JPH0724554B2 - Manufacturing method of powdered food material - Google Patents
Manufacturing method of powdered food materialInfo
- Publication number
- JPH0724554B2 JPH0724554B2 JP14426186A JP14426186A JPH0724554B2 JP H0724554 B2 JPH0724554 B2 JP H0724554B2 JP 14426186 A JP14426186 A JP 14426186A JP 14426186 A JP14426186 A JP 14426186A JP H0724554 B2 JPH0724554 B2 JP H0724554B2
- Authority
- JP
- Japan
- Prior art keywords
- water
- minutes
- powder
- gel
- hours
- 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
- 239000000463 material Substances 0.000 title claims description 38
- 235000013305 food Nutrition 0.000 title claims description 16
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 229920002752 Konjac Polymers 0.000 claims description 17
- 235000010485 konjac Nutrition 0.000 claims description 17
- 229920001285 xanthan gum Polymers 0.000 claims description 15
- 239000000230 xanthan gum Substances 0.000 claims description 15
- 235000010493 xanthan gum Nutrition 0.000 claims description 15
- 229940082509 xanthan gum Drugs 0.000 claims description 15
- 229920000057 Mannan Polymers 0.000 claims description 14
- 238000010438 heat treatment Methods 0.000 claims description 13
- 238000001035 drying Methods 0.000 claims description 12
- 230000008961 swelling Effects 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 claims description 6
- 230000002378 acidificating effect Effects 0.000 claims description 4
- 229940025902 konjac mannan Drugs 0.000 claims description 4
- 230000007935 neutral effect Effects 0.000 claims description 4
- 238000000227 grinding Methods 0.000 claims description 3
- 238000010298 pulverizing process Methods 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 34
- 239000000843 powder Substances 0.000 description 33
- 239000000499 gel Substances 0.000 description 25
- 239000000203 mixture Substances 0.000 description 14
- 239000000796 flavoring agent Substances 0.000 description 7
- 230000000704 physical effect Effects 0.000 description 7
- 239000011812 mixed powder Substances 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 241000251468 Actinopterygii Species 0.000 description 5
- 235000019634 flavors Nutrition 0.000 description 5
- 235000015110 jellies Nutrition 0.000 description 5
- 239000008274 jelly Substances 0.000 description 5
- 238000001816 cooling Methods 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- -1 amino acid salts Chemical class 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 235000011194 food seasoning agent Nutrition 0.000 description 3
- 238000007710 freezing Methods 0.000 description 3
- 230000008014 freezing Effects 0.000 description 3
- 150000004676 glycans Chemical class 0.000 description 3
- 238000007602 hot air drying Methods 0.000 description 3
- 235000013372 meat Nutrition 0.000 description 3
- 229920001282 polysaccharide Polymers 0.000 description 3
- 239000005017 polysaccharide Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 229940024606 amino acid Drugs 0.000 description 2
- 235000001014 amino acid Nutrition 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 235000013355 food flavoring agent Nutrition 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 235000018102 proteins Nutrition 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 229940013618 stevioside Drugs 0.000 description 2
- OHHNJQXIOPOJSC-UHFFFAOYSA-N stevioside Natural products CC1(CCCC2(C)C3(C)CCC4(CC3(CCC12C)CC4=C)OC5OC(CO)C(O)C(O)C5OC6OC(CO)C(O)C(O)C6O)C(=O)OC7OC(CO)C(O)C(O)C7O OHHNJQXIOPOJSC-UHFFFAOYSA-N 0.000 description 2
- 235000019202 steviosides Nutrition 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- 235000019465 surimi Nutrition 0.000 description 2
- FTLYMKDSHNWQKD-UHFFFAOYSA-N (2,4,5-trichlorophenyl)boronic acid Chemical compound OB(O)C1=CC(Cl)=C(Cl)C=C1Cl FTLYMKDSHNWQKD-UHFFFAOYSA-N 0.000 description 1
- LUEWUZLMQUOBSB-FSKGGBMCSA-N (2s,3s,4s,5s,6r)-2-[(2r,3s,4r,5r,6s)-6-[(2r,3s,4r,5s,6s)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2r,4r,5s,6r)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound O[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@H](O[C@@H](OC3[C@H](O[C@@H](O)[C@@H](O)[C@H]3O)CO)[C@@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O LUEWUZLMQUOBSB-FSKGGBMCSA-N 0.000 description 1
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 1
- 244000291564 Allium cepa Species 0.000 description 1
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
- 240000007087 Apium graveolens Species 0.000 description 1
- 235000015849 Apium graveolens Dulce Group Nutrition 0.000 description 1
- 235000010591 Appio Nutrition 0.000 description 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
- 108010011485 Aspartame Proteins 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 244000056139 Brassica cretica Species 0.000 description 1
- 235000003351 Brassica cretica Nutrition 0.000 description 1
- 235000003343 Brassica rupestris Nutrition 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
- 244000000626 Daucus carota Species 0.000 description 1
- 235000002767 Daucus carota Nutrition 0.000 description 1
- 239000004129 EU approved improving agent Substances 0.000 description 1
- 239000004278 EU approved seasoning Substances 0.000 description 1
