JPS6359670B2 - - Google Patents
Info
- Publication number
- JPS6359670B2 JPS6359670B2 JP56103737A JP10373781A JPS6359670B2 JP S6359670 B2 JPS6359670 B2 JP S6359670B2 JP 56103737 A JP56103737 A JP 56103737A JP 10373781 A JP10373781 A JP 10373781A JP S6359670 B2 JPS6359670 B2 JP S6359670B2
- Authority
- JP
- Japan
- Prior art keywords
- raw material
- dipeptide sweetener
- dipeptide
- powder raw
- sweetener
- 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
- 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 33
- 239000000843 powder Substances 0.000 claims description 22
- 239000002994 raw material Substances 0.000 claims description 20
- 229930006000 Sucrose Natural products 0.000 claims description 15
- 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 claims description 15
- 239000005720 sucrose Substances 0.000 claims description 15
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 claims description 6
- 239000008101 lactose Substances 0.000 claims description 6
- 235000013923 monosodium glutamate Nutrition 0.000 claims description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 4
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 claims description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- 150000007524 organic acids Chemical class 0.000 claims description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 2
- 235000010216 calcium carbonate Nutrition 0.000 claims 1
- PXEDJBXQKAGXNJ-QTNFYWBSSA-L disodium L-glutamate Chemical compound [Na+].[Na+].[O-]C(=O)[C@@H](N)CCC([O-])=O PXEDJBXQKAGXNJ-QTNFYWBSSA-L 0.000 claims 1
- 239000011736 potassium bicarbonate Substances 0.000 claims 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 claims 1
- 235000015497 potassium bicarbonate Nutrition 0.000 claims 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 claims 1
- 235000017550 sodium carbonate Nutrition 0.000 claims 1
- 229940073490 sodium glutamate Drugs 0.000 claims 1
- 235000003599 food sweetener Nutrition 0.000 description 20
- 239000003765 sweetening agent Substances 0.000 description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 108010016626 Dipeptides Proteins 0.000 description 12
- 238000001125 extrusion Methods 0.000 description 11
- 239000000203 mixture Substances 0.000 description 5
- 230000000704 physical effect Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000004375 Dextrin Substances 0.000 description 3
- 229920001353 Dextrin Polymers 0.000 description 3
- 239000004278 EU approved seasoning Substances 0.000 description 3
- 235000019425 dextrin Nutrition 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 235000011194 food seasoning agent Nutrition 0.000 description 3
