水洗、ろ過、乾燥して各種の置換度
のヒドロキシプロピル澱粉を得る。
参考例 2
水120部にコーンスターチ100部を撹拌下に分散
させ、無水酢酸2〜20部を徐々に滴下し、希水酸
化ナトリウム溶液を用い、PH8〜9に維持しなが
ら30℃で10時間反応する。反応終了後、希塩酸で
中和し、水洗、ろ過、乾燥して各種の置換度の酢
酸澱粉を得る。
参考例 3
プロピレンオキシドの代わりにエチレンオキシ
ドを用いる以外は参考例1と同様にして、各種の
置換度のヒドロキシエチル澱粉を得る。
参考例 4
プロピレンオキシドの代わりにモノクロル酢酸
ナトリウムを用いる以外は参考例1と同様にして
各種の置換度のカルボキシメチル澱粉を得る。
参考例 5
無水酢酸の代わりに無水コハク酸を用いる以外
は参考例2と同様にして各種の置換度の澱粉コハ
ク酸エステルを得る。
参考例 6
無水酢酸の代わりに無水オクテニルコハク酸を
用いる以外は参考例2と同様にして各種の置換度
の澱粉オクテニルコハク酸エステルを得る。
参考例 7
無水酢酸の代わりに無水マレイン酸を用いる以
外は参考例2と同様にして各種の置換度の澱粉マ
レイン酸エステルを得る。
以上参考例1、2、3、4、5、6および7で
本発明のエーテル化澱粉およびエステル化澱粉の
各種置換度のものを得た。
実施例 1
参考例1で得たヒドロキシプロピル澱粉90部に
活性グルテン10部を混合後、食塩2部およびかん
すい末0.2部を水32部に溶解したものを加え、充
分混合した後、厚さ1mmに圧延し、線切を18番の
切刃で行い生麺線を得る。これを約95℃で2分間
蒸煮した後、約100℃の空気浴中で水分が5%程
度になるまで熱風乾燥してノンフライ即席麺を得
る。
実施例 2
参考例1で得たヒドロキシプロピル澱粉の代わ
りに参考例2で得た酢酸澱粉を用いて実施例1と
同様にしてノンフライ即席麺を得る。
実施例 3
参考例1で得たヒドロキシプロピル澱粉の代り
に参考例3で得たヒドロキシエチル澱粉および参
考例4で得たカルボキシメチル澱粉を用いて実施
例1と同様にしてノンフライ即席麺を得る。
実施例 4
参考例1で得たヒドロキシプロピル澱粉の代り
に参考例5で得た澱粉コハク酸エステル、参考例
6で得た澱粉オクテニルコハク酸エステルおよび
参考例7で得た澱粉マレイン酸エステルを用いて
実施例1と同様にしてノンフライ即席麺を得る。
以上実施例1〜4で本発明の各種置換度のヒド
ロキシプロピル澱粉、酢酸澱粉、カルボキシメチ
ル澱粉、澱粉コハク酸エステル、澱粉オクテニル
コハク酸エステルおよび澱粉マレイン酸エステル
を単独使用したものについてノンフライ即席麺を
得た。
比較例 1
小麦粉100部を参考例1で得たヒドロキシプロ
ピル澱粉90部および活性グルテン10部の代りに用
いる以外、実施例1と同様にしてノンフライ即席
麺を得る。
比較例 2
コーンスターチ90部を参考例1で得たヒドロキ
シプロピル化澱粉90部の代りに用いる以外、実施
例1と同様にしてノンフライ即席麺を得る。
比較例 3
小麦粉80部、馬鈴薯澱粉18部および活性グルテ
ン2部を参考例1で得たヒドロキシプロピル澱粉
90部および活性グルテン10部の代りに用いる以
外、実施例1と同様にしてノンフライ即席麺を得
る。
以上、比較例1〜3で本発明のヒドロキシプロ
ピル澱粉、ヒドロキシエチル澱粉、カルボキシメ
チル澱粉、酢酸澱粉、澱粉コハク酸エステル、澱
粉オクテニルコハク酸エステルおよび澱粉マレイ
ン酸エステルの代りに小麦粉、コーンスターチ、
馬鈴薯澱粉を使用したものについてノンフライ即
席麺を得た。
次に、このようにして得られたノンフライ即席
麺についての各物性値を測定し、第1〜6表に示
す結果を得た。
第1表および第2表には、ノンフライ即席麺の
製造に使用した各種澱粉および小麦粉の糊化開始
温度および置換度を示す。尚、糊化開始温度と
は、2.7%食塩水溶液を用い、5%澱粉懸濁液を
調整して、ブラベンダーアミログラフにおいて加
熱したときの粘度増加開始時の温度を示す。
第3表および第4表には、第1表および第2表
に示した澱粉等を使用して製造したノンフライ即
席麺のα化度および食感を示す。
尚、α化度の測定は酵素(ジアスターゼ)法に
よる。実施例および比較例で得たノンフライ即席
麺を100メツシユ以下に粉砕し試料として以下の
通り測定する。測定は100ml三角フラスコを1点
につき5個用意し、これをA1〜A4およびBとす
る。上記の調整試料1.00gをA1〜A4の4個の三角
フラスコにそれぞれはかり取る。但し、4秤取量
相互間のばらつき±0.5%以内とする。
5個のフラスコに水50mlずつ加え、そのうち
A1およびA2を15分間加熱沸騰させた後、氷水中
で常温まで急冷する。
一方、A1、A3およびBにそれぞれ5%ジアス
ターゼ溶液5mlずつを加え、5個のフラスコ全部
を恒温水槽中で振とうしながら、37℃±1℃に90
分間保つた後ただちに1N塩酸を全部のフラスコ
に2mlずつ加えて、ジアスターゼの反応を停止さ
せ、夫々100mlのメスフラスコに移し、水を加え
て定容とする。
乾燥ろ紙を用いて各々の溶液をろ過し、A1〜
A4およびBから得たろ液をピペツトで10mlずつ
共栓三角フラスコに取り、これらをそれぞれa1〜
a4およびbとする。
この時点で別に水10mlをピペツトで採取した共
栓三角フラスコの各々にN/10ヨウ素溶液10mlず
つを加える。
次にストツプウオツチを用いて等時間間隔で、
N/10水酸化ナトリウム溶液18mlずつを順次6個
のフラスコに加え、密栓して振り混ぜ、正確に15
分間置く。最初のフラスコが15分経過したら、先
にN/10水酸化ナトリウム水溶液を加えた時と同
じ順序、同じ等時間間隔で、10%硫酸2mlずつ
を、栓を開けると同時に手早く加える。これらの
溶液をN/10チオ硫酸ナトリウム溶液で滴定し、
a1〜a4およびbの滴定値をそれぞれP1〜P4およ
びQまたは空試験の滴定値をγとし次式によりα
化度(%)を求める。
α化度(%)
=(γ−P3)−(γ−P4)−(γ−Q)/(γ−
P1)−(γ−P2)−(γ−Q)×100
次に、食感については、即席麺70gに熱湯を
400ml注ぎ、3分間復元した後、水切を行ないソ
ースを15mlを加えたものについて、10人のパネラ
ーが食して評価した官能値である。
食感の項目において、麺線の結着および膠着、
歯に対する付着性、生感(小麦様の生感がある状
態をいう、以下同じ)についてはその性質の強さ
を最高10点から最低0点までの範囲で評価。その
他の項目については、好適なものを5.0点、過剰
なものには加点、不足のものには減点して評価し
た。
第5表および第6表には、即席麺製造直後およ
び6ケ月保存(室温にて)した後、第2表の食感
テストと同様に即席麺を復元、調味し官能テスト
を行なつた値を示した。
尚、フライ即席麺についても比較し、製造直後
および6ケ月後の官能テスト値を併記する。ここ
でフライ即席麺は、比較例1における熱風乾燥の
代りに油揚げ処理を油温140℃で3分間行なつて
得たものである。
第5表および第6表における総合評価について
は、食感の項目の他、風味などを加味した総合評
価でパネラーの意見を総合して採点した値であ
る。
第1〜6表の結果から明らかなように本発明の
エーテル化澱粉またはエステル化澱粉を用いて、
ノンフライ即席麺を製造したもの(実施例1〜
4)はそうでないもの(比較例1〜3)よりα化
度、食感等において優れている。また、フライ即
席麺、比較例1と長期保存性を比較すると、フラ
イ即席麺は6ケ月保存後、著しく食感が低下し、
また比較例1は直後、6ケ月後とも食感が悪く生
感が強い。これに対し、本発明によるノンフライ
即席麺は直後、6ケ月後ともに好適な食感を有す
ることが明らかで長期保存に対しても安定である
ことがわかる。
また、第2表においては本発明のエーテル化澱
粉およびエステル化澱粉は一定の置換度の範囲に
おいて効果があることがわかる。
実施例 5
実施例1、2および比較例1で得られたノンフ
ライ即席麺(第1表における試料番号2、4、
7、9、14)の復元時間を測定した。
復元時間はノンフライ即席麺に熱湯を注いだ後
30秒毎にサンプリングしナイフで切り、切り口の
復元状態を観察し完全に復元されるまでの時間を
復元時間とした。結果を第7表に示す。
TECHNICAL FIELD The present invention relates to a method for producing non-fried instant noodles that have excellent long-term storage stability and hot water restorability, are smooth, and have good texture and flavor. Conventionally, in instant noodles, after steaming raw noodle strings,
