Enzymatic method to determine biomass in skim milk whey permeate medium

1995 ◽  
Vol 9 (2) ◽  
Author(s):  
H. Choi ◽  
L. Laleye ◽  
G.F. Amantea ◽  
R.E. Simard
1996 ◽  
Vol 79 (6) ◽  
pp. 956-963 ◽  
Author(s):  
H. Choi ◽  
L. Laleye ◽  
G.F. Amantea ◽  
R.E. Simard

1984 ◽  
Vol 67 (3) ◽  
pp. 637-640 ◽  
Author(s):  
David O Biltcliffe ◽  
Dick H Kleyn ◽  
J Richard Trout ◽  
◽  
D Azzara ◽  
...  

Abstract Collaborators in 8 dairy and food industry laboratories performed one lactose determination on each of 8 unknown samples of milk, lowfat milk, or skim milk, as 3 pairs of blind duplicates. Two known samples were provided to gain experience prior to analysis of the unknown samples. All of the above samples were also analyzed for lactose content by the official AOAC gravimetric method (16.507) by a commercial laboratory. From the overall mean of results on all samples, determinations by the enzymatic method averaged 0.49% lower than by the AOAC method. This difference was significant by the t-test (P = 0.05), which indicated a lack of agreement between the compared methods in determining lactose content. Standard deviations were similar for the 3 sets of blind duplicates which ranged between 3.67 and 4.55% lactose content. F-values revealed that variations between means obtained by laboratories differed significantly as compared with variations within laboratory means. The method has been adopted official first action.


1982 ◽  
Vol 65 (12) ◽  
pp. 2274-2280 ◽  
Author(s):  
Nancy L. Keim ◽  
Judith A. Marlett ◽  
Clyde H. Amundson ◽  
Linda D. Hagemann

2020 ◽  
pp. 59-68
Author(s):  
Svetlana Ryabtseva ◽  
Yulia Tabakova ◽  
Andrey Khramtsov ◽  
Georgy Anisimov ◽  
Vitalii Kravtsov

Introduction. Microorganisms of dairy raw materials tend to adhere to the surfaces of processing equipment and form sustainable biofilms, which is a serious issue in the dairy industry. The goal of the present work was to investigate formation of biofilms on a glass surface in static model conditions, and removal of such biofilms by cleaning. Study objects and methods. The study objects were the permeates of skim milk, sweet whey and acid whey, as well as the biofilms formed and washings from glass slides. Biofilms were removed from the glass with detergents used in the dairy industry. Standard methods of determining microbiological and physicochemical properties were used to characterize the permeates. The biofilm structure and morphology of microorganisms participating in biofilm formation were investigated with a light spectroscopy. The efficiency of biofilm removal in a cleaning process was quantified with optical density of washings. Results and discussion. Biofilms in whey permeates formed slower compared to those in skimmed milk permeate during the first 24 h. Yeasts contributed significantly to the biofilm microflora in acid whey permeate throughout 5 days of biofilm growth. Well adhered biofilm layers were the most stable in skimmed milk permeate. The highest growth of both well and poorly adhered biofilm layers was observed in sweet whey permeate after 3–5 days. It was established that the primary attachment of microorganisms to a glass surface occurred within 8 h, mature multicultural biofilms formed within 48 h, and their partial destruction occurred within 72 h. Conclusion. The research results can be used to improve the cleaning equipment procedures in processing secondary dairy raw materials.