- 102000002322 Egg Proteins Human genes 0.000 description 1
- 108010000912 Egg Proteins Proteins 0.000 description 1
- 108010028690 Fish Proteins Proteins 0.000 description 1
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 1
- 229920002581 Glucomannan Polymers 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- 108010070551 Meat Proteins Proteins 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 102000014171 Milk Proteins Human genes 0.000 description 1
- 108010011756 Milk Proteins Proteins 0.000 description 1
- 241001098054 Pollachius pollachius Species 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 108010073771 Soybean Proteins Proteins 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- UEDUENGHJMELGK-HYDKPPNVSA-N Stevioside Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@]12C(=C)C[C@@]3(C1)CC[C@@H]1[C@@](C)(CCC[C@]1([C@@H]3CC2)C)C(=O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O UEDUENGHJMELGK-HYDKPPNVSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 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 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 241000589634 Xanthomonas Species 0.000 description 1
- YGCFIWIQZPHFLU-UHFFFAOYSA-N acesulfame Chemical compound CC1=CC(=O)NS(=O)(=O)O1 YGCFIWIQZPHFLU-UHFFFAOYSA-N 0.000 description 1
- 229960005164 acesulfame Drugs 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- AEMOLEFTQBMNLQ-WAXACMCWSA-N alpha-D-glucuronic acid Chemical compound O[C@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O AEMOLEFTQBMNLQ-WAXACMCWSA-N 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 239000000605 aspartame Substances 0.000 description 1
- 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 description 1
- 235000010357 aspartame Nutrition 0.000 description 1
- 229960003438 aspartame Drugs 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
- 235000008429 bread Nutrition 0.000 description 1
- 229940041514 candida albicans extract Drugs 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 229940109275 cyclamate Drugs 0.000 description 1
- HCAJEUSONLESMK-UHFFFAOYSA-N cyclohexylsulfamic acid Chemical compound OS(=O)(=O)NC1CCCCC1 HCAJEUSONLESMK-UHFFFAOYSA-N 0.000 description 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 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 229940046240 glucomannan Drugs 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000000845 maltitol Substances 0.000 description 1
- 235000010449 maltitol Nutrition 0.000 description 1
- VQHSOMBJVWLPSR-WUJBLJFYSA-N maltitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-WUJBLJFYSA-N 0.000 description 1
- 229940035436 maltitol Drugs 0.000 description 1
- 235000010746 mayonnaise Nutrition 0.000 description 1
- 239000008268 mayonnaise Substances 0.000 description 1
- 235000021239 milk protein Nutrition 0.000 description 1
- 235000013923 monosodium glutamate Nutrition 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000002336 ribonucleotide Substances 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 229940085605 saccharin sodium Drugs 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 235000020183 skimmed milk Nutrition 0.000 description 1
- 229940073490 sodium glutamate Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 235000019710 soybean protein Nutrition 0.000 description 1
- 235000013599 spices 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
- 239000005720 sucrose Substances 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000012138 yeast extract Substances 0.000 description 1
Landscapes
- Preparation Of Fruits And Vegetables (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は水に溶解したときに簡単に可逆性のゲルを製造
することのできるコンニャクマンナン含有可逆性ゲルと
なる粉末食品素材の製造法に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method for producing a powdered food material to be a konjak mannan-containing reversible gel capable of easily producing a reversible gel when dissolved in water. .
本発明者らは以前コンニャクマンナンとキサンタンガム
とを含有せしめることにより熱可逆性のゲルが得られる
ことを見い出した。このゲルはアルカリ剤を含有せずに
強固でかつ安定なゲルであり、保水性、凍結耐性、製造
加工適性に優れているものである。しかしこのゲルを得
るためには、コンニャクマンナン及びキサンタンガムを
含有する水溶液を加熱、冷却、必要に応じては摩砕を行
うが、加熱、または摩砕の前に、コンニャクマンナンを
十分に膨潤させるのに時間を要した。The present inventors have previously found that the inclusion of konjac mannan and xanthan gum results in a thermoreversible gel. This gel is a strong and stable gel that does not contain an alkaline agent, and is excellent in water retention, freeze resistance and suitability for manufacturing and processing. However, in order to obtain this gel, an aqueous solution containing konjak mannan and xanthan gum is heated, cooled, and, if necessary, ground, but the konjak mannan is sufficiently swelled before heating or grinding. Took a while.
本発明者らは、上記欠点を改良する為種々検討した結
果、予め、コンニャクマンナン及びキサンタンガムを水
に溶解膨潤した後乾燥し、更に粉砕して粉末食品素材を
得ることによって、この素材を水に溶解したときに膨潤
に長時間必要としないことを見い出し本発明を完成し
た。The present inventors, as a result of various studies to improve the above drawbacks, in advance, konjak mannan and xanthan gum were dissolved and swelled in water, then dried, and further pulverized to obtain a powdered food material, and this material was added to water. The present invention has been completed by finding that it does not require a long time for swelling when dissolved.