- LPUQAYUQRXPFSQ-DFWYDOINSA-M monosodium L-glutamate Chemical compound [Na+].[O-]C(=O)[C@@H](N)CCC(O)=O LPUQAYUQRXPFSQ-DFWYDOINSA-M 0.000 description 3
- 239000004223 monosodium glutamate Substances 0.000 description 3
- 239000000546 pharmaceutical excipient Substances 0.000 description 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 235000013615 non-nutritive sweetener Nutrition 0.000 description 2
- 238000001694 spray drying Methods 0.000 description 2
- 235000019640 taste Nutrition 0.000 description 2
- YZQCXOFQZKCETR-UWVGGRQHSA-N Asp-Phe Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 YZQCXOFQZKCETR-UWVGGRQHSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 241000567769 Isurus oxyrinchus Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- NKWPZUCBCARRDP-UHFFFAOYSA-L calcium bicarbonate Chemical compound [Ca+2].OC([O-])=O.OC([O-])=O NKWPZUCBCARRDP-UHFFFAOYSA-L 0.000 description 1
- 229910000020 calcium bicarbonate Inorganic materials 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000000504 effect on taste Effects 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 235000012437 puffed product Nutrition 0.000 description 1
- 235000021067 refined food Nutrition 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 235000012094 sugar confectionery Nutrition 0.000 description 1
- 235000021147 sweet food Nutrition 0.000 description 1
- 230000008961 swelling Effects 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
- 239000003232 water-soluble binding agent Substances 0.000 description 1
Landscapes
- Seasonings (AREA)
Description
本発明は、溶解性及び分散性が改善された高比
容でポーラスな構造を有するジペプチド甘味料の
製造法に関する。
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、APと略記する)に代表
されるジペプチド甘味料は、その原末が一般に細
かい針状の結晶で、比容が大きく、飛散し易い。
更にまた、水に対する分散性、溶解度がともに低
い。このため、原末のままで使用する場合には、
溶解時いわゆるママコを生成し、溶解が困難な物
性を呈する。従つて、例えば、蔗糖のような原末
のままでの甘味料としての使用には種々の制約が
ある。
一方、ジペプチド甘味料は、例えばAPの場合
で蔗糖の約200倍程度(その濃度又は共存する物
質等により変化する)という高い甘味度をもつ。
これは、重量基準にすると、蔗糖の約1/200の使
用量で蔗糖と同等の甘味が得られることとなる。
従つて、所望する甘味度を得るために、極少量の
ジペプチド甘味料を他の比較的多量の成分と混合
して、粉末形の食品、例えば粉末ジユース等を製
造する場合においては、粉末の系全体に甘味料が
均一に分散し、かつその状態を維持するための技
術を要するし、或いは、卓上用甘味料として、上
記の如き高甘味度のジペプチド甘味料を使用する
場合には、計量上の問題を生じる。
このような、ジペプチド甘味料を加工食品、卓
上用調味料等に利用する場合における種々の制約
を解消する目的で、例えば、賦形剤等と共に錠剤
化し、或いは顆粒化する方法が種々提案されてい
るが、熱及び水分に不安定で甘味のロスを生じ易
いという、ジペプチド甘味料利用上の最も大きな
制約の一つを十分に克服して、物性上も満足でき
るものを提供するには非常に困難なものがある。
一例を挙げれば、ジペプチド甘味料を一旦、デキ
ストリン等の賦形・増量剤と共に水に溶解し又は
スラリー化して、主として、スプレー・ドライで
加熱乾燥することにより、溶解性、分散性を改善
する方法では、溶解性、分散性の悪いジペプチド
甘味料を溶解し、又はスラリー化するため、その
操作が困難なことや、スプレー・ドライ等の乾燥
工程において、熱によりジペプチド甘味料が分解
し、甘味のロスを生ずること、更には、比較的多
量の水を蒸発する必要があるため、エネルギー・
コスト的にも不利な点等が予想される。
本発明者らは、以上の点に鑑み、ジペプチド甘
味料の化学的性質、すなわち、熱が水分に対する
不安定さに由来する甘味のロスを伴わず、また、
エネルギー・コスト的にも有利で、溶解性及び分
散性、特に冷水に対する溶解・分散性が良好で、
種々の甘味食品・調味料に応用可能なジペプチド
