TWI617245B - Method for extending the shelf life of chilled fresh milk - Google Patents
Method for extending the shelf life of chilled fresh milk Download PDFInfo
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- TWI617245B TWI617245B TW103130373A TW103130373A TWI617245B TW I617245 B TWI617245 B TW I617245B TW 103130373 A TW103130373 A TW 103130373A TW 103130373 A TW103130373 A TW 103130373A TW I617245 B TWI617245 B TW I617245B
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- Dairy Products (AREA)
Abstract
本發明揭示一種用於延長冷藏乳製品保存期限之方法,其製造方法包括:分離生乳之鮮乳油並獲得一脫脂生乳;將前述脫脂生乳經由濾膜過濾,以得到一膜過濾後之脫脂生乳;將前述鮮乳油,經超高溫瞬間殺菌法進行殺菌,以獲得一殺菌鮮乳油;將前述膜過濾後之脫脂生乳與前述殺菌鮮乳油混合後,獲得一生乳半成品;將前述鮮乳半成品經由前述超高溫瞬間殺菌法進行殺菌,以獲得一鮮乳成品;將前述鮮乳成品降低溫度,並進行無菌充填,以獲得一冷藏鮮乳。本發明所製成之前述冷藏鮮乳可減少超高溫殺菌所造成風味之改變,且可於冷藏儲存至少六個月。 The invention discloses a method for extending the shelf life of a chilled dairy product, which comprises the steps of: separating raw milk of raw milk and obtaining a defatted raw milk; filtering the defatted raw milk through a filter to obtain a membrane-filtered defatted raw milk; The fresh emulsifiable oil is sterilized by an ultra-high temperature instant sterilization method to obtain a sterilized fresh emulsifiable concentrate; the defatted raw milk filtered by the membrane is mixed with the sterilized fresh emulsifiable oil to obtain a raw milk semi-finished product; and the fresh milk semi-finished product is passed through the aforementioned super The high-temperature instant sterilization method is sterilized to obtain a fresh milk product; the fresh milk product is lowered in temperature and aseptically filled to obtain a fresh milk. The aforementioned refrigerated fresh milk produced by the present invention can reduce the change in flavor caused by ultra-high temperature sterilization and can be stored in cold storage for at least six months.
Description
本發明係關於一種用以延長冷藏超高溫瞬間殺菌乳製品之保存期限之方法,尤指一種可保留前述鮮乳新鮮風味之方法。 The present invention relates to a method for extending the shelf life of a sterilized ultra-high temperature instant sterilized dairy product, and more particularly to a method for retaining the fresh flavor of the aforementioned fresh milk.
一般市售鮮乳之殺菌方法係以低溫長時間巴氏德殺菌法(Low-temperature long-time pasteurization,LTLT pasteurization)、高溫短時間巴氏德殺菌法(High-temperature short-time pasteurization,HTST pasteurization)以及超高溫瞬間殺菌法(Ultrahigh temperature pasteurization,UHT-pasteurization);而保久乳則採用超高溫滅菌法(Ultrahigh temperature sterilization,UHT-sterilization)。不同的殺菌方法將會影響前述鮮乳品之保存期限以及原始風味。 Generally, the sterilization method of fresh milk is based on low-temperature long-time pasteurization (LTLT pasteurization) and high-temperature short-time pasteurization (HTST pasteurization). And ultrahigh temperature pasteurization (UHT-pasteurization); while the long-term milk is UHT-sterilization. Different sterilization methods will affect the shelf life and original flavor of the aforementioned fresh dairy products.
