JPH0461623B2 - - Google Patents
Info
- Publication number
- JPH0461623B2 JPH0461623B2 JP58145482A JP14548283A JPH0461623B2 JP H0461623 B2 JPH0461623 B2 JP H0461623B2 JP 58145482 A JP58145482 A JP 58145482A JP 14548283 A JP14548283 A JP 14548283A JP H0461623 B2 JPH0461623 B2 JP H0461623B2
- Authority
- JP
- Japan
- Prior art keywords
- composition
- emulsifier
- weight
- lactone
- glucono delta
- 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 - Lifetime
Links
- 239000000203 mixture Substances 0.000 claims description 36
- PHOQVHQSTUBQQK-SQOUGZDYSA-N D-glucono-1,5-lactone Chemical compound OC[C@H]1OC(=O)[C@H](O)[C@@H](O)[C@@H]1O PHOQVHQSTUBQQK-SQOUGZDYSA-N 0.000 claims description 28
- 235000012209 glucono delta-lactone Nutrition 0.000 claims description 28
- 239000000182 glucono-delta-lactone Substances 0.000 claims description 28
- 229960003681 gluconolactone Drugs 0.000 claims description 28
- IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 claims description 25
- 239000003995 emulsifying agent Substances 0.000 claims description 20
- 229920001282 polysaccharide Polymers 0.000 claims description 10
- 239000005017 polysaccharide Substances 0.000 claims description 10
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 14
- 239000003921 oil Substances 0.000 description 13
- 235000019198 oils Nutrition 0.000 description 13
- 235000014113 dietary fatty acids Nutrition 0.000 description 12
- 239000000194 fatty acid Substances 0.000 description 12
- 229930195729 fatty acid Natural products 0.000 description 12
- -1 glycerin fatty acid ester Chemical class 0.000 description 11
- 206010047642 Vitiligo Diseases 0.000 description 10
- 239000000546 pharmaceutical excipient Substances 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- 239000003925 fat Substances 0.000 description 9
- 235000019197 fats Nutrition 0.000 description 9
- 230000000704 physical effect Effects 0.000 description 9
- 235000003599 food sweetener Nutrition 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- 239000003765 sweetening agent Substances 0.000 description 8
- 108010011485 Aspartame Proteins 0.000 description 7
- 229920000858 Cyclodextrin Polymers 0.000 description 7
- 239000001116 FEMA 4028 Substances 0.000 description 7
- 235000021355 Stearic acid Nutrition 0.000 description 7
- 239000000605 aspartame Substances 0.000 description 7
- 235000010357 aspartame Nutrition 0.000 description 7
- 229960003438 aspartame Drugs 0.000 description 7
- WHGYBXFWUBPSRW-FOUAGVGXSA-N beta-cyclodextrin Chemical compound OC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)CO)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1CO WHGYBXFWUBPSRW-FOUAGVGXSA-N 0.000 description 7
- 235000011175 beta-cyclodextrine Nutrition 0.000 description 7
- 229960004853 betadex Drugs 0.000 description 7
- 230000006866 deterioration Effects 0.000 description 7
- 239000001530 fumaric acid Substances 0.000 description 7
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 7
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 7
- 150000007524 organic acids Chemical class 0.000 description 7
- 239000008117 stearic acid Substances 0.000 description 7
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 7
- 108010016626 Dipeptides Proteins 0.000 description 6