Fried food obtained by frying in oil (aburaage)
Noodles and non-fried noodles obtained by drying with hot air after steaming are known. Although fried noodles have relatively good hot water restorability, long-term storage causes the oil contained in the noodle strings to deteriorate and deteriorate, significantly reducing the texture and flavor. On the other hand, non-fried noodles do not have the disadvantages of fried noodles because they are not fried, but they require long drying times and are difficult to work with, and there is a risk that the noodle strings will not be gelatinized sufficiently or become uneven. . For this reason, there is a problem in that the restoration with hot water is insufficient, resulting in deterioration of texture and flavor. In order to solve such problems, the present inventors
As a result of extensive research, the present invention was completed by discovering that the above-mentioned problems with non-fried noodles can be solved by using etherified starch and esterified starch having a certain degree of substitution. The etherified starch and esterified starch used in the present invention have a degree of substitution (degree of substitution DS mole per mole of anhydroglucose residue) DS = 0.005 to 0.3, preferably 0.01 to 0.2. These usually have a gelatinization initiation temperature lowered by about 1 to 30°C compared to unmodified starch, making gelatinization (gelatinization) easier. Therefore, if the etherified starch or esterified starch is used as noodle strings for non-fried instant noodles,
In the steaming process, the noodle strings are sufficiently gelatinized and a high degree of gelatinization is obtained. Moreover, since a high degree of gelatinization can be obtained in a short time, the time required for the steaming process can be shortened. Furthermore, the non-fried instant noodles obtained by drying them with hot air have excellent thermal permeability, so they can be restored with hot water in a much shorter time than conventional non-fried instant noodles. For example 80
It can be fully restored even with hot water (about 30°F (°C)), and has excellent texture and flavor. The etherified starch and esterified starch of the present invention may be unmodified starch or other modified starch (e.g.
It has better stability after gelatinization (resistance to aging) than gelatinization (acid treatment, oxidation, moist heat treatment, etc.). Therefore, when reheated, it has good heat permeability and can be used in a short time. will be restored. Therefore, it is thought that products with good texture and flavor can be obtained. The gist of the present invention is to provide a method for producing non-fried noodles, characterized in that at least one type of etherified starch or esterified starch having a degree of substitution (DS) of 0.00.5 to 0.3 is used in the non-fried noodles production process. Exists. The etherified starch and esterified starch referred to herein include starches such as wheat starch, potato starch, rice starch, tapioca starch, sago starch, sweet potato starch, corn starch, waxy corn starch, and high amylose corn starch, as well as wheat flour, corn flour,
