TWI287434B - Method for producing germinated seeds - Google Patents

Method for producing germinated seeds Download PDF

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TWI287434B
TWI287434B TW95110285A TW95110285A TWI287434B TW I287434 B TWI287434 B TW I287434B TW 95110285 A TW95110285 A TW 95110285A TW 95110285 A TW95110285 A TW 95110285A TW I287434 B TWI287434 B TW I287434B
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water
aqueous solution
acid
less
rice
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TW95110285A
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TW200735762A (en
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Yi-Long Lee
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Yi-Long Lee
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Abstract

The present invention is related to a method for producing germinated seeds comprising germinating seeds by an acidic solution. The present invention provides a method for preparing a lower microbial count, a higher germination ratio, and a less off-flavor germinated seeds.

Description

1287434 九、發明說明: 【發明所屬之技術領域】 本發明係一種發芽處理方法,尤指利用電解酸性水催 芽以生產低微生物汙染及無泡水臭味的發芽種子的方法。 【先前技術】 水稻是台灣最主要的糧食作物,米飯則是國人之主 艮近年來’由於健康的追求及報章雜誌、的報導,國人對 於食品的要求,雖然在外觀與口感之外,同時也追求吃的 營養,導致市面上出現許多糙米商品,然而即使已有文獻 祖只越米本身比白米具有較多的營養成分,如:半纖維素、 維生素E、肌醇和米糠醇等,但是由於白米飯口感較好, 所以國人仍然以食用白米的人為多;另一方面,自從加入 WT〇後,東南亞的稻米也陸續在市面上販售,對我國的稻 米農業及市場造成相當的衝擊,所以為了增加我國的稻米 市場競爭能力,並顧及國人的健康,勢必要發展出比一般 糙米更具機能性、更營養的產品。 而糙米發芽後除含糙米原有之多種營養成分外,藉由 發芽帶動的生化代謝作用,蛋白質及醣類等大分子一定程 度的降解為更易消化吸收的醣類、胺基酸等小分子物質, 其中糙米發芽後,更使内含的一個機能性成*_gaba(7_ 胺基丁酸,Gamma-amin〇bUtyric acid)含量大為提升,由 於GABA已被證實具有安定精神、改善失眠、降血壓、促 進子宮及卵巢血液循環、減少更年期障礙及降低初老期症 狀等保健效果,現代台灣社會,生活緊張、銀髮族增多, 4 1287434 較佳 的 是 ,酸性水係 由 方式產生 0 更佳 的 是 ,酸 性水係 由 生。 較佳 的 是 ,酸 性水係 由 更佳 的 是 ,酸 性水係 由 麵胺酸的 方 式產生 〇 電解含有電解質離子水溶液的 電解氣化鈉水溶液的方式產 添加食用有機酸方式產生。 添加醋酸、檸檬酸、蘋果酸或1287434 IX. Description of the invention: [Technical field to which the invention pertains] The present invention relates to a method for germination treatment, and more particularly to a method for producing germinated seeds having low microbial contamination and no odor of water by utilizing electrolytic acidic water germination. [Prior Art] Rice is the main food crop in Taiwan, and rice is the mainstay of the Chinese people. In recent years, due to the pursuit of health and newspapers and magazines, the requirements of the food for the Chinese people, in addition to the appearance and taste, The pursuit of eating nutrition has led to the emergence of many brown rice products on the market. However, even if the ancestors of the literature have more nutrients than white rice, such as hemicellulose, vitamin E, inositol and rice sterol, Rice tastes better, so the Chinese still use more people who eat white rice. On the other hand, since joining WT, Southeast Asian rice has also been sold in the market, which has caused considerable impact on China's rice agriculture and market, so To increase the competitiveness of China's rice market and take into account the health of Chinese people, it is necessary to develop products that are more functional and nutritious than ordinary brown rice. After germination of brown rice, in addition to the various nutrients contained in brown rice, macromolecules such as proteins and sugars are degraded to a more digestible and absorbing sugar, amino acid and other small molecular substances by germination-driven biochemical metabolism. After the germination of brown rice, the content of a functional one is *_gaba (7-aminobutyric acid, Gamma-amin〇bUtyric acid) is greatly increased, because GABA has been confirmed to have a stable spirit, improve insomnia, lower blood pressure It promotes the blood circulation of the uterus and ovaries, reduces menopausal disorders, and reduces the health effects of aging symptoms. In modern Taiwanese society, life is tense and the number of silver-haired people increases. 4 1287434 Preferably, the acidic water system produces 0. More preferably, The acidic water system is produced by nature. Preferably, the acid water system is more preferably produced by the method of adding an acid organic acid to an aqueous solution of an aqueous solution of an electrolytic solution containing an aqueous solution of an electrolytic solution. Add acetic acid, citric acid, malic acid or