- 150000004676 glycans Chemical class 0.000 description 6
- 229920002261 Corn starch Polymers 0.000 description 5
- 239000008120 corn starch Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 230000002209 hydrophobic effect Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 229940023462 paste product Drugs 0.000 description 4
- 241000723346 Cinnamomum camphora Species 0.000 description 3
- 229930006000 Sucrose Natural products 0.000 description 3
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 3
- 229960000846 camphor Drugs 0.000 description 3
- 229930008380 camphor Natural products 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 235000019614 sour taste Nutrition 0.000 description 3
- 239000005720 sucrose Substances 0.000 description 3
- 235000019465 surimi Nutrition 0.000 description 3
- 235000019484 Rapeseed oil Nutrition 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 235000009508 confectionery Nutrition 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- 230000005923 long-lasting effect Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 235000014594 pastries Nutrition 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000001953 sensory effect Effects 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 230000004083 survival effect Effects 0.000 description 2
- JLPULHDHAOZNQI-ZTIMHPMXSA-N 1-hexadecanoyl-2-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC JLPULHDHAOZNQI-ZTIMHPMXSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 239000004278 EU approved seasoning Substances 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- RGHNJXZEOKUKBD-SQOUGZDYSA-N Gluconic acid Natural products OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 229920001218 Pullulan Polymers 0.000 description 1
- 239000004373 Pullulan Substances 0.000 description 1
- 241000519995 Stachys sylvatica Species 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000008429 bread Nutrition 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 229940113118 carrageenan Drugs 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 229940099112 cornstarch Drugs 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 235000011194 food seasoning agent Nutrition 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 235000021110 pickles Nutrition 0.000 description 1
- 108010022457 polysaccharide peptide Proteins 0.000 description 1
- 235000019423 pullulan Nutrition 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000004170 rice bran wax Substances 0.000 description 1
- 235000019384 rice bran wax Nutrition 0.000 description 1
- 235000013580 sausages Nutrition 0.000 description 1
- 235000014102 seafood Nutrition 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000008347 soybean phospholipid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 235000019605 sweet taste sensations Nutrition 0.000 description 1
- 238000010257 thawing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Landscapes
- Seasonings (AREA)
- Fish Paste Products (AREA)
- Meat, Egg Or Seafood Products (AREA)
Description
本発明は、蒲鉾、ソーセージ等の練製品の製造
において、熱や分解酸素に対し、ジペプチド甘味
料を安定に保持するジペプチド甘味料組成物に関
する。
練製品の製造において甘味料として、α−L−
アスパルチル−L−フエニルアラニンメチルエス
テル(以下、アルパルテームと略記する。)に代
表されるジペプチド甘味料を直接添加すると、そ
の殆どが分解されて、甘味を呈さなくなる。
その主な理由は、練製品では、その特有の物性
(いわゆる“足”等)を発現するため、原料すり
身類がPH6.8〜7.5程度の比較的高PHの領域で加熱
(蒲鉾の場合で、PH7.0付近、80℃、40分間程度)