本発明で用いるコンニャクマンナンとは、コンニャクの
もつ多糖類の主成分であるグルコマンナンをいい、特定
の構造の物質に限定されるものではない。一方キサンタ
ンガムとしてはキサントモナス属細菌がブドウ糖を含有
する培地中に生産するD−グルコース、D−マンノー
ス、D−グルクロン酸を主成分とする多糖類糊料をい
い、いずれも市販のものを使用することができる。コン
ニャクマンナンとキサンタンガムの配合比率(重量)は
95:5ないし5:95、より好ましくは80:20〜20:80であれば
よい。The konjak mannan used in the present invention means glucomannan, which is the main component of the polysaccharide of konjak, and is not limited to a substance having a specific structure. On the other hand, xanthan gum refers to a polysaccharide paste containing D-glucose, D-mannose, and D-glucuronic acid as main components, which is produced by a bacterium belonging to the genus Xanthomonas in a medium containing glucose. You can The mixing ratio (weight) of konjac mannan and xanthan gum is
It may be 95: 5 to 5:95, more preferably 80:20 to 20:80.
又、コンニャクマンナン及びキサンタンガムを含有する
水溶液のPHは酸性〜中性域であればよい。これらの粉末
を水に溶解膨潤させる。本発明は後に乾燥するので水の
量は特に限定する必要はないが固型分濃度が0.2%ない
し50%程度にしておくのが膨潤及び乾燥の効率から好ま
しい。水にコンニャクマンナン及びキサンタンガムを添
加後膨潤するまで30分ないし24時間放置する。放置させ
たものはゾル状であるが、これを乾燥後粉砕し粉末食品
素材とすることができる。The PH of the aqueous solution containing konjak mannan and xanthan gum may be in the acidic to neutral range. These powders are dissolved and swelled in water. Since the present invention will be dried later, the amount of water is not particularly limited, but it is preferable to keep the solid content concentration at about 0.2% to 50% from the viewpoint of swelling and drying efficiency. After adding konjac mannan and xanthan gum to water, leave for 30 minutes to 24 hours until it swells. What is left to stand is in the form of a sol, but this can be dried and then pulverized into a powdered food material.
更に、この乾燥前のゾル状物を、加熱後、好ましくは冷
却してゲル化物とした後、乾燥、粉砕しても、同様の粉
末食品素材を得ることができる。加熱条件は特に限定さ
れるものではなく、加熱時間、配合比率、その他の条件
により加熱温度の下限が異なるが、70℃以上に加熱する
ことが好ましい。Further, the same powdered food material can be obtained by heating the sol-like substance before drying, preferably by cooling to give a gelled product, and then drying and pulverizing. The heating conditions are not particularly limited, and the lower limit of the heating temperature varies depending on the heating time, the blending ratio, and other conditions, but it is preferable to heat to 70 ° C or higher.
又、加熱前のゾル状物を摩砕することによりゲル化物が
得られる。摩砕に使用する装置は特に限定されるもので
はなく、市販のミキサー、ジューサー、ホモジナイザ
ー、フードカッター、スピードニーダー、ロボクープミ
キサー等を用いることができる。Further, a gelled product can be obtained by grinding the sol before heating. The apparatus used for milling is not particularly limited, and a commercially available mixer, juicer, homogenizer, food cutter, speed kneader, robo coup mixer or the like can be used.
この摩砕したゲル化物を乾燥、粉砕して、粉末食品素材
とすることができる。更に、摩砕したゲル化物を加熱後
好ましくは冷却した後、乾燥、粉砕しても、粉末食品素
材が得られる。The ground gel product can be dried and pulverized to obtain a powdered food material. Furthermore, a powdered food material can be obtained by heating and preferably cooling the ground gelled product, and then drying and crushing it.
乾燥方法は、熱風乾燥、天日乾燥、気流乾燥、凍結乾燥
など一般に知られている方法を適用することができる
が、熱風乾燥法が得られる粉末の物性上好ましい。熱風
乾燥の条件は30℃ないし80℃にて6時間ないし36時間が
好ましい。乾燥後の水分は5%ないし15%程度であって
保存、流通に適している。As the drying method, generally known methods such as hot air drying, sun drying, air flow drying and freeze drying can be applied, but the hot air drying method is preferable in terms of physical properties of the powder. The hot air drying conditions are preferably 30 ° C. to 80 ° C. for 6 hours to 36 hours. The water content after drying is about 5% to 15%, which is suitable for storage and distribution.
乾燥後のものは乾燥方法によってシート状、多孔質状、
粒状などの形状であり、溶解性が必ずしも好ましくない
ので粉砕し水への溶解性を高める。粉砕する方法は一般
の粉砕機による方法を適用することができ、種々の粒径
の粉末を得ることができる。一般には粒径が小さいとダ
マを形成しやすいので40μmないし1000μm、より好ま
しくは100μmないし600μmにして、分散性を高めると
共に溶解性を保ったものが好適である。After drying, sheet-like, porous, and
Since it has a granular shape and the solubility is not always preferable, it is pulverized to improve the solubility in water. As a method for crushing, a method using a general crusher can be applied, and powders having various particle sizes can be obtained. Generally, if the particle size is small, lumps are likely to form, so 40 μm to 1000 μm, more preferably 100 μm to 600 μm, is preferable because the dispersibility is improved and the solubility is maintained.