較佳的是,酸性水為PH 2.3至pH 6.5。 更佳的是,酸性水為pH3 〇 5 〇 較佳的是’種子為花生、綠豆、黃豆或糙米。 種經由前述之方法所獲製的發芽種 本發明另相關於一 子0 由上所述,可了解本發明所提供之發芽處理方法,使 用電解酸性水進行發芽種子的製作,由於能有效降低生菌 數y;肖除泡水臭味,進而提高發芽率,並避免可能使用化 鲁學藥劑的情形,例如漂白水;因而建立比傳統發芽種子生 產製程更符合衛生要求且品質更好的發芽種子產品,更進 一步,由f驗結果可以發現,經本發明之酸性水處理的種 子錢芽率變異係數小,亦即發芽率均一,所生產的種子 負一致,因此,藉由本發明的發芽處理方法可推出具市 %潛力之發芽種子類產品,以提升國產農產品之競爭力。 【實施方式】 本發明係相關於一種發芽處理方法,其係利用酸性水 抑制微生物生長以使種子發芽的方法,更進一步藉由具有 1287434 因此可以有效抑制微生物 弱酸性的電解水提供殺菌效果 生長。 本發明所利用的酸性水,其可Λ 人 馬添加食用有機酸或其 他可s用的酸性物質,諸如醋酸、 Λ^ 頻果®文、彳争樣酸或麩胺 酉欠寻,以達到本發明所欲的酸性水。 在本發明中較佳的是, …係精由電解含有低濃度電解質離 库卞的水溶液,以獲取酸 性水。本發明的較佳具體實施例中,係以低濃度氣化納水 浴液’利肖電解原理將戈化納水溶液經由電極的分解,使 得水中微量的金屬離子平衡產生變化,在陽極產生ρΗ值 較低’供外用消毒的『酸性水』。Preferably, the acidic water is from pH 2.3 to pH 6.5. More preferably, the acidic water is pH 3 〇 5 〇 Preferably, the seed is peanut, mung bean, soybean or brown rice. A germinated seed obtained by the above method. The present invention is further related to a sub-zero. From the above, the germination treatment method provided by the present invention can be understood, and the production of germinated seeds using electrolytic acidic water can effectively reduce the growth. The number of bacteria y; in addition to soaking water odor, thereby increasing the germination rate, and avoiding the possibility of using chemical agents, such as bleach; thus establishing a germinating seed that is more hygienic and of better quality than the traditional germinated seed production process. The product, further, can be found from the results of the test, the seed milk bud rate variation coefficient of the treated by the acidic water of the invention is small, that is, the germination rate is uniform, and the produced seeds are negatively consistent, and therefore, the germination treatment method of the present invention can be used. Launched sprouted seed products with the potential of the market to enhance the competitiveness of domestically produced agricultural products. [Embodiment] The present invention relates to a germination treatment method which is a method for inhibiting the growth of microorganisms by using acidic water to germination of seeds, and further provides a bactericidal effect growth by electrolyzed water having 1287434 which can effectively suppress microbial weak acidity. The acidic water utilized in the present invention can be added to an edible organic acid or other acidic substance such as acetic acid, 频 ® 彳, 彳 样 或 or glutamine to find the present invention. The desired acidic water. In the present invention, it is preferred that the system extracts an aqueous solution containing a low concentration of electrolyte from the reservoir to obtain acid water. In a preferred embodiment of the present invention, the decomposition of the aqueous solution of Gehuana via the electrode is carried out by using a low-concentration gasification nano-water bath 'Lee Xiao electrolysis principle, so that a trace amount of metal ions in the water changes, and a value of ρ 在 is generated at the anode. Low 'acidic water' for external disinfection.

電解酸性水目前已知具殺菌效能,其殺菌功能除來自 其低ΡΗ值外,主要是成分中包括有效氣成分如^(氯氣)、 H/CI (次氯酸)及〇cr(次氯酸根離子)(了才_夕_研究 彙、為’ 1 997)’次氣酸為主要之有效氯且殺菌效果最強。H〇c| 是一種具揮發性的物質,在電解後氣氣與水反應形成 H〇CI,隨PH值逐漸降低,使得ci2揮發致有效氣不斷減 少。故在一開放系統中,可利用的氯亦會逐漸揮發消失。 根據文獻指出電解酸性水具有下列特點: (1) 酸性水在室溫密閉下能維持2至3天穩定。 (2) 具瞬間殺菌效果可殺死致病的細菌。 (3) 由食鹽加水電解而成,成本低廉。 (4) 經過許多醫院檢試,對眼睛、皮膚、口腔、食道、 月黏膜%•’不會造成刺激與傷害。 (5) 酸性水作用後會還原為普通水,不會造成殘留而污 7 J287434 染環境。 而目前電解酸性水在產業上之應用,包括有廚房、餐 廳、食品加工廠中作業員手部、環境或食品清潔…的 洗務(砧板、刀、碗盤及毛巾等),在醫院則是對内部感染 的預防及醫藥設備的清洗與衛生。而在農業上,有文獻則 是使用在蛋殼與洗務消毒或家畜類糞便除臭。而目前在水 產業中的使用包括有魚的清洗消毒及除臭,並且比較電解 酸,水與自來水分別對不同水產物如娃魚片及田螺等之水 產=進行清洗試驗,發現電解酸性水對水產物的殺菌效果 稍同於自來水;同時也發現經電解酸性水處理過的魚肉之 κ值及彻上升較為緩慢,進而可延長保存期限。根據日 本電解水機製造商的技術資料(Ann〇nym〇us,1 997),顯示 電解酸性水對如三甲基胺(TMA)及甲基硫醇等惡臭物質, 可藉由電解酸性水對其之氧化作用而達到除臭效果。而Electrolyzed acidic water is currently known to have bactericidal efficacy. In addition to its low enthalpy value, its bactericidal function mainly includes effective gas components such as ^ (chlorine), H/CI (hypochlorous acid) and 〇cr (hypochlorite). Ion) (the only _ _ _ research sink, for '1 997) 'secondary acid is the main effective chlorine and the sterilization effect is the strongest. H〇c| is a volatile substance. After electrolysis, the gas reacts with water to form H〇CI, which gradually decreases with the pH value, so that the effective gas of ci2 is continuously reduced. Therefore, in an open system, the available chlorine will gradually disappear and disappear. According to the literature, electrolytic acidic water has the following characteristics: (1) Acidic water can be stable for 2 to 3 days at room temperature. (2) Instant bactericidal effect kills pathogenic bacteria. (3) It is made by electrolysis of salt and water, and the cost is low. (4) After many hospital tests, there will be no irritation or injury to the eyes, skin, mouth, esophagus, and mucous membranes. (5) After the action of acidic water, it will be reduced to ordinary water, which will not cause residue and pollution. 7 J287434 Dyeing environment. At present, the application of electrolytic acid water in the industry includes washing (chopper, knife, dish and towel) in the kitchen, restaurant, hand of the food processing factory, the environment or food cleaning... in the hospital. Prevention of internal infections and cleaning and sanitation of medical equipment. In agriculture, there is literature on the use of eggshells and decontamination or defecation of livestock manure. At present, the use in the aquaculture industry includes the cleaning, disinfection and deodorization of fish, and compares the electrolytic acid, water and tap water to the aquatic products of different water products such as squid and snails, respectively, and the electrolytic acid water is found. The bactericidal effect of the water product is slightly the same as that of the tap water; it is also found that the κ value of the fish treated with the electrolytic acid water is relatively slow and the storage period is extended. According to the technical data of the manufacturer of Japanese water ionizers (Ann〇nym〇us, 1 997), it is shown that electrolytic acidic water is used to treat malodorous substances such as trimethylamine (TMA) and methyl mercaptan. Its oxidation effect achieves the deodorizing effect. and

