WO2014020717A1 - Spherical gel and manufacturing process therefor - Google Patents
Spherical gel and manufacturing process therefor Download PDFInfo
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- WO2014020717A1 WO2014020717A1 PCT/JP2012/069550 JP2012069550W WO2014020717A1 WO 2014020717 A1 WO2014020717 A1 WO 2014020717A1 JP 2012069550 W JP2012069550 W JP 2012069550W WO 2014020717 A1 WO2014020717 A1 WO 2014020717A1
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- Prior art keywords
- gel
- liquid
- heat
- glucan
- spherical
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/0052—Preparation of gels
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
- A23L29/20—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents
- A23L29/206—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents of vegetable origin
- A23L29/231—Pectin; Derivatives thereof
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
- A23L29/20—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents
- A23L29/269—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents of microbial origin, e.g. xanthan or dextran
- A23L29/271—Curdlan; beta-1-3 glucan; Polysaccharides produced by agrobacterium or alcaligenes
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
- A23L29/20—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents
- A23L29/269—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents of microbial origin, e.g. xanthan or dextran
- A23L29/272—Gellan
Definitions
- the present invention relates to a spherical gel having an excellent texture and capable of stably maintaining the shape, and a method for producing the same.
- Patent Document 1 Japanese Patent Application Laid-Open No. 55-99177 (Patent Document 1) reports a granular gel prepared by dropping sodium alginate into a calcium chloride solution, and an artificial salmon roe is described as its utilization method. .
- the texture is determined by the properties of calcium alginate, and the granular gel is not sticky and has a brittle texture.
- Patent Document 2 JP-A-8-80166 discloses, as a method for preparing a granular gel, an aqueous polysaccharide solution that forms a gel by reacting with a polyvalent metal ion, a thermocoagulable ⁇ -1,3- A method for producing a granular gel, characterized in that it is dropped into an aqueous solution containing glucan and a polyvalent metal salt and then heated, has been reported.
- the obtained granular gel is mainly mixed with two types of gelling agents. For example, in the case of a mixture of curdlan and other gelling agents, the breaking load (maximum) The gel strength indicated by (load) decreases, and the gel viscosity indicated by the breaking strain ratio decreases.
- Patent Document 3 discloses that a solution containing a salt and a gelling agent and a solution containing another salt and a gelling agent are brought into contact with each other to provide a solution between different species.
- Patent Document 3 discloses that a method for preparing a jelly that is made to gel by reacting with a mixture of different gels.
- Patent Document 4 JP-A-9-275915 discloses a gelling agent that solidifies by heating and does not solidify with calcium ions and a dispersion containing a calcium compound, and a gelling agent that solidifies with calcium ions.
- the granular gel is made to exist in other jelly to compensate for the low stability of the granular gel, and it is difficult to take out the granular jelly alone.
- granular gels are widely applied in various fields including food texture or aesthetics in the food field.
- an effective texture and aesthetic appearance are taken into consideration, an excellent texture with hardness and stickiness and a gel that can stably retain its shape and its simple and rapid manufacturing method still remain. It can be said that it is required.
- the object of the present invention is to provide a spherical gel having excellent texture and hardness and having a stable shape, and a method for producing the same.
- a gelling agent that gels a dispersion containing a heat-coagulating ⁇ -1,3-glucan and a polyvalent metal salt and having a viscosity of 130 to 3600 mPa ⁇ s by reacting with a polyvalent metal ion. And dropping into a solution having a temperature equal to or higher than the heat irreversible solidification temperature of the heat-coagulable ⁇ -1,3-glucan.
- the gelling agent is alginate, wax methoxyl pectin or gellan gum.
- a spherical gel having excellent texture with hardness and stickiness and capable of maintaining a stable shape can be easily and quickly produced in one step. It can be advantageously used in industrial production.
- the spherical gel and the production method of the present invention can be advantageously used in giving food texture and aesthetics in the food field and in industrial production.
- the method for producing a spherical gel of the present invention comprises a dispersion liquid (hereinafter also referred to as “liquid A”) containing heat-coagulating ⁇ -1,3-glucan and a polyvalent metal salt and having a viscosity of 130 to 3600 ⁇ mPa ⁇ s. .)
- liquid A a dispersion liquid
- the liquid A of the present invention can be obtained by dispersing heat-coagulating ⁇ -1,3-glucan and a polyvalent metal salt in a solvent using a known method.
- the viscosity of the liquid A is adjusted to 130 to 3600 mPa ⁇ s.
- Such a viscosity range of the liquid A is advantageous in securing the fluidity of the liquid A and stably producing a spherical gel.
- the viscosity range of the liquid A is preferably 150 to 3600 mPa ⁇ s, more preferably 150 to 2600 mPa ⁇ s.
- Such a viscosity range is particularly preferable for imparting a texture and a true spherical shape with hardness and stickiness to the gel.
- the said viscosity of A liquid can be determined by the method as described in Example 1 mentioned later, for example.
- the viscosity of the liquid A can be appropriately adjusted by a known technique.
- Such methods include, for example, a method of increasing viscosity by dispersing heat-coagulable ⁇ -1,3-glucan and then cooling (see: Development and application of food hydrocolloids, editor Katsuyoshi Shonishi), heat-coagulating ⁇ -1 , An alkali swelling / dissolution method in which viscosity is increased by swelling or dissolving 3,3-glucan in an alkali, and a method in which starch is added to heat-coagulating ⁇ -1,3-glucan to impart viscosity.
- the alkali swelling / dissolving method is preferred.
- heat-coagulating ⁇ -1,3-glucan is a polysaccharide having D-glucose as a constituent sugar and ⁇ -1,3-glucoside bond, and having heat-coagulating properties.
- the origin of heat-coagulating ⁇ -1,3-glucan is not particularly limited, such as microorganisms, animals or plants.
- Examples of the heat-coagulating ⁇ -1,3-glucan include curdlan, paramylon, and pachyman, and curdlan is preferable.
- the amount of heat-coagulating ⁇ -1,3-glucan in the liquid A is not particularly limited, but considering the fluidity of the liquid A, it is 0.1 to 8 parts by weight with respect to 100 parts by weight of the liquid A. More preferably, it is 0.5 to 5 parts by weight.
- Edible salts are preferably used as the polyvalent metal salt in the liquid A.
- the polyvalent metal salt includes, for example, a group IIa (alkaline earth metal) (eg, calcium), a group VIII (eg, iron), a group Ib (eg, copper), a group IIb ( Examples include salts of metals and acids belonging to Group IIIa (aluminum, etc.), etc., preferably calcium salts.
- the acid that forms the polyvalent metal salt is not particularly limited, but inorganic acids (e.g., hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, etc.) and organic acids (e.g., acetic acid, lactic acid, gluconic acid, thioglycolic acid, Ascorbic acid and the like).
- inorganic acids e.g., hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, etc.
- organic acids e.g., acetic acid, lactic acid, gluconic acid, thioglycolic acid, Ascorbic acid and the like.