甘味料を取得すべく鋭意研究を重ね、ジペプチド
甘味料を賦形剤と共に加圧下加熱押出処理し、ポ
ーラスな構造を付与することにより、甘味のロス
を伴わず、物性的にも改善された汎用性のあるロ
ーカロリー甘味料が得られるとの知見に至り、本
発明を完成したものである。
すなわち、本発明は、ジペプチド甘味料を0.5
〜30重量%含有する粉末原料を水分1.0〜10.0%
に調湿した後、エクストルーダーにより品温80〜
160℃で加圧下加熱押出処理することを特徴とす
るポーラスな構造を有するジペプチド甘味料の製
造法である。
次に、本発明を具体的に説明する。
本発明で使用するジペプチド甘味料は、α−L
−アスパルチル−L−フエニルアラニン低級アル
キルエステルであり、好ましくはAPである。ジ
ペプチド甘味料の他に粉末原料を構成する成分
は、澱粉、デキストリン、乳糖その他、水溶性の
物質であれば特にその種類を限定されないが、甘
味料構成成分として呈味質に悪影響を及ぼさず、
又、押出し処理がスムーズに行れるものとして、
蔗糖及び/又は乳糖の使用が望ましい。また、少
量の他の呈味成分、例えばグルタミン酸ナトリウ
ム(MSG)を併用することが、呈味上好ましく、
この他、炭酸ナトリウム、炭酸カルシウム、重炭
酸ナトリウム又は重炭酸カルシウムを有機酸と共
に添加併用すると、押出処理が非常にスムーズに
行える。
上記粉末原料中に占めるジペプチド甘味料の割
合は、粉末原料全体に対し、ジペプチド甘味料が
0.5〜30重量%である。ジペプチド甘味料の占め
る割合が少なすぎる場合には、ローカロリー甘味
料としての特徴を失うし、逆にジペプチド甘味料
の割合が多すぎると溶解性及び分散性の改善が望
めなくなる。従つて上記0.5〜30%好ましくは2
〜5%が至適の範囲である。また、粉末原料中に
MSGを添加する場合には、(含有するAPに対し
て10〜100重量%)、粉末原料全体に対して0.1〜
10重量%が好ましい。
上記粉末原料を水分1〜10%に調湿する。具体
的には、例えば、水、蔗糖水溶液その他水溶性の
結合剤を添加混和して調湿するが、原料粉末自体
の水分含量が高い場合には、特に結合剤の使用を
必須としないことはいうまでもない。水分量がこ
の程度であり、エクストルーダーの運転条件が下
に示すものであれば、押出・乾燥工程における甘
味のロスも殆ど生せず、かつ、安定した膨化品が
得られる。尚、調湿の程度は、使用する賦形剤の
種類に応じて異なるが、蔗糖の場合で水分1〜3
%とし、乳糖の場合で5.0〜10.0%とすることが
好ましく、水分を1.5%程度に調湿し、蔗糖と共
に押出処理した場合に、比容が大きく、冷水に対
する溶解度も極めて高いものが得られる。
調湿した粉末原料をエクストルーダーにより、
温度80〜160℃で加圧下加熱処理する。エクスト
ルーダーは、どのようなタイプのものでもよく、
スクリユー圧縮比、スクリユー形状、ノズルの有
無、押出速度等も適宜選択決定するが、圧力とし
ては具体的には50〜150Kg/cm2程度でよい。上記
温度は品温を示し、160℃以下では褐変を生ずる
事なく白色製品を得る事ができ、逆に160℃を越
すと、褐変が進み、甘味のロスも大きいため、上
記品温80〜160℃好ましくは130℃前後で押出処理
する。なお、押出処理の方法は一般的には大気圧
中へ射出するが、真空中への射出も運転条件の中
に含まれる。
このように押出処理したジペプチド甘味料は比
容が3〜5以上で、ポーラスな構造のものとな
り、水、特に冷水への分散性、溶解性が原末に比
べて著しく向上する。従つて、水に溶かす場合は
もちろん、そのまま食べる場合でもソフトで非常
に口溶けのよい製品が得られる。また、高比容な
ため、卓上甘味料として使用する場合に、蔗糖に
比べ、1/10以下のローカロリーで同じ甘味度かつ
甘味質のものが、同程度の容積で得られることと
なり、薬品的なイメージを与えず、甘味料として
異和感が殆どなく使用でき、個人の嗜好に合せた
微妙な甘味度の調整も極めて容易に行うことがで
きる。更に、他の同程度のカサ密度の物質と混合
して用いる場合にも、比重差によりジペプチド甘
味料が分離して、均一な混合を妨げることもな
く、配合粉末系食品・調味料への利用上有利であ
る。
尚、押出処理した本発明のジペプチド甘味料
は、エクストルーダーのノズルの形状や大きさに
応じ、種々の形態のものが得られ、従つて、微細
な顆粒状のものから、砂糖菓子様のものまで、目
的に応じ、各種大きさ、形状を対象とすることが
可能である。
以下、実施例により、本発明を更に説明する。
実施例 1
AP2重量部及び蔗糖98重量部から成る粉末原料
を万能ミキサーで混練し、水分2.03%に調湿した
後、エクストルーダー(20m/mΦ、スクリユ
ー:フルフライト型、ピツチ:一定、圧縮比:
1:3、ノズル:4.4m/mΦ)により品温120〜
130℃で30〜40秒間(滞留時間)押出処理し、ジ
ペプチド甘味料(A)を調製した。
同一の配合で、水分1.8%に調湿し、同一のエ
クストルーダーで品温160℃で30〜40秒間押出処
理し、ジペプチド甘味料(B)を調製し、更に蔗糖の
1部をデキストリン5.0部に代え、水分4.0%に調
湿し、ジペプチド甘味料(A)と同一の押出し条件で
ジペプチド甘味料(C)を調製し、得られた3種類の
ジペプチド甘味料につき物性等を測定評価した。
結果を第1表に示す。
The present invention relates to a method for producing a dipeptide sweetener having a high specific volume and porous structure with improved solubility and dispersibility. Dipeptide sweeteners, represented by α-L-aspartyl-L-phenylalanine methyl ester (hereinafter abbreviated as AP), are generally fine needle-shaped crystals with a large specific volume and are easily scattered. .