前述低溫長時間巴氏德殺菌法係以62℃至65℃溫度,進行殺菌30分鐘;高溫短時間巴氏德殺菌法係以72℃溫度,進行殺菌15秒,前述低溫長時間殺菌法和高溫短時間殺菌法可令前述鮮乳保有原始風味,且前述鮮乳於低溫儲存具有10天至14天之保存期限。前述超高溫瞬間殺菌法係利用120℃至134℃溫度,進行殺菌1秒至4秒, 前述超高溫瞬間殺菌法會導致前述鮮乳之原始風味遭中度破壞,若充填於近乎無菌之包裝,可使前述鮮乳於低溫儲存之保存期限延長至30天至60天,一般我國之國產鮮乳係利用前述超高溫瞬間殺菌法進行殺菌。前述超高溫滅菌法係利用135℃至145℃溫度,進行殺菌2秒至10秒,前述超高溫滅菌法會嚴重破壞前述鮮乳之原始風味,但搭配無菌充填,可令前述鮮乳於常溫儲存條件下具有至少六個月的保存期限,市售保久乳便是利用前述超高溫滅菌法進行殺菌,並於常溫進行包裝。 The low-temperature long-time pasteurization sterilization method is performed at a temperature of 62 ° C to 65 ° C for 30 minutes; the high temperature short-time pasteurization sterilization method is performed at a temperature of 72 ° C for 15 seconds, and the aforementioned low-temperature long-time sterilization method and high temperature The short-time sterilization method allows the aforementioned fresh milk to retain the original flavor, and the aforementioned fresh milk has a shelf life of 10 days to 14 days at low temperature storage. The ultra-high temperature instant sterilization method utilizes a temperature of 120 ° C to 134 ° C for sterilization for 1 second to 4 seconds. The above-mentioned ultra-high temperature instant sterilization method may cause the original flavor of the fresh milk to be moderately damaged. If the package is filled in a nearly aseptic package, the storage period of the fresh milk in the low temperature storage may be extended to 30 days to 60 days, generally domestically produced in China. The fresh milk is sterilized by the above-described ultra-high temperature instant sterilization method. The ultra-high temperature sterilization method utilizes a temperature of 135 ° C to 145 ° C for sterilization for 2 seconds to 10 seconds. The above-mentioned ultra-high temperature sterilization method may seriously damage the original flavor of the fresh milk, but with aseptic filling, the fresh milk may be stored at room temperature. Under the condition, there is a shelf life of at least six months, and the commercially available long-lasting milk is sterilized by the above-mentioned ultra-high temperature sterilization method, and packaged at normal temperature.
前述鮮乳之原始風味之改變主要來自於前述鮮乳於加熱殺菌過程中所產生的梅納反應(Maillard reaction)。前述梅納反應之初期階段係前述鮮乳之胺基酸(amino acid)之親核胺基(nucleophilic amino group)與乳糖之羰基(carbonyl group)間所產生之化學反應,前述親核胺基與前述羰基先進行胺羰縮合反應,以形成希夫鹼(Schiff base),之後再進行安瑪多立重排反應(Amadori rearrangement)。前述梅納反應之中期階段會引起蛋白質之史崔克降解反應(Strecker degradation),此時胺基酸裂解,並產生二氧化碳及醛類。前述梅納反應之終期階段會進行醛類與醇類之縮合反應,並產生黑色素物質,此反應中所產生的許多中間產物,將會影響牛乳的顏色與風味。 The change in the original flavor of the aforementioned fresh milk is mainly derived from the Maillard reaction produced by the aforementioned fresh milk in the heat sterilization process. The initial stage of the Mena reaction is a chemical reaction between the nucleophilic amino group of the amino acid of the fresh milk and the carbonyl group of the lactose, and the nucleophilic amine group and the nucleophilic group The aforementioned carbonyl group is subjected to an amine carbonyl condensation reaction to form a Schiff base, followed by an Amadori rearrangement. The intermediate phase of the aforementioned Mena reaction causes a Strecker degradation of the protein, at which time the amino acid cleaves and produces carbon dioxide and aldehydes. In the final stage of the aforementioned Mena reaction, a condensation reaction of an aldehyde with an alcohol is carried out, and a melanin substance is produced, and many intermediate products produced in the reaction will affect the color and flavor of the milk.
因此,為了兼顧保留前述鮮乳之原始風味以及延長其保存期限,現有技術對於前述鮮乳之殺菌方式,目前仍然存在許多尚待改進的地方。 Therefore, in order to balance the original flavor of the fresh milk and to extend the shelf life thereof, the prior art still has many places for improvement in the sterilization method of the aforementioned fresh milk.
有鑑於現有技術之缺失,本發明之目的在於利用將一脫脂生乳經由濾膜過濾法(membrane filtration)技術,並結合較溫和之殺菌條件,再於低溫下進行無菌充填包裝,藉以克服前述鮮乳之原始風味之保留以及其保存期限之延長無法兼顧之問題。 In view of the absence of the prior art, the object of the present invention is to overcome the aforementioned fresh milk by using a defatted raw milk through a membrane filtration technique in combination with mild sterilizing conditions and then performing aseptic filling and packaging at a low temperature. The retention of the original flavor and the extension of its shelf life cannot be balanced.