されるためと推察される。即ち、ジペプチド甘味
料はPH4.0〜5.0付近で最も安定であり、中性乃至
はアルカリ性では不安定で、特にこの比較的高PH
値と加熱とが組合された場合、アスパルテームが
極めて不安定な条件に置かれ、急速に甘味力を失
うことが考えられる。
一方、ジペプチド甘味料、例えば、アスパルテ
ームは蔗糖の約300〜500倍(食塩含有食品)の甘
味強度で、甘味の持続性を有することから、練製
品においては、加熱終了時点でのジペプチド甘味
料残存率の15〜30%の増加であつても、甘味付与
効果としては一定の満足な結果をもたらす。
上述のように、ジペプチド甘味料の残存率の向
上は、PHの関与が大きいと考えられるため、一定
のPH低下によるジペプチド甘味料の安定化が有効
な方法として想定できるが、この方法には、練製
品によつて極めて重大な別の問題を生じてしま
う。
即ち、本発明者らがPH低下の最も一般的方法で
ある、クエン酸、フマール酸等の固型有機酸を用
いて蒲鉾のPH低下を試みたところ、アスパルテー
ム残存率の向上は認められたものの、物性劣化、
白斑現象発現、酸味発現等の新たな重大なデリメ
リツトの発生がみられたものである。
本発明者らは、上記の一般には相反するものと
思料される二つの効果、即ち、ジペプチド甘味料
の安定化と練製品の物性、官能等の維持を同時に
満足する方法につき鋭意検討した結果、先ず、白
斑現象については、グルコノデルタラクトンを用
いるか、又は、固型有機酸を水溶液で用いれば解
消可能であり、特に、グルコノデルタラクトンを
用いてPH6.5〜6.0に調整すると、白斑現象解消の
他に物性劣化や酸味発現がかなり押えられるとの
知見を得た。
本発明者らは、かかる知見に基づき更に鋭意研
究を重ねた結果、グルコノデルタラクトンと油
脂、乳化剤、更に必要に応じ多糖類とを一定の比
率で組合せることにより、練製品中におけるジペ
プチド甘味料残存率を向上させ、白斑現象は勿
論、物性劣化及び酸味発現のない練製品等用ジペ
プチド甘味料組成物が得られることを見出し、本
発明を完成するに至つたものである。
即ち、本発明は、(1)グルコノデルタラクトン15
〜60重量%、(2)油脂、乳化剤、油脂−乳化剤又は
油脂−乳化剤−多糖類30〜80重量%及び(3)ジペプ
チド甘味料20重量%以下から成ることを特徴とす
るジペプチド甘味料組成物であり、練製品のPHを
6.7〜5.5程度に規制する量の本組成物を添加する
ことにより、白斑現象、ゲル強度低下及び酸味発
現がなく、ジペプチド甘味料の残存率が向上し、
ジペプチド甘味料の練製品への実用化が可能とな
る。
以下、本発明を具体的に説明する。
本発明に使用するグルコノデルタラクトンは、
粉末、顆粒等の固型品の使用が望ましく、本発明
のジペプチド甘味料組成物に占める割合は、重量
比で15〜60%、好ましくは20〜40%である。
グルコノデルタラクトンが60重量%を越える場
合、官能(甘味)を満足させる本ジペプチド甘味
料組成物の添加量範囲では、PHが5.5以下に低下
するので、物性の劣化や酸味の発現を生じる。逆
に15%より少ないと、ジペプチド甘味料の残存向
上効果に欠け、所期の目的は達成し得なくなる。
従つて、グルコノデルタラクトンが15〜60重量%
である本組成物を用い、練製品のPHを6.7〜5.5に
調整することが好ましく、更に望ましくは、グル
コノデルタラクトン含量20〜40重量%の本組成物
により、練製品のPHを6.5〜6.0に調整すれば最大
の効果を奏ずることができる。
グルコノデルタラクトンと組合せる第2成分
は、油脂、乳化剤、油脂−乳化剤又は油脂−乳化
剤−多糖類である。
油脂類は液体油脂、硬化油、高級脂肪酸、高級
アルコール、ヘツド、ろう、樹脂等が挙げられ
る。好ましくは融点50℃以上のもので、具体例と
して硬化ナタネ油、ステアリン酸がある。
乳化剤としてはグリセリン脂肪酸エステル、ソ
ルビタン脂肪酸エステル、シヨトウ脂肪酸エステ
ル、ダイズリン脂質等の常用の乳化剤を使用出来
るがソルビタン脂肪酸エステル、シヨトウ脂肪酸
エステルが好ましい。
多糖類として澱粉、デキストリン、β−シクロ
デキストリン、プルラン、ペクチン、カラゲーナ
ン、タマミンド等が挙げられるがモチトウモロコ
シ澱粉、β−シクロデキストリンが好ましい。
油脂、乳化剤、油脂−乳化剤又は油脂−乳化剤
−多糖類のジペプチド甘味料組成物に占める割合
は重量比30〜80%で、好ましくは60%前後であ
る。80%以上では目的量のグルコノデルタラクト
ンやアスパルテームが含有されず、30%以下では
アスパルテーム残存率向上が計れない。
尚、油脂−乳化剤の構成割合は重量比で2:
1、油脂−乳化剤−多糖類のそれは2:1:1が
好ましい。
本発明のジペプチド甘味料組成分は前記グルコ
ノデルタラクトン、油脂、乳化剤、多糖類及びジ
ペプチド甘味料を均一に混合することにより調製
できる。
具体的には、例えば、低融点の油脂又は乳化剤
使用の場合は油脂、乳化剤、多糖類、ジペプチド
甘味料、グルコノデルタラクトンを順次混合して
ペースト状のものを得るか、m.p.50℃以上の油脂
又は乳化剤使用の場合は加熱溶融した固型油脂、
乳化剤、固型油脂−乳化剤に多糖類、ジペプチド
甘味料、グルコノデルタラクトンを順次混合し、
冷却した後、ミキサー等で粉砕する。又、いずれ
の場合も溶融混合物をスプレードライヤーにかけ
て乾燥粉末化してもよい。粉末粒子の大きさは好
ましく12メツシユ以下とする。
上記で得られたジペプチド甘味料組成物は、練
製品は勿論、加熱を要する食品乃至酵素を失活し
てない食品、例えば練製品類、漬物類、つくだ煮
類、くん製魚介類・肉類、和菓子・洋菓子類、ガ
ム類、パン類、各種調味類なとに配合されること
により、その効果を最大限に発現するものであ
る。
以下、実験例、実施例により、本発明を更に説
明する。
(尚、実験例、実施例中のAPはアスパルテーム
である。)
比較実施例 1
クエン酸又はグルコノデルタラクトン添加蒲鉾
を下記により試作し、評価した。
レシピー;冷凍スリミ(SA)6.04Kg、食塩0.18
Kg、「味の素」0.06Kg、「新エスサン澱粉」0.60
Kg、氷水2.12Kg、計9.00Kg、AP3.0g使用。
製造方法;冷凍スリミ→解凍→ミンチ→荒ズリ10
分→塩ズリ15分→「味の素」、AP、氷水添加→
本ズリ20分→ケーシング詰→加熱80℃40分→冷
却。
結果を表−1、表−2に示す。
尚、AP分析は液体クロマトグラフイー法によ
る。
The present invention relates to a dipeptide sweetener composition that stably retains a dipeptide sweetener against heat and decomposed oxygen in the production of pastry products such as kamaboko and sausages. α-L- is used as a sweetener in the production of pastry products.
When a dipeptide sweetener represented by aspartyl-L-phenylalanine methyl ester (hereinafter abbreviated as aspartame) is directly added, most of it is decomposed and no longer exhibits sweetness. The main reason for this is that raw surimi products are heated in a relatively high PH region of about 6.8 to 7.5 (in the case of kamaboko , pH around 7.0, 80℃, about 40 minutes)
