TW201343074A - Milk fat cream and method of manufacturing same - Google Patents
Milk fat cream and method of manufacturing same Download PDFInfo
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Abstract
Description
本發明係關於新穎的乳脂肪奶油及其製造方法。又,本發明中,「乳脂肪奶油」係指乳及乳製品的成分規格等相關的省令(昭和26年12月27日厚生省令第52號、以下稱為「乳等省令」。)所規範之「分類 奶油」定義者。 The present invention relates to novel milk fat creams and methods of making the same. In the present invention, the term "milk fat cream" refers to a provincial order related to the composition specifications of the milk and the dairy product (December 27, 26th, December 26th, 26th, and the Ministry of Health and Welfare, No. 52, hereinafter referred to as "milk and other provincial orders"). The definition of "category cream".
一般而言,被稱為奶油(cream)者,除了僅由乳脂肪構成之乳脂肪奶油以外,尚有於乳脂肪添加乳化劑及安定劑者、於植物性脂肪添加乳化劑及安定劑者、於乳脂肪與植物性脂肪的混合脂肪添加乳化劑及安定劑者。乳等省令上,僅乳脂肪奶油被定義為「分類 奶油」,其他添加了乳化劑、安定劑者(以下,稱為「合成奶油」。)被定義為「以乳或乳製品為主要原料之食品」。 In general, what is called cream, in addition to milk fat cream composed only of milk fat, there are emulsifiers and stabilizers added to milk fat, emulsifiers and stabilizers added to vegetable fats, Add emulsifier and stabilizer to the mixed fat of milk fat and vegetable fat. In the case of milk and other provincial orders, only milk fat cream is defined as "classified cream", and other emulsifiers and stabilizers (hereinafter referred to as "synthetic cream") are defined as "milk or dairy products as the main raw material." food".
製造糕點糖果、製造麵包、製造甜點時,乳脂肪奶油、合成脂肪都會使用,但近年來從完全不使用添加劑的觀點,有偏好乳脂肪奶油的傾向。合成奶油的配合油脂的選擇自由度高,且乳化劑及安定劑的組合也有各式各樣的選擇,故具有可提供攪打性與乳化安定性優異之製品的優點,然而,相較於乳脂肪奶油,缺乏芳醇且新鮮的乳風味,有風味方面不佳的缺點。 When making confectionery, making bread, and making desserts, milk fat cream and synthetic fat are used, but in recent years, there is a tendency to prefer milk fat cream from the viewpoint of not using additives at all. Synthetic cream has a high degree of freedom in the selection of fats and oils, and a combination of emulsifiers and stabilizers has various advantages, so it has the advantage of providing products excellent in whipping and emulsifying stability, however, compared to milk Fat cream, lacking aromatic alcohol and fresh milk flavor, has the disadvantage of poor flavor.
乳脂肪奶油一般係將由乳分離之奶油、或將由乳分離之脂肪經殺菌處 理而得者以生乳調整脂肪後進行均質、殺菌、再均質、冷卻而製造者。乳脂肪奶油具有乳脂肪獨特的風味及濃醇,在風味上較合成奶油佳,定義上,因為不能添加用以提供安定性的乳化劑及安定劑,為了賦予攪打性及乳化安定性等的物性,必須完全藉由製造條件的控制而實施。因此,有攪打性及乳化安定性不如合成奶油的問題。關於乳脂肪奶油之乳化安定性的改善,有人提出:在利用超高溫殺菌法(UHT法)之殺菌步驟的前後進行均質化藉以抑制脂肪層上浮的方法(專利文獻1),但該方法中無法得到充份的乳化安定性。又,有人提出在奶油加熱殺菌處理後之冷卻步驟,先急速冷卻至7℃~25℃,在該溫度保持1分鐘~30分鐘,之後急速冷卻至3℃~5℃,藉以賦予乳化安定性的方法(專利文獻2)。然而,該方法中,賦予了冷藏保存時之振動耐性,但未賦予溫度處理耐性,在乳化安定性方面並不理想。 Milk fat cream is generally a cream that is separated from milk, or a fat that is separated from milk. The rationale is that the fat is adjusted by raw milk, and then homogenized, sterilized, rehomogenized, and cooled. Milk fat cream has a unique flavor and concentrated alcohol of milk fat, and is superior in flavor to synthetic cream. In definition, emulsifier and stabilizer for providing stability cannot be added, in order to impart whipping property and emulsion stability. Physical properties must be implemented entirely by the control of manufacturing conditions. Therefore, there is a problem that the whipping property and the emulsion stability are inferior to those of the synthetic cream. Regarding the improvement of the emulsion stability of the milk fat cream, there has been proposed a method of suppressing the fat layer by homogenizing before and after the sterilization step by the UHT method (Patent Document 1), but this method cannot Ample emulsion stability is obtained. Moreover, it has been proposed to cool the step after the heat treatment of the cream, first rapidly cooling to 7 ° C ~ 25 ° C, at this temperature for 1 minute ~ 30 minutes, then rapidly cooling to 3 ° C ~ 5 ° C, thereby giving emulsion stability Method (Patent Document 2). However, in this method, the vibration resistance at the time of cold storage is given, but the temperature treatment resistance is not given, and it is not preferable in terms of emulsion stability.
此外,關於乳脂肪奶油的製造,也有人提出將生乳藉由膜濃縮處理、脫氧處理之風味與物性優異的奶油製造方法(專利文獻3),然而,該方法除了在製造上需要特別裝置及複雜步驟以外,所得到的乳脂肪奶油雖然改善了風味但乳化安定性並不充份。 In addition, a cream manufacturing method which is excellent in flavor and physical properties of raw milk by membrane concentration treatment and deoxidation treatment has been proposed for the production of milk fat cream (Patent Document 3). However, this method requires special equipment and complexity in manufacturing. In addition to the steps, although the obtained milk fat cream has improved flavor, the emulsion stability is not sufficient.