Furthermore, both the dispersibility and solubility in water are low. Therefore, when using the raw powder as is,
When dissolved, it produces so-called mako, which exhibits physical properties that are difficult to dissolve. Therefore, there are various restrictions on the use of raw powders such as sucrose as sweeteners. On the other hand, dipeptide sweeteners, for example in the case of AP, have a sweetness level as high as about 200 times that of sucrose (varies depending on its concentration, coexisting substances, etc.).
This means that on a weight basis, the same sweetness as sucrose can be obtained with approximately 1/200 the amount of sucrose.
Therefore, when producing a powdered food, such as powdered juice, by mixing a very small amount of a dipeptide sweetener with a relatively large amount of other ingredients in order to obtain a desired degree of sweetness, it is necessary to A technique is required to uniformly disperse the sweetener throughout and maintain that state, or when using a dipeptide sweetener with a high sweetness such as the one mentioned above as a tabletop sweetener, it is difficult to measure the sweetener. This causes problems. In order to overcome various restrictions when using dipeptide sweeteners in processed foods, table seasonings, etc., various methods have been proposed, such as forming tablets or granules with excipients, etc. However, it is very difficult to fully overcome one of the biggest constraints on the use of dipeptide sweeteners, which is that they are unstable to heat and moisture and easily cause loss of sweetness, and to provide products with satisfactory physical properties. There are some difficult things.
One example is a method of improving solubility and dispersibility by first dissolving a dipeptide sweetener in water or slurrying it together with a filler/filler such as dextrin, and then heating and drying it mainly by spray drying. In this method, dipeptide sweeteners with poor solubility and dispersibility are dissolved or made into a slurry, which is difficult to operate, and in drying processes such as spray drying, dipeptide sweeteners are decomposed by heat and the sweetness is reduced. In addition, because a relatively large amount of water needs to be evaporated, energy consumption is
Disadvantages are also expected in terms of cost. In view of the above points, the present inventors have discovered that the chemical properties of dipeptide sweeteners, that is, do not involve loss of sweetness due to instability with respect to heat and moisture, and
It is advantageous in terms of energy and cost, and has good solubility and dispersibility, especially in cold water.
We have conducted intensive research to obtain dipeptide sweeteners that can be applied to various sweet foods and seasonings, and by heat-extruding dipeptide sweeteners together with excipients under pressure to give them a porous structure, we have reduced the loss of sweetness. The present invention has been completed based on the finding that a versatile low-calorie sweetener with improved physical properties can be obtained without the addition of alcohol. That is, the present invention uses a dipeptide sweetener of 0.5
Powder raw material containing ~30% by weight with moisture content of 1.0~10.0%
After adjusting the humidity to
This is a method for producing a dipeptide sweetener having a porous structure, which is characterized by carrying out a heat extrusion treatment under pressure at 160°C. Next, the present invention will be specifically explained. The dipeptide sweetener used in the present invention is α-L
-Aspartyl-L-phenylalanine lower alkyl ester, preferably AP. In addition to the dipeptide sweetener, the ingredients constituting the powder raw material are not particularly limited in type as long as they are water-soluble substances such as starch, dextrin, lactose, etc., but as sweetener constituents, they do not have a negative effect on taste quality,
In addition, as the extrusion process can be carried out smoothly,
The use of sucrose and/or lactose is preferred. In addition, it is preferable to use a small amount of other flavor components, such as monosodium glutamate (MSG), in terms of taste.