It is speculated that this is because the In other words, dipeptide sweeteners are most stable at pH levels around 4.0 to 5.0, and are unstable at neutral or alkaline conditions, especially at this relatively high pH.
It is believed that the combination of temperature and heating would place the aspartame in extremely unstable conditions, causing it to rapidly lose its sweetening power. On the other hand, dipeptide sweeteners such as aspartame have a sweetness intensity approximately 300 to 500 times that of sucrose (salt-containing foods) and have a long-lasting sweetness. Even an increase of 15 to 30% in the sweetening rate results in a certain satisfactory sweetening effect. As mentioned above, it is thought that the improvement of the residual rate of dipeptide sweeteners is largely related to pH, so it can be assumed that stabilizing dipeptide sweeteners by a certain level of pH reduction is an effective method. The refined product creates another very serious problem. That is, when the present inventors attempted to lower the pH of kamaboko using solid organic acids such as citric acid and fumaric acid, which is the most common method for lowering the pH, although an improvement in the aspartame residual rate was observed. , physical property deterioration,
New serious demerits such as vitiligo and acidity were observed. As a result of intensive study by the present inventors on a method that simultaneously satisfies the above-mentioned two effects that are generally considered to be contradictory, that is, stabilizing the dipeptide sweetener and maintaining the physical properties and sensory properties of the paste product, First, the vitiligo phenomenon can be resolved by using glucono delta lactone or by using a solid organic acid in an aqueous solution.In particular, if glucono delta lactone is used to adjust the pH to 6.5 to 6.0, vitiligo can be resolved. In addition to eliminating the phenomenon, it was found that the deterioration of physical properties and the development of sourness were considerably suppressed. As a result of further intensive research based on this knowledge, the present inventors have found that by combining glucono delta-lactone, fats and oils, emulsifiers, and, if necessary, polysaccharides at a certain ratio, dipeptide sweetness in pasted products can be improved. The inventors have discovered that it is possible to obtain a dipeptide sweetener composition for paste products, etc., which improves the residual rate of sweeteners and does not cause vitiligo, physical property deterioration, or sourness, and has led to the completion of the present invention. That is, the present invention provides (1) glucono delta lactone 15
~60% by weight, (2) 30 to 80% by weight of fat, oil, emulsifier, fat-emulsifier or fat-emulsifier-polysaccharide, and (3) 20% by weight or less of dipeptide sweetener. and the pH of the paste product is
By adding the present composition in an amount regulated to about 6.7 to 5.5, there is no vitiligo phenomenon, decrease in gel strength, and sour taste, and the residual rate of the dipeptide sweetener is improved.