- calcium and acid salts include, for example, salts with inorganic acids such as calcium chloride, calcium hydroxide, calcium oxide, calcium sulfate, calcium nitrate, and calcium phosphate, calcium acetate, calcium lactate, calcium gluconate,
- inorganic acids such as calcium chloride, calcium hydroxide, calcium oxide, calcium sulfate, calcium nitrate, and calcium phosphate
- organic acids such as calcium thioglycolate and calcium ascorbate
- calcium chloride, calcium hydroxide, calcium oxide, or calcium lactate more preferably calcium chloride, calcium lactate, Preferably, it is calcium lactate.
- the amount of the polyvalent metal salt in the liquid A is not particularly limited as long as the gelling agent in the liquid B can be gelled, and can be appropriately determined by those skilled in the art.
- the amount of the polyvalent metal salt is, for example, 0.1 to 5 parts by weight, preferably 0.3 to 3 parts by weight as the polyvalent metal per 100 parts by weight of Liquid A. May be. Such an amount is particularly preferred when calcium lactate is used.
- the solvent in the liquid A is not particularly limited as long as ⁇ -1,3-glucan and a polyvalent metal salt can be dispersed, but is preferably an aqueous medium, more preferably water or an alcohol-containing aqueous solution (for example, about 0.1. 1-10 v / v% alcohol-containing water), more preferably water.
- the temperature of the liquid A can be appropriately determined by those skilled in the art so as to keep the liquid A in a suitable viscosity range.
- the temperature of the liquid A is preferably lower than the solidification temperature (gelation temperature) of the heat-coagulating ⁇ -1,3-glucan, and the temperature at which the viscosity of the liquid A is maintained in the above numerical range. More specifically, the temperature of the liquid A is preferably less than 80 ° C., and more preferably 50 to 60 ° C. Such a temperature is particularly preferred when the heat-coagulating ⁇ -1,3-glucan is curdlan.
- the pH of solution A is appropriately determined by those skilled in the art in consideration of the type and properties of heat-coagulating ⁇ -1,3-glucan. Specifically, the pH of the solution A is desirably 11 or less, preferably pH 1.0 to pH 11.0. Such a suitable pH is advantageous in effectively dispersing the curdlan in the solvent without dissolving the curdlan when the heat-coagulating ⁇ -1,3-glucan is curdlan.
- the liquid B of the present invention is obtained by dispersing a gelling agent that reacts with polyvalent metal ions and gels in a solvent by a conventional method, and heat irreversible heat-solidifying ⁇ -1,3-glucan in the liquid A. It can prepare by setting it as the temperature more than a sexual coagulation (gelation) temperature.
- the temperature of the liquid B is preferably 80 ° C. or higher, more preferably 80 to 150 ° C. Such a temperature is particularly advantageous in forming a spherical gel when the heat-coagulating ⁇ -1,3-glucan is curdlan.
- the gelling agent in the B liquid is not particularly limited as long as it reacts with a polyvalent metal ion to gel, but is preferably a polysaccharide, more preferably alginic acid, wax methoxyl pectin, gellan gum or a salt thereof, and the like. More preferred is alginic acid or a salt thereof, more preferred is an alkali metal alginate, and still more preferred is sodium alginate or potassium alginate.
- the amount of the gelling agent in the B liquid is not particularly limited, but is, for example, 0.01 to 5 parts by weight, preferably 0.1 to 2 parts by weight with respect to 100 parts by weight of the B liquid.
- the solvent and pH used for the B liquid are not particularly limited, and can be the same as the A liquid.
- the liquid A and the liquid B may appropriately contain additives as long as they do not interfere with the formation of the spherical gel of the present invention.
- additives include, but are not limited to, fragrances, pigments, fruit juices, extracts, seasonings or pH adjusters.
- the method of dropping the A liquid into the B liquid is not particularly limited, and may be performed continuously or intermittently using a known device such as a perforated plate or a nozzle.
- the shape and size of the spherical gel can be adjusted by appropriately adjusting the aperture and shape of a known device such as a perforated plate and a nozzle, the dropping amount of the liquid A, the dropping speed, the viscosity, or the specific gravity. The length is appropriately adjusted by those skilled in the art.
- the gel of a shape like a noodle-like gel or a shark fin section can also be prepared, and this aspect is also included by this invention.
- the liquid B may be left standing or stirred.
- the temperature of the B liquid after the dropping of the A liquid is not particularly limited, but considering the stable production of the spherical gel, the heat irreversible solidification (gelation) temperature of the heat coagulable ⁇ -1,3-glucan It is preferable to maintain above.
- the holding time of such temperature is preferably 10 minutes or more.
- the spherical gel comprises a core mainly composed of heat-coagulating ⁇ -1,3-glucan, and optionally a reaction product of a polyvalent metal salt and a gelling agent. It can be provided as a gel having an outer membrane as a main component. Such a spherical gel can be obtained in a state where the binding property peculiar to ⁇ -1,3-glucan is reduced, and prevents polymerization due to contact that is usually generated in the production of ⁇ -1,3-glucan gel. This is advantageous in maintaining a stable shape.
- the spherical gel of the present invention has an outer membrane that can be peeled by hand by appropriately adjusting the concentration of the polyvalent metal salt in the A liquid, the concentration of the gelling agent in the B liquid, and the reaction time. It is possible to provide from a spherical gel having a spherical gel having no outer membrane.
- the outer membrane may be removed by immersing the spherical gel in an alkaline agent aqueous solution such as sodium carbonate.
- the present invention includes such an embodiment.
- the spherical gel is substantially composed of heat-coagulating ⁇ -1,3-glucan.
- “consisting essentially of heat-coagulating ⁇ -1,3-glucan” means other components different from the heat-coagulating ⁇ -1,3-glucan mixed in the production process and use process of the spherical gel.
- the content of heat-coagulating ⁇ -1,3-glucan is preferably 0.5% by weight or more, more preferably 0.8% by weight of the entire spherical gel. It means wt% or more, more preferably 1 wt% or more.
- the size of the spherical gel is not particularly limited, but is preferably 2 to 20 mm, more preferably 3 to 15 mm, and further preferably 3 to 10 mm. Such a size is particularly advantageous when the spherical gel is used as a food.
- the spherical gel of this invention can have the food texture provided with hardness and stickiness as above-mentioned.
- the maximum load is preferably 0.3 to 3.0 N when the product temperature is 20 ° C.
- the breaking strain rate is preferably 65% or more when the product temperature is 20 ° C.
- the said maximum load and breaking strain rate can be determined with the method as described in (2) of Example 1 of this-application specification (It measured using the Yamaden Corporation creep meter RE2-3300S. Measurement. Conditions: Plunger: cylindrical shape with a diameter of 3 mm and a height of 22 mm, maximum measurement distortion: 98%, measurement speed: 0.5 mm / second).
- the spherical gel of this invention can show the outstanding retort tolerance and freezing tolerance.
- the maximum load of the spherical gel is preferably 100 to 300% of the maximum load before retort sterilization.
- the maximum load of the spherical gel is preferably 100 to 600% of the maximum load of the spherical gel before freezing.
- the spherical gel of the present invention may be used as it is as a food or as a raw material for food.