本発明の粉末食品素材は、いずれも水分散性に優れ、か
つ、ただちに膨潤する。また、水に溶解し放置するだけ
でゲル化してくるが、好ましくは熱水に溶解するか、水
に溶解後加熱することによって、コンニャクマンナン及
びキサンタンガムを混合して調製して得たゲルと同等以
上のゲルを得ることができる。All of the powder food materials of the present invention have excellent water dispersibility and immediately swell. Also, it dissolves in water and gels just by leaving it, but preferably it dissolves in hot water or is dissolved in water and heated to be equivalent to a gel obtained by mixing konjak mannan and xanthan gum. The above gel can be obtained.
また、コンニャクマンナン及びキサンタンガムとの併用
により得られるゲルの特徴である熱可逆性を有するこ
と、アルカリ処理を経ないためアルカリ臭がないこと、
酸性〜中性で安定な物性を呈すること、保存時における
離水が少なく、凍結耐性に優れている等の、一般食品へ
の幅広い加工適性はいうまでもなく維持されている。Further, it has thermoreversibility which is a characteristic of the gel obtained by using konjak mannan and xanthan gum together, and has no alkaline odor because it does not undergo alkali treatment,
Needless to say, it has a wide range of processability for general foods, such as stable acidic to neutral physical properties, little water separation during storage, and excellent freezing resistance.
本発明の粉末食品素材は水溶解性に優れているので、目
的とする食品によって他の食品素材を併用することがで
きる。具体的には、調味料(グルタミン酸、グルタミン
酸ナトリウムその他のアミノ酸、アミノ酸塩、5′−リ
ボヌクレチオド類、食塩、塩化カリウム等)、酸味料
(各種有機酸、ビネガー類)、甘味料(蔗糖その他の
糖、ソルビトール、マルチトールその他の糖アルコー
ル、アスパルテーム、アセサルファム、サイクラメー
ト、サッカリン、サッカリンナトリウム、ステビオサイ
ド、グリコシルステビオサイドその他)、その他の呈味
料、各種エキス類(動植物エキス、HAP、HVP、酵母エキ
ス等)、フレーバー、香辛料、等の風味料、着香料、ビ
タミン類、その他の栄養強化成分、各種の医薬成分、着
色料等の粉末素材の中から選ばれた1種以上を併用する
ことができ、更に、蛋白質(大豆たん白、小麦たん白、
乳たん白、卵たん白、魚肉たん白、蓄肉たん白等)、多
糖類(でん粉類、各種糊料、セルロース等)及び油脂の
中から選ばれた1種以上を組合せることにより、各種の
物性を呈する粉末原料を得ることが可能である(保存料
その他の各種の品質改良剤の加配が可能なことはいうま
でもない。)。Since the powdered food material of the present invention has excellent water solubility, other food materials can be used in combination depending on the intended food. Specifically, seasonings (glutamic acid, sodium glutamate and other amino acids, amino acid salts, 5'-ribonucleotides, salt, potassium chloride, etc.), acidulants (various organic acids, vinegars), sweeteners (sucrose and other sugars). , Sorbitol, maltitol and other sugar alcohols, aspartame, acesulfame, cyclamate, saccharin, saccharin sodium, stevioside, glycosyl stevioside, etc., other flavors, various extracts (animal and plant extracts, HAP, HVP, yeast extract, etc.), One or more selected from powder materials such as flavors, spices, flavoring agents, flavoring agents, vitamins, other nutrition-enhancing ingredients, various medicinal ingredients, coloring agents, and the like can be used in combination. Protein (soybean protein, wheat protein,
By combining one or more selected from milk protein, egg protein, fish protein, meat protein etc.), polysaccharides (starch, various pastes, cellulose etc.) and fats and oils, It is possible to obtain a powder raw material having physical properties (it goes without saying that a preservative and various other quality improving agents can be added).
コンニャクマンナン及びキサンタンガムを含有する酸性
〜中性の水溶液を乾燥後粉砕することによる本発明の粉
末食品素材は、コンニャクマンナン、キサンタンガムの
配合、混合の手間を省き、水分散性にすぐれ、コンニャ
クマンナンの膨潤に要する時間を大幅に短縮することが
できる。また水に溶解、もしくは熱水に溶解及び簡単な
加熱によりゲルを形成し、即席簡便性に大いに優れてい
る。なおかつ従来のコンニャクマンナン、キサンタンガ
ムを混合し調製して得たゲルの数々の特徴を維持、ある
いはさらに改良し得るものであり、新しい粉末食品素材
としてその有用性は明らかである。Powdered food material of the present invention by pulverizing after drying an acidic to neutral aqueous solution containing konjak mannan and xanthan gum, konjak mannan, compounding of xanthan gum, save the labor of mixing, excellent water dispersibility, konjak mannan. The time required for swelling can be greatly reduced. In addition, it dissolves in water, or dissolves in hot water and forms a gel by simple heating, and is extremely excellent in instant convenience. In addition, it is possible to maintain or further improve various characteristics of the gel obtained by mixing conventional konjak mannan and xanthan gum, and its usefulness as a new powdered food material is clear.