IzUmi ( 1 999 )運用4G倍量的電解酸性水清洗蘿萄、获菜 及馬鈴薯等蔬菜,發現皆可有效的降低生菌數及大腸桿菌 =數二另外Suzuki(1 996)利用酸性水試驗於各種病原菌 ’毋之試驗,試驗結果表示酸性水對於廚房_般性 ,和主要食物中毒菌-鏈黴菌屬(加咖野⑽)有殺 菌效果。 由於電解酸性水具有抑菌作用,故本發明採用電解酸 性水進行種子浸泡,讓該電解酸性水在浸泡過程中對微生 物產生抑制作用;所以在發芽過程中’可解決浸泡過程生 菌數過高的問題。 8 1287434 具體而言,電解酸性水之Η佶总人μ 〈PH值係介於ρΗ2 〇到ρΗ7 〇 之間’而使用pH 4.0之電解酸性水當作浸泡水,對發芽種 子之營養成分r·胺基丁酸及維生素E並無不良影響,同 時又擁有較低的生菌數及較高的發芽率。 因此’本發明所提供之發穿步 < %牙處理方法,主要的特點在 於:將種子以電解酸性水催芽以冷 丨隹才Μ生產發芽種子,以期產生 术又函效果並消除泡水引發的臭味, 六不且具有良好的外觀而能IzUmi (1 999) used 4G times of electrolytic acid water to clean vegetables such as radish, vegetables and potatoes, and found that it can effectively reduce the number of bacteria and E. coli = number two. Suzuki (1 996) used acidic water test. The test of various pathogens, the test results indicate that the acidic water has a bactericidal effect on the kitchen, and the main food poisoning bacteria - Streptomyces (Gaya (10)). Since the electrolytic acidic water has a bacteriostatic action, the present invention uses electrolytic acidic water for seed immersion, so that the electrolytic acidic water inhibits microorganisms during the immersion process; therefore, the number of bacteria in the immersion process can be solved too high during the germination process. The problem. 8 1287434 Specifically, the total amount of 电解 电解 〈 〈 〈 〈 〈 〈 Η佶 Η佶 Η佶 Η佶 Η佶 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解 电解Aminobutyric acid and vitamin E have no adverse effects, while having a lower number of bacteria and a higher germination rate. Therefore, the hair threading method provided by the present invention has the main features of: germination of seeds with electrolytic acidic water to produce germinated seeds by cold sputum, in order to produce a surgical effect and eliminate the initiation of water soaking. The smell, six does not have a good appearance and can

提供品質更優秀的發芽種子。 在本發明中所指白勺『種子』意指各類植物的種子,不 限於可食用或不可食用之種子,較佳的是,可食用的種子 包含雙子葉植物種子及單子夜植物種子,例如:黃豆、綠 豆、花生、糙米。由於種子經發芽後,其種子内所含的營 養成分較發芽前不同,據研究顯示,發芽種子含有較高的 機能性物質,例如r -胺基丁酸(GABA),因此,食用發芽 種子可進一步提供攝食者不同於未發芽種子的營養成分。 由文獻可知,在植物組織遇到不同刺激時,這些刺激 的壓力會引發一條信號傳遞之路徑,藉增加細胞漿鈣含量 來活化Ca2+/攜舞蛋白依賴型麩胺酸去魏酶(ca|m〇d山independent glutamate decarboxylase)活性 ,促進 GABA 合成,如觸碰等緊迫因子誘發之GABA蓄積反應,即是利 用此種增加細胞質的Ca2+含量方式。此外提高H+和受質 含量也可刺激GAD (glutamate decarboxylase麵胺酸去叛 酶)活性,GAD乃細胞漿的酵素,其活性與發芽率呈高度 正相關,GABA蓄積主要是由GAD所調節。體外GAD最 9 1287434 適PH為酸性約pH5 5, n κ 、PH7.0缺乏ca2 +下則僅具有_ 妓活性。不論胞内和 頁季二 刺激GAD活性蓄積,體外= 象均暗示降低細胞質卟會 較GAD蓄積為先 ::已證明細胞質H +增加程度 pq & 數展境因素刺激GABA蓄積均為 間接的利用細胞質pH降低 ^ , …Provide better quality germinating seeds. The term "seed" as used in the present invention means a seed of various plants, and is not limited to edible or inedible seeds. Preferably, the edible seeds comprise dicotyledon seeds and single-night plant seeds, for example : Soy beans, mung beans, peanuts, brown rice. Since the seeds are germinated, the nutrients contained in the seeds are different from those before germination. According to research, the germinated seeds contain higher functional substances, such as r-aminobutyric acid (GABA). Therefore, the edible germinated seeds can be used. Further providing the nutrients of the ingestor different from the ungerminated seeds. It is known from the literature that when plant tissues encounter different stimuli, the pressure of these stimuli triggers a signalling pathway to activate Ca2+/carrying protein-dependent glutamate deferase (ca|m) by increasing cytosolic calcium content. Ind mountain independent glutamate decarboxylase) activity, promote GABA synthesis, such as contact and other agonistic factors induced by GABA accumulation, that is, the use of this way to increase the cytoplasmic Ca2+ content. In addition, increasing H+ and substrate content can also stimulate GAD (glutamate decarboxylase) activity. GAD is a cytoplasmic enzyme whose activity is highly positively correlated with germination rate. GABA accumulation is mainly regulated by GAD. The in vitro GAD of the most 9 1287434 is suitable for acidic pH of about 5 5, n κ, PH7.0 lack of ca2 + only _ 妓 activity. Regardless of intracellular and squamous stimulating GAD activity accumulation, in vitro = elephants suggest that lowering cytoplasmic sputum is more important than GAD accumulation:: cytoplasmic H + increase has been demonstrated pq & number of context factors stimulate GABA accumulation are indirect use Cytoplasmic pH is lowered ^, ...

