ISO 13082-2011 Milk and milk products - Determination of the lipase activity of pregastric lipase preparation《牛奶和奶制品 预先制备的胃脂肪酶活性测定》.pdf

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1、 Reference numbers ISO 13082:2011(E) IDF 218:2011(E) ISO and IDF 2011INTERNATIONAL STANDARD ISO 13082 IDF 218 First edition 2011-11-15 Milk and milk products Determination of the lipase activity of pregastric lipase preparation Lait et produits laitiers Dtermination de lactivit de lipase de la prpar

2、ation de lipase prgastrique ISO 13082:2011(E) IDF 218:2011(E) COPYRIGHT PROTECTED DOCUMENT ISO and IDF 2011 All rights reserved. Unless otherwise specified, no part of this publication may be reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying and mic

3、rofilm, without permission in writing from either ISO or IDF at the respective address below. ISO copyright office International Dairy Federation Case postale 56 CH-1211 Geneva 20 Silver Building Boulevard Auguste Reyers 70/B B-1030 Brussels Tel. + 41 22 749 01 11 Tel. + 32 2 733 98 88 Fax + 41 22 7

4、49 09 47 Fax + 32 2 733 04 13 E-mail copyrightiso.org E-mail infofil-idf.org Web www.iso.org Web www.fil-idf.org Published in Switzerland ii ISO and IDF 2011 All rights reservedISO 13082:2011(E) IDF 218:2011(E) ISO and IDF 2011 All rights reserved iiiForeword ISO (the International Organization for

5、Standardization) is a worldwide federation of national standards bodies (ISO member bodies). The work of preparing International Standards is normally carried out through ISO technical committees. Each member body interested in a subject for which a technical committee has been established has the r

6、ight to be represented on that committee. International organizations, governmental and non-governmental, in liaison with ISO, also take part in the work. ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization. Internation

7、al Standards are drafted in accordance with the rules given in the ISO/IEC Directives, Part 2. The main task of technical committees is to prepare International Standards. Draft International Standards adopted by the technical committees are circulated to the member bodies for voting. Publication as

8、 an International Standard requires approval by at least 75 % of the member bodies casting a vote. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. ISO shall not be held responsible for identifying any or all such patent rights. IS

9、O 13082 IDF 218 was prepared by Technical Committee ISO/TC 34, Food products, Subcommittee SC 5, Milk and milk products, and the International Dairy Federation (IDF). It is being published jointly by ISO and IDF. ISO 13082:2011(E) IDF 218:2011(E) iv ISO and IDF 2011 All rights reservedForeword IDF (

10、the International Dairy Federation) is a non-profit organization representing the dairy sector worldwide. IDF membership comprises National Committees in every member country as well as regional dairy associations having signed a formal agreement on cooperation with IDF. All members of IDF have the

11、right to be represented on the IDF Standing Committees carrying out the technical work. IDF collaborates with ISO in the development of standard methods of analysis and sampling for milk and milk products. The main task of Standing Committees is to prepare International Standards. Draft Internationa

12、l Standards adopted by the Standing Committees are circulated to the National Committees for endorsement prior to publication as an International Standard. Publication as an International Standard requires approval by at least 50 % of IDF National Committees casting a vote. Attention is drawn to the

13、 possibility that some of the elements of this document may be the subject of patent rights. IDF shall not be held responsible for identifying any or all such patent rights. ISO 13082 IDF 218 was prepared by the International Dairy Federation (IDF) and Technical Committee ISO/TC 34, Food products, S

14、ubcommittee SC 5, Milk and milk products. It is being published jointly by IDF and ISO. All work was carried out by the Joint ISO-IDF Project Group Lipase activity of the Standing Committee on Analytical methods for processing aids and indicators under the aegis of its project leaders, Mrs M. Harboe

15、 (DK) and Dr J. Jacobsen (DK). ISO 13082:2011(E) IDF 218:2011(E) ISO and IDF 2011 All rights reserved vIntroduction Lipases (EC 3.1.1.3) are the group of esterases that hydrolyse emulsified triacylglycerolesters, which are the main component of milk fat. Commercial pregastric lipase and some rennet

16、preparations (paste or liquid) contain lipases from calf, kid- goat or lamb sources. These lipase preparations are used particularly in the production of Italian type cheeses, e.g. in Romano, Provolone, and Asiago and in other similar cheese varieties and in enzyme-modified dairy products as describ

17、ed in IDF Bulletin 294 6 . Lipase is not allowed in Feta, but it is often used in Feta-type cheese. The method is based on the principle of the FCCIV method for forestomach lipase activity 7 , but in its current form the FCCIV method is not sufficiently developed. As such, it does not provide adequa

18、te details in several critical areas, most notably in sample and substrate preparation. However, the FCCIV method served as a useful model for the development of this International Standard. INTERNATIONAL STANDARD ISO 13082:2011(E) IDF 218:2011(E) ISO and IDF 2011 All rights reserved 1Milk and milk

19、products Determination of the lipase activity of pregastric lipase preparation 1 Scope This International Standard specifies a method for the determination of the lipase activity. It is intended for the preparation of pregastric lipase and rennet paste, both of animal origin. NOTE No reference metho

20、d was used to check this method as no stable standard can be found. On the other hand, a reference method can be omitted as the substrate is reproducible and well defined. 2 Terms and definitions For the purposes of this document, the following terms and definitions apply. 2.1 international lipase u