為達到上述之目的,本發明提供一種用以延長冷藏鮮乳之保存期限之方法,其步驟包含:(a)將鮮乳油自生乳中分離,藉以獲得前述脫脂生乳;(b)將前述步驟(a)之脫脂生乳通過一濾膜(membrane filter)進行過濾,藉以去除微生物,並獲得一膜過濾後之脫脂生乳;(c)將前述步驟(a)之鮮乳油,經由超高溫瞬間殺菌法進行殺菌,藉以獲得一殺菌鮮乳油,再將前述殺菌鮮乳油降低溫度;(d)將前述步驟(b)之膜過濾後之脫脂生乳與前述殺菌鮮乳油混合後,獲得一生乳半成品;(e)將前述生乳半成品經由前述超高溫瞬間殺菌法進行殺菌,藉以獲得一鮮乳成品;(f)將前述鮮乳成品降低溫度,並進行無菌充填,藉以獲得一冷藏鮮乳。 In order to achieve the above object, the present invention provides a method for extending the shelf life of chilled fresh milk, the steps comprising: (a) separating fresh emulsifiable milk from raw milk to obtain the aforementioned defatted raw milk; (b) the aforementioned steps ( a) the defatted raw milk is filtered through a membrane filter to remove microorganisms, and a membrane-filtered defatted raw milk is obtained; (c) the fresh emulsifiable concentrate of the above step (a) is subjected to ultra-high temperature instant sterilization Sterilizing, obtaining a sterilized fresh emulsifiable oil, and then lowering the sterilizing fresh emulsifiable concentrate; (d) mixing the defatted raw milk after filtering the membrane of the above step (b) with the sterilized fresh emulsifiable concentrate to obtain a raw milk semi-finished product; (e) The raw milk semi-finished product is sterilized by the above-mentioned ultra-high temperature instant sterilization method to obtain a fresh milk product; (f) the fresh milk product is lowered in temperature and aseptically filled to obtain a chilled fresh milk.
依據本發明,前述步驟(b)之濾膜係一0.8μm孔徑之濾膜。 According to the present invention, the filter of the above step (b) is a filter having a pore size of 0.8 μm.
依據本發明,前述步驟(c)之超高溫瞬間殺菌法係選擇可快速加熱且快速降低溫度之方式,包括,但不限於板式加熱法以及管式加熱法,並利用120℃至134℃溫 度,進行殺菌2秒至10秒。在較佳的實施例中,前述步驟(c)之超高溫瞬間殺菌法係板式加熱法。 According to the present invention, the ultra-high temperature instant sterilization method of the foregoing step (c) selects a method for rapidly heating and rapidly reducing the temperature, including, but not limited to, a plate heating method and a tube heating method, and using a temperature of 120 ° C to 134 ° C. Sterilize for 2 seconds to 10 seconds. In a preferred embodiment, the ultra-high temperature instant sterilization method of the aforementioned step (c) is a plate heating method.
依據本發明,前述步驟(c)之降低溫度係降低至50℃至60℃之間。 According to the present invention, the lowering temperature of the aforementioned step (c) is lowered to between 50 ° C and 60 ° C.
依據本發明,前述步驟(e)之超高溫瞬間殺菌法係利用120℃至134℃溫度,進行殺菌3秒至10秒。 According to the present invention, the ultra-high temperature instantaneous sterilization method of the above step (e) is sterilized by using a temperature of 120 ° C to 134 ° C for 3 seconds to 10 seconds.
較佳的,前述步驟(f)之鮮乳成品係降低溫度至10℃以下。 Preferably, the fresh milk product of the aforementioned step (f) is lowered to a temperature below 10 °C.
更佳的,前述步驟(f)之鮮乳成品係降低溫度至8℃以下。 More preferably, the fresh milk product of the aforementioned step (f) is lowered to a temperature below 8 °C.
較佳的,前述步驟(f)之鮮乳成品係無菌充填至一無菌包材中。 Preferably, the fresh milk product of the aforementioned step (f) is aseptically filled into a sterile packaging material.