In addition, when sodium carbonate, calcium carbonate, sodium bicarbonate, or calcium bicarbonate is added together with an organic acid, extrusion processing can be carried out very smoothly. The proportion of the dipeptide sweetener in the powder raw material above is as follows:
It is 0.5-30% by weight. If the proportion of the dipeptide sweetener is too small, it will lose its characteristics as a low-calorie sweetener, and conversely, if the proportion of the dipeptide sweetener is too large, it will not be possible to improve solubility and dispersibility. Therefore, the above 0.5 to 30% preferably 2
~5% is the optimum range. In addition, in powder raw materials
When adding MSG (10-100% by weight based on the AP contained), 0.1-100% based on the total powder raw material
10% by weight is preferred. The moisture content of the above powdered raw material is adjusted to 1 to 10%. Specifically, for example, water, a sucrose aqueous solution, or other water-soluble binder is added and mixed to adjust the humidity, but if the raw material powder itself has a high moisture content, it is not necessary to use a binder. Needless to say. If the moisture content is within this range and the extruder operating conditions are as shown below, there will be almost no loss of sweetness during the extrusion/drying process, and a stable puffed product can be obtained. The degree of humidity control varies depending on the type of excipient used, but in the case of sucrose, the moisture content is 1 to 3.
%, preferably 5.0 to 10.0% in the case of lactose, and when the moisture is adjusted to about 1.5% and extruded with sucrose, a product with a large specific volume and extremely high solubility in cold water can be obtained. . The moisture-adjusted powder raw material is processed using an extruder.
Heat treatment under pressure at a temperature of 80 to 160°C. The extruder can be of any type.
The screw compression ratio, screw shape, presence or absence of a nozzle, extrusion speed, etc. are also selected and determined as appropriate, but the pressure may specifically be about 50 to 150 kg/cm 2 . The above temperature indicates the product temperature. If the temperature is below 160℃, a white product can be obtained without browning. On the other hand, if it exceeds 160℃, browning will progress and the loss of sweetness will be large. The extrusion treatment is carried out at a temperature of preferably around 130°C. In addition, although the extrusion treatment method generally involves injection into atmospheric pressure, injection into vacuum is also included in the operating conditions. The dipeptide sweetener thus extruded has a specific volume of 3 to 5 or more and has a porous structure, and its dispersibility and solubility in water, especially cold water, are significantly improved compared to bulk powder. Therefore, a product that is soft and melts in the mouth very well can be obtained not only when dissolved in water but also when eaten as is. In addition, due to its high specific volume, when used as a tabletop sweetener, it can be used as a tabletop sweetener, with less than 1/10 the calories and the same sweetness and sweetness as sucrose, and can be used as a drug. It can be used as a sweetener without giving off any unpleasant impression, and the sweetness level can be very easily adjusted to suit individual tastes. Furthermore, even when mixed with other substances of similar bulk density, the dipeptide sweetener will not separate due to the difference in specific gravity and prevent uniform mixing, making it suitable for use in blended powder foods and seasonings. It is advantageous. The extruded dipeptide sweetener of the present invention can be obtained in various forms depending on the shape and size of the extruder nozzle, ranging from fine granules to sugar confectionery. It is possible to target various sizes and shapes depending on the purpose. The present invention will be further explained below with reference to Examples. Example 1 A powdered raw material consisting of 2 parts by weight of AP and 98 parts by weight of sucrose was kneaded with a universal mixer, and the moisture content was adjusted to 2.03%. :
1:3, nozzle: 4.4m/mΦ), product temperature 120 ~
Dipeptide sweetener (A) was prepared by extrusion treatment at 130°C for 30 to 40 seconds (residence time). Using the same formulation, adjust the moisture content to 1.8%, extrude using the same extruder at a product temperature of 160°C for 30 to 40 seconds to prepare a dipeptide sweetener (B), and further add 1 part of sucrose to 5.0 parts of dextrin. Instead, the moisture content was adjusted to 4.0% and a dipeptide sweetener (C) was prepared under the same extrusion conditions as the dipeptide sweetener (A), and the physical properties etc. of the three types of dipeptide sweeteners obtained were measured and evaluated.
The results are shown in Table 1.