21、nit ILU amount of lipase activity that releases butanoic acid, also known as butyric acid, at a rate of 1,25 mol/min under specified conditions NOTE 1 Lipase activity is expressed either in international lipase units (ILU) per gram of product or ILU per millilitre of product. NOTE 2 The definition i

22、s based on the direct consumption of titrant while not considering that a small molar fraction of the butyric acid (4 %) is not dissociated and thus cannot be titrated. As such, that creates a small error in the definition. 3 Principle Triglyceride esters are hydrolysed by lipase. The free fatty aci

23、ds (as butyric acid) released from the substrate tributyrin are titrated in a pH-stat with sodium hydroxide. The amount of sodium hydroxide consumed within a defined period is used to calculate the activity in ILU per millilitre or ILU per gram. Due to the non-existence of a reference standard, it i

24、s recommended that a control (known) sample be included in the test. 4 Reagents During the analysis, unless otherwise stated, use only reagents of recognized analytical grade and distilled water or demineralized water or water of equivalent purity. The brand of chemicals can affect the result. There

25、fore, before using a brand other than the one mentioned, verify whether it gives the same result. ISO 13082:2011(E) IDF 218:2011(E) 2 ISO and IDF 2011 All rights reserved4.1 Tributyrin (glycerintributyrate or glyceryl tributyrate), e.g. Merck No. 1.01958.0100 1)or similar. 4.2 Sodium caseinate, e.g.

26、 Sigma C8654 1)or similar. 4.3 Lecithin, from soya bean, e.g. BDH Prod. 29863 1)or similar. 4.4 Liquid paraffin. Use paraffin which is highly liquid (or similar light mineral oil), e.g. Merck No. 7174.1000 1) , or similar. 4.5 Soda lime granules Carbosorb 1) , e.g, BDH no 331104 1)or similar. 4.6 So

27、dium hydroxide solution, c(NaOH) 0,025 mol/l, which can either be purchased or be prepared as follows. Using a pipette (5.1), add 25,00 ml of 1 mol/l sodium hydroxide with an accurately known titre into a container. Dilute with water to 1 000 ml. The 0,025 mol/l NaOH solution can be kept in a closed

28、 container, protected against carbon dioxide in the air by use of a CO 2trap with soda lime (4.5) at room temperature for at least 1 month. If necessary, seek advice from the supplier of the equipment or reagent. Change the soda lime at least once a year. When changing the sodium hydroxide batch, ch

29、eck the actual stability of the titre by comparing the old and new titrant, e.g. using a control sample. For samples with low activity and manual titrations, use a 0,010 mol/l NaOH instead of a 0,025 mol/l NaOH solution. As such, the 0,010 mol/l NaOH solution gives a higher and more useful consumpti

30、on of titrant. Prepare the 0,010 mol/l NaOH solution freshly before use (unless the titre has been checked) as it is unstable. If using the 0,010 mol/l NaOH solution, correct the calculation according to the formulae in 8.1. 4.7 Lecithin solution, with a mass per volume fraction of 10 %. Weigh 10,0

31、g of lecithin in a suitable bottle. Use magnetic stirring to dissolve it in approx. 95 ml of liquid paraffin, which may take between 1 day and 2 days of mixing. When the lecithin is completely dissolved, make it up to a total volume of 100 ml with the liquid paraffin. When stored in a refrigerator,

32、the lecithin solution is stable for 1 year. 4.8 Control sample. Include a control sample of known activity in each series of test for lipase samples. Collect the results and use them for the evaluation of the variation of the test. The control sample can be the last sample analysed or another well-k

33、nown sample. When carrying out the method for the very first time, use a control sample obtained from another laboratory or the first sample analysed being kept as control sample for the next series of analyses. If needed, store the control sample(s) in a freezer. NOTE It can be difficult to get a s

34、uitable control sample for rennet paste. 5 Apparatus Usual laboratory equipment and, in particular, the following. The laboratory equipment can be substituted by other equipment verified as giving similar results. 5.1 Micropipette or any other pipette, of capacities 1 ml and 10 ml with a repeatabili

35、ty of 0,5 % or higher. 1) Example of a suitable product available commercially. This information is given for the benefit of users of this document and does not constitute an endorsement by ISO of this product. ISO 13082:2011(E) IDF 218:2011(E) ISO and IDF 2011 All rights reserved 35.2 One-mark volu

36、metric flasks, of required capabilities, ISO 1042 3class A. 5.3 Water bath, capable of circulating the water externally and of maintaining a constant temperature in the reaction vessel of 42 C 0,5 C. 5.4 Blender, Warren 1) , Ultraturax 1)or any equivalent apparatus. 5.5 pH stated equipment, includin

37、g the following components: a) a thermostated reaction vessel capable of stirring effectively, e.g. mechanical or magnetic stirring; b) a burette for titration; c) a recorder, printer or computer. A Metrohm 718 Stat Titrino 1)is suitable for the purpose. A manual titration set-up may also be used bu

38、t that can reduce the precision of the method. For control purposes, therefore, mention the equipment used in the test report. 5.6 Stomacher and stomacher bags, for dissolving rennet paste, e.g. standard bags BA 6041 from Seward 1)or equivalent. 6 Sampling A representative sample should have been se

39、nt to the laboratory. It should not have been damaged or changed during transport or storage. Sampling is not part of the