【先前技術文獻】 [Previous Technical Literature]
【專利文獻】 [Patent Literature]
專利文獻1:日本特開2007-259831號公報 Patent Document 1: Japanese Laid-Open Patent Publication No. 2007-259831
專利文獻2:日本特開2006-325426號公報 Patent Document 2: Japanese Laid-Open Patent Publication No. 2006-325426
專利文獻3:日本特開2006-141273號公報 Patent Document 3: Japanese Laid-Open Patent Publication No. 2006-141273
本發明之課題為提供一種乳化安定性優異,且具有良好攪打性之乳脂肪奶油。 An object of the present invention is to provide a milk fat cream which is excellent in emulsion stability and has good whipping properties.
本發明如以下所示。 The present invention is as follows.
(1)一種乳脂肪奶油,其特徵為:脂肪球之中位直徑為2.4μm以下,且在脂肪球皮膜中,酪蛋白相對於乳白蛋白質的質量比為3.5以下。 (2)一種乳脂肪奶油的製造方法,包含以下步驟:奶油分離步驟,由原料乳分離奶油;奶油殺菌步驟,將藉由該奶油分離步驟分離的分離奶油進行殺菌;其特徵為:在該奶油分離步驟前包含將原料乳進行均質處理之原料乳均質步驟。 (1) A milk fat cream characterized in that the median diameter of the fat globule is 2.4 μm or less, and in the fat globule membrane, the mass ratio of casein to milk protein is 3.5 or less. (2) A method for producing a milk fat cream comprising the steps of: a cream separation step of separating the cream from the raw milk; and a cream sterilization step of sterilizing the separated cream separated by the cream separation step; characterized in that: the cream Before the separation step, a raw material milk homogenization step of homogenizing the raw material milk is included.
(3)如(2)之乳脂肪奶油的製造方法,其中,該原料乳均質步驟之均質處理的均質壓力為2.0MPa~5.0MPa。 (3) The method for producing a milk fat cream according to (2), wherein the homogenization pressure of the raw material milk homogenization step is 2.0 MPa to 5.0 MPa.
(4)如(2)或(3)之乳脂肪奶油的製造方法,其中,在該奶油殺菌步驟前及/或該奶油殺菌步驟後,包含將分離後的奶油進行均質處理的奶油均質處理步驟。 (4) The method for producing a milk fat cream according to (2) or (3), wherein before the cream sterilization step and/or after the cream sterilization step, a cream homogenization treatment step of homogenizing the separated cream is included .
藉由本發明可得到乳化安定性優異,且具有良好攪打性之乳脂肪奶油。 According to the present invention, a milk fat cream excellent in emulsification stability and having good whipping property can be obtained.
以下,更詳細說明本發明。 Hereinafter, the present invention will be described in more detail.
本發明之乳脂肪奶油係指乳等省令上之「分類 奶油」,不含乳化劑及安定劑等的添加物。乳脂肪奶油,通常經由以下步驟製造:奶油分離步驟,將原料乳通過圓盤型之離心分離機,分離奶油與脫脂乳;奶油殺菌步驟,將已分離的奶油殺菌;奶油冷卻步驟,將殺菌後的奶油冷卻。又,也可根據需要在殺菌步驟前及/或殺菌步驟後進行將奶油均質化的奶油均質步驟。本發明之乳脂肪奶油,其特徵為:在前述步驟以外尚在奶油分離步驟前進行對原料乳實施均質處理的原料乳均質步驟。 The milk fat cream of the present invention refers to a "classified cream" such as milk, and does not contain an additive such as an emulsifier or a stabilizer. Milk fat cream, usually produced by the following steps: a cream separation step, passing the raw milk through a disc-type centrifuge, separating the cream and skim milk; a cream sterilization step, sterilizing the separated cream; a cream cooling step, after sterilization The cream is cooled. Further, a cream homogenizing step of homogenizing the cream may be performed before the sterilization step and/or after the sterilization step as needed. The milk fat cream of the present invention is characterized in that a raw material milk homogenizing step of performing homogenization treatment on the raw material milk is carried out before the cream separation step in addition to the above steps.
本發明之乳脂肪奶油,其特徵為:藉由經原料乳均質步驟,使脂肪球之中位直徑為2.4μm以下、且脂肪球皮膜中酪蛋白相對於乳白蛋白質之質量比(以下,稱為「酪蛋白/乳白蛋白質比」。)為3.5以下。本發明中所謂中位直徑係指相當於利用體積基準之累積分佈曲線之50%的粒子徑,例如可使用雷射繞射式粒度分佈測定裝置(SALD-3100、島津製作所製)測定。 The milk fat cream of the present invention is characterized in that the median diameter of the fat globule is 2.4 μm or less and the mass ratio of casein to milk protein in the fat globule membrane is obtained by a homogenization step of the raw material milk (hereinafter referred to as The "casein/lactal protein ratio" is 3.5 or less. In the present invention, the median diameter is a particle diameter corresponding to 50% of the cumulative distribution curve based on the volume, and can be measured, for example, by a laser diffraction type particle size distribution measuring apparatus (SALD-3100, manufactured by Shimadzu Corporation).