次に本発明の実施例を示す(尚、実施例においてコンニ
ャクマンナンはKm、キサンタンガムはXnと略す。)。Next, examples of the present invention will be shown (herein, konjak mannan is abbreviated as Km and xanthan gum is abbreviated as Xn).
実施例1 Km37.5g、Xn12.5gを混合したもの(混合粉末)に加水し
て全量を2500gとし、十分に膨潤させた。この時のPHは
6.7であった。この半量をそのまま熱風乾燥機で40℃に
て18時間乾燥させた後、卓上粉砕機で粉砕し、粉末素材
(I)を得た。Example 1 A mixture of 37.5 g of Km and 12.5 g of Xn (mixed powder) was added with water to a total amount of 2500 g, and the mixture was sufficiently swollen. PH at this time is
It was 6.7. This half amount was dried as it was with a hot air dryer at 40 ° C. for 18 hours and then pulverized with a table pulverizer to obtain a powder material (I).
また、残り半量は90℃で30分間加熱した後、同様に乾
燥、粉砕を行い、粉末素材(II)とした。The other half was heated at 90 ° C. for 30 minutes, dried and pulverized in the same manner to obtain a powder material (II).
この粉末素材(I)、(II)およびKmとXnの混合粉末に
ついて、それぞれ4gを水196gに加え、品温を20℃に保
ち、ケミスターラー(800rpm)で攪拌しながら膨潤させ
た。経時的に粘度計を用いてみかけの粘度を測定して膨
潤の具合をみた。4 g of each of the powder materials (I) and (II) and the mixed powder of Km and Xn was added to 196 g of water, the product temperature was kept at 20 ° C., and the mixture was swollen while being stirred with a Chemistrer (800 rpm). The apparent viscosity was measured with time using a viscometer to check the swelling condition.
混合粉末では十分な膨潤を得るのに時間がかかったのに
対し、粉末素材(I)、(II)はともにすばやく膨潤し
た。結果を第1表に示した。It took time for the mixed powder to obtain sufficient swelling, whereas the powder materials (I) and (II) swollen quickly. The results are shown in Table 1.
実施例2 実施例1と同様にKmとXnを膨潤させた水溶液2500gをホ
モジナイザー中で10,000rpm、5分間摩砕処理した。半
量はそのまま、残り半量は90℃で30分加熱処理後、とも
に熱風乾燥機を用い40℃で22時間乾燥させた。これらを
粉砕し、粉末素材(III)と粉末素材(IV、加熱処理し
たもの)を得た。 Example 2 In the same manner as in Example 1, 2500 g of an aqueous solution in which Km and Xn were swollen was ground in a homogenizer at 10,000 rpm for 5 minutes. Half the amount was left as it was, and the other half was heat-treated at 90 ° C. for 30 minutes and then dried at 40 ° C. for 22 hours using a hot air dryer. These were crushed to obtain a powder material (III) and a powder material (IV, heat-treated).
実施例1で得た粉末素材(I)、(II)、およびこの粉
末素材(III)、(IV)の4点につき、それぞれ5gを水2
45gに加えたところ、ただちに分散、膨潤した。これら
を90℃で30分加熱後、冷却(20℃)して得られたゲルの
物性を測定した。また、Km、Xnの混合粉末5gを水245gに
1時間半膨潤させた後、90℃で30分加熱し、冷却して得
たゲルについても物性を測定した。物性の測定には、レ
オメーターを使用し、プランジャー(直径7mm球体)の
球部全体が試料(30mmφ×30mmφの大きさ)に入りきっ
た時点のチャート上の値から硬さ(g/cm2)を求めた。For each of the four powder materials (I) and (II) obtained in Example 1 and the four powder materials (III) and (IV), 5 g of water was added.
When added to 45 g, it immediately dispersed and swelled. These were heated at 90 ° C for 30 minutes and then cooled (20 ° C), and the physical properties of the obtained gel were measured. Further, the physical properties of the gel obtained by swelling 5 g of a mixed powder of Km and Xn in 245 g of water for 1 hour and half and then heating at 90 ° C. for 30 minutes and cooling were also measured. A rheometer was used to measure the physical properties, and the hardness (g / cm) was calculated from the value on the chart when the entire spherical part of the plunger (7 mm diameter sphere) entered the sample (30 mmφ x 30 mmφ size). 2 ) asked.
結果を第2表に示した。混合粉末から調製したゲルに比
べ、粉末素材(I)〜(IV)によるものはいずれも、強
固なゲルであった。The results are shown in Table 2. All of the powder materials (I) to (IV) were stronger gels than the gel prepared from the mixed powder.
実施例3 Km45g、Xn15gに水1440g添加し、2時間膨潤させた。こ
の時のPHは6.4であった。 Example 3 1440 g of water was added to 45 g of Km and 15 g of Xn and swollen for 2 hours. The PH at this time was 6.4.