- the food of the present invention is not particularly limited, and examples thereof include fish egg-like foods such as imitation salmon, tapioca pearl-like foods, spherical jelly foods, and cold foods such as ice and frozen desserts.
- Example 1 Water and curdlan were sufficiently dispersed at the ratio shown in Formula 1 of the a-1 solution in Table 1 to obtain 50 parts by weight of the a-1 solution composed of water and curdlan. Next, a solution obtained by dissolving 0.5 parts by weight of trisodium phosphate in 25 parts by weight of water was added to the a-1 solution while stirring the a-1 solution (300 rpm). Next, a solution obtained by dissolving 0.4 parts by weight of lactic acid in 3.6 parts by weight of water was added to the above mixture while stirring the obtained mixture at 50 to 55 ° C. (600 rpm). While maintaining the obtained mixed liquid at 55 to 60 ° C.
- liquid A 1 a solution obtained by dissolving 1 part by weight of calcium lactate in 19.5 parts by weight of water was added to the above mixed liquid.
- the obtained mixed liquid was maintained at 55 to 60 ° C. and stirred (800 rpm) to obtain a dispersion of curdlan and calcium ions (liquid A 1).
- liquids A 2 to 6 were obtained in the same manner as liquid A 1, except that the liquid a-1 was prepared according to formulations 2 to 6 in Table 1. When liquids 1 to 6 were prepared, the viscosities of liquids 1 to 6 were measured. ). The results are shown in Table 1.
- solution B sodium alginate solution
- the A liquid 1 with which the syringe was filled was dripped at 95 degreeC B liquid with which the container was filled at the speed
- the liquid B was held at 95 ° C. for 60 minutes, and a 3 to 6 mm granular gel was formed.
- the granular gel was separated from the liquid B, cooled and washed with water, and a test product 1 was obtained.
- test products 2 to 6 were produced using the A liquids 2 to 6.
- the moldability of the test product was judged as follows. ⁇ : True spherical granular gel is formed. ⁇ : Although granular gel is formed, it is not true spherical. ⁇ : Since the viscosity is high and cannot be dripped, the granular gel cannot be formed.
- the obtained spherical gel A (hereinafter also referred to as “spherical gel B”) was obtained.
- the spherical gel A was filled in a suitable container and sealed.
- the container was allowed to stand together with the spherical gel A at ⁇ 20 ° C. for 7 days. Seven days later, the container was thawed with running water at a temperature of 20 ° C.
- spherical gel C a frozen spherical gel A
- the texture of the spherical gels B and C was compared with the texture of the spherical gel A.
- the measurement results and comparison results are shown in Table 2. Even after retort sterilization and after freezing and thawing, the texture was firm and sticky.
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Description
本発明は、優れた食感を有し、かつ安定に形状を保持しうる球状ゲルおよびその製造方法に関する。 The present invention relates to a spherical gel having an excellent texture and capable of stably maintaining the shape, and a method for producing the same.
イクラ、スジコ、キャビア等の魚卵食品やタピオカティに含まれるタピオカパール等は、球状であるという外観と弾力のある食感が好まれ、様々な食品に使用されている。さらに、それらを模した人工イクラ等の粒状ゲルの食品も広く利用されている。 </ I> Fish egg foods such as salmon roe, sujiko, caviar and tapioca pearls contained in tapiocaty are preferred for various foods because of their spherical appearance and elastic texture. In addition, granular gel foods such as artificial salmon roe imitating them are also widely used.
各種ゲル化剤を用いて、粒状ゲルを調製する様々な方法が報告されている。例えば、特開昭55-99177号公報(特許文献1)には、アルギン酸ナトリウムを塩化カルシウム溶液に滴下することにより調製される粒状ゲルが報告され、その利用方法としては人工イクラが記載されている。しかしながら、この方法では、食感はアルギン酸カルシウムの性質によって決定され、粒状ゲルは粘りがなくもろい食感となる。 Various methods for preparing granular gels using various gelling agents have been reported. For example, Japanese Patent Application Laid-Open No. 55-99177 (Patent Document 1) reports a granular gel prepared by dropping sodium alginate into a calcium chloride solution, and an artificial salmon roe is described as its utilization method. . However, in this method, the texture is determined by the properties of calcium alginate, and the granular gel is not sticky and has a brittle texture.
また、特開平8-80166号公報(特許文献2)には、粒状ゲル調製する方法として、多価金属イオンと反応してゲルを形成する多糖類水溶液を、熱凝固性β-1,3-グルカンおよび多価金属塩含有水溶液に滴下し、ついで加熱することを特徴とする粒状ゲルの製造法が報告されている。しかしながら、得られる粒状ゲルは主に2種のゲル化剤が混合ざれた状態となり、たとえば、カードランとそれ以外のゲル化剤の混合物の場合、カードラン単独の場合に比べ、破断荷重(最大荷重)で示されるゲル強度が低下し、破断歪率で示されるゲルの粘りが低下してしまう。 JP-A-8-80166 (Patent Document 2) discloses, as a method for preparing a granular gel, an aqueous polysaccharide solution that forms a gel by reacting with a polyvalent metal ion, a thermocoagulable β-1,3- A method for producing a granular gel, characterized in that it is dropped into an aqueous solution containing glucan and a polyvalent metal salt and then heated, has been reported. However, the obtained granular gel is mainly mixed with two types of gelling agents. For example, in the case of a mixture of curdlan and other gelling agents, the breaking load (maximum) The gel strength indicated by (load) decreases, and the gel viscosity indicated by the breaking strain ratio decreases.
また、ゼリー食品を製造する種々の方法が報告されている。例えば、特開昭63-230041号公報(特許文献3)には、塩類およびゲル化剤を含有する溶液と、それとは別の塩類およびゲル化剤を含有する溶液とを接触させ、異種間溶液で反応させることによりゲル化させ、異種ゲルが混在したゼリーを調製する方法が報告されている。 Also, various methods for producing jelly foods have been reported. For example, Japanese Patent Laid-Open No. 63-230041 (Patent Document 3) discloses that a solution containing a salt and a gelling agent and a solution containing another salt and a gelling agent are brought into contact with each other to provide a solution between different species. There has been reported a method for preparing a jelly that is made to gel by reacting with a mixture of different gels.
また、特開平9-275915号公報(特許文献4)には、加熱により固化し、かつカルシウムイオンでは固化しないゲル化剤およびカルシウム化合物を含有する分散液と、カルシウムイオンで固化するゲル化剤を含有する溶液とを接触させた後、加熱することを特徴とする異種ゼリーが混在するゼリー食品の製造方法が報告されている。 JP-A-9-275915 (Patent Document 4) discloses a gelling agent that solidifies by heating and does not solidify with calcium ions and a dispersion containing a calcium compound, and a gelling agent that solidifies with calcium ions. A method for producing a jelly food mixed with different kinds of jelly, which is heated after contacting with the contained solution, has been reported.
しかしながら、上記のゼリー食品の製造方法ではいずれも、粒状ゲルを他のゼリーの中に存在させることにより粒状ゲルの安定性の低さを補っており、粒状ゼリーを単独で取り出すことは難しい。 However, in any of the above jelly food production methods, the granular gel is made to exist in other jelly to compensate for the low stability of the granular gel, and it is difficult to take out the granular jelly alone.