It becomes possible to put dipeptide sweeteners to practical use in paste products. The present invention will be explained in detail below. The glucono delta lactone used in the present invention is
It is desirable to use solid products such as powders and granules, and their proportion in the dipeptide sweetener composition of the present invention is 15 to 60%, preferably 20 to 40% by weight. When glucono delta lactone exceeds 60% by weight, the pH decreases to 5.5 or less within the range of addition amount of the present dipeptide sweetener composition that satisfies sensory (sweet taste), resulting in deterioration of physical properties and development of sour taste. On the other hand, if it is less than 15%, the dipeptide sweetener will not have the effect of improving the persistence of the sweetener, and the intended purpose will not be achieved.
Therefore, 15-60% by weight of glucono delta-lactone
It is preferable to adjust the pH of the paste product to 6.7 to 5.5 using the present composition, and more preferably, to adjust the pH of the paste product to 6.5 to 5.5 using the present composition having a glucono delta lactone content of 20 to 40% by weight. Adjusting to 6.0 will give you the maximum effect. The second component to be combined with glucono delta lactone is a fat, an emulsifier, a fat-emulsifier, or a fat-emulsifier-polysaccharide. Examples of the oils and fats include liquid oils, hardened oils, higher fatty acids, higher alcohols, heads, waxes, and resins. Preferably, it has a melting point of 50° C. or higher, and specific examples include hardened rapeseed oil and stearic acid. As the emulsifier, commonly used emulsifiers such as glycerin fatty acid ester, sorbitan fatty acid ester, camphor fatty acid ester, and soybean phospholipid can be used, but sorbitan fatty acid ester and camphor fatty acid ester are preferred. Examples of the polysaccharide include starch, dextrin, β-cyclodextrin, pullulan, pectin, carrageenan, tamamine, and waxy corn starch and β-cyclodextrin are preferred. The proportion of fat, oil, emulsifier, fat-emulsifier, or fat-emulsifier-polysaccharide in the dipeptide sweetener composition is 30 to 80% by weight, preferably around 60%. If it is more than 80%, it will not contain the desired amount of glucono delta-lactone or aspartame, and if it is less than 30%, it will not be possible to improve the aspartame residual rate. The composition ratio of oil and fat to emulsifier is 2:
1. The ratio of oil/fat/emulsifier/polysaccharide is preferably 2:1:1. The dipeptide sweetener composition of the present invention can be prepared by uniformly mixing the glucono delta lactone, oil, emulsifier, polysaccharide, and dipeptide sweetener. Specifically, for example, in the case of using a low-melting point oil or emulsifier, the oil, emulsifier, polysaccharide, dipeptide sweetener, and glucono delta-lactone are mixed in order to obtain a paste, or the oil or fat with an mp of 50°C or higher is used. Or, if using an emulsifier, heat-melted solid oil or fat,
Emulsifier, solid fat-emulsifier, polysaccharide, dipeptide sweetener, glucono delta-lactone are mixed in sequence,
After cooling, pulverize with a mixer or the like. In either case, the molten mixture may be dried and powdered using a spray dryer. The size of the powder particles is preferably 12 mesh or less. The dipeptide sweetener composition obtained above can be used not only for paste products, but also for foods that require heating or foods whose enzymes have not been deactivated, such as paste products, pickles, boiled fish, smoked seafood/meat, Japanese sweets, etc. Its effects can be maximized by incorporating it into Western confectionery, gum, bread, and various seasonings. The present invention will be further explained below using experimental examples and examples. (AP in the Experimental Examples and Examples is aspartame.) Comparative Example 1 A prototype kamaboko with citric acid or glucono delta-lactone added was produced and evaluated as follows. Recipe: Frozen surimi (SA) 6.04Kg, salt 0.18
Kg, “Ajinomoto” 0.06Kg, “New Essan Starch” 0.60
Kg, ice water 2.12Kg, total 9.00Kg, AP 3.0g used. Manufacturing method: Frozen surimi → thawing → minced → Arasuri 10
Minutes → Salt slurry 15 minutes → “Ajinomoto”, AP, ice water addition →
Stirring for 20 minutes → Stuffing in casings → Heating at 80℃ for 40 minutes → Cooling. The results are shown in Table-1 and Table-2. Note that AP analysis is based on liquid chromatography.