これを熱風乾燥機で60℃にて11時間乾燥させた。これを
卓上粉砕機で粉砕し、粉末素材(V)を得た。また、同
様に膨潤させたKm、Xnの混合物を100℃で30分間加熱し
た後、室温で20分放置し、同じく乾燥、粉砕して得た粉
末を粉末素材(VI)とした。This was dried with a hot air dryer at 60 ° C. for 11 hours. This was crushed with a table crusher to obtain a powder material (V). Further, the similarly swollen mixture of Km and Xn was heated at 100 ° C. for 30 minutes, then left at room temperature for 20 minutes, and similarly dried and pulverized to obtain a powder material (VI).
これら粉末素材(V)および(VI)を、各々6gを194gの
熱水(92℃)に溶解し、流水中で30分間冷却したとこ
ろ、両者ともしっかりとしたゲルを形成した(ゲルV−
A、VI−A)。6 g of each of these powder materials (V) and (VI) was dissolved in 194 g of hot water (92 ° C.) and cooled in running water for 30 minutes, and both formed a firm gel (gel V-
A, VI-A).
同じく各々6gを水(20℃)194gに加え、そのまま室温に
放置したところ、ともにゲル化した(ゲルV−B、VI−
B)ので、以上を、実施例2と同一の条件でゲル強度
(硬さg/cm2として測定)を測定した。結果を第3表に
示した。Similarly, when 6 g of each was added to 194 g of water (20 ° C.) and allowed to stand at room temperature, both gelled (Gels V-B, VI-
Therefore, the gel strength (measured as hardness g / cm 2 ) was measured under the same conditions as in Example 2. The results are shown in Table 3.
実施例4 Km60g、Xn60gを混合したもの(混合粉末)に加水して全
量を5000gとし、2時間膨潤させた。尚、この溶液はク
エン酸でPH3.8に調製した。この溶液を4等分し、その
内の1画分はそのまま熱風乾燥機で40℃、18時間乾燥さ
せた後、卓上粉砕機で粉砕し、粉末素材(VIII)を得
た。 Example 4 A mixture of 60 g of Km and 60 g of Xn (mixed powder) was hydrated to a total amount of 5000 g and swollen for 2 hours. This solution was adjusted to pH 3.8 with citric acid. This solution was divided into 4 equal parts, and one fraction thereof was dried as it was with a hot air dryer at 40 ° C. for 18 hours and then pulverized with a table pulverizer to obtain a powder material (VIII).
また、ある1画分は90℃で30分間加熱した後、同様に乾
燥し、粉砕を行い、粉末素材(IX)を得た。One fraction was heated at 90 ° C. for 30 minutes, dried in the same manner, and pulverized to obtain a powder material (IX).
また、別の1画分はホモジナイザー中で10,000rpm、5
分間摩砕処理した後、VIIIを調製した時と同様に乾燥、
粉砕を行い粉末素材(X)を得た。残りの1画分はホモ
ジナイザー中で10,000rpm、5分間摩砕処理を行い、更
に90℃で30分間加熱した後、同様に乾燥、粉砕を行い粉
末素材(XI)を得た。In addition, another fraction was 10,000 rpm for 5 minutes in a homogenizer.
After milling for minutes, dry as in VIII preparation,
Crushing was performed to obtain a powder material (X). The remaining 1 fraction was ground in a homogenizer at 10,000 rpm for 5 minutes, further heated at 90 ° C. for 30 minutes, dried and ground in the same manner to obtain a powder material (XI).
このようにして得られた粉末素材(VIII)(IX)(X)
(XI)の4点につき、それぞれ5gを水245gに加えたとこ
ろ、ただちに分散、膨潤した。これらを90℃で30分加熱
後、冷却(20℃)して得られたゲルの物性を実施例2の
方法に従ってゲル強度を測定した。その結果は表4に示
した。表4に示す如く、いずれも強いゲル強度を示し
た。Powder material (VIII) (IX) (X) thus obtained
When 5 g of each of the four points of (XI) was added to 245 g of water, it immediately dispersed and swelled. These were heated at 90 ° C. for 30 minutes and then cooled (20 ° C.), and the physical properties of the obtained gel were measured according to the method of Example 2 for gel strength. The results are shown in Table 4. As shown in Table 4, all showed strong gel strength.
利用例1(オレンジゼリーミックス) Km14g、Xn18gを水3000mlに加え膨潤させ、アスコルビン
4gを添加し(PH4.2)、ミキサーで1分間摩砕処理を行
った。これを35℃で12時間、ひきつづき40℃で9時間熱
風乾燥して、さらに粉砕し、粉末素材を約30g得た。 Use example 1 (orange jelly mix) Km14g, Xn18g was added to 3000 ml of water to swell, and ascorbin
4 g was added (PH4.2) and the mixture was milled for 1 minute with a mixer. This was dried at 35 ° C. for 12 hours and then at 40 ° C. for 9 hours with hot air, and further pulverized to obtain about 30 g of a powder material.
この粉末素材に味の素(株)製「Pal Sweet 1/60」100
g、オレンジパウダー5gを配合し、オレンジゼリーミッ
クス粉末を得た。"Pal Sweet 1/60" 100 from Ajinomoto Co., Inc.
g and 5 g of orange powder were mixed to obtain orange jelly mix powder.