— 命低。在本發明中較佳的酸性水pH— Life is low. Preferred acidic water pH in the present invention

值乾圍為PH3.0-5.0。 P 以下揭露本發明之齡The value of the dry circumference is PH3.0-5.0. P discloses the age of the present invention

— aι枚佳具體實施例,以說明本發明之 貫施方法及所達到的效果。 所有在本說明書中引述之專利及發表刊物均併入本發 明作為參考資料。 [儀器設備] 本實施例所採用的儀器設備包括有: 1·迴轉式振盪培養箱(shaking incubator) : S300R, Firstek,臺灣。 2·無菌操作檯(laminar flow) : 2ht-24,淳美(股)公司, 臺灣。 3·恆溫水槽(water bath) : BC-2D,WISDOM,臺灣。 4 ·高效率液相層析儀(Η P L C): 幫浦(pump) : L-6200,Hitachi, Co.Ltd·,Tokyo, Japan. 檢測器(UV-VIS detector): L-4200,Hitachi, Co.Ltd., Tokyo, Japan. 管柱(〇〇丨11»11门):尺卩-18,6卩250-4.6(5/7〇1),關東化學 株式會社,Japan. 5·高速冷凍離心機(centrifuge): All eg ra 64R Backman 1287434— a specific embodiment to illustrate the method of the present invention and the effects achieved. All patents and publications cited in this specification are incorporated herein by reference. [Instrument Equipment] The equipment used in this embodiment includes: 1. Rotary incubator (Singapore incubator): S300R, Firstek, Taiwan. 2. Aseptic console (laminar flow): 2ht-24, comparable to the company, Taiwan. 3. Water bath: BC-2D, WISDOM, Taiwan. 4 · High-efficiency liquid chromatograph (Η PLC): Pump: L-6200, Hitachi, Co.Ltd,, Tokyo, Japan. Detector (UV-VIS detector): L-4200, Hitachi, Co.Ltd., Tokyo, Japan. Pipe column (〇〇丨11»11门): Ruler -18,6卩250-4.6(5/7〇1), Kanto Chemical Co., Ltd., Japan. 5·High speed freezing Centrifuge: All eg ra 64R Backman 1287434