又,從以往就一直實施的奶油均質步驟,因為係對高脂肪奶油實施均質處理,若例如以2.0MPa以上之高均質壓力實施均質處理,要被覆因微粒子化造成表面積有增加的脂肪球的蛋白質量不足,發生脂肪球間的凝集或合而為一。因此,奶油均質步驟中,一般係利用未達2.0MPa之低均質壓力實施均質處理,但以如此的均質壓力反覆實施均質使脂肪球之中位直徑成為2.4μm以下時,脂肪球皮膜之酪蛋白/乳白蛋白質變得較3.5大。相反地,為了使脂肪球皮膜之酪蛋白/乳白蛋白質比小於3.5,而降低均質壓力、減少均質次數時,脂肪球之中位直徑無法變成2.4μm以下。 In the cream homogenization step which has been carried out in the past, the high-fat cream is subjected to a homogenization treatment, and if the homogenization treatment is carried out at a high homogenization pressure of, for example, 2.0 MPa or more, the protein of the fat globule having an increased surface area due to the pulverization is coated. Insufficient amount, agglomeration or union between fat globules occurs. Therefore, in the cream homogenization step, the homogenization treatment is generally performed using a low homogenization pressure of less than 2.0 MPa, but when the homogenization pressure is repeatedly performed so that the median diameter of the fat globule becomes 2.4 μm or less, the casein of the fat globule membrane is used. / Milky white protein becomes larger than 3.5. On the contrary, in order to reduce the homogenization pressure and reduce the number of homogenizations when the casein/lactoprotein ratio of the fat globule membrane is less than 3.5, the median diameter of the fat globule cannot be 2.4 μm or less.
本發明中藉由利用將原料乳進行均質處理的原料乳均質步驟,可使脂肪球之中位直徑為2.4μm以下,且脂肪球皮膜之酪蛋白/乳白蛋白質比為3.5以下,並且藉由滿足如此的條件,可得到兼具乳化安定性、攪打性的乳脂肪奶油。 In the present invention, by using a raw material milk homogenizing step of homogenizing the raw material milk, the median diameter of the fat globule can be 2.4 μm or less, and the casein/lactoprotein ratio of the fat globule membrane is 3.5 or less, and by satisfying Under such conditions, a milk fat cream having both emulsion stability and whipping property can be obtained.
原料乳均質步驟中,將原料乳加熱使成為特定的均質化溫度後,利用均質機進行均質化。原料乳的加溫,可使用平板式熱交換機、批式加熱機等。其中,就原料乳的加溫效率的觀點而言,較佳為使用平板式熱交換機。又,均質化時,均質機(homogenizer)等的均質機以外,也可使用高壓納米均質機(Microfluidizer)、膠體研磨機(colloid mill)等。就原料乳之均質化效率及處理量的能力的觀點而言,較佳為使用均質機,其中又以使用二段均質機較佳。又,均質化壓力可根據均質機的種類、原料乳的處理流量及均質閥(homo valve)的形狀、均質化溫度等製造條件的不同適當變更,例如也可以2.0MPa以上之高均質壓力進行處理。 In the raw material milk homogenization step, the raw material milk is heated to a specific homogenization temperature, and then homogenized by a homogenizer. For the heating of the raw material milk, a flat type heat exchanger, a batch type heating machine, or the like can be used. Among them, from the viewpoint of the heating efficiency of the raw material milk, it is preferred to use a flat plate heat exchanger. Further, in the case of homogenization, a homogenizer such as a homogenizer or the like may be used, such as a high-pressure nano-homogenizer or a colloid mill. From the viewpoint of the homogenization efficiency of the raw milk and the ability to handle the amount, it is preferred to use a homogenizer, and it is preferable to use a two-stage homogenizer. Further, the homogenization pressure can be appropriately changed depending on the type of the homogenizer, the treatment flow rate of the raw material milk, the shape of the homo valve, the homogenization temperature, and the like, and for example, it can be treated with a high homogenization pressure of 2.0 MPa or more. .
又,奶油分離步驟、奶油殺菌步驟,可利用適宜之既有的方法實施, 奶油分離步驟中,利用圓盤型離心分離機等實施即可。又,奶油殺菌步驟中以下列條件實施即可,例如:保持殺菌法為63℃ 30分鐘、平板式熱交換殺菌法為72~75℃ 15秒、82~85℃ 10秒之高溫短時間殺菌法(HTST法)或130~140℃ 2秒的超高溫殺菌法(UHT法)等。又,通常,將經過殺菌步驟的奶油立即冷卻至10℃以下,但也可在該奶油殺菌步驟前後實施奶油均質步驟。奶油均質步驟,依既有的方法實施即可,例如:可於約1.0MPa之均質壓力實施均質處理。 Moreover, the cream separation step and the cream sterilization step can be carried out by using a suitable method. In the cream separation step, it may be carried out by a disk type centrifugal separator or the like. Moreover, the cream sterilization step can be carried out under the following conditions, for example, maintaining a sterilization method of 63 ° C for 30 minutes, a plate type heat exchange sterilization method of 72 to 75 ° C for 15 seconds, and 82 to 85 ° C for 10 seconds of high-temperature short-time sterilization. (HTST method) or ultra-high temperature sterilization method (UHT method) of 130 to 140 ° C for 2 seconds. Further, in general, the cream subjected to the sterilization step is immediately cooled to 10 ° C or lower, but the cream homogenization step may be carried out before and after the cream sterilization step. The cream homogenization step can be carried out according to the existing method. For example, the homogenization treatment can be carried out at a homogenization pressure of about 1.0 MPa.
以下舉實施例、參考例、試驗例為例說明本發明,但本發明不限於此等。 Hereinafter, the present invention will be described by way of examples, reference examples and test examples, but the present invention is not limited thereto.