上記のように、粒状ゲルは、食品分野において食感または美観付与をはじめとする様々な用途に広く適用されている。しなしながら、効果的な食感および美観付与を勘案すれば、硬さと粘りとを備えた優れた食感を有しかつ安定に形状を保持しうるゲルおよびその簡易かつ迅速な製造方法が依然として求められているといえる。 As described above, granular gels are widely applied in various fields including food texture or aesthetics in the food field. However, if an effective texture and aesthetic appearance are taken into consideration, an excellent texture with hardness and stickiness and a gel that can stably retain its shape and its simple and rapid manufacturing method still remain. It can be said that it is required.
本発明は、硬さと粘りとを備えた優れた食感を有しかつ形状の安定した球状ゲルおよびその製造方法を提供することをその目的とする。 The object of the present invention is to provide a spherical gel having excellent texture and hardness and having a stable shape, and a method for producing the same.
本発明によれば、以下の発明が提供される。
(1)加熱凝固性β-1,3-グルカンおよび多価金属塩を含み、かつ粘度が130~3600 mPa・sである分散液を、多価金属イオンと反応してゲル化するゲル化剤を含み、かつ加熱凝固性β-1,3-グルカンの熱不可逆性凝固温度以上の温度である溶液に滴下することを含んでなる、球状ゲルの製造方法。
(2)加熱凝固性β-1,3-グルカンがカードランである、(1)に記載の方法。
(3)上記ゲル化剤が、アルギン酸塩、ロウメトキシルペクチンまたはジェランガムである、(1)または(2)に記載の方法。
(4)多価金属イオンが、カルシウムイオン、鉄イオンまたはマグネシウムイオンである、(1)~(3)のいずれか一つに記載の方法。
(5)(1)~(4)のいずれか一つに記載の方法により得られる、球状ゲル。
(6)加熱凝固性β-1,3-グルカンから実質的になる、球状ゲル。
According to the present invention, the following inventions are provided.
(1) A gelling agent that gels a dispersion containing a heat-coagulating β-1,3-glucan and a polyvalent metal salt and having a viscosity of 130 to 3600 mPa · s by reacting with a polyvalent metal ion. And dropping into a solution having a temperature equal to or higher than the heat irreversible solidification temperature of the heat-coagulable β-1,3-glucan.
(2) The method according to (1), wherein the heat-coagulating β-1,3-glucan is curdlan.
(3) The method according to (1) or (2), wherein the gelling agent is alginate, wax methoxyl pectin or gellan gum.
(4) The method according to any one of (1) to (3), wherein the polyvalent metal ion is calcium ion, iron ion or magnesium ion.
(5) A spherical gel obtained by the method according to any one of (1) to (4).
(6) A spherical gel substantially composed of heat-coagulating β-1,3-glucan.
本発明によれば、硬さと粘りとを備えた優れた食感を有しかつ安定した形状を保持しうる球状ゲルを1ステップで簡易かつ迅速に製造することができる。工業生産上有利に利用することができる。また、かかる本発明の球状ゲルおよび製造方法は、食品分野における食感および美観付与や工業的生産において有利に利用できる。 According to the present invention, a spherical gel having excellent texture with hardness and stickiness and capable of maintaining a stable shape can be easily and quickly produced in one step. It can be advantageously used in industrial production. In addition, the spherical gel and the production method of the present invention can be advantageously used in giving food texture and aesthetics in the food field and in industrial production.
本発明の球状ゲルの製造方法は、加熱凝固性β-1,3-グルカンおよび多価金属塩を含み、かつ粘度が130~3600 mPa・sである分散液(以下、「A液」ともいう。)を、多価金属イオンと反応してゲル化するゲル化剤を含み、かつ加熱凝固性β-1,3-グルカンの熱不可逆性凝固温度以上の温度である溶液(以下、「B液」ともいう。)に滴下することを一つの特徴としている。 The method for producing a spherical gel of the present invention comprises a dispersion liquid (hereinafter also referred to as “liquid A”) containing heat-coagulating β-1,3-glucan and a polyvalent metal salt and having a viscosity of 130 to 3600 μmPa · s. .) Is a solution containing a gelling agent that reacts with a polyvalent metal ion to form a gel and has a temperature equal to or higher than the heat irreversible solidification temperature of heat-coagulable β-1,3-glucan (hereinafter referred to as “liquid B”). It is also one of the features of dripping.
本発明のA液は、加熱凝固性β-1,3-グルカンおよび多価金属塩を溶媒中で公知手法を用いて分散することにより得ることができる。 The liquid A of the present invention can be obtained by dispersing heat-coagulating β-1,3-glucan and a polyvalent metal salt in a solvent using a known method.
また、A液の粘度は130~3600 mPa・sに調製されている。かかるA液の粘度範囲は、A液の流動性を確保し、球状ゲルを安定に製造する上で有利である。また、A液の粘度範囲は、好ましくは150~3600mPa・sであり、より好ましくは150~2600mPa・sである。かかる粘度範囲は、硬さと粘りとのある食感や真球形状をゲルに付与する上で特に好ましい。
A液の上記粘度は、例えば、後述する実施例1に記載の方法により決定することができる。
The viscosity of the liquid A is adjusted to 130 to 3600 mPa · s. Such a viscosity range of the liquid A is advantageous in securing the fluidity of the liquid A and stably producing a spherical gel. The viscosity range of the liquid A is preferably 150 to 3600 mPa · s, more preferably 150 to 2600 mPa · s. Such a viscosity range is particularly preferable for imparting a texture and a true spherical shape with hardness and stickiness to the gel.
The said viscosity of A liquid can be determined by the method as described in Example 1 mentioned later, for example.
A液の粘度は、公知技術により適宜調製することができる。かかる手法としては、例えば、加熱凝固性β-1,3-グルカンを分散させた後、冷却する高粘度化法(参照:食品ハイドロコロイドの開発と応用 編者 西成 勝好)、加熱凝固性β-1,3-グルカンをアルカリに膨潤または溶解させることで高粘度化を行うアルカリ膨潤/溶解法、加熱凝固性β-1,3-グルカンに、でんぷん等を添加して粘度を付与する方法等が挙げられるが、好ましくはアルカリ膨潤/溶解法である。 The viscosity of the liquid A can be appropriately adjusted by a known technique. Such methods include, for example, a method of increasing viscosity by dispersing heat-coagulable β-1,3-glucan and then cooling (see: Development and application of food hydrocolloids, editor Katsuyoshi Shonishi), heat-coagulating β-1 , An alkali swelling / dissolution method in which viscosity is increased by swelling or dissolving 3,3-glucan in an alkali, and a method in which starch is added to heat-coagulating β-1,3-glucan to impart viscosity. The alkali swelling / dissolving method is preferred.