Coulter, USA 6·粉碎機(crusher) : DM-6,佑崎機械,臺灣。 7.超音波振盪器(ultrasonic cleaner) : D-78224,El ma, Germany. 8·ρΗ 測定儀(ph meter) : SP-2200, Suntex,臺灣。 9.植物生長箱(growth chamber) : 747FH,WISDOM, 台灣 1〇_手&型超酸化水生成器:AL-700,Mettle r-Toledo, _ Switzerland 在本發明所使用的縫米,係由台中農業改良場提供, 為台梗9號糖米,民國93年二期稻。 貫施例一:發芽縫米的催芽方法 製備杳芽糙米之方法為:取縫米1 〇〇粒,置於5〇毫 升k杯中"沿著杯壁緩緩加A 3〇冑升經過超音波震盈除 氣處里20刀4里的自來水,將浮在液面上的趟米以玻棒壓 入液面下’並輕輕㈣’使附著於糖米表面的空氣排出, 後放入一層發泡塑膠膜於液面上,以隔絕外界空氣進入 燒杯中。將經過上述處理後的㈣移人抓、叫95%的 黑暗植物生長箱中,進行催芽24小時,收集芽長〇5·,麵 之發芽糙米。 實施例二:浸泡用水對發芽糙米之影響 2·1不同浸泡用水處理糙米之處理方法 席=酸性水⑼ectrolyzed acidic wate「),是利用電解 原里將W通自來水或加入低濃度的氣化納溶液再經由電極 11 1287434 的分解,使得水中金屬離子平衡產生變化,在陽極產生pH 值較低,供外用消毒的『酸性水』。電解酸性水目前已知 具殺菌效能,主要是成分中包括有效氣成分如ci2(氣氣)、 H0C1 (次氯酸)及〇cr(次氯酸根離子),次氣酸為主 要之有效氣且殺菌效果最強。 為瞭解浸泡用水對發芽糙米的影響,本發明人以自來 水及電解酸性水分別處理糙米,並進行試驗比較其差異。 製、備一自來水浸泡發芽糙米及一電解酸性i浸泡發芽糙 米’並進行試驗以比較縫米、該自來水浸泡發芽輪米及該 電解酸性水浸泡發芽趟米在生菌數、發芽率及gaba含量 和品評得分方面的差異。 取2_5克(約1〇〇粒)的台梗9號趟米以脫氣2〇分鐘的 自來水或脫氣20分鐘的ρΗ 4·〇電解酸性水分別進行浸泡, 將脫氣水緩緩倒入糙米中,於浸泡的燒杯頂部覆蓋一層泡 棉’以隔絕空氣;接著將之移入黑暗的植物生長箱中^显声 及濕度控制於25。〇嶋%,經催芽24小時後,得到該: 來水浸泡發芽糙米及該電解酸性水浸泡發芽糙米。〆 2 · 2不同浸泡用水處理糙米之試驗結果 2·2·1生菌數分析 將縫米、自來水浸泡發芽縫米及電解酸性水浸泡發芽 糙米絞碎後,以無菌水稀釋至適當倍數’再利用pca培養 ,(Merck, Germany)於3rc下進行培養48小時後:計 算其菌落數。每個處理作六重複。所得結果如表,所示。 表1 ·不同浸泡用水處理糙米所得的生菌數 12 .1287434 樣品種類 台梗9號糙米 自來水浸泡發 芽糙米 電解酸性水浸 泡發芽糙米 生菌數(106/g) ----- 2. 98±〇. 65a 7· 45±〇· 25b 2· 92±〇· 6la 表中所列數值為平均值±標準差 同項目中標有不同英文字母者其值有明顯差異 (P<0.05) 由表1的數據來看,可知於溫度25r下,以自來水浸 =24小時之後’其生菌數明顯比未催芽之糙米增加了 2: 倍’而利用pH 4.G的酸性水浸泡24小時後,其生菌數不 :明顯低於自來水浸泡的發芽糙米’甚至還比:催芽的糙 米的生菌數低些’確可改善傳統發芽糖米生產方法之催芽 過程中可能導致生g數過高以致^引發衛生疑慮的問題。 2 · 2 · 2發芽率比較 在本發明中,發芽率係以下式計算: ^芽率(% ) ·(發芽縫米數/取樣糙米數)χ彳〇〇% # ^ 糙米、自來水浸泡發芽糙米及電解酸性水浸泡發 米之發芽率。每個處理作三重複。所得結果如表 yj\ 〇 * 樣品種類Coulter, USA 6. Crusher: DM-6, Yusaki Machinery, Taiwan. 7. Ultrasonic cleaner: D-78224, El ma, Germany. 8·ρΗ analyzer (ph meter): SP-2200, Suntex, Taiwan. 9. Plant growth chamber: 747FH, WISDOM, Taiwan 1〇_Hand & type super acidified water generator: AL-700, Mettle r-Toledo, _ Switzerland The sewing rice used in the present invention is The Taichung Agricultural Improvement Field provides the No. 9 sugar rice in Taiwan, and the second rice in the Republic of China in 1993. Example 1: The germination method of germinated seam rice The method for preparing axillary bud brown rice is as follows: take the seam rice 1 〇〇 granules and place it in a 5 〇 ml k cup " slowly add A 3 沿着 along the wall of the cup Ultrasonic shock and degassing 20 knives of 4 tap water in the degassing place, the glutinous rice floating on the liquid surface is pressed into the liquid surface with a glass rod 'and gently (four)' so that the air attached to the surface of the sugar rice is discharged, and then placed A layer of foamed plastic film is placed on the liquid surface to insulate the outside air into the beaker. After the above treatment (4), it was transferred to a 95% dark plant growth box, and germinated for 24 hours to collect the germinated brown rice. Example 2: Effect of soaking water on germinated brown rice 2. Treatment of brown rice by different soaking water treatments = acidic water (9) ectrolyzed acidic wate "), using electrolysis raw materials to pass W tap water or adding low concentration gasification nano solution Then, through the decomposition of the electrode 11 1287434, the balance of the metal ions in the water changes, and the "acid water" which is low in pH value for external use is sterilized at the anode. The electrolytic acid water is currently known to have bactericidal efficacy, mainly including effective gas in the composition. Ingredients such as ci2 (air gas), H0C1 (hypochlorous acid) and 〇cr (hypochlorite ion), hypogastric acid is the main effective gas and has the strongest bactericidal effect. In order to understand the effect of soaking water on germinated brown rice, the inventor The brown rice was treated separately with tap water and electrolytic acid water, and the difference was tested. The preparation and preparation of a tap water soaked germinated brown rice and an electrolytic acid i soaked germinated brown rice were tested to compare the sewn rice, the tap water soaked fermented rice and the The difference in the number of bacteria, germination rate, gaba content and evaluation score of immersed glutinous rice in electrolytic acid water. Take 2_5 grams ( 1 〇〇 ) 的 台 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 9 The top of the beaker is covered with a layer of foam to isolate the air; then it is moved into a dark plant growth box. The sound and humidity are controlled at 25. 〇嶋%. After 24 hours of germination, the water is obtained. The electrolytic acid water soaks the germinated brown rice. 试验2 · 2 test results of different immersion water treatment of brown rice 2·2·1 bacteria number analysis After sewing rice, tap water soaked germinated seam rice and electrolytic acid water soaked germinated brown rice, Dilute the sterile water to the appropriate multiples and re-use pca culture (Merck, Germany) for 48 hours at 3 rc: calculate the number of colonies. Each treatment was repeated six times. The results are shown in the table. The number of bacteria obtained by soaking water to treat brown rice 12.1287434 Sample type Taiwan stalk 9th brown rice tap water soaked germinated brown rice electrolytic acid water soaked germinated brown rice bacteria number (106/g) ----- 2. 98±〇. 65a 7 · 45±〇· 25b 2· 92±〇· 6la The values listed in the table are the mean±standard deviation. The values marked with different English letters in the project are significantly different (P<0.05). From the data in Table 1, it can be seen that at temperature 25r, After tap water immersion = 24 hours, the number of bacteria was significantly increased by 2: times than that of ungerminated brown rice. After soaking for 24 hours with acidic water of pH 4.G, the number of bacteria was not: significantly lower than that of tap water. Germinated brown rice is even better than the fact that the number of bacteria in the germinated brown rice is lower, which can improve the problem that the gypsum process of the traditional germinated sugar rice production method may cause the g-growth to be too high and cause health concerns. 2 · 2 · 2 germination rate comparison In the present invention, the germination rate is calculated by the following formula: ^ bud rate (%) · (germination seam number / sampled brown rice number) χ彳〇〇 % # ^ brown rice, tap water soaked germinated brown rice And germination rate of soaked rice in electrolytic acid water. Each process is repeated three times. The results obtained are shown in the table yj\ 〇 * sample type