It is obtained in granular or pregelatinized form by using a starch-containing substance such as rice flour as a raw material and treating it with an etherifying agent or an esterifying agent according to a conventional method. All conventional etherification agents and esterification agents can be used. For example, examples of the etherification agent include ethylene oxide, propylene oxide, and monochloroacetic acid, and examples of the esterification agent include acetic anhydride, vinyl acetate monomer, maleic anhydride, succinic anhydride, and 1-octenylsuccinic anhydride. Cheap corn starch and tapioca starch, which were conventionally considered not to be very suitable for instant noodles, can be used satisfactorily if they are etherified or esterified according to the present invention and an appropriate amount of active gluten is added. was discovered. Furthermore, the non-fried instant noodles obtained by using the etherified starch or esterified starch of the present invention as the main ingredient and adding an appropriate amount of active gluten have a significantly longer restoring time than conventional noodles made from wheat flour as the main ingredient. We found that it can be shortened. Furthermore, in producing the non-fried instant noodles of the present invention, it is possible not only to use at least one type of etherified starch or esterified starch, but also to use in combination with unmodified starch such as wheat starch, potato starch, and sweet potato starch. , can be produced according to a conventional method by adding an appropriate amount of active gluten. Next, the present invention will be further explained in detail by giving Reference Examples, Examples, and Comparative Examples. Reference example 1 Dissolve 1 part of sodium hydroxide and 30 parts of sodium sulfate in 120 parts by weight of water (abbreviated as "parts" below),
100 parts of corn starch is dispersed in this while stirring, 2 to 20 parts of propylene oxide is further added, and the mixture is reacted at 40°C for 20 hours. After the reaction is completed, it is neutralized with dilute hydrochloric acid, washed with water, filtered, and dried to obtain hydroxypropyl starch with various degrees of substitution. Reference Example 2 100 parts of cornstarch is dispersed in 120 parts of water with stirring, 2 to 20 parts of acetic anhydride is gradually added dropwise, and the reaction is carried out at 30°C for 10 hours while maintaining the pH at 8 to 9 using dilute sodium hydroxide solution. do. After the reaction is completed, the mixture is neutralized with dilute hydrochloric acid, washed with water, filtered, and dried to obtain starch acetate with various degrees of substitution. Reference Example 3 Hydroxyethyl starches with various degrees of substitution are obtained in the same manner as Reference Example 1 except that ethylene oxide is used instead of propylene oxide. Reference Example 4 Carboxymethyl starches with various degrees of substitution were obtained in the same manner as in Reference Example 1, except that sodium monochloroacetate was used instead of propylene oxide. Reference Example 5 Starch succinate esters with various degrees of substitution are obtained in the same manner as in Reference Example 2 except that succinic anhydride is used instead of acetic anhydride. Reference Example 6 Starch octenyl succinic acid esters having various degrees of substitution were obtained in the same manner as in Reference Example 2, except that octenyl succinic anhydride was used instead of acetic anhydride. Reference Example 7 Starch maleic esters with various degrees of substitution were obtained in the same manner as in Reference Example 2, except that maleic anhydride was used instead of acetic anhydride. In Reference Examples 1, 2, 3, 4, 5, 6 and 7, etherified starches and esterified starches of the present invention with various degrees of substitution were obtained. Example 1 After mixing 10 parts of active gluten with 90 parts of the hydroxypropyl starch obtained in Reference Example 1, 2 parts of common salt and 0.2 parts of kansui powder dissolved in 32 parts of water were added, and after thorough mixing, a mixture with a thickness of 1 mm was added. Roll it and cut it with a No. 