このオレンジゼリーミックス20gを水200mlに加えたとこ
ろすぐに溶けた。軽く火にかけゼリー型に流し冷やし固
めて、簡単にオレンジゼリーをつくることができた。こ
れは低カロリーなうえ、食感も非常に好ましいとの評価
を得た。20 g of this orange jelly mix was added to 200 ml of water and immediately dissolved. I could easily make orange jelly by lightly heating it, pouring it in a jelly mold, cooling and hardening. It was evaluated that it has a low calorie and a very pleasant texture.
利用例2(ラクトアイス) Km45g、Xn15gを水1440gで2時間膨潤させた後、熱風乾
燥機で60℃にて11時間乾燥させた。これを卓上粉砕機で
粉砕し、粉末素材を得た。Utilization Example 2 (Lactic ice) Km 45 g and Xn 15 g were swollen with 1440 g of water for 2 hours, and then dried with a hot air dryer at 60 ° C. for 11 hours. This was crushed with a table crusher to obtain a powder material.
このように調製されたKm−Xnの粉末5g、脱脂粉乳40g、
モノグリセリド1.5gに水780gを添加し、攪拌しながら加
熱し70℃になってからさらに5分間加熱した。この溶液
にヤシ油20gを添加して混合し、この混合液をオステラ
イザーで5分間処理を行い均質化させた後、70℃で30分
間加熱殺菌を行った。Thus prepared Km-Xn powder 5 g, skim milk powder 40 g,
780 g of water was added to 1.5 g of monoglyceride, and the mixture was heated with stirring to 70 ° C. and further heated for 5 minutes. 20 g of coconut oil was added to and mixed with this solution, and the mixture was homogenized by treatment with an Osterizer for 5 minutes and then heat-sterilized at 70 ° C. for 30 minutes.
このようにして調製したアイスクリームミックスを冷却
させ、5℃で一晩エージングした。エージング後、味の
素(株)製「Pal Sweet 1/60」35g、東和化成(株)製
「Po40」75g、及び林原(株)製「カップリングシュガ
ー」75gを添加、混合し、−3℃でオーバーランが80%
になるまで数分間フリージングを行った。The ice cream mix thus prepared was cooled and aged at 5 ° C. overnight. After aging, Ajinomoto Co., Inc. "Pal Sweet 1/60" 35g, Towa Kasei Co., Ltd. "Po40" 75g, and Hayashibara Co., Ltd. "Coupling sugar" 75g were added and mixed, and at -3 ° C. 80% overrun
Freezing was carried out for several minutes.
フリージング後、常法どおりカップ採り、硬化(−40
℃、24時間)を行ってラクトアイスを得た。After freezing, take a cup as usual and cure (-40
℃, 24 hours) was performed to obtain lacto ice.
このようにして調製したラクトアイスを訓練された10名
のパネルによる官能評価を行ったところ風味、食感とも
好ましいとの結果を得た。The thus-prepared lacto ice was subjected to a sensory evaluation by a panel of 10 trained persons, and it was found that the taste and texture were favorable.
利用例3(フィリング) Km37.5gとXn12.5gに加水して全量を2500gとし、2時間K
m,Xnを膨潤させた。この水溶液(PH6.6)をホモジナイ
ザー中で10,000rpm、5分間摩砕した後90℃で30分間加
熱処理を行った。Usage example 3 (Filling) Add 37.5 g of Km and 12.5 g of Xn to bring the total amount to 2500 g. K for 2 hours
The m and Xn were swollen. This aqueous solution (PH6.6) was ground in a homogenizer at 10,000 rpm for 5 minutes and then heat-treated at 90 ° C. for 30 minutes.
この加熱処理物を次に、40℃で20時間熱風乾燥を行い、
これを粉砕してKm−Xnの粉末素材を得た。Next, this heat-treated product is dried with hot air at 40 ° C. for 20 hours,
This was crushed to obtain a powder material of Km-Xn.
このKm−Xn粉末物20g、薄切りしたじゃがいも170g、ダ
イス切りした人参50g、みじん切りしたたまねぎ及びセ
ロリをそれぞれ85gと50g、食塩3g、マスタード9g、味の
素(株)製「味の素」2g、マヨネーズ14g、及び水110g
を添加してよく混合した後、レトルトパウチに厚さが約
6mmになる様に詰めた。20 g of this Km-Xn powdered product, 170 g of sliced potatoes, 50 g of diced carrots, 85 g and 50 g of chopped onion and celery, respectively, 3 g of salt, mustard 9 g, Ajinomoto Co., Inc. 2 g, mayonnaise 14 g, and 110g water
After adding well and mixing well, the thickness of the retort pouch is approx.
Packed to be 6 mm.
これを80℃で15分間、湯浴中で加熱した後、取り出し、
熱い内に内容物を外部から圧して混合し、平らにした状
態で冷蔵庫で1日保存した。After heating this at 80 ℃ for 15 minutes in a hot water bath, take it out,
While the contents were hot, the contents were externally pressed and mixed, and the contents were kept flat in the refrigerator for 1 day.