【表】
表−1の如く、固型の有機酸使用では白斑現象
がある。固型有機酸を水溶液にして使用しれば白
斑現象はないが物性劣化等により適当でない。[Table] As shown in Table 1, there is a vitiligo phenomenon when solid organic acids are used. If a solid organic acid is used in the form of an aqueous solution, there will be no white spots, but this is not appropriate due to deterioration of physical properties.
【表】【table】
【表】
表−2の如く、グルコノデルタラクトン使用に
より、白斑現象が解消し、物性劣化も比較的せ
ず、酸味も比較的感ぜられずクエン酸の場合より
比較的PHをより下げることができ、AP残存率の
向上が計られる。
尚、表−1の固型有機酸使用の場合、AP残存
率が高い傾向にあるが、これは白斑現象との関連
と考えられる。
比較実施例 2
固型有機酸使用による白斑現象解消の為に親水
性賦形剤、疎水性賦形剤による有機酸−APのコ
ーデイングを行つた。
新水性賦形剤使用の場合は混合物に同量の水を
加えてホモナイズし、40℃、24時間減圧乾燥後、
粉砕し、粒子の大きさを65〜150メツシユとした。
疎水性賦形剤使用の場合はその油脂又は乳化剤を
加熱溶融し、フマール酸とAPを十分混練し、冷
却後粉砕し、粒子の大きさを65〜150メツシユと
した。
賦形剤コーデイング組成物
組成物(A)
アラビアゴム 50.0%重量
フマール酸 35.7 〃
AP 14.3 〃
組成物(B)
モチトウモロコシ澱粉 50.0%重量
フマール酸 35.7 〃
AP 14.3 〃
組成物(C)
β−シクロデキストリン 50.0%重量
フマール酸 35.7 〃
AP 14.3 〃
組成物(D)
シヨトウ脂肪酸エステル 66.7%重量
フマール酸 23.8 〃
AP 9.5 〃
組成物(E)
ステアリン酸 66.7%重量
フマール酸 23.8 〃
AP 9.5 〃
組成物(A)〜(E)につき比較実験例1と同様にして
蒲鉾を試作し、評価した。
尚、組成物中のAP分析は困難な為に組成物使
用の場合のAP残存率には全て組成物調製物と蒲
鉾製造時を加味したものである。
結果は表−3に示す。[Table] As shown in Table 2, the use of glucono delta lactone eliminates the vitiligo phenomenon, causes relatively no deterioration of physical properties, has relatively no sour taste, and lowers the pH comparatively more than in the case of citric acid. This will improve the AP remaining rate. In addition, in the case of using the solid organic acid shown in Table 1, the AP residual rate tends to be high, but this is considered to be related to the vitiligo phenomenon. Comparative Example 2 In order to eliminate the vitiligo phenomenon caused by the use of a solid organic acid, an organic acid-AP was coded using a hydrophilic excipient and a hydrophobic excipient. When using a new aqueous excipient, add the same amount of water to the mixture, homogenize, dry at 40℃ for 24 hours under reduced pressure,
It was ground to a particle size of 65 to 150 mesh.