來水浸泡發 芽糙米 水處理糙米所得的發芽率 κ 一 發芽率 (%) 51. 67±11. 841 (CV= 22. 91%) 13 1287434 79. 〇±4· 32丨 46%) 電解酸性水浸 泡發芽糖米 -----~----- 表中所列數值為平均值土標準差 同項目中標有不同英 (p<0.05) 央文予母者其值有明顯差異 有較面广表2可!現經酸性水處理_, / 2的數據還顯示電解酸性水處理的糙 變異係數(cv)只有5.46%,而以自 二 =率之變異係數則為22.91%,由此可見以電解酸性者 水處理所得發諸米之μ較 管與生產作業是較為有利的。 牙‘未之品 2·2.3 胺基丁酸之定量分析 [r -胺基丁酸萃取] 取縫米粉末1克置於35毫升之離心管中,再加入1〇 毫升75%的乙醇,搖動離心管使縫米粉末均句分散,於7〇 。(:下水浴振i(15〇 rpm)1小時後,以離心力2q,刪%, 冷凍離心20分鐘,收集上澄液,沉澱物再加入1〇毫升75% 的乙醇進行第二次水浴振i萃取,重複上述步驟後,將兩 次所得之上澄液合併,即得初步萃取液,此萃取液在45乞 下,以減壓濃縮機濃縮至乾,加入0.5毫升,〇 〇2N Hc丨 (Merck,Germany)溶液,將濃縮物洗出收集之,再以 離心力20,〇〇〇xg,在4°C離心20分鐘,移出上澄液,即 為7 -胺基丁酸萃取液,將其置於冰箱中儲存,待7 _ 胺基丁酸測定。 [T -胺基丁酸定量] 14 1287434 本實施例採柱前衍生化之方法,以高效液相層析儀 (HPLC) ’對7 -胺基丁酸進行分析。取彳〇"L厂胺基丁酸萃 取液加入70以衍生化試劑(AQC)專用緩衝液(AccQ Tag WAT052880 ’ Waters)與 20/yL 衍生化試劑(AccQ. Tag WA1T052880 ’ Waters),總體積為100//L,使其均勻混合 後,靜置1分鐘,使未與樣品中7 _胺基丁酸作用的AQc 試劑自行分解後,在50°C水浴中加熱1 〇分鐘,使7 •胺基 丁酸與衍生化試劑結合,冷卻至室溫,以〇 2/Vm過濾膜免 濾’取20/vl進行HPLC分析,以標準曲線求得7 -胺基丁 酸含量。每個處理作三重複。 高效液相層析條件: 幫浦:L-6200 (Hitachi) 管柱·· RP_18, GP250-4.6 (5//m),關東化學株式會社, Japan ° 檢測器· L-7485,Hitachi, Co. Ltd·,Tokyo, Japan 螢光檢測器 >iex=295nm,Mem = 395nm 移動相: A液 母升溶液中含19.0g醋酸納-3-水合物(sodium acetate-3-hydrate)、6·0 g 正構酸(ortho-phosphoric acid) 與2_0 g三乙胺(triethylamine),再調pH至5.15,以純水 定量至1升。 B液 60% acetoitrile/ H2〇 15 1287434 流速·· 1 ml/min 表3· r-胺基丁酸HPLC分析之移動相梯度混合比例Germination rate κ germination rate (%) obtained by immersing germinated brown rice water in water treatment 51. 67±11. 841 (CV= 22.91%) 13 1287434 79. 〇±4· 32丨46%) Electrolyzed acidic water Soaked germinated sugar rice-----~----- The values listed in the table are the average standard deviation of the soil. The standard is different from the standard in English (p<0.05). The value of the parent is significantly different.广表2可! The data of acid water treatment _, / 2 also shows that the coefficient of variation (cv) of electrolytic acid water treatment is only 5.46%, and the coefficient of variation from the two = rate is 22.91%. It is advantageous to treat the resulting rice with the electrolytic acid water treatment and the production operation. Quantitative analysis of the tooth '2'2.3 Aminobutyric acid [r-Aminobutyric acid extraction] 1 gram of the split rice powder was placed in a 35 ml centrifuge tube, and then 1 liter of 75% ethanol was added and shaken. The centrifuge tube disperses the split rice powder at 7〇. (: After 1 hour of water bathing vibration i (15 rpm), centrifuge 2%, remove %, freeze and centrifuge for 20 minutes, collect the supernatant, and add 1 liter of 75% ethanol to the second water bath. After the above steps are repeated, the obtained supernatants are combined twice to obtain a preliminary extract. The extract is concentrated to dryness under a reduced pressure of 45 Torr, and 0.5 ml of 〇〇2N Hc丨 is added. Merck, Germany) solution, the concentrate is washed out and collected, centrifuged at 20 °, g xg, centrifuged at 4 ° C for 20 minutes, remove the supernatant, which is 7-aminobutyric acid extract, Store in a refrigerator and store with 7 _ aminobutyric acid. [T-Aminobutyric acid quantitation] 14 1287434 This example is a pre-column derivatization method using high performance liquid chromatography (HPLC) '7 -Aminobutyric acid was analyzed. Add 彳〇"L plant aminobutyric acid extract to 70 to derivatization reagent (AQC) special buffer (AccQ Tag WAT052880 'Waters) and 20/yL derivatization reagent (AccQ. Tag WA1T052880 'Waters), the total volume is 100//L, so that it is evenly mixed, let stand for 1 minute, so that it is not in the sample 7 _ The amino acid butyric acid-reactive AQc reagent is decomposed by itself and heated in a 50 ° C water bath for 1 , minutes to combine 7 • aminobutyric acid with a derivatizing reagent, cooled to room temperature, and filtered at 〇 2/Vm filter. ' Take 20/vl for HPLC analysis and determine the 7-aminobutyric acid content from the standard curve. Each treatment is repeated three times. High performance liquid chromatography conditions: Pump: L-6200 (Hitachi) Column ·· RP_18 , GP250-4.6 (5//m), Kanto Chemical Co., Ltd., Japan ° Detector · L-7485, Hitachi, Co. Ltd., Tokyo, Japan Fluorescence Detector >iex=295nm, Mem = 395nm Mobile Phase : A liquid mother solution contains 19.0g of sodium acetate-3-hydrate, 6.00g of ortho-phosphoric acid and 2_0g of triethylamine. Adjust pH to 5.15, quantify to 1 liter of pure water. B solution 60% acetoitrile / H2 〇 15 1287434 flow rate · · 1 ml / min Table 3 · r-aminobutyric acid HPLC analysis of mobile phase gradient mixing ratio