【表】
尚、溶解度については200c.c.ビーカーに水を張
り、マグネチツクスターラーでやわらかく撹拌
(250rpm)しながら、試料約2.0gを投入し、溶
解時間を測定した。また同様な方法によりAP原
末の溶解速度を測定したところ、温水の場合にお
いてもAP原末がママコになり、5分間経過後も
完全溶解に至らなかつた。また、AP原末の添加
量を極端に減少しても同様の傾向を示した。
実施例 2ジペプチド甘味料(D)の配合
AP 2重量部
乳 糖 98 〃
上記配合の粉末原料に加水して、水分7.5%に、
万能ミキサーで混練調湿した後、実施例1と同一
のエクストルーダーにより品温120〜130℃で押出
処理した。
得られたジペプチド甘味料(D)は粗比容が3.5、
密比容が2.8であり、ジペプチド甘味料(A)及び(B)
に比べて膨化度はやや低いが、エクストルーダー
における運転が、これらに比べて詰りが少なくス
ムーズで、褐変も少なかつた。溶解性及び分散性
は、実施例1と同様良好であつた。
実施例 3ジペプチド甘味料(E)の配合
AP 2重量部
蔗 糖 93.5
MSG 0.5
重 曹 2.0
フマール酸 2.0
上記配合の粉末原料を万能ミキサーで混練し、
水分2.67%に調湿した後、実施例1と同一のエク
ストルーダーにより品温120〜130℃で20〜30秒の
滞留時間で押出処理した。
得られたジペプチド甘味料(E)は比容が、粗比容
3.03及び密比容2.34で、溶解性は、実施例1と同
一の条件で60℃温水で約18秒、2℃の冷水で2分
間であり、ジペプチド甘味料(A)、(B)及び(D)に比べ
劣るが、エクストルーダーの運転は、全く詰りを
生じず、これらに比べてよりスムースな運転で膨
化品が得られた。
実施例 4ジペプチド甘味料(F)の配合
AP 2.0重量部
蔗 糖 97.5
MSG 0.5
上記配合の粉末原料を万能ミキサーで混練して
水分1.56%に調湿した後、実施例1と同一のエク
ストルーダーにより品温130℃で30〜40秒間押出
処理した。
得られたジペプチド甘味料(F)は、ひなあられ状
の形状で、粗比容が5.0であつた。また、実施例
1と同一の条件で溶解度を測定したところ、60℃
温水で8秒、2℃冷水においても25〜30秒で溶解
し、極めて良好な溶解性を示した。[Table] Regarding solubility, a 200 c.c. beaker was filled with water, and while gently stirring (250 rpm) with a magnetic stirrer, about 2.0 g of the sample was added, and the dissolution time was measured. In addition, when the dissolution rate of the AP bulk powder was measured using the same method, it was found that the AP bulk powder became lumpy even in the case of hot water, and did not completely dissolve even after 5 minutes had elapsed. Furthermore, a similar trend was observed even when the amount of AP bulk powder added was extremely reduced. Example 2 Combination of dipeptide sweetener (D) AP 2 parts by weight Lactose 98 Water was added to the powdered raw material of the above combination to make the water content 7.5%,
After kneading and controlling the humidity using a universal mixer, the mixture was extruded using the same extruder as in Example 1 at a product temperature of 120 to 130°C. The obtained dipeptide sweetener (D) has a crude specific volume of 3.5,
Dense specific volume is 2.8, dipeptide sweeteners (A) and (B)
Although the degree of swelling was slightly lower than that of the extruder, the operation in the extruder was smoother with less clogging, and there was less browning. The solubility and dispersibility were as good as in Example 1. Example 3 Composition of dipeptide sweetener (E) AP 2 parts by weight Sucrose 93.5 MSG 0.5 Baking soda 2.0 Fumaric acid 2.0 The powdered raw materials of the above composition were kneaded with a universal mixer,
After adjusting the moisture content to 2.67%, extrusion treatment was performed using the same extruder as in Example 1 at a product temperature of 120 to 130° C. and a residence time of 20 to 30 seconds. The specific volume of the dipeptide sweetener (E) obtained is
3.03 and dense specific volume of 2.34, the solubility was about 18 seconds in 60°C hot water and 2 minutes in 2°C cold water under the same conditions as Example 1, and the dipeptide sweeteners (A), (B) and ( Although inferior to D), the extruder operation did not cause any clogging, and the expanded product was obtained with smoother operation compared to these. Example 4 Combination of dipeptide sweetener (F) AP 2.0 parts by weight Sucrose 97.5 MSG 0.5 After kneading the powdered raw materials of the above composition with a universal mixer and adjusting the moisture content to 1.56%, using the same extruder as in Example 1. Extrusion treatment was performed at a material temperature of 130°C for 30 to 40 seconds. The obtained dipeptide sweetener (F) had a chickpea-like shape and a rough specific volume of 5.0. In addition, when solubility was measured under the same conditions as in Example 1, it was found that 60℃
It dissolved in 8 seconds in hot water and in 25 to 30 seconds in cold water at 2°C, showing extremely good solubility.