When a hydrophobic excipient is used, the oil or fat or emulsifier is heated and melted, fumaric acid and AP are sufficiently kneaded, cooled, and then ground to give a particle size of 65 to 150 mesh. Excipient Coding Composition Composition (A) Gum Arabic 50.0% by weight fumaric acid 35.7 〃 AP 14.3 〃 Composition (B) Waxy corn starch 50.0% by weight fumaric acid 35.7 〃 AP 14.3 〃 Composition (C) β-cyclo Dextrin 50.0% weight fumaric acid 35.7 〃 AP 14.3 〃 Composition (D) Shoots fatty acid ester 66.7% weight fumaric acid 23.8 〃 AP 9.5 〃 Composition (E) Stearic acid 66.7% weight fumaric acid 23.8 〃 AP 9.5 〃 Composition (A ) to (E), kamaboko was prototyped and evaluated in the same manner as in Comparative Experiment Example 1. Incidentally, since it is difficult to analyze AP in the composition, all AP residual rates when using the composition take into account the composition preparation and the time of kamaboko production. The results are shown in Table-3.
【表】【table】
【表】
表−3の如く、賦形剤でコーテイングしても白
斑現象は解消できない。しかし、賦形剤がモチト
ウモロコシ澱粉、β−シクロデキストリン、シヨ
トウ脂肪酸エステル、ステアリン酸の場合AP残
存率の向上が認められる。
実施例 1
有機酸材としてグルコノデルタラクトンを用
い、これをAPと共に疎水性賦形剤でコーテイン
グした。その調製方法は比較実施例2の場合と同
様である。
親水性賦形剤(組成物(F)の場合)についてはグ
ルコノデルタラクトンは水存圧下でグルコン酸に
分解するのでβ−シクロデキストリンコーテイン
グAPのみを採り上げ、グルコノデルタラクトン
を別添とした。
又、疎水性賦形剤使用でグルコノデルタラクト
ン別添の例を組成物(J)に示した。
グルコノデルタラクトン含有組成物
組成物(F)
β−シクロデキストリン 80.0%重量
AP 20.0 〃
(β−シクロデキストリン及びAPの総重量15部
に対し、グルコノデルタラクトンを23.1部の比率
で併用)
組成物(G)
シヨトウ脂肪酸エステル 66.7%重量
グルコノデルタラクトン 29.5 〃
AP 3.8 〃
組成物(H)
硬化ナタネ油 66.7%重量
グルコノデルタラクトン 29.5 〃
AP 3.8 〃
組成物(I)
米ぬかろう 66.7%重量
グルコノデルタラクトン 29.5 〃
AP 3.8 〃
組成物(J)
ステアリン酸 40.0%重量
ソルタビン脂肪酸エステル 20.0 〃
モチトウモロコシ澱粉 20.0 〃
AP 20.0 〃
(グルコノデルタラクトンは別添)
組成物(K)
ステアリン酸 44.4%重量
ソルタビン脂肪酸エステル 22.3 〃
グルコノデルタラクトン 29.5 〃
AP 3.8 〃
組成物(L)
ステアリン酸 33.3%重量
ソルタビン脂肪酸エステル 16.7 〃
モチトウモロコシ澱粉 16.7 〃
グルコノデルタラクトン 29.5 〃
AP 3.8 〃
組成物(F)〜(L)につき、実験例1の場合と同様に
して蒲鉾を試作し、評価した。
結果を表−4に示す。[Table] As shown in Table 3, the vitiligo phenomenon cannot be resolved even by coating with excipients. However, when the excipients are waxy corn starch, β-cyclodextrin, camphor fatty acid ester, and stearic acid, an improvement in the AP residual rate is observed. Example 1 Glucono delta-lactone was used as the organic acid material and coated with AP and a hydrophobic excipient. The preparation method is the same as in Comparative Example 2. Regarding hydrophilic excipients (in the case of composition (F)), since glucono delta-lactone decomposes into gluconic acid under aqueous pressure, only β-cyclodextrin-coated AP was selected, and glucono delta-lactone was added separately. . In addition, an example of using a hydrophobic excipient and adding glucono delta lactone is shown in Composition (J). Composition containing glucono delta lactone Composition (F) β-cyclodextrin 80.0% Weight AP 20.0 (Glucono delta lactone is used in combination at a ratio of 23.1 parts to 15 parts of total weight of β-cyclodextrin and AP) Composition Product (G) Blackberry fatty acid ester 66.7% glucono delta lactone by weight 29.5 〃 AP 3.8 〃 Composition (H) Hydrogenated rapeseed oil 66.7% glucono