Author(s):  
А.Г. ХРАМЦОВ

Рассмотрена проблема сохранения и направленного регулирования качества молочной сыворотки путем кондиционирования. Предложены три направления переработки молочной сыворотки на основе кондиционирования: полное использование в нативном и/или модифицированном виде, извлечение компонентов, синтез производных. В рамках каждого из направлений разработаны нанобиомембранные технологии, по которым получены молочные продукты нового поколения: пребиотический концентрат Лактобел для кормовых и пищевых целей на основе изомеризованных сгущенных молочной сыворотки и обезжиренного молока с оптимизированным составом при соотношении 60 : 40 соответственно по массовой доле сухих веществ компонентов, ЛипКА – липидный казеиново-альбуминный концентрат и линейка продуктов бренда МиЛа с пониженным содержанием лактозы: из творожной сыворотки – МиЛа-С; из обезжиренного молока – МиЛа-О; из смеси творожной сыворотки и обезжиренного молока – МиЛа-ОС. Установлено, что сочетание ферментативного гидролиза лактозы со сквашиванием молочнокислыми бактериями позволяет получать кисломолочные продукты с низким содержанием молочного сахара, которые целесообразно рекомендовать для включения в рацион лактозозависимых людей. Разработанные по инновационным технологиям продукты на основе молочной сыворотки являются функциональными продуктами нового поколения для здорового питания. The problem of preservation and directed regulation of whey quality by conditioning is considered. Three directions of processing of whey on the basis of conditioning are offered: full use in native and/or modified form, extraction of components, synthesis of derivatives. Within each of the directions nanobiomembrane technologies are developed, on which dairy products of new generation are obtained: prebiotic concentrate of Lactobel for feed and food purposes on the basis of isomerized condensed milk whey and skimmed milk with optimized composition in the ratio of 60 : 40, respectively, by the mass fraction of dry matter components, LipKa – lipid casein-albumin concentrate and a line of products of the brand MiLa with a reduced content of lactose: from curd serum – MiLa-S; from skimmed milk – MiLa-O; from a mixture of curd whey and skim milk – MiLa-OS. It was found that the combination of enzymatic hydrolysis of lactose with lactic acid bacteria fermentation allows to obtain dairy products with a low content of milk sugar, which is advisable to recommend for inclusion in the diet of lactose-dependent people.


2007 ◽  
Vol 2 (1) ◽  
pp. 80-88 ◽  
Author(s):  
Mohammed Aider ◽  
Damien de Halleux ◽  
Inna Melnikova
Keyword(s):  

1989 ◽  
Vol 52 (7) ◽  
pp. 459-465 ◽  
Author(s):  
DEMETRIOS K. PAPAGEORGIOU ◽  
ELMER H. MARTH

The ability of Listeria monocytogenes to grow during the manufacture of blue cheese and to survive during its ripening was examined. Pasteurized skim milk was standardized to a milk fat content of 3.7% by addition of pasteurized homogenized cream (35% milk fat), was inoculated to contain ca. 1.0–2.0 × 103 L. monocytogenes [strain Scott A or California (CA)] cfu/ml, and was made into blue cheese according to the modified Iowa method. Blue cheese was ripened at 9–12°C and a relative humidity of 90–98% for 84 d, and then cheese was stored at 4°C. Duplicate samples of milk, curd, whey, and cheese were tested for pH and for numbers of Listeria by surface plating of appropriate dilutions [made in Tryptose Broth (TB) with 2% sodium citrate] on McBride Listeria Agar (MLA). Initial TB dilutions were stored at 4°C and surface-plated on MLA after 2, 4, 6, and 8 weeks, if the pathogen was not quantitated in the original sample. Selected Listeria colonies were confirmed biochemically. L. monocytogenes was entrapped in curd during cheese-making with the population in curd before hooping being ca. 1.0 log10 cfu/g greater than in the inoculated milk; whey contained an average of 3.6% of the cells in the initial inoculum. L. monocytogenes in cheese increased in numbers by 0.58 to 1.22 log10 cfu/g during the first 24 h of the cheese-making process. Only modest growth (0.12 to 0.30 log10 cfu/g) was noted in two lots with rapid acid production. Growth of L. monocytogenes ceased when the pH of cheese dropped below 5.0. Populations of both strains of the pathogen decreased significantly (P≤ 0.005) during the first 50 d of ripening, by an average of 2.68 log10 cfu/g compared to populations of 1-d-old cheese. From days 50 to 120 the environment of blue cheese became more favorable (pH of cheese increased because of growth by Penicillium roqueforti), and this resulted in improved survival but no growth of the pathogen. Strain Scott A survived without any more substantial decrease in numbers during days 50 to 120 of storage. Strain CA survived during days 50 to 80, and then populations of the pathogen decreased gradually so that direct plating at 110 d (one trial) and 120 d gave negative results, but the same samples gave positive results after cold enrichment.


2017 ◽  
Vol 66 (1) ◽  
pp. 306-314 ◽  
Author(s):  
Sara J. Lupton ◽  
Nancy W. Shappell ◽  
Weilin L. Shelver ◽  
Heldur Hakk

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