更佳的,前述無菌包材係一利樂包材(Tetra Pak),其由外向內係由雙層聚乙烯(polyethylene,PE)、鋁箔(aluminum foil)以及聚乙烯所組成。 More preferably, the aforementioned sterile packaging material is a Tetra Pak which is composed of a double-layer polyethylene (polyethylene), an aluminum foil and polyethylene from the outside to the inside.
藉由本發明所製備之前述冷藏鮮乳,其最具創新的關鍵點在於經由前述濾膜過濾法技術,去除微生物,再結合較超高溫滅菌法溫和之殺菌條件,藉以降低因高溫所產生之梅納反應,以保留前述生乳之原始風味。最後將前述鮮乳於低溫下進行無菌充填包裝,藉以延長前述鮮乳之保存期限,使前述冷藏鮮乳於4℃至8℃溫度環境下,可儲存至少6個月。本發明對於兼顧前述冷藏鮮乳之原始風味之保留以及其保存期限之延長確實提供了有效改善。 The most innovative key point of the above-mentioned refrigerated fresh milk prepared by the invention is that the microorganisms are removed through the above-mentioned filter membrane filtration technology, and combined with the mild sterilization conditions of the ultra-high temperature sterilization method, thereby reducing the plum produced by the high temperature. The reaction is carried out to retain the original flavor of the aforementioned raw milk. Finally, the fresh milk is aseptically packaged at a low temperature to extend the shelf life of the fresh milk, and the chilled fresh milk can be stored for at least 6 months at a temperature of 4 ° C to 8 ° C. The present invention provides an effective improvement in maintaining both the retention of the original flavor of the chilled fresh milk and the extension of its shelf life.
圖1係本發明之流程圖。 Figure 1 is a flow chart of the present invention.
下列實施例用於示範說明本發明。所述之實施例不以任何方式意欲限制本發明之範圍,但用於例示如何實施本發明的材料及方法。 The following examples are intended to illustrate the invention. The examples are not intended to limit the scope of the invention in any way, but are used to illustrate the materials and methods of the invention.
將鮮乳油自生乳中分離,以獲得一脫脂生乳。藉由板式加熱法,將前述鮮乳油經由超高溫瞬間殺菌,於120℃-134℃環境下,加熱2秒至10秒,以獲得一殺菌鮮乳油,再將前述殺菌鮮乳油降低溫度至50℃至60℃之間。將前述脫脂生乳通過一孔徑為0.8μm濾膜進行過濾,並獲得一膜過濾後之脫脂生乳。 The fresh cream is separated from the raw milk to obtain a skim milk. The fresh milk is sterilized by ultra-high temperature by a plate heating method, and heated at 120 ° C - 134 ° C for 2 seconds to 10 seconds to obtain a sterilized fresh emulsifiable concentrate, and then the temperature of the sterilized fresh emulsifiable concentrate is lowered to 50 ° C. Up to 60 ° C. The aforementioned defatted raw milk was filtered through a filter having a pore size of 0.8 μm, and a membrane-filtered defatted raw milk was obtained.
將前述殺菌鮮乳油與前述膜過濾後之脫脂生乳進行混合成一生乳半成品,並經由超高溫瞬間殺菌,於120℃-134℃環境下,加熱3秒至10秒,藉以獲得一鮮乳成品。降低前述鮮乳成品之溫度至10℃以下,並進行無菌充填至一無菌包材中,以獲得一冷藏鮮乳。前述無菌包材係一利樂包材,其由外向內係由雙層聚乙烯、鋁箔以及聚乙烯所組成。 The sterilized fresh emulsifiable concentrate is mixed with the defatted raw milk filtered by the membrane to form a raw milk semi-finished product, and is rapidly sterilized by ultra-high temperature, and heated at 120 ° C - 134 ° C for 3 seconds to 10 seconds to obtain a fresh milk product. The temperature of the fresh milk product is lowered to below 10 ° C, and aseptically filled into a sterile package to obtain a fresh milk. The aforementioned aseptic packaging material is a Tetra Pak material which is composed of a double-layer polyethylene, an aluminum foil and polyethylene from the outside to the inside.
將前述冷藏鮮乳儲存於8℃以及12℃環境下,於儲存0個月至6個月分別檢測前述冷藏鮮乳之微生物總數量。前述微生物之檢測包括每毫升所形成之總生菌數(Colony forming units/ml,CFU/ml)、黴菌/酵母菌數(CFU/ml)、大腸桿菌群(CFU/ml)、大腸桿菌數(CFU/ml)、80℃耐熱性孢子菌數(CFU/ml)以及100℃耐熱性孢子菌數(CFU/ml)。 The chilled fresh milk was stored at 8 ° C and 12 ° C, and the total amount of microorganisms of the aforementioned chilled fresh milk was separately detected for 0 months to 6 months. The detection of the aforementioned microorganisms includes the total number of bacteria formed per ml (Colony forming units/ml, CFU/ml), mold/yeast count (CFU/ml), Escherichia coli (CFU/ml), and Escherichia coli ( CFU/ml), heat-resistant spores at 80 °C (CFU/ml) and heat-resistant spores at 100 °C (CFU/ml).
前述總生菌數之檢測方法係將前述冷藏鮮乳 經系列稀釋後,以無菌操作方式分取0.1毫升注入一平板計數培養基(Plate count agar,PCA)上,迅速利用無菌之曲玻璃棒將前述系列稀釋之冷藏鮮乳均勻塗抹散佈,並於35℃環境下進行培養48±2小時。前述稀釋方法係吸取10倍稀釋之前述冷藏鮮乳10毫升加至90毫升稀釋液中,以依序作成100倍、1000倍、10000倍等一系列稀釋檢測液。前述稀釋液係一0.1%蛋白胴稀釋液(0.1% peptone diluents);前述平板計數培養基包含0.5%胰化蛋白胴(tryptone)、0.25%酵母抽出物(yeast extract)、0.1%葡萄糖(glucose)以及1.5%洋菜。前述冷藏鮮乳經培養後,選取25至250個菌落之兩個前述平板計數培養基進行計數,將前述兩個平板計數培養基之菌落數平均值乘以稀釋倍數,及得前述微生物總數量。 The above method for detecting the total number of bacteria is the aforementioned fresh milk After serial dilution, 0.1 ml was dispensed into a plate count agar (PCA) by aseptic operation, and the above-mentioned serially diluted fresh milk was quickly spread and spread at 35 ° C using a sterile curved glass rod. The culture was carried out for 48 ± 2 hours under the environment. In the above dilution method, 10 ml of the above-mentioned chilled fresh milk diluted 10 times is added to 90 ml of the dilution liquid, and a series of dilution detection liquids such as 100 times, 1000 times, and 10000 times are sequentially prepared. The aforementioned dilution is a 0.1% peptone diluents; the aforementioned plate count medium contains 0.5% tryptone, 0.25% yeast extract, 0.1% glucose, and 1.5% amaranth. After the chilled fresh milk is cultured, two of the aforementioned plate counting mediums of 25 to 250 colonies are selected for counting, and the average number of colonies of the two plate counting mediums is multiplied by the dilution factor, and the total number of microorganisms is obtained.
前述黴菌/酵母菌數之檢測方法係將前述冷藏鮮乳經系列稀釋後,以無菌操作方式分取0.1毫升注入一二氯喃玫瑰紅氯黴素培養基(Dichloran rose bengal chloramphenicol agar,DRBC)上,迅速利用無菌之曲玻璃棒將前述系列稀釋之冷藏鮮乳均勻塗抹散佈,並於25℃黑暗環境下進行培養5天。前述稀釋方法係吸取10倍稀釋之前述冷藏鮮乳10毫升加至90毫升稀釋液中,以依序作成100倍、1000倍、10000倍等一系列稀釋檢測液。前述稀釋液係一0.1%蛋白胴稀釋液;前述二氯喃玫瑰紅氯黴素培養基包含0.5%蛋白胴、1%葡萄糖、0.1%磷酸二氫鉀(KH2PO4)、0.05%硫酸鎂(MgSO4‧7H2O)、0.25%孟加拉玫瑰紅(rose bengal)、0.02%二氯喃(dichloran)、1.5%洋菜以及0.01%氯 黴素。前述冷藏鮮乳經培養後,選取25至250個菌落之兩個前述平板計數培養基進行計數,將前述兩個平板計數培養基之菌落數平均值乘以稀釋倍數,及得前述微生物總數量。 The method for detecting the number of molds/yeasts is to serially dilute the chilled fresh milk, and 0.1 ml of the solution into the Dichloran rose bengal chloramphenicol agar (DRBC) is aseptically operated. The above-mentioned serially diluted chilled fresh milk was quickly spread and spread using a sterile curved glass rod, and cultured in a dark environment at 25 ° C for 5 days. In the above dilution method, 10 ml of the above-mentioned chilled fresh milk diluted 10 times is added to 90 ml of the dilution liquid, and a series of dilution detection liquids such as 100 times, 1000 times, and 10000 times are sequentially prepared. The aforementioned dilution is a 0.1% peptone dilution; the dichloropyranine chloramphenicol medium comprises 0.5% peptone, 1% glucose, 0.1% potassium dihydrogen phosphate (KH 2 PO 4 ), 0.05% magnesium sulfate ( MgSO 4 ‧7H 2 O), 0.25% rose bengal, 0.02% dichloran, 1.5% amaranth, and 0.01% chloramphenicol. After the chilled fresh milk is cultured, two of the aforementioned plate counting mediums of 25 to 250 colonies are selected for counting, and the average number of colonies of the two plate counting mediums is multiplied by the dilution factor, and the total number of microorganisms is obtained.
前述大腸桿菌群以及前述大腸桿菌之檢測方法係將前述冷藏鮮乳經系列稀釋後,以無菌操作方式分取0.1毫升注入一科瑪嘉培養基(CHROMagar ECC)上,迅速利用無菌之曲玻璃棒將前述系列稀釋之冷藏鮮乳均勻塗抹散佈,並於37±1℃環境下進行培養24小時。前述稀釋方法係吸取10倍稀釋之前述冷藏鮮乳10毫升加至90毫升稀釋液中,以依序作成100倍、1000倍、10000倍等一系列稀釋檢測液。前述稀釋液係一0.1%蛋白胴稀釋液;前述科瑪嘉培養基包含3.28%DHROMagar。前述冷藏鮮乳經培養後,選取25至250個菌落之兩個前述平板計數培養基進行計數,將前述兩個平板計數培養基之菌落數平均值乘以稀釋倍數,及得前述微生物總數量。藉由觀察培養後之菌落數顏色來判斷前述微生物之種類,若前述菌落呈現藍色,其為大腸桿菌;若前述菌落呈現紅色,其為其他(糞便的)大腸桿菌群細菌;若前述菌落呈現無色,其為其他革蘭氏陰性菌。 The above-mentioned Escherichia coli group and the above-mentioned Escherichia coli detection method are obtained by serially diluting the above-mentioned chilled fresh milk, and 0.1 ml of the sterilized fresh milk is injected into a Kromagar medium (CHROMagar ECC), and the sterile curved glass rod is quickly used. The above-mentioned serially diluted fresh milk was evenly spread and incubated at 37±1 ° C for 24 hours. In the above dilution method, 10 ml of the above-mentioned chilled fresh milk diluted 10 times is added to 90 ml of the dilution liquid, and a series of dilution detection liquids such as 100 times, 1000 times, and 10000 times are sequentially prepared. The aforementioned dilution is a 0.1% peptone dilution; the aforementioned coma medium contains 3.28% DHROMagar. After the chilled fresh milk is cultured, two of the aforementioned plate counting mediums of 25 to 250 colonies are selected for counting, and the average number of colonies of the two plate counting mediums is multiplied by the dilution factor, and the total number of microorganisms is obtained. The species of the microorganism is determined by observing the color of the colony after the culture, and if the colony is blue, it is Escherichia; if the colony is red, it is other (fecal) bacteria of the E. coli; if the colony is present Colorless, it is another Gram-negative bacteria.
前述80℃耐熱性孢子菌數之檢測方法係將前述冷藏鮮乳利用0.1%蛋白胴稀釋液稀釋10倍,以無菌操作方式分取10毫升、1毫升以及0.1毫升注入100毫升之平板計數培養基,前述平板計數培養基包含0.5%胰化蛋白胴、0.25%酵母抽出物、0.1%葡萄糖以及1.5%洋菜,於80 ℃水浴槽加熱30分鐘,之後迅速置於一冷卻水中。將前述含有冷藏鮮乳之平板計數培養基均分為五份,分別倒入五個平板培樣盤中,於35℃環境下進行培養48小時,並計算菌落數。 The method for detecting the heat-resistant spores of 80 ° C is to dilute the chilled fresh milk by 10 times with a 0.1% peptone dilution, and to dispense 10 ml, 1 ml, and 0.1 ml into 100 ml of the plate counting medium by aseptic operation. The aforementioned plate counting medium contains 0.5% tryptone, 0.25% yeast extract, 0.1% glucose and 1.5% amaranth, at 80 The °C water bath was heated for 30 minutes and then quickly placed in a cooling water. The above-mentioned plate counting medium containing chilled fresh milk was divided into five portions, and each was poured into five plate-shaped plate samples, and cultured at 35 ° C for 48 hours, and the number of colonies was counted.
前述100℃耐熱性孢子菌數之檢測方法係將前述冷藏鮮乳利用0.1%蛋白胴稀釋液稀釋10倍,以無菌操作方式分取10毫升、1毫升以及0.1毫升注入100毫升之DTA培養基(Destrose tryptone agar),於100℃水浴槽加熱5分鐘,之後迅速置於一冷卻水中。將前述含有冷藏鮮乳之DTA培養基均分為五份,分別倒入五個平板培樣盤中,於55℃環境下進行培養48小時,並計算菌落數。 The method for detecting the heat-resistant spores of 100 ° C is to dilute the chilled fresh milk by 10 times with 0.1% peptone dilution, and to dispense 10 ml, 1 ml and 0.1 ml into 100 ml of DTA medium (Destrose) by aseptic operation. Tryptone agar), heated in a 100 ° C water bath for 5 minutes, then quickly placed in a cooling water. The above-mentioned DTA medium containing chilled fresh milk was divided into five portions, and each was poured into five plate culture samples, and cultured at 55 ° C for 48 hours, and the number of colonies was counted.
前述冷藏鮮乳之微生物數量分析結果如表1所示。 The results of microbial analysis of the aforementioned chilled fresh milk are shown in Table 1.
一般前述冷藏鮮乳之殺菌方式以及保存期限,如表2所示(Tamime,A.Y.(Ed.).2009.Milk processing and quality management.p.196.John Wiley & Sons)。 Generally, the sterilization method and shelf life of the aforementioned fresh milk are as shown in Table 2 (Tamime, A.Y. (Ed.). 2009. Milk processing and quality management. p. 196. John Wiley & Sons).
經由比較表1以及表2之結果可知,前述冷藏鮮乳於8℃以及12℃環境下儲存0個月至6個月,並未檢測出任何前述微生物。此結果顯示,藉由本發明之方法,可有效地延長前述冷藏鮮乳之保存期限。 As a result of comparing Table 1 and Table 2, it was found that the aforementioned chilled fresh milk was stored at 8 ° C and 12 ° C for 0 months to 6 months, and no microorganisms were detected. This result shows that the shelf life of the aforementioned chilled fresh milk can be effectively extended by the method of the present invention.
綜上所述,經過本發明所製成之鮮乳,藉由前述濾膜過濾方式,先除去微生物,再配合較溫和之殺菌條件進行殺菌,藉以降低前述鮮乳因高溫所產生之梅納反應,並保留前述鮮乳之原始風味。最後將前述鮮乳於低溫 環境下進行無菌充填包裝,藉以延長前述鮮乳之保存期限。藉由本發明所製造之前述冷藏鮮乳,可避免超高溫瞬間殺菌所造成前述冷藏鮮乳之原始風味之改變,且可使前述冷藏鮮乳於4℃至8℃的環境下,具有至少6個月之保存期限。 In summary, the fresh milk produced by the invention is firstly removed by the filter membrane filtration method, and then sterilized by mild sterilization conditions, thereby reducing the Mena reaction of the fresh milk due to high temperature. And retain the original flavor of the aforementioned fresh milk. Finally, the aforementioned fresh milk is at a low temperature. Sterile filling and packaging in the environment to extend the shelf life of the aforementioned fresh milk. According to the chilled fresh milk manufactured by the present invention, the change of the original flavor of the chilled fresh milk caused by the ultra-high temperature instant sterilization can be avoided, and the chilled fresh milk can have at least 6 in an environment of 4 ° C to 8 ° C. The shelf life of the month.
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