また、加熱凝固性β-1,3-グルカンは、D-グルコースを構成糖とし、β-1,3-グルコシド結合してなり、加熱凝固性を有する多糖類である。加熱凝固性β-1,3-グルカンの起源は、微生物、動物あるいは植物等、特に限定されない。加熱凝固性β-1,3-グルカンとしては、例えば、カードラン、パラミロン、パキマン等を挙げることができ、好ましくはカードランである。 In addition, heat-coagulating β-1,3-glucan is a polysaccharide having D-glucose as a constituent sugar and β-1,3-glucoside bond, and having heat-coagulating properties. The origin of heat-coagulating β-1,3-glucan is not particularly limited, such as microorganisms, animals or plants. Examples of the heat-coagulating β-1,3-glucan include curdlan, paramylon, and pachyman, and curdlan is preferable.
A液中の加熱凝固性β-1,3-グルカンの量は、特に限定されないが、A液の流動性を勘案すると、A液100重量部に対して、0.1~8重量部であり、より好ましくは0.5~5重量部である。 The amount of heat-coagulating β-1,3-glucan in the liquid A is not particularly limited, but considering the fluidity of the liquid A, it is 0.1 to 8 parts by weight with respect to 100 parts by weight of the liquid A. More preferably, it is 0.5 to 5 parts by weight.
A液中の多価金属塩は、可食性の塩類が好ましく用いられる。また、多価金属塩は、例えば、元素周期表でIIa族(アルカリ土類金属)(例、カルシウム等)、VIII族(例、鉄等)、Ib族(例、銅等)、IIb族(例、亜鉛等)、IIIa族(アルミニウム等)等に属する金属と酸との塩が挙げられるが、好ましくはカルシウム塩である。 Edible salts are preferably used as the polyvalent metal salt in the liquid A. The polyvalent metal salt includes, for example, a group IIa (alkaline earth metal) (eg, calcium), a group VIII (eg, iron), a group Ib (eg, copper), a group IIb ( Examples include salts of metals and acids belonging to Group IIIa (aluminum, etc.), etc., preferably calcium salts.
また、多価金属塩を形成する酸としては、特に限定されないが、無機酸(例、塩酸、硫酸、硝酸、リン酸等)および有機酸(例、酢酸、乳酸、グルコン酸、チオグリコール酸、アスコルビン酸等)が挙げられる。 In addition, the acid that forms the polyvalent metal salt is not particularly limited, but inorganic acids (e.g., hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, etc.) and organic acids (e.g., acetic acid, lactic acid, gluconic acid, thioglycolic acid, Ascorbic acid and the like).
より具体的には、カルシウムと酸の塩は、例えば、塩化カルシウム、水酸化カルシウム、酸化カルシウム、硫酸カルシウム、硝酸カルシウム、リン酸カルシウム等の無機酸との塩、酢酸カルシウム、乳酸カルシウム、グルコン酸カルシウム、チオグリコール酸カルシウム、アスコルビン酸カルシウム等の有機酸との塩が挙げられるが、好ましくは塩化カルシウム、水酸化カルシウム、酸化カルシウム、または乳酸カルシウムであり、より好ましくは塩化カルシウム、乳酸カルシウムであり、さらに好ましくは、乳酸カルシウムである。 More specifically, calcium and acid salts include, for example, salts with inorganic acids such as calcium chloride, calcium hydroxide, calcium oxide, calcium sulfate, calcium nitrate, and calcium phosphate, calcium acetate, calcium lactate, calcium gluconate, Examples include salts with organic acids such as calcium thioglycolate and calcium ascorbate, preferably calcium chloride, calcium hydroxide, calcium oxide, or calcium lactate, more preferably calcium chloride, calcium lactate, Preferably, it is calcium lactate.
A液中の多価金属塩の量は、B液中のゲル化剤をゲル化しうる限り特に限定されず、当業者が適宜決定することができる。具体的には、多価金属塩の量は、例えば、A液100重量部当り、多価金属として0.1~5重量部であり、好ましくは0.3~3重量部の範囲で適宜選択してもよい。かかる量は、乳酸カルシウムを用いた場合に特に好ましい。 The amount of the polyvalent metal salt in the liquid A is not particularly limited as long as the gelling agent in the liquid B can be gelled, and can be appropriately determined by those skilled in the art. Specifically, the amount of the polyvalent metal salt is, for example, 0.1 to 5 parts by weight, preferably 0.3 to 3 parts by weight as the polyvalent metal per 100 parts by weight of Liquid A. May be. Such an amount is particularly preferred when calcium lactate is used.
A液中の溶媒は、β-1,3-グルカンおよび多価金属塩を分散しうる限り特に限定されないが、好ましくは水性媒体であり、より好ましくは水または含アルコール水溶液(例えば、約0.1~10v/v%アルコール含有水)であり、さらに好ましくは水である。 The solvent in the liquid A is not particularly limited as long as β-1,3-glucan and a polyvalent metal salt can be dispersed, but is preferably an aqueous medium, more preferably water or an alcohol-containing aqueous solution (for example, about 0.1. 1-10 v / v% alcohol-containing water), more preferably water.
また、A液の温度は、A液を好適な粘度範囲に保つように当業者が適宜決定することができる。かかるA液の温度は、好ましくは加熱凝固性β-1,3-グルカンの凝固温度(ゲル化温度)未満であり、かつA液の粘度が上述の数値範囲に保たれる温度である。より具体的には、A液の温度は、好ましくは80℃未満であり、より好ましくは50~60℃である。かかる温度は、加熱凝固性β-1,3-グルカンがカードランである場合に特に好ましい。 Further, the temperature of the liquid A can be appropriately determined by those skilled in the art so as to keep the liquid A in a suitable viscosity range. The temperature of the liquid A is preferably lower than the solidification temperature (gelation temperature) of the heat-coagulating β-1,3-glucan, and the temperature at which the viscosity of the liquid A is maintained in the above numerical range. More specifically, the temperature of the liquid A is preferably less than 80 ° C., and more preferably 50 to 60 ° C. Such a temperature is particularly preferred when the heat-coagulating β-1,3-glucan is curdlan.
A液のpHは、加熱凝固性β-1,3-グルカンの種類・性質を勘案して、当業者により適宜決定される。具体的には、A液のpHは、11以下が望ましく、好ましくは、pH1.0~pH11.0である。かかる好適なpHは加熱凝固性β-1,3-グルカンがカードランである場合、カードランを溶解させずに効果的に溶媒中に分散させる上で有利である。 The pH of solution A is appropriately determined by those skilled in the art in consideration of the type and properties of heat-coagulating β-1,3-glucan. Specifically, the pH of the solution A is desirably 11 or less, preferably pH 1.0 to pH 11.0. Such a suitable pH is advantageous in effectively dispersing the curdlan in the solvent without dissolving the curdlan when the heat-coagulating β-1,3-glucan is curdlan.
また、本発明のB液は、多価金属イオンと反応してゲル化するゲル化剤を溶媒中で常法により分散させ、A液中の加熱凝固性β-1,3-グルカンの熱不可逆性凝固(ゲル化)温度以上の温度とすることにより調製することができる。 In addition, the liquid B of the present invention is obtained by dispersing a gelling agent that reacts with polyvalent metal ions and gels in a solvent by a conventional method, and heat irreversible heat-solidifying β-1,3-glucan in the liquid A. It can prepare by setting it as the temperature more than a sexual coagulation (gelation) temperature.