【實施例1】 [Example 1]
將已加溫至60℃之原料乳以均質壓力2.0MPa進行均質處理,之後以離心分離機分離脂肪率45%的奶油。將所得到的奶油通入平板式殺菌機,實施120℃、2秒的殺菌處理。殺菌後,進行平板冷卻至約50℃後,採集奶油700g至袋中,進行冷卻而得到乳脂肪奶油(實施例品1)。所得到的乳脂肪奶油以5℃保存。 The raw material milk which had been heated to 60 ° C was homogenized at a homogenization pressure of 2.0 MPa, and then a cream having a fat percentage of 45% was separated by a centrifugal separator. The obtained cream was passed through a plate sterilizer, and sterilizing treatment was performed at 120 ° C for 2 seconds. After the sterilization, the plate was cooled to about 50 ° C, and then 700 g of cream was collected in a bag and cooled to obtain a milk fat cream (Example 1). The resulting milk fat cream was stored at 5 °C.
【實施例2】 [Example 2]
將已加溫至60℃之原料乳在均質機中以均質壓力2.0MPa進行均質處理,之後以離心分離機分離脂肪率45%的奶油。將所得到的奶油以均質壓力1.0MPa進行均質處理後,通入平板式殺菌機,實施120℃、2秒的殺菌處理。之後,進行平板冷卻至約50℃後,採集奶油700g至袋中,進行冷卻而得到乳脂肪奶油(實施例品2)。所得到的乳脂肪奶油以5℃保存。 The raw material milk which had been heated to 60 ° C was homogenized in a homogenizer at a homogenization pressure of 2.0 MPa, and then a cream having a fat percentage of 45% was separated by a centrifugal separator. The obtained cream was homogenized at a homogenization pressure of 1.0 MPa, and then passed through a plate sterilizer to carry out sterilization treatment at 120 ° C for 2 seconds. Thereafter, after cooling the plate to about 50 ° C, 700 g of cream was collected into a bag and cooled to obtain a milk fat cream (Example 2). The resulting milk fat cream was stored at 5 °C.
【實施例3】 [Example 3]
將已加溫至60℃之原料乳以均質壓力2.0MPa進行均質處理,之後以離心分離機分離脂肪率45%的奶油。將所得到的奶油以均質壓力1.0MPa進行均質處理後,通入平板式殺菌機,實施120℃、2秒的殺菌處理。之後,進行平板冷卻至約50℃後,再度以均質壓力1.0MPa進行均質處理,採集奶 油700g至袋中,進行冷卻而得到乳脂肪奶油(實施例品3)。所得到的乳脂肪奶油以5℃保存。 The raw material milk which had been heated to 60 ° C was homogenized at a homogenization pressure of 2.0 MPa, and then a cream having a fat percentage of 45% was separated by a centrifugal separator. The obtained cream was homogenized at a homogenization pressure of 1.0 MPa, and then passed through a plate sterilizer to carry out sterilization treatment at 120 ° C for 2 seconds. Thereafter, after the plate was cooled to about 50 ° C, the homogenization treatment was again performed at a homogenization pressure of 1.0 MPa, and milk was collected. 700 g of oil was placed in a bag and cooled to obtain a milk fat cream (Example 3). The resulting milk fat cream was stored at 5 °C.
【實施例4】 [Embodiment 4]
將已加溫至60℃之原料乳以均質壓力2.0MPa進行均質處理,之後以離心分離機分離脂肪率45%的奶油。將所得到的奶油通入平板式殺菌機,實施120℃、2秒的殺菌處理,之後,進行平板冷卻至約50℃後,以均質壓力1.0MPa進行均質處理,採集均質處理後的奶油700g至袋中,進行冷卻而得到乳脂肪奶油(實施例品4)。所得到的乳脂肪奶油以5℃保存。 The raw material milk which had been heated to 60 ° C was homogenized at a homogenization pressure of 2.0 MPa, and then a cream having a fat percentage of 45% was separated by a centrifugal separator. The obtained cream was passed through a plate sterilizer, and subjected to sterilization treatment at 120 ° C for 2 seconds. Thereafter, the plate was cooled to about 50 ° C, and then homogenized at a homogenization pressure of 1.0 MPa, and 700 g of the cream after homogenization treatment was collected. The bag was cooled to obtain milk fat cream (Example 4). The resulting milk fat cream was stored at 5 °C.
[比較例1] [Comparative Example 1]
將原料乳加溫至60℃後,以離心分離機分離脂肪率45%的奶油。將所得到的奶油通入平板式殺菌機,實施120℃、2秒的殺菌處理,之後,進行平板冷卻至約50℃後,以均質壓力1.0MPa進行均質處理,採集均質處理後的奶油700g至袋中,進行冷卻而得到乳脂肪奶油(比較例品1)。所得到的乳脂肪奶油以5℃保存。 After the raw milk was warmed to 60 ° C, the cream having a fat percentage of 45% was separated by a centrifugal separator. The obtained cream was passed through a plate sterilizer, and subjected to sterilization treatment at 120 ° C for 2 seconds. Thereafter, the plate was cooled to about 50 ° C, and then homogenized at a homogenization pressure of 1.0 MPa, and 700 g of the cream after homogenization treatment was collected. The bag was cooled to obtain milk fat cream (Comparative Example 1). The resulting milk fat cream was stored at 5 °C.
[比較例2] [Comparative Example 2]
將原料乳加溫至60℃後,以離心分離機分離脂肪率45%的奶油。將所得到的奶油以均質壓力1.0MPa進行均質處理後,通入平板式殺菌機,實施120℃、2秒的殺菌處理。之後,進行平板冷卻至約50℃,以均質壓力1.0MPa進行均質處理。採集均質處理後的奶油700g至袋中,進行冷卻而得到乳脂肪奶油(比較例品2)。所得到的乳脂肪奶油以5℃保存。 After the raw milk was warmed to 60 ° C, the cream having a fat percentage of 45% was separated by a centrifugal separator. The obtained cream was homogenized at a homogenization pressure of 1.0 MPa, and then passed through a plate sterilizer to carry out sterilization treatment at 120 ° C for 2 seconds. Thereafter, the plate was cooled to about 50 ° C, and homogenization was carried out at a homogenization pressure of 1.0 MPa. 700 g of the cream after the homogenization treatment was collected in a bag, and cooled to obtain a milk fat cream (Comparative Example 2). The resulting milk fat cream was stored at 5 °C.