土 4·不同浸泡用水處理糙米所得的Gaba含量 樣品種類Soil 4·Gaba content obtained by treating brown rice with different soaking waters

台梗9號糖米 自來水浸泡發 芽糙:米 電解酸性水浸 泡發芽糙米 10·42±0.88a 10.98±1. 〇9a 表中所列數值為平均值±標準差 * * 同項目中標有不同英文字母者其值有明顯差異 (Ρ<0·05) 由表4可知,r -胺基丁酸蓄積主要可能是由麩胺酸去 羧酶所調節,其是細胞質内之酵素,其活性與發芽率成高 度正相關。故糙米發芽後,其r •胺基丁酸含量增加了約2 七’以自來水與酸性水浸泡者分別由5·25增加為1 〇 42 及1 0.98 mg/1 〇〇g d.b.(表4),兩者浸泡水處理後之發芽 糙米r-胺基丁酸含量無顯著差異,實驗結果顯示pH4之 16 1287434 電解酸性水對發芽糙米7 _胺基丁酸含量的提升與自來水浸 泡之影響並無差異。 2.2.4電解酸性水與自來水浸泡發芽糙米之氣味喜好 性品評 本實驗以20位品評員採九分制進行氣味喜好性之感 官品評,其中九分代表最喜歡,五分代表不喜歡也不討厭, 一分代表最不喜歡,每位品評員均須同時品評上述兩種種 樣品。品評時就發芽糙米之氣味(〇d〇r)進行評分。 供品評發芽糖米樣本係將自來水浸泡及電解酸性水浸 泡各24小時之發芽糙未經濾紙輕輕吸乾其表面水份後, 各取約20公克,放入50m丨玻璃燒杯,其上以保鮮膜蓋住 並以橡皮筋綁緊,於品評時,請品評員鬆開保鮮膜,就發 芽糙米氣味之喜好性加以品評,又,品評係在室溫下進行。 品評結果如表5所示,由該表發現利用pH4〇的酸 性水浸泡處理後之發芽糙米的喜好性評分為6 33分高於自 來水浸泡的4.97分’故電解酸性水應可預防在催芽:間因 雜菌生長而造成不良氣味產生或一些不好的代謝產物味道 生成。 樣品種類 自來水浸泡發 芽糙米 電解酸性水浸 泡發芽糙米 不―泡用水處理見能品評 品評得分 --------- 4. 92±〇· 76b 6· 33±1· 6〇a 表中所列數值為平均值±標準差 17Taiwan stalk 9 sugar rice tap water germination rough: rice electrolytic acid water soaked germinated brown rice 10·42±0.88a 10.98±1. 〇9a The values listed in the table are mean ± standard deviation * * The same item is marked with different English letters The values are significantly different (Ρ<0·05). As can be seen from Table 4, the accumulation of r-aminobutyric acid may be mainly regulated by glutamate decarboxylase, which is an enzyme in the cytoplasm, its activity and germination rate. It is highly positively correlated. Therefore, after germination of brown rice, the content of r-aminobutyric acid increased by about 2 VII', and the soaking of tap water and acidic water increased from 5·25 to 1 〇42 and 1 0.98 mg/1 〇〇g db, respectively (Table 4). There was no significant difference in the content of r-aminobutyric acid in the germinated brown rice after soaking with water. The experimental results showed that the pH of 16 1687434 electrolytic acid water had no effect on the content of germinated brown rice 7-aminobutyric acid and tap water soaking. difference. 2.2.4 Electrolytic acid water and tap water soaked germinated brown rice scent preference product evaluation This experiment uses 20 people to take the nine-point system for the sensory evaluation of odor preference, of which nine points represent the most favorite, five points do not like or hate One point represents the least favorite, and each reviewer must evaluate both samples. The scent of germinated brown rice (〇d〇r) was scored during the evaluation. The product evaluation of the germinated sugar rice sample was immersed in tap water and electrolytic acid water for 24 hours. The germinated brown water was gently blotted to the surface water without filter paper, and then about 20 grams was taken into a 50m glass beaker. The plastic wrap is covered and tied with a rubber band. During the evaluation, the reviewer is asked to loosen the wrap and evaluate the taste of the germinated brown rice. The evaluation is carried out at room temperature. The results of the evaluation are shown in Table 5. It is found that the preference score of the germinated brown rice after soaking with acidic water of pH 4〇 is 6 33 points higher than 4.97 points of tap water soaking. Therefore, the electrolytic acidic water should be prevented from germination: A bad odor is generated due to the growth of the bacteria or some bad metabolites are produced. Sample type, tap water, germinated, germinated brown rice, electrolytic acid water, soaked germinated brown rice, not treated with water, see the evaluation of the quality evaluation grade --------- 4. 92±〇· 76b 6· 33±1· 6〇a Column values are mean ± standard deviation 17