具体的には、B液の温度は、好ましくは80℃以上であり、さらに好ましくは80~150℃である。かかる温度は、加熱凝固性β-1,3-グルカンがカードランの場合、球状ゲルを形成する上で特に有利である。 Specifically, the temperature of the liquid B is preferably 80 ° C. or higher, more preferably 80 to 150 ° C. Such a temperature is particularly advantageous in forming a spherical gel when the heat-coagulating β-1,3-glucan is curdlan.
B液中のゲル化剤は、多価金属イオンと反応してゲル化する限り特に限定されないが、好ましくは多糖類であり、より好ましくはアルギン酸、ロウメトキシルペクチン、ジェランガムまたはその塩等であり、さらに好ましくはアルギン酸またはその塩であり、さらに好ましくはアルギン酸アルカリ金属塩であり、さらに一層好ましくはアルギン酸ナトリウムまたはアルギン酸カリウムである。 The gelling agent in the B liquid is not particularly limited as long as it reacts with a polyvalent metal ion to gel, but is preferably a polysaccharide, more preferably alginic acid, wax methoxyl pectin, gellan gum or a salt thereof, and the like. More preferred is alginic acid or a salt thereof, more preferred is an alkali metal alginate, and still more preferred is sodium alginate or potassium alginate.
B液中のゲル化剤の量は、特に限定されないが、B液100重量部に対して、例えば、0.01~5重量部であり、好ましくは0.1~2重量部である。 The amount of the gelling agent in the B liquid is not particularly limited, but is, for example, 0.01 to 5 parts by weight, preferably 0.1 to 2 parts by weight with respect to 100 parts by weight of the B liquid.
B液に用いられる溶媒およびpHは、特に限定されず、A液と同様とすることができる。 The solvent and pH used for the B liquid are not particularly limited, and can be the same as the A liquid.
上記の他、A液およびB液は、本発明の球状ゲルの形成を妨げない範囲で適宜添加剤を含んでいてもよい。かかる添加剤としては、特に限定されないが、香料、色素、果汁、エキス、調味料またはpH調節剤等が挙げられる。 In addition to the above, the liquid A and the liquid B may appropriately contain additives as long as they do not interfere with the formation of the spherical gel of the present invention. Such additives include, but are not limited to, fragrances, pigments, fruit juices, extracts, seasonings or pH adjusters.
また、A液をB液に滴下する方法は、特に限定されず、多孔板やノズル等の公知装置を用いて連続的または断続的に行ってよい。また、A液の滴下の際には、多孔板、ノズル等の公知装置の口径・形状やA液の滴下量、滴下速度、粘度または比重などを適宜調節することにより、球状ゲルの形や大きさは当業者によって適宜調節される。なお、A液をノズル等から連続的にB液に注入する場合、麺状のゲルやフカヒレ切片のような形状のゲルを調製することもでき、本発明にはかかる態様も包含される。 Further, the method of dropping the A liquid into the B liquid is not particularly limited, and may be performed continuously or intermittently using a known device such as a perforated plate or a nozzle. In addition, when the liquid A is dropped, the shape and size of the spherical gel can be adjusted by appropriately adjusting the aperture and shape of a known device such as a perforated plate and a nozzle, the dropping amount of the liquid A, the dropping speed, the viscosity, or the specific gravity. The length is appropriately adjusted by those skilled in the art. In addition, when inject | pouring A liquid into B liquid continuously from a nozzle etc., the gel of a shape like a noodle-like gel or a shark fin section can also be prepared, and this aspect is also included by this invention.
また、A液の滴下の際、B液は静置していてもよく、撹拌していてもよい。 In addition, when the liquid A is dropped, the liquid B may be left standing or stirred.
また、A液の滴下後のB液の温度は、特に限定されないが、球状ゲルの安定な製造を勘案すれば、加熱凝固性β-1,3-グルカンの熱不可逆性凝固(ゲル化)温度以上に維持することが好ましい。かかる温度の保持時間は、好ましくは10分以上である。 Further, the temperature of the B liquid after the dropping of the A liquid is not particularly limited, but considering the stable production of the spherical gel, the heat irreversible solidification (gelation) temperature of the heat coagulable β-1,3-glucan It is preferable to maintain above. The holding time of such temperature is preferably 10 minutes or more.
上記のような本発明の製造方法によれば、球状ゲルは、加熱凝固性β-1,3-グルカンを主成分とするコアと、所望により、多価金属塩およびゲル化剤の反応物を主成分とする外膜とを具備するゲルとして提供しうる。かかる球状ゲルは、β-1,3-グルカン特有の結着性の低減した状態で取得することができ、β-1,3-グルカンゲルの製造で通常発生しやすい接触による重合を防止して安定した形状を保持する上で有利である。 According to the production method of the present invention as described above, the spherical gel comprises a core mainly composed of heat-coagulating β-1,3-glucan, and optionally a reaction product of a polyvalent metal salt and a gelling agent. It can be provided as a gel having an outer membrane as a main component. Such a spherical gel can be obtained in a state where the binding property peculiar to β-1,3-glucan is reduced, and prevents polymerization due to contact that is usually generated in the production of β-1,3-glucan gel. This is advantageous in maintaining a stable shape.
また、本発明の球状ゲルは、A液の多価金属塩濃度、B液のゲル化剤濃度および反応時間等を当業者が適宜調節することによって、手で剥離することが可能な外膜を有する球状ゲルから外膜を有していない球状ゲルまで提供することが可能である。なお、上記外膜は、球状ゲルを炭酸ナトリウム等のアルカリ剤水溶液に浸漬することによって除去してもよく、本発明には、かかる態様も包含される。 In addition, the spherical gel of the present invention has an outer membrane that can be peeled by hand by appropriately adjusting the concentration of the polyvalent metal salt in the A liquid, the concentration of the gelling agent in the B liquid, and the reaction time. It is possible to provide from a spherical gel having a spherical gel having no outer membrane. The outer membrane may be removed by immersing the spherical gel in an alkaline agent aqueous solution such as sodium carbonate. The present invention includes such an embodiment.
また、一つの態様によれば、球状ゲルは、加熱凝固性β-1,3-グルカンから実質的になる。ここで、「加熱凝固性β-1,3-グルカンから実質的になる」とは、球状ゲルの製造工程および使用工程に際して混入した加熱凝固性β-1,3-グルカンとは異なる他の成分が含まれてもよいことを意味し、具体的には、加熱凝固性β-1,3-グルカンの含有量が、球状ゲル全体の好ましくは0.5重量%以上、より好ましくは0.8重量%以上、さらに好ましくは1重量%以上を意味する。 Further, according to one embodiment, the spherical gel is substantially composed of heat-coagulating β-1,3-glucan. Here, “consisting essentially of heat-coagulating β-1,3-glucan” means other components different from the heat-coagulating β-1,3-glucan mixed in the production process and use process of the spherical gel. Specifically, the content of heat-coagulating β-1,3-glucan is preferably 0.5% by weight or more, more preferably 0.8% by weight of the entire spherical gel. It means wt% or more, more preferably 1 wt% or more.