このようにして調製したフィリングを厚さ約9mmの食パ
ンにはさみ、サンドイッチの形として訓練されたパネル
に供したところ、風味、食感とも好ましい結果を得た。When the filling thus prepared was sandwiched between bread pieces having a thickness of about 9 mm and subjected to a trained panel in the form of a sandwich, favorable results were obtained in terms of flavor and texture.
利用例4(かまぼこ) Km4.5g、Xn1.5gに水300mlを加え、1時間膨潤させた。
これを40℃、22時間熱風乾燥して、さらに粉砕し、粉末
素材を約3g得た。Utilization Example 4 (Kamaboko) 300 ml of water was added to 4.5 g of Km and 1.5 g of Xn and swelled for 1 hour.
This was dried at 40 ° C. for 22 hours with hot air and further pulverized to obtain about 3 g of a powder material.
スケソウタラ冷凍すり身80gに食塩3g、氷30g、調味料適
当量にこの粉末素材を1g加えて、らいかい機で5分間混
練し、魚肉すり身を得た。この魚肉すり身を85℃、30分
間加熱し、冷却してかまぼこを得た。80 g of frozen minced cod roe, 3 g of salt, 30 g of ice, and 1 g of this powder material in an appropriate amount of seasoning were kneaded for 5 minutes with a raikai machine to obtain a fish surimi. This ground fish meat was heated at 85 ° C. for 30 minutes and cooled to obtain kamaboko.
こうして得たかまぼこは、従来品かまぼこと比べて食
感、風味とも変わらず、また魚肉の使用量を20%節減す
ることができた。Compared with the conventional kamaboko, the kamaboko obtained in this way had the same texture and flavor, and was able to reduce the amount of fish meat used by 20%.
利用例5(コンニャクが点在したタイプのかまぼこ) 利用例4で得た粉末素材1gを熱水50gに溶解し、ゲル化
した後、ミンチした。Use Example 5 (Kamaboko of a type in which konjak is scattered) 1 g of the powder material obtained in Use Example 4 was dissolved in 50 g of hot water, gelled, and then minced.
スケソウタラ冷凍すり身100gに食塩3g、氷30g及び調味
料適当量を混練し、魚肉すり身を調製した。この魚肉す
り身にミンチしたKm−Xnゲルを30g加えて軽く混合し、8
5℃、30分間加熱後、冷却し、Km−Xnゲルが点在したか
まぼこを得た。A fish meat surimi was prepared by kneading 100 g of frozen pollack pollack with 3 g of salt, 30 g of ice and an appropriate amount of seasoning. Add 30 g of minced Km-Xn gel to this fish paste and mix gently,
After heating at 5 ° C for 30 minutes, the mixture was cooled to obtain a kamaboko scattered with Km-Xn gel.
こうして得たかまぼこは、通常のコンニャクをそのまま
点在させたものと異なり、アルカリ臭が全くなく、食
感、風味共に良好であった。The thus-obtained kamaboko had no alkaline odor at all, and had a good texture and flavor, unlike the one in which ordinary konjak was scattered as it was.
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭59−113867(JP,A) 特開 昭48−56846(JP,A) ─────────────────────────────────────────────────── ─── Continuation of the front page (56) References JP-A-59-113867 (JP, A) JP-A-48-56846 (JP, A)
Claims (3)
酸性〜中性の水溶液中で膨潤させた後に乾燥し、そして
粉砕することを特徴とする粉末食品素材の製造法。1. A method for producing a powdered food material, which comprises swelling konjak mannan and xanthan gum in an acidic to neutral aqueous solution, followed by drying and pulverizing.
重量比率が95:5〜5:95である特許請求の範囲(1)項記
載の製造法。2. The method according to claim 1, wherein the weight ratio of konjac mannan and xanthan gum is 95: 5 to 5:95.
熱することを特徴とする特許請求の範囲第(1)項記載
の製造法。3. The method according to claim 1, wherein the swelling is followed by grinding and / or heating before drying.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13814885 | 1985-06-25 | ||
| JP60-138148 | 1985-06-25 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6296061A JPS6296061A (en) | 1987-05-02 |
| JPH0724554B2 true JPH0724554B2 (en) | 1995-03-22 |
Family
ID=15215129
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14426186A Expired - Lifetime JPH0724554B2 (en) | 1985-06-25 | 1986-06-20 | Manufacturing method of powdered food material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0724554B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7408057B2 (en) | 2000-07-03 | 2008-08-05 | Marine Bioproducts Intenational | Clarified hydrocolloids of undiminished properties and method of producing same |
| JP4616203B2 (en) * | 2006-03-27 | 2011-01-19 | 伊那食品工業株式会社 | Konjac modifier and modified konjac |
| JP5088867B2 (en) * | 2007-06-08 | 2012-12-05 | 松谷化学工業株式会社 | Chewing / swallowing aid |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5545173B2 (en) * | 1971-11-15 | 1980-11-17 | ||
| JPS59113867A (en) * | 1982-12-20 | 1984-06-30 | Kiichiro Sarui | Preparation of powdery mannan of konjak (devil's tongue) bonded with protecting colloidal agent, etc. or its partial decomposition product |
-
1986
- 1986-06-20 JP JP14426186A patent/JPH0724554B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6296061A (en) | 1987-05-02 |
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