18 cutting blade to obtain raw noodle strings. This is steamed at about 95°C for 2 minutes and then dried with hot air in an air bath at about 100°C until the moisture content is about 5% to obtain non-fried instant noodles. Example 2 Non-fried instant noodles were obtained in the same manner as in Example 1 except that the acetic acid starch obtained in Reference Example 2 was used instead of the hydroxypropyl starch obtained in Reference Example 1. Example 3 Non-fried instant noodles were obtained in the same manner as in Example 1 except that the hydroxyethyl starch obtained in Reference Example 3 and the carboxymethyl starch obtained in Reference Example 4 were used instead of the hydroxypropyl starch obtained in Reference Example 1. Example 4 Starch succinate obtained in Reference Example 5, starch octenyl succinate obtained in Reference Example 6, and starch maleate obtained in Reference Example 7 were used in place of the hydroxypropyl starch obtained in Reference Example 1. Non-fried instant noodles are obtained in the same manner as in Example 1. In Examples 1 to 4 above, non-fried instant noodles were obtained using hydroxypropyl starch, acetate starch, carboxymethyl starch, starch succinate, starch octenyl succinate and starch maleate of the present invention with various degrees of substitution alone. Ta. Comparative Example 1 Non-fried instant noodles are obtained in the same manner as in Example 1, except that 100 parts of wheat flour are used in place of 90 parts of hydroxypropyl starch and 10 parts of active gluten obtained in Reference Example 1. Comparative Example 2 Non-fried instant noodles were obtained in the same manner as in Example 1, except that 90 parts of corn starch was used instead of 90 parts of hydroxypropylated starch obtained in Reference Example 1. Comparative Example 3 Hydroxypropyl starch obtained in Reference Example 1 with 80 parts of wheat flour, 18 parts of potato starch, and 2 parts of active gluten
Non-fried instant noodles are obtained in the same manner as in Example 1, except that 90 parts of active gluten and 10 parts of active gluten are used instead. As mentioned above, in Comparative Examples 1 to 3, wheat flour, cornstarch,
Non-fried instant noodles were obtained using potato starch. Next, each physical property value of the non-fried instant noodles thus obtained was measured, and the results shown in Tables 1 to 6 were obtained. Tables 1 and 2 show the gelatinization initiation temperature and degree of substitution of various starches and wheat flours used in the production of non-fried instant noodles. Note that the gelatinization start temperature refers to the temperature at which viscosity starts to increase when a 5% starch suspension is prepared using a 2.7% saline solution and heated in a Brabender amylograph. Tables 3 and 4 show the degree of gelatinization and texture of non-fried instant noodles produced using the starches shown in Tables 1 and 2. The degree of gelatinization is measured by an enzyme (diastase) method. The non-fried instant noodles obtained in the Examples and Comparative Examples were ground into pieces of 100 mesh or less, and the samples were measured as follows. For the measurement, prepare five 100 ml Erlenmeyer flasks for each point and call them A1 to A4 and B. Weigh 1.00 g of the above prepared sample into four Erlenmeyer flasks A1 to A4. However, the variation between the four weighed amounts shall be within ±0.5%. Add 50ml of water to each of the 5 flasks, and
Heat A1 and A2 to boiling temperature for 15 minutes, then rapidly cool to room temperature in ice water. On the other hand, add 5 ml of 5% diastase solution to each of A1, A3, and B, and heat all five flasks to 37°C ± 1°C for 90°C while shaking in a thermostatic water bath.