また、球状ゲルの大きさは、特に限定されないが、好ましくは2~20mmであり、より好ましくは3~15mmであり、さらに好ましくは3~10mmである。かかる大きさは、球状ゲルを食品として用いる場合に特に有利である。 The size of the spherical gel is not particularly limited, but is preferably 2 to 20 mm, more preferably 3 to 15 mm, and further preferably 3 to 10 mm. Such a size is particularly advantageous when the spherical gel is used as a food.
また、本発明の球状ゲルは、上述の通り、硬さと粘りとを備えた食感を奏することができる。
球状ゲルの硬さを、最大荷重(ゲル強度)を用いて表す場合、最大荷重は、品温20℃のとき、好ましくは最大荷重0.3~3.0Nである。
また、球状ゲルの粘りを、破断歪率を用いて表す場合、破断歪率は、品温20℃のとき、好ましくは65%以上である。
なお、上記最大荷重および破断歪率は、本願明細書の実施例1の(2)に記載の手法により、決定することができる(山電社製クリープメーターRE2-3300Sを使用して測定。測定条件:プランジャー:直径3mm、高さ22mmの円柱型、最大測定歪率:98%、測定速度:0.5mm/秒)。
Moreover, the spherical gel of this invention can have the food texture provided with hardness and stickiness as above-mentioned.
When the hardness of the spherical gel is expressed using the maximum load (gel strength), the maximum load is preferably 0.3 to 3.0 N when the product temperature is 20 ° C.
Further, when the stickiness of the spherical gel is expressed using a breaking strain rate, the breaking strain rate is preferably 65% or more when the product temperature is 20 ° C.
In addition, the said maximum load and breaking strain rate can be determined with the method as described in (2) of Example 1 of this-application specification (It measured using the Yamaden Corporation creep meter RE2-3300S. Measurement. Conditions: Plunger: cylindrical shape with a diameter of 3 mm and a height of 22 mm, maximum measurement distortion: 98%, measurement speed: 0.5 mm / second).
また、本発明の球状ゲルは、優れたレトルト耐性および冷凍耐性を奏することができる。
例えば、121℃ F=20のレトルト条件の場合、球状ゲルの最大荷重は、好ましくはレトルト殺菌前の最大荷重の100~300%である。
また、-20℃、7日間冷凍して解凍した場合、球状ゲルの最大荷重は、好ましくは冷凍前の球状ゲルの最大荷重の100~600%である。
Moreover, the spherical gel of this invention can show the outstanding retort tolerance and freezing tolerance.
For example, in the case of 121 ° C. F = 20 retort conditions, the maximum load of the spherical gel is preferably 100 to 300% of the maximum load before retort sterilization.
Further, when frozen and thawed at −20 ° C. for 7 days, the maximum load of the spherical gel is preferably 100 to 600% of the maximum load of the spherical gel before freezing.
また、本発明の球状ゲルは、本発明の球状ゲルは、そのまま食品として用いてもよくまたは食品の原料として用いてもよい。本発明の食品としては、特に限定されないが、模造イクラなどの魚卵様食品、タピオカパール様食品、球状のゼリー食品、アイスや冷菓などの冷製食品、等が挙げられる。 In addition, the spherical gel of the present invention may be used as it is as a food or as a raw material for food. The food of the present invention is not particularly limited, and examples thereof include fish egg-like foods such as imitation salmon, tapioca pearl-like foods, spherical jelly foods, and cold foods such as ice and frozen desserts.
以下、本発明を実施例により具体的に説明するが、本発明はこれらの例示に限定されない。 Hereinafter, the present invention will be specifically described by way of examples, but the present invention is not limited to these examples.
実施例1
(1)
表1のa-1液の配合1に示される割合で、水とカードランを充分に分散させ、水とカードランからなるa-1液50重量部を得た。次に、a-1液を撹拌(300rpm)しながら、リン酸3ナトリウム0.5重量部を水25重量部に溶解させた溶解液をa-1液に添加した。次に、得られた混合液を50~55℃で撹拌(600rpm)しながら、乳酸0.4重量部を水3.6重量部に溶解させた溶解液を上記混合液に添加した。得られた混合液を55~60℃に維持して撹拌(800rpm)しながら、乳酸カルシウム1重量部を水19.5重量部に溶解させた溶解液を上記混合液に添加した。得られた混合液を55~60℃に維持して撹拌(800rpm)することにより、カードランとカルシウムイオンの分散液(A液1)を得た。同様にして、表1の配合2~6でa-1液を調製する以外、A液1と同様にして、A液2~6を得た。
A液1~6を調製した時点で、A液1~6の粘度を測定した(測定機器:東機産業ビスコメーター TVB-10 ロータNo.23(M4)、60rpm、60秒後の数値を測定)。その結果は、表1に示す。
Example 1
(1)
Water and curdlan were sufficiently dispersed at the ratio shown in Formula 1 of the a-1 solution in Table 1 to obtain 50 parts by weight of the a-1 solution composed of water and curdlan. Next, a solution obtained by dissolving 0.5 parts by weight of trisodium phosphate in 25 parts by weight of water was added to the a-1 solution while stirring the a-1 solution (300 rpm). Next, a solution obtained by dissolving 0.4 parts by weight of lactic acid in 3.6 parts by weight of water was added to the above mixture while stirring the obtained mixture at 50 to 55 ° C. (600 rpm). While maintaining the obtained mixed liquid at 55 to 60 ° C. and stirring (800 rpm), a solution obtained by dissolving 1 part by weight of calcium lactate in 19.5 parts by weight of water was added to the above mixed liquid. The obtained mixed liquid was maintained at 55 to 60 ° C. and stirred (800 rpm) to obtain a dispersion of curdlan and calcium ions (liquid A 1). Similarly, liquids A 2 to 6 were obtained in the same manner as liquid A 1, except that the liquid a-1 was prepared according to formulations 2 to 6 in Table 1.
When liquids 1 to 6 were prepared, the viscosities of liquids 1 to 6 were measured. ). The results are shown in Table 1.
次に、水99.5重量部にアルギン酸ナトリウム0.5重量部に添加し、撹拌(800rpm)・溶解することにより、アルギン酸ナトリウム溶液(以下、「B液」ともいう)を得た。
次に、容器に充填した95℃のB液に、シリンジに充填したA液1を約 25g/sの速度で滴下した。その後B液を95℃で60分保持したところ、3~6mmの粒状ゲルが生成した。次に、該粒状ゲルをB液より分離し、水を用いて冷却・洗浄し、試験品1を得た。同様にして、A液2~6を用いて、試験品2~6の製造を行った。
Next, 0.5 part by weight of sodium alginate was added to 99.5 parts by weight of water, stirred (800 rpm) and dissolved to obtain a sodium alginate solution (hereinafter also referred to as “solution B”).
Next, the A liquid 1 with which the syringe was filled was dripped at 95 degreeC B liquid with which the container was filled at the speed | rate of about 25 g / s. Thereafter, the liquid B was held at 95 ° C. for 60 minutes, and a 3 to 6 mm granular gel was formed. Next, the granular gel was separated from the liquid B, cooled and washed with water, and a test product 1 was obtained. In the same manner, test products 2 to 6 were produced using the A liquids 2 to 6.