delta lactone by weight 29.5 〃 AP 3.8 〃 Composition (I) Rice bran wax 66.7% glucono delta lactone by weight Nodelta-lactone 29.5 〃 AP 3.8 〃 Composition (J) Stearic acid 40.0% by weight Sortabin fatty acid ester 20.0 〃 Waxy corn starch 20.0 〃 AP 20.0 〃 (Glucono-delta-lactone is attached separately) Composition (K) Stearic acid 44.4% by weight Sortavin fatty acid ester 22.3 〃 Glucono delta lactone 29.5 〃 AP 3.8 〃 Composition (L) Stearic acid 33.3% by weight Sortavin fatty acid ester 16.7 〃 Waxy corn starch 16.7 〃 Glucono delta lactone 29.5 〃 AP 3.8 〃 Composition (F) ~( Regarding L), a prototype of kamaboko was produced and evaluated in the same manner as in Experimental Example 1. The results are shown in Table 4.
【表】
表−4からステアリン酸使用の場合は蒲鉾PHが
6.5より若干低くなることもあつてAP残存率が高
い。又、PHが低くなる割合には物性劣化もない。
特に(L)の場合が最もAP残存率が高く、蒲鉾物
性もよい。
(L)の場合のAP残存率30.4%蒲鉾は蔗糖3.74%
含有蒲鉾に相当(AP甘味度369対蔗糖1.0)し、
甘味の持続性もあつて、蒲鉾への甘味付与の目的
は充分達せられるものである。[Table] From Table 4, when using stearic acid, kamaboko PH is
The AP survival rate is high, as it is slightly lower than 6.5. In addition, there is no deterioration in physical properties at a rate where the PH decreases. In particular, case (L) has the highest AP survival rate and good kamaboko physical properties. (L) AP residual rate is 30.4%, kamaboko is sucrose 3.74%
Equivalent to kamaboko containing (AP sweetness level 369 vs. sucrose 1.0),
The sweetness is long-lasting, and the purpose of adding sweetness to kamaboko can be fully achieved.
Claims (1)
物。 (1) グルコノデルタラクトン15〜60重量% (2) 油脂、乳化剤、油脂−乳化剤又は油脂−乳化
剤−多糖類30〜80重量% 及び (3) ジペプチド甘味料20重量%。[Claims] 1. A dipeptide sweetener composition comprising the following composition. (1) 15 to 60% by weight of glucono delta lactone, (2) 30 to 80% by weight of oil, emulsifier, fat-emulsifier or fat-emulsifier-polysaccharide, and (3) 20% by weight of dipeptide sweetener.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58145482A JPS6037948A (en) | 1983-08-09 | 1983-08-09 | Dipeptide sweetener composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58145482A JPS6037948A (en) | 1983-08-09 | 1983-08-09 | Dipeptide sweetener composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6037948A JPS6037948A (en) | 1985-02-27 |
| JPH0461623B2 true JPH0461623B2 (en) | 1992-10-01 |
Family
ID=15386272
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58145482A Granted JPS6037948A (en) | 1983-08-09 | 1983-08-09 | Dipeptide sweetener composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6037948A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6156795A (en) * | 1997-12-22 | 2000-12-05 | Oklahoma Medical Research Foundation | N-L-alpha-aspartyl-L-phenylalanine 1-methyl ester and its derivatives for appetite enhancement |
| US6326400B1 (en) | 1999-08-27 | 2001-12-04 | Allen B. Edmundson | N-L-alpha-aspartyl-L-phenylalanine 1-methyl ester and its derivatives for appetite enhancement |
-
1983
- 1983-08-09 JP JP58145482A patent/JPS6037948A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6037948A (en) | 1985-02-27 |
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