將原料乳加溫至60℃後,以離心分離機分離脂肪率45%的奶油。將所得到的奶油以均質壓力1.0MPa進行均質處理,通入平板式殺菌機,實施120℃、2秒的殺菌處理。之後,進行平板冷卻至約50℃,採集奶油700g至袋中,進行冷卻而得到乳脂肪奶油(比較例品3)。所得到的乳脂肪奶油以5℃保存。 After the raw milk was warmed to 60 ° C, the cream having a fat percentage of 45% was separated by a centrifugal separator. The obtained cream was homogenized at a homogenization pressure of 1.0 MPa, passed through a plate sterilizer, and subjected to sterilization treatment at 120 ° C for 2 seconds. Thereafter, the plate was cooled to about 50° C., and 700 g of cream was collected in a bag and cooled to obtain a milk fat cream (Comparative Example 3). The resulting milk fat cream was stored at 5 °C.
[比較例4] [Comparative Example 4]
將原料乳加溫至60℃後,以離心分離機分離脂肪率45%的奶油。將所得到的奶油通入平板式殺菌機,實施120℃、2秒的殺菌處理。之後,進行平板冷卻至約50℃,以均質壓力2.0MPa進行均質處理後,採集奶油700g至袋中,進行冷卻而得到乳脂肪奶油(比較例品4)。所得到的乳脂肪奶油以5℃保存。 After the raw milk was warmed to 60 ° C, the cream having a fat percentage of 45% was separated by a centrifugal separator. The obtained cream was passed through a plate sterilizer, and sterilizing treatment was performed at 120 ° C for 2 seconds. Thereafter, the plate was cooled to about 50° C., and after homogenization treatment at a homogenization pressure of 2.0 MPa, 700 g of cream was collected into a bag and cooled to obtain a milk fat cream (Comparative Example 4). The resulting milk fat cream was stored at 5 °C.
[比較例5] [Comparative Example 5]
將原料乳加溫至60℃後,以離心分離機分離脂肪率45%的奶油。將所得到的奶油通入平板式殺菌機,實施120℃、2秒的殺菌處理。之後,進行平板冷卻至約50℃,以均質壓力5.0MPa進行均質處理後,採集奶油700g至袋中,進行冷卻而得到乳脂肪奶油(比較例品5)。所得到的乳脂肪奶油以5℃保存。 After the raw milk was warmed to 60 ° C, the cream having a fat percentage of 45% was separated by a centrifugal separator. The obtained cream was passed through a plate sterilizer, and sterilizing treatment was performed at 120 ° C for 2 seconds. Thereafter, the plate was cooled to about 50° C., and homogenized at a homogenization pressure of 5.0 MPa, and then 700 g of cream was collected in a bag and cooled to obtain a milk fat cream (Comparative Example 5). The resulting milk fat cream was stored at 5 °C.
[試驗例1] [Test Example 1]
對於實施例品1~4、比較例品1~5,測定脂肪球的中位直徑。又,進行脂肪球皮膜的蛋白質組成分析,算出脂肪球皮膜之酪蛋白/乳白蛋白質比。 For the example products 1 to 4 and the comparative examples 1 to 5, the median diameter of the fat globule was measured. Further, the protein composition analysis of the fat globule membrane was carried out to calculate the casein/lactal protein ratio of the fat globule membrane.
脂肪球之中位直徑的測定,使用雷射繞射式粒度分佈測定裝置(SALD-3100、島津製作所製)。 For the measurement of the median diameter of the fat globule, a laser diffraction type particle size distribution measuring apparatus (SALD-3100, manufactured by Shimadzu Corporation) was used.
脂肪球皮膜之蛋白質組成分析係藉由以下的方法實施。 The protein composition analysis of the fat globule membrane was carried out by the following method.