Immediately after incubating for 1 minute, add 2 ml of 1N hydrochloric acid to each flask to stop the diastase reaction, transfer each flask to a 100 ml volumetric flask, and add water to make the volume constant. Filter each solution using dry filter paper and
Pipette 10 ml of the filtrate obtained from A4 and B into a stoppered Erlenmeyer flask, and transfer these from a1 to
Let them be a4 and b. At this point, add 10 ml of N/10 iodine solution to each of the stoppered Erlenmeyer flasks from which 10 ml of water was separately pipetted. Then, at equal time intervals using a stopwatch,
Add 18 ml of N/10 sodium hydroxide solution to six flasks one by one, cap tightly, and shake to make exactly 15 ml of N/10 sodium hydroxide solution.
Leave for a minute. After 15 minutes have elapsed in the first flask, quickly add 2 ml of 10% sulfuric acid at the same time interval and in the same order as when the N/10 aqueous sodium hydroxide solution was added, as soon as the stopper is opened. These solutions were titrated with N/10 sodium thiosulfate solution,
The titration values of a1 to a4 and b are respectively P1 to P4 and Q or the titration value of the blank test is γ, and α is calculated by the following formula.
Find the degree of conversion (%). Degree of α-ization (%) = (γ-P3)-(γ-P4)-(γ-Q)/(γ-
P1)-(γ-P2)-(γ-Q)×100 Next, for the texture, add boiling water to 70g of instant noodles.
This is the sensory value evaluated by 10 panelists after pouring 400ml of the sauce, reconstitution for 3 minutes, draining the water, and adding 15ml of the sauce. In terms of texture, noodle string binding and adhesion;
Regarding adhesion to teeth and raw texture (meaning a state with a wheat-like raw texture, the same applies hereinafter), the strength of the properties is evaluated from a maximum of 10 points to a minimum of 0 points. Other items were evaluated by adding 5.0 points for those that were suitable, adding points for excessive items, and deducting points for insufficient items. Tables 5 and 6 show the values obtained when the instant noodles were reconstituted and seasoned and subjected to a sensory test in the same manner as the texture test in Table 2, immediately after the instant noodles were produced and after being stored for 6 months (at room temperature). showed that. A comparison was also made for fried instant noodles, and the sensory test values immediately after production and 6 months later are also listed. Here, the fried instant noodles were obtained by performing deep-frying treatment at an oil temperature of 140° C. for 3 minutes instead of hot air drying in Comparative Example 1. The overall evaluation in Tables 5 and 6 is a value obtained by combining the opinions of the panelists in an overall evaluation that takes into account flavor and other factors in addition to the texture items. As is clear from the results in Tables 1 to 6, using the etherified starch or esterified starch of the present invention,
Non-fried instant noodles manufactured (Example 1~
4) is superior to other products (Comparative Examples 1 to 3) in terms of degree of gelatinization, texture, etc. Furthermore, when comparing the long-term storage stability with fried instant noodles and Comparative Example 1, the texture of fried instant noodles significantly deteriorated after being stored for 6 months.