試験品の成形性は、下記のように判断した。
○:真球状の粒状ゲルが成形できている
△:粒状ゲルが成形できているが、真球状ではない
×:粘度が高く、滴下できないため、粒状ゲルが成形できない。
The moldability of the test product was judged as follows.
◯: True spherical granular gel is formed. Δ: Although granular gel is formed, it is not true spherical. ×: Since the viscosity is high and cannot be dripped, the granular gel cannot be formed.
また、試験品の食感を訓練されたパネラー3名により評価した。結果を表1に示す。 Also, the texture of the test product was evaluated by three trained panelists. The results are shown in Table 1.
(2)
(1)の球状の試験品3(以下、「球状ゲルA」ともいう)をレトルト殺菌用の容器に充填し、密閉し、121℃、F=20にて、レトルト殺菌を行い、レトルト殺菌処理された球状ゲルA(以下、「球状ゲルB」ともいう)を得た。
また、球状ゲルAを適当な容器に充填し、密閉した。次に、該容器を球状ゲルAごと、-20℃に7日間、静置した。7日後、該容器を20℃の水温で流水解凍し、冷凍処理された球状ゲルA(以下、「球状ゲルC」ともいう)を得た。
次に、球状ゲルA~Cの食感を比較するために、最大荷重(ゲル強度)と破断歪率(ゲルの粘り)を山電社製クリープメーターRE2‐3300Sにて、N数=4~5にて測定した(測定温度:20℃、プランジャー:直径3mm、高さ22mmの円柱型、最大測定歪率:98%、測定速度:0.5mm/秒)。
また、球状ゲルBおよびCの食感を、球状ゲルAの食感と比較した。測定結果と比較結果は表2に示す。レトルト殺菌後、冷凍解凍後においても、硬さ、粘りのある食感であった。
(2)
A spherical test product 3 of (1) (hereinafter also referred to as “spherical gel A”) is filled in a retort sterilization container, hermetically sealed, retort sterilized at 121 ° C. and F = 20, and retort sterilized. The obtained spherical gel A (hereinafter also referred to as “spherical gel B”) was obtained.
Moreover, the spherical gel A was filled in a suitable container and sealed. Next, the container was allowed to stand together with the spherical gel A at −20 ° C. for 7 days. Seven days later, the container was thawed with running water at a temperature of 20 ° C. to obtain a frozen spherical gel A (hereinafter also referred to as “spherical gel C”).
Next, in order to compare the textures of the spherical gels A to C, the maximum load (gel strength) and the breaking strain rate (gel stickiness) were measured using a Yamaden Corporation creep meter RE2-3300S with N number = 4 (Measurement temperature: 20 ° C., plunger: cylindrical shape with a diameter of 3 mm, height of 22 mm, maximum measurement distortion: 98%, measurement speed: 0.5 mm / second).
Further, the texture of the spherical gels B and C was compared with the texture of the spherical gel A. The measurement results and comparison results are shown in Table 2. Even after retort sterilization and after freezing and thawing, the texture was firm and sticky.
Claims (6)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
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| HK15109562.2A HK1208784A1 (en) | 2012-08-01 | 2012-08-01 | Spherical gel and manufacturing process therefor |
| PCT/JP2012/069550 WO2014020717A1 (en) | 2012-08-01 | 2012-08-01 | Spherical gel and manufacturing process therefor |
| CN201280074848.8A CN104507330A (en) | 2012-08-01 | 2012-08-01 | Spherical gel and manufacturing process therefor |
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| Application Number | Priority Date | Filing Date | Title |
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| PCT/JP2012/069550 WO2014020717A1 (en) | 2012-08-01 | 2012-08-01 | Spherical gel and manufacturing process therefor |
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| WO2014020717A1 true WO2014020717A1 (en) | 2014-02-06 |
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| PCT/JP2012/069550 Ceased WO2014020717A1 (en) | 2012-08-01 | 2012-08-01 | Spherical gel and manufacturing process therefor |
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| CN (1) | CN104507330A (en) |
| HK (1) | HK1208784A1 (en) |
| WO (1) | WO2014020717A1 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105476065A (en) * | 2015-12-16 | 2016-04-13 | 贵州中烟工业有限责任公司 | Production system for hollow alginate capsule for cigarette |
| CN105559139A (en) * | 2015-12-16 | 2016-05-11 | 贵州中烟工业有限责任公司 | Production system for hollow alginate capsules for cigarettes |
| JPWO2016152729A1 (en) * | 2015-03-24 | 2018-01-18 | ニュートリー株式会社 | Gelling composition |
| JP2021031785A (en) * | 2019-08-20 | 2021-03-01 | 株式会社ユーグレナ | Paramylum-containing rayon fiber and method of producing paramylum-containing rayon fiber |
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| JPH06276965A (en) * | 1993-03-30 | 1994-10-04 | Takeda Chem Ind Ltd | Gel-state food and its production |
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| CN102429137A (en) * | 2011-11-10 | 2012-05-02 | 上海统益生物科技有限公司 | Preparation method of novel curdlan gel particles |
| JP2012157278A (en) * | 2011-01-31 | 2012-08-23 | Kirin Kyowa Foods Co Ltd | Globular gel and method for producing the same |
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| CN102613446A (en) * | 2012-03-08 | 2012-08-01 | 山东中科生物科技股份有限公司 | Preparation method of curdlan gel particles |
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- 2012-08-01 WO PCT/JP2012/069550 patent/WO2014020717A1/en not_active Ceased
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- 2012-08-01 CN CN201280074848.8A patent/CN104507330A/en active Pending
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| JPH06276965A (en) * | 1993-03-30 | 1994-10-04 | Takeda Chem Ind Ltd | Gel-state food and its production |
| JPH0880166A (en) * | 1994-07-12 | 1996-03-26 | Takeda Chem Ind Ltd | Production of granular gel |
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPWO2016152729A1 (en) * | 2015-03-24 | 2018-01-18 | ニュートリー株式会社 | Gelling composition |
| EP3266315A4 (en) * | 2015-03-24 | 2018-08-29 | Nutri Co., Ltd. | Gelling composition |
| US10806167B2 (en) | 2015-03-24 | 2020-10-20 | Nutri Co., Ltd. | Gelling composition |
| JP7114253B2 (en) | 2015-03-24 | 2022-08-08 | ニュートリー株式会社 | Gelling composition |
| CN105476065A (en) * | 2015-12-16 | 2016-04-13 | 贵州中烟工业有限责任公司 | Production system for hollow alginate capsule for cigarette |
| CN105559139A (en) * | 2015-12-16 | 2016-05-11 | 贵州中烟工业有限责任公司 | Production system for hollow alginate capsules for cigarettes |
| JP2021031785A (en) * | 2019-08-20 | 2021-03-01 | 株式会社ユーグレナ | Paramylum-containing rayon fiber and method of producing paramylum-containing rayon fiber |
Also Published As
| Publication number | Publication date |
|---|---|
| HK1208784A1 (en) | 2016-03-18 |
| CN104507330A (en) | 2015-04-08 |
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