相對於各水準的奶油150g添加超純水250g進行稀釋,以2500rpm、5℃進行20分鐘離心分離,捨棄下層的水層。於剩下的奶油層添加超純水300g進行稀釋再次進行離心分離,捨棄下層。再進行此操作2次回收奶油層。於回收的奶油層25g添加己烷15g並混合後,以1000rpm、25℃進行5分鐘進行離心分離,去除上層的己烷與奶油層中的脂質做為試樣。將所得到的試樣10g使用Amicon Ultra Ultrace-3K,以15000r pm、5℃進行30分鐘離心分離並濃縮。精秤經濃縮的試樣4g,添加含有5.37mM檸檬酸鈉及6M胍鹽酸鹽之0.1MBis Tris緩衝液(pH6.8)5000μl與1MDTT300μl並混合,將試樣可溶化。以1N-NaOH調整至pH8.2後,添加蒸餾水定容至10ml。之 後,取1ml至1.5ml微量試管,在沸水加熱3分鐘放冷至室溫。之後,取300μl與稀釋液900μl混合,注入高效能液相層析儀(HPLC)。稀釋液組成係在以下記載之移動相A中溶解胍鹽酸鹽使其最終濃度為4.5M後使用。高效能液相層析儀裝置係將ELITE Lachrom(L2000、Hitachi High-Technologies公司製)連接於PDA檢測器(L7490、Hitachi High-Technologies公司製)後使用。管柱使用ODS-3管柱(直徑4.6mm×長度250mm、GL Sciences公司製)。試樣注入量為40μl、管柱溫度為25℃、流速為1.2ml/min,在220nm進行偵測。移動相使用含0.1%TFA之乙腈/水=1/9(移動相A)、含0.1%TFA之乙腈/水=9/1(移動相B),將移動相B之比例由開始27%至4分鐘後32%、12分鐘後34%、17分鐘後36.5%、35分鐘後39%、50分鐘後43.5%、52分鐘後80%的濃度梯度沖提管柱,進行洗脫。洗脫之各波峰係由標準品(Sigma-Aldrich)的洗脫位置判定。α-乳白蛋白、β-乳球蛋白、κ-酪蛋白,係由波峰面積值利用由各標準品求得的檢量線算出各別的質量。α-酪蛋白、β-酪蛋白係由注入HPLC之試樣的所有蛋白質量扣除前述之α-乳白蛋白、β-乳球蛋白、κ-酪蛋白之質量的值定為α-酪蛋白、β-酪蛋白的總質量。由所得到的α-乳白蛋白、β-乳球蛋白之合計質量,與α-酪蛋白、β-酪蛋白、κ-酪蛋白之合計質量的比,可算出酪蛋白相對於乳白蛋白質的質量比(酪蛋白/乳白蛋白質比)。 250 g of ultrapure water was added to 150 g of each level of cream, diluted, and centrifuged at 2,500 rpm and 5 ° C for 20 minutes to discard the lower aqueous layer. 300 g of ultrapure water was added to the remaining cream layer, diluted, and centrifuged again, and the lower layer was discarded. This operation was carried out twice to recover the cream layer. After 15 g of hexane was added to 25 g of the recovered cream layer and mixed, the mixture was centrifuged at 1000 rpm and 25 ° C for 5 minutes to remove the lipid in the upper layer of hexane and the cream layer as a sample. 10 g of the obtained sample was centrifuged at 15,000 rpm and 5 ° C for 30 minutes using Amicon Ultra Ultrace-3K, and concentrated. 4 g of the concentrated sample was weighed, and 5000 μl of 0.1 MBis Tris buffer (pH 6.8) containing 5.37 mM sodium citrate and 6 M guanidine hydrochloride was added to 300 μl of 1 MDTT and mixed, and the sample was solubilized. After adjusting to pH 8.2 with 1 N-NaOH, distilled water was added to make a volume to 10 ml. It Thereafter, 1 ml to 1.5 ml microtubes were taken and allowed to cool to room temperature by heating in boiling water for 3 minutes. Thereafter, 300 μl of the mixture was mixed with 900 μl of the diluent, and injected into a high performance liquid chromatography (HPLC). The dilution composition was used after dissolving hydrazine hydrochloride in the mobile phase A described below to have a final concentration of 4.5 M. A high performance liquid chromatograph apparatus was used by connecting ELITE Lachrom (manufactured by Hitachi High-Technologies Co., Ltd.) to a PDA detector (manufactured by Hitachi High-Technologies Co., Ltd.). The column was an ODS-3 column (diameter: 4.6 mm × length: 250 mm, manufactured by GL Sciences). The sample injection amount was 40 μl, the column temperature was 25 ° C, the flow rate was 1.2 ml/min, and detection was performed at 220 nm. The mobile phase uses acetonitrile/water = 1/9 (mobile phase A) containing 0.1% TFA, acetonitrile/water = 9/1 (mobile phase B) containing 0.1% TFA, and the ratio of mobile phase B is from the beginning of 27% to After 32 minutes, 32% after 12 minutes, 34% after 12 minutes, 36.5% after 17 minutes, 39% after 35 minutes, 43.5% after 50 minutes, and 80% concentration gradient after 52 minutes, the column was eluted. The elution peaks were determined by the elution position of the standard (Sigma-Aldrich). Α-lactalbumin, β-lactoglobulin, and κ-casein are calculated from the peak area values using the calibration lines obtained from the respective standards. Α-casein and β-casein are the values of all the protein amounts of the samples injected into the HPLC, minus the masses of α-lactalbumin, β-lactoglobulin, and κ-casein, which are defined as α-casein, β. - the total mass of casein. From the total mass of α-lactalbumin and β-lactoglobulin obtained, and the ratio of the total mass of α-casein, β-casein, and κ-casein, the mass ratio of casein to milk protein can be calculated. (casein/lactal protein ratio).
[試驗例2] [Test Example 2]
對於實施例品1~4、比較例品1~5,實施作為乳化安定性之指標的振動耐性試驗,與作為攪打性指標之攪打時的起泡性試驗。 In Examples 1 to 4 and Comparative Examples 1 to 5, a vibration resistance test as an index of emulsification stability and a foaming test at the time of whipping as a whipping property index were carried out.
(振動耐性試驗) (Vibration tolerance test)
振動耐性試驗,係將奶油調製後以5℃保存24小時者,與進行暫時的溫度處理(25℃、1小時溫浴)後在5℃保存24小時者(熱震(HS)25℃處理品)各200g加入250ml容量之紙盒(carton)容器,求出施在20℃施以167次/分時的振動時直到脂肪凝固為止的次數。 The vibration resistance test is a case where the cream is prepared and stored at 5 ° C for 24 hours, and after being subjected to temporary temperature treatment (25 ° C, 1 hour warm bath) and stored at 5 ° C for 24 hours (thermal shock (HS) 25 ° C treated product Each of 200 g was placed in a carton container having a capacity of 250 ml, and the number of times until the fat was solidified when the vibration was applied at 167 times/min at 20 ° C was determined.