In addition, Comparative Example 1 had poor texture both immediately and after 6 months, and had a strong raw texture. In contrast, it is clear that the non-fried instant noodles according to the present invention have a suitable texture both immediately and after 6 months, and are stable even during long-term storage. Furthermore, Table 2 shows that the etherified starch and esterified starch of the present invention are effective within a certain degree of substitution. Example 5 Non-fried instant noodles obtained in Examples 1 and 2 and Comparative Example 1 (sample numbers 2, 4, and
7, 9, 14) were measured. The restoration time is after pouring boiling water into the non-fried instant noodles.
Samples were taken every 30 seconds, cut with a knife, and the restoration state of the cut end was observed, and the time required for complete restoration was defined as the restoration time. The results are shown in Table 7.
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】【table】
Claims (1)
チル澱粉、ヒドロキシプロピル澱粉およびカルボ
キシメチル澱粉より選ばれるエーテル化澱粉また
は酢酸澱粉、コハク酸澱粉、オクテニルコハク酸
澱粉およびマレイン酸澱粉より選ばれるエステル
化澱粉の少なくとも1種に活性グルテンを添加す
ることを特徴とするノンフライ即席麺の製造方
法。1 Etherified starch selected from hydroxyethyl starch, hydroxypropyl starch and carboxymethyl starch with a degree of substitution (DS) of 0.005 to 0.3, or esterified starch selected from acetic acid starch, succinic acid starch, octenyl succinic acid starch and maleic acid starch. A method for producing non-fried instant noodles, characterized in that active gluten is added to at least one kind.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57166794A JPS5955156A (en) | 1982-09-25 | 1982-09-25 | Preparation of non-fried instant noodle |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57166794A JPS5955156A (en) | 1982-09-25 | 1982-09-25 | Preparation of non-fried instant noodle |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5955156A JPS5955156A (en) | 1984-03-30 |
JPS6240980B2 true JPS6240980B2 (en) | 1987-09-01 |
Family
ID=15837793
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57166794A Granted JPS5955156A (en) | 1982-09-25 | 1982-09-25 | Preparation of non-fried instant noodle |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5955156A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04101667U (en) * | 1991-02-04 | 1992-09-02 | 株式会社ヨンマルゴ | teapot stand |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3649532B2 (en) * | 1996-07-29 | 2005-05-18 | 日清製粉株式会社 | Method for producing frozen noodles |
JPH1128067A (en) * | 1997-07-11 | 1999-02-02 | Kumamoto Seifun Kk | Production of raw chinese noodle or semiraw chinese noodle and cooking thereof |
JP6099031B2 (en) * | 2012-07-18 | 2017-03-22 | 日清製粉株式会社 | Method for producing retort noodles |
CA2896456C (en) * | 2013-01-16 | 2018-05-22 | Sanyo Foods Co., Ltd. | Method for manufacturing instant noodle |
-
1982
- 1982-09-25 JP JP57166794A patent/JPS5955156A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04101667U (en) * | 1991-02-04 | 1992-09-02 | 株式会社ヨンマルゴ | teapot stand |
Also Published As
Publication number | Publication date |
---|---|
JPS5955156A (en) | 1984-03-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPH0491744A (en) | Production of bread | |
KR101986841B1 (en) | Process for preparing noodle with starches | |
JPH0763324B2 (en) | Noodle manufacturing method | |
JPS6240980B2 (en) | ||
JP4957379B2 (en) | Processed starch production method, food and feed | |
CN114401644B (en) | High acetylated pea starch for instant noodles | |
JP3968714B2 (en) | Polysaccharide-coated starch and method for producing the same | |
JPS6142546B2 (en) | ||
JPS6262137B2 (en) | ||
JP5936880B2 (en) | Rice cracker quality improver and rice cracker | |
JPS6136897B2 (en) | ||
JPS633572B2 (en) | ||
JPS6136898B2 (en) | ||
EP0910957B1 (en) | Starch-based water-binding composition for foods | |
US3878196A (en) | Process for modifying starch to obtain a thixotropic starch | |
JP4150691B2 (en) | Instant noodle powder composition and instant noodles | |
JP2015136311A (en) | Texture improver for laminar swelled food and use thereof | |
JPS6211076A (en) | Production of fibrous boiled fish paste | |
JP3109893B2 (en) | Manufacturing method of non-fried instant noodles | |
KR101303864B1 (en) | Starch Octenyl Succinate for noodles, manufacturing method of the same, and noodles composition comprising the same | |
JP2796537B2 (en) | Production method of fishery products | |
JPS62248470A (en) | Production of meat paste product | |
JPH05328921A (en) | Production of raw chinese noodle | |
JPH04311359A (en) | Noodles blended with acetylated potato starch | |
JPS5921335A (en) | Production of sausages |