Claims (1)
粉末原料を、水分1−10%に調湿した後、エクス
トルーダーにより、品温80−160℃で加圧下加熱
押出処理することを特徴とするポーラスな構造を
有するジペプチド甘味料の製造法。 2 粉末原料が蔗糖及び/又は乳糖とジペプチド
甘味料を含有して成ることを特徴とする特許請求
の範囲第1項記載のジペプチド甘味料の製造法。 3 粉末原料として更にグルタミン酸ナトリウム
を0.1−10重量%含有することを特徴とする特許
請求の範囲第1項又は第2項記載のジペプチド甘
味料の製造法。 4 粉末原料として更に炭酸ナトリウム、炭酸カ
ルシウム、重炭酸ナトリウム又は重炭酸カリウム
と有機酸とを含有することを特徴とする特許請求
の範囲第1項、第2項又は第3項記載のジペプチ
ド甘味料の製造法。 5 粉末原料の一部として蔗糖を使用し、粉末原
料を水分1.0−3.0%に調湿することを特徴とする
特許請求の範囲第1項、第2項、第3項又は第4
項記載のジペプチド甘味料の製造法。 6 粉末原料の一部として乳糖を使用し、粉末原
料を水分5.0−10.0%に調湿することを特徴とす
る特許請求の範囲第1項、第2項、第3項又は第
4項記載のジペプチド甘味料の製造法。[Scope of Claims] 1. A powder raw material containing 0.5-30% dipeptide sweetener by weight is adjusted to a moisture content of 1-10%, and then heat-extruded under pressure using an extruder at a material temperature of 80-160°C. A method for producing a dipeptide sweetener having a porous structure. 2. The method for producing a dipeptide sweetener according to claim 1, wherein the powder raw material contains sucrose and/or lactose and a dipeptide sweetener. 3. The method for producing a dipeptide sweetener according to claim 1 or 2, which further contains 0.1-10% by weight of sodium glutamate as a powder raw material. 4. The dipeptide sweetener according to claim 1, 2, or 3, which further contains sodium carbonate, calcium carbonate, sodium bicarbonate, or potassium bicarbonate and an organic acid as a powder raw material. manufacturing method. 5. Claims 1, 2, 3, or 4, characterized in that sucrose is used as a part of the powder raw material, and the moisture content of the powder raw material is adjusted to 1.0-3.0%.
2. Method for producing the dipeptide sweetener described in Section 1. 6. The method according to claim 1, 2, 3, or 4, characterized in that lactose is used as a part of the powder raw material, and the moisture content of the powder raw material is adjusted to 5.0-10.0%. Method for producing dipeptide sweetener.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56103737A JPS585160A (en) | 1981-07-02 | 1981-07-02 | Preparation of dipeptide sweetener having porous structure |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56103737A JPS585160A (en) | 1981-07-02 | 1981-07-02 | Preparation of dipeptide sweetener having porous structure |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS585160A JPS585160A (en) | 1983-01-12 |
JPS6359670B2 true JPS6359670B2 (en) | 1988-11-21 |
Family
ID=14361933
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56103737A Granted JPS585160A (en) | 1981-07-02 | 1981-07-02 | Preparation of dipeptide sweetener having porous structure |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS585160A (en) |
-
1981
- 1981-07-02 JP JP56103737A patent/JPS585160A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS585160A (en) | 1983-01-12 |
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