關於乳化安定性,藉由振動耐性試驗(5℃保存品、熱震(HS)25℃處理品),以○、╳的2階段進行評價。具體而言,5℃保存品振動次數10,000 次以上、且HS25℃處理品振動次數8,000次以上者評為○,不滿足該等條件的任一種者評為╳。 The evaluation of the emulsion stability was carried out in two stages of ○ and ╳ by a vibration resistance test (5° C. preserved product, thermal shock (HS) 25° C. treated product). Specifically, the number of vibrations of the stored product at 5 ° C is 10,000. The number of times of vibration of the HS25°C treated product of 8,000 or more was evaluated as ○, and any one who did not satisfy the above conditions was rated as ╳.
(攪打時起泡性試驗) (Foaming test at the time of whipping)
攪打時之起泡性試驗中,將奶油以混合器(GENERAL ELECTRIC製)攪打時顯示最適造花性的負荷設定為攪打終點,測定到達此終點的時間(攪打時間)及攪打起泡開始至終點為止的時間(△攪打時間)。又,測定攪打前後一定容積的奶油重量,藉由下式求出到達攪打終點的奶油的膨脹率(overrun)。 In the foaming test at the time of whipping, the load indicating the optimum flowering property when the cream was whipped with a mixer (manufactured by GENERAL ELECTRIC) was set as the end point of the whipping, and the time to reach the end point (whipping time) and the whipping were measured. The time from the start of the bubble to the end point (△ whipping time). Further, the weight of the cream in a predetermined volume before and after the whipping was measured, and the expansion ratio of the cream reaching the end of the whipping was determined by the following formula.
膨脹率=((W1-W2)/W2)×100(%) Expansion ratio = ((W1-W2)/W2) × 100 (%)
W1:一定容積之攪打前的奶油重量 W1: the weight of the cream before the whipping of a certain volume
W2:一定容積之攪打後的奶油重量 W2: the weight of the cream after a certain volume of whipping
又,將到達攪打終點之奶油的硬度利用流變儀(CR-200D、SUN SCIENTIFIC公司製),以柱塞(plunger)直徑20mm、侵入深度10mm、架台速度60mm/min的條件進行測定。 In addition, the hardness of the cream which reached the end of the whipping was measured by a rheometer (CR-200D, manufactured by SUN SCIENTIFIC Co., Ltd.) under the conditions of a plunger diameter of 20 mm, an intrusion depth of 10 mm, and a gantry speed of 60 mm/min.
評價時綜合攪打時間、△攪打時間、膨脹率、硬度,以○、╳的2階段進行評價。具體而言,攪打時間為18分鐘以內、△攪打時間為2分鐘以上、膨脹率為100%以上、硬度為20gf以上未達30gf者評為○,不滿足該等條件者評為╳。又,△攪打時間係表示由攪打鮮奶油之設定硬度(負荷25gf)之1/10的值起至到達設定硬度為止的時間。將試驗例1、試驗例2的結果彙整如表1所示。 In the evaluation, the whipping time, the whipping time, the expansion ratio, and the hardness were comprehensively evaluated in two stages of ○ and ╳. Specifically, the whipping time is 18 minutes or less, the Δ whipping time is 2 minutes or more, the expansion ratio is 100% or more, the hardness is 20 gf or more and less than 30 gf is evaluated as ○, and those not satisfying the conditions are evaluated as ╳. Further, the Δ whipping time indicates the time from the value of 1/10 of the set hardness (load 25 gf) of the whipped cream to the time when the set hardness is reached. The results of Test Example 1 and Test Example 2 are summarized as shown in Table 1.
如表1所示,關於實施例品1~4,相較於比較例品1~3,在5℃保存品及HS25℃處理品的兩條件下,乳化安定性飛躍性地提升。又,起泡性評價 中,相較於比較例品1及比較例品3,△攪打時間長,膨脹率也提升,容易攪打成所預期的硬度。了解:在實施例品1~4中並未見到很大的差異,均質化的次數幾乎不影響奶油物性,僅進行原料乳均質即可得到目標效果。又,從比較例品4可知:奶油分離後進行均質處理時,即使提高均質壓力縮小脂肪球徑,乳化安定性仍降低。此外,從比較例品5可知:奶油分離後若以均質壓力5.0Mpa實施均質處理,均質過程出現凝集,無法調製奶油。 As shown in Table 1, with respect to the examples 1 to 4, the emulsion stability was drastically improved under the conditions of the 5 ° C preserved product and the HS 25 ° C treated product as compared with the comparative examples 1 to 3. Also, foaming evaluation In the comparison with Comparative Example 1 and Comparative Example 3, the Δ whipping time was long, the expansion ratio was also increased, and the desired hardness was easily whipped. Understand: In the examples 1 to 4, no significant difference was observed. The number of homogenizations hardly affected the cream properties, and only the raw milk was homogenized to obtain the desired effect. Moreover, it is understood from the comparative example 4 that when the homogenization treatment is performed after the cream is separated, the emulsion stability is lowered even if the homogenization pressure is increased to reduce the fat globule diameter. Further, from Comparative Example 5, it was found that homogenization treatment was carried out at a homogenization pressure of 5.0 MPa after separation of the cream, and aggregation occurred during the homogenization process, and the cream could not be prepared.
【實施例5】 [Embodiment 5]
將已加溫至60℃的原料乳以均質壓力5.0Mpa進行均質處理,之後以離心分離機分離脂肪率45%的奶油。將所得到的奶油通入平板式殺菌機,實施120℃、2秒的殺菌處理。殺菌後,進行平板冷卻至約50℃後,採集奶油700g至袋中,進行冷卻而得到乳脂肪奶油(實施例品5)。所得到的乳脂肪奶油以5℃保存。 The raw material milk which had been heated to 60 ° C was homogenized at a homogenization pressure of 5.0 MPa, and then a cream having a fat percentage of 45% was separated by a centrifugal separator. The obtained cream was passed through a plate sterilizer, and sterilizing treatment was performed at 120 ° C for 2 seconds. After the sterilization, the plate was cooled to about 50 ° C, and then 700 g of cream was collected into a bag and cooled to obtain a milk fat cream (Example 5). The resulting milk fat cream was stored at 5 °C.
[比較例6] [Comparative Example 6]
將原料乳加溫至60℃後,以均質壓力0.0Mpa進行均質處理,之後以離心分離機分離脂肪率45%的奶油。將所得到的奶油通入平板式殺菌機,實施120℃、2秒的殺菌處理。殺菌後,進行平板冷卻至約50℃後,採集奶油700g至袋中,進行冷卻而得到乳脂肪奶油(比較例品6)。所得到的乳脂肪奶油以5℃保存。 After the raw milk was warmed to 60 ° C, homogenization treatment was carried out at a homogenization pressure of 0.0 MPa, and then a cream having a fat percentage of 45% was separated by a centrifugal separator. The obtained cream was passed through a plate sterilizer, and sterilizing treatment was performed at 120 ° C for 2 seconds. After the sterilization, the plate was cooled to about 50 ° C, and then 700 g of cream was collected in a bag and cooled to obtain a milk fat cream (Comparative Example 6). The resulting milk fat cream was stored at 5 °C.
[比較例7] [Comparative Example 7]
將原料乳加溫至60℃後,以均質壓力1.0Mpa進行均質處理,之後以離心分離機分離脂肪率45%的奶油。將所得到的奶油通入平板式殺菌機,實施120℃、2秒的殺菌處理。殺菌後,進行平板冷卻至約50℃後,採集奶油700g至袋中,進行冷卻而得到乳脂肪奶油(比較例品7)。所得到的乳脂肪奶油以5℃保存。 After the raw material milk was warmed to 60 ° C, homogenization treatment was carried out at a homogenization pressure of 1.0 Mpa, and then a cream having a fat percentage of 45% was separated by a centrifugal separator. The obtained cream was passed through a plate sterilizer, and sterilizing treatment was performed at 120 ° C for 2 seconds. After the sterilization, the plate was cooled to about 50 ° C, and then 700 g of cream was collected in a bag and cooled to obtain a milk fat cream (Comparative Example 7). The resulting milk fat cream was stored at 5 °C.
[比較例8] [Comparative Example 8]
將已加溫至60℃的原料乳以均質壓力8.0Mpa進行均質處理,之後以 離心分離機分離脂肪率45%的奶油。將所得到的奶油通入平板式殺菌機,實施120℃、2秒的殺菌處理。殺菌後,進行平板冷卻至約50℃後,採集奶油700g至袋中,進行冷卻而得到乳脂肪奶油(比較例品8)。所得到的乳脂肪奶油以5℃保存。 The raw milk which has been heated to 60 ° C is homogenized at a homogenization pressure of 8.0 MPa, and then The centrifuge separates the cream with a fat percentage of 45%. The obtained cream was passed through a plate sterilizer, and sterilizing treatment was performed at 120 ° C for 2 seconds. After the sterilization, the plate was cooled to about 50 ° C, and then 700 g of cream was collected in a bag and cooled to obtain a milk fat cream (Comparative Example 8). The resulting milk fat cream was stored at 5 °C.
[比較例9] [Comparative Example 9]
將已加溫至60℃的原料乳以均質壓力10.0Mpa進行均質處理,之後以離心分離機分離脂肪率45%的奶油。將所得到的奶油通入平板式殺菌機,實施120℃、2秒的殺菌處理。殺菌後,進行平板冷卻至約50℃後,採集奶油700g至袋中,進行冷卻而得到乳脂肪奶油(比較例品9)。所得到的乳脂肪奶油以5℃保存。 The raw material milk which had been heated to 60 ° C was homogenized at a homogenization pressure of 10.0 MPa, and then a cream having a fat percentage of 45% was separated by a centrifugal separator. The obtained cream was passed through a plate sterilizer, and sterilizing treatment was performed at 120 ° C for 2 seconds. After the sterilization, the plate was cooled to about 50 ° C, and then 700 g of cream was collected in a bag and cooled to obtain a milk fat cream (Comparative Example 9). The resulting milk fat cream was stored at 5 °C.
[試驗例3] [Test Example 3]
關於實施例品1、實施例品5、比較例品6~9,藉由與試驗例1及試驗例2相同的方法,實施脂肪球之中位直徑的測定、脂肪球皮膜之酪蛋白/乳白蛋白質比的計算、振動耐性試驗及攪打時之起泡性試驗。結果如表2所示。 With respect to Example 1, Example 5, and Comparative Examples 6 to 9, the measurement of the median diameter of the fat globule and the casein/white of the fat globule membrane were carried out by the same method as Test Example 1 and Test Example 2. Calculation of protein ratio, vibration resistance test and foaming test during whipping. The results are shown in Table 2.
如表2所示,關於實施例品1及5,相較於比較例品6及7,在5℃保存品及HS25℃處理品的兩條件,乳化安定性飛躍性地提升。又,起泡性評價中,△攪打時間長,膨脹率也提升,容易攪打成所預期的硬度。比較例品8及9,相較於實施例品1及5,乳化安定性提升,但攪打時間明顯延長,故不適合作為攪打奶油。 As shown in Table 2, in the examples 1 and 5, the emulsion stability was drastically improved in comparison with the comparative examples 6 and 7, under the conditions of the 5 ° C preserved product and the HS 25 ° C treated product. Further, in the evaluation of the foaming property, the Δ whipping time was long, the expansion ratio was also improved, and the desired hardness was easily whipped. In Comparative Examples 8 and 9, the emulsion stability was improved as compared with the examples 1 and 5, but the whipping time was remarkably extended, so that it was not suitable as a whipping cream.
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