【圖式簡單說明】 無 ,1287434 同項目中標有不同英文字母者其值有明顯差異 (P<0.05) 2 · 3結論 八综/上述結果可知,經浸泡催芽之發㈣米之營養成 =私基丁 g文均有所提升,同時使用pH 4 〇之電解酸性 ▲ t /又泡水者又擁有比自來水浸泡者較低的生菌數及較 :且較均句的發芽率’同時喜好性感官品評之氣味品評, 也是電解酸性水的評分高於自、來水。 根據本發明可竹> Τ π ^ .了作之不同修正及變化對於熟悉該項技術 者而&均顯然不會偏離本發 Μ明的耗圍與精神。雖然本發明 已敘述特定的較佳且艚塞 干狂w體事貫,必須 不當地限制於該等特定且體事奋卜卜疋本土月不應被 權★太品似▲ 、體事只上。在貫施本發明之已述 、:,子於熟習該項技術者而言顯而易知之不同佟正 亦被涵蓋於τ列巾請專利範圍之内。 Μ正 【主要元件符號說明】[Simple description of the schema] None, 1287434 There are significant differences in the values of different English letters in the same project (P<0.05) 2 · 3 Conclusions Eight comprehensives / The above results show that the immersion germination hair (four) meters of nutrition into private The Keding G text has been improved, and the acidity of pH 4 〇 is also used. ▲ t / and soaked water have a lower number of bacteria than the tap water soaking person: and the germination rate of the more uniform sentence 'also likes sexy The odor evaluation of the official evaluation is also higher than that of the self-supplied water. According to the present invention, the different modifications and variations of the bamboo can be made to the skilled person and the invention obviously does not deviate from the cost and spirit of the present invention. Although the present invention has described a particular preferred and defamatory affair, it must be unduly limited to such specific and enthusiasm. The local month should not be entitled to ★Taiwan like ▲, physical affairs only . Having described the invention as described above, the differences that are readily apparent to those skilled in the art are also covered by the scope of the τ lining. Μ正 [Main component symbol description]

Ml 18Ml 18

Claims (1)

1287434 、申請專利範圍·· 1 . 一種發芽處理方法,其係包含: 提供種子;以及 種 子 ❹子㈣PH值小於7·0之水溶液内以獲取發芽 包含: •如申請專利範圍第1項所述之方 法,其更進一 步 乾燥該發$種子以獲取乾燥發芽種子。 3 .如申請專利範圍第1項所述之方法,其中ρΗ值 小於7_0之水溶液係由電解含有電解f離子水溶液 產生。 式 4 .如申請專利範圍第3項所述之方法,其中卟值 小於7.0之水溶液係由電解氯化鈉水溶液的方式產生。 5 .如中請專利範圍第1項所述之方法/其中叫值 小於7.0之水溶液係由添加可食用的酸性物質方式產生。 6 .如申請專利範圍第5項所述之方法:其中卟值 小於7.0之水溶液係由添加醋酸、檸檬酸、顏果酸或麵胺 酸的方式產生。 7 ·如申明專利範圍第1項所述之方法,其中種子浸 於pH值小於7·〇之水溶液内的時間係為j 2小時到36小 時0 8 .如申請專利範圍第1至7項中任—項所述之方 法,其中pH值小於7.0之水溶液為pH 2 3至pH 6 5。 9 ·如申請專利範圍第8項所述之方法,其中pH值 19 1287434’1287434, the scope of patent application · 1. A method for germination, comprising: providing seeds; and seed tweezers (4) in an aqueous solution having a pH of less than 7.5 to obtain germination: • as described in claim 1 The method further dries the hair seed to obtain dried germinating seeds. 3. The method of claim 1, wherein the aqueous solution having a ρ Η value of less than 7 _0 is produced by electrolysis containing an aqueous solution of electrolytic f ions. The method of claim 3, wherein the aqueous solution having a enthalpy of less than 7.0 is produced by electrolyzing an aqueous solution of sodium chloride. 5. The method of claim 1 or wherein the aqueous solution having a value of less than 7.0 is produced by adding an edible acidic substance. 6. The method of claim 5, wherein the aqueous solution having a enthalpy of less than 7.0 is produced by adding acetic acid, citric acid, anaphoric acid or a face acid. 7. The method of claim 1, wherein the time during which the seed is immersed in the aqueous solution having a pH of less than 7 〇 is from 2 hours to 36 hours 0 8 as in the patent claims 1 to 7. The method according to any one of the preceding claims, wherein the aqueous solution having a pH of less than 7.0 is pH 2 3 to pH 6 5 . 9 · The method described in claim 8 wherein the pH is 19 1287434’ 小於7.0之水溶液為pH 3.0至pH 5.0。 1 0 ·如申請專利範圍第8項所述之方法,其中種子 為花生、.綠豆、黃豆或糙米。 1 1 ·如申請專利範圍第1項所述之方法,其中種子 為花生、綠豆、黃豆或縫米。 1 2 · —種經由申請專利範圍第1項至第1 1項中任 一項所述之方法所獲製發芽率均一的發芽種子。 十一、圖式: 無An aqueous solution of less than 7.0 is pH 3.0 to pH 5.0. 1 0. The method of claim 8, wherein the seed is peanut, mung bean, soybean or brown rice. 1 1 The method of claim 1, wherein the seed is peanut, mung bean, soybean or rice. 1 2 - A germinated seed having a uniform germination rate obtained by the method according to any one of claims 1 to 11. XI. Schema: None 2020
TW95110285A 2006-03-24 2006-03-24 Method for producing germinated seeds TWI287434B (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115024045A (en) * 2022-07-11 2022-09-09 浙江大学 A kind of method to improve the vigor of sweet corn seeds

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115024045A (en) * 2022-07-11 2022-09-09 浙江大学 A kind of method to improve the vigor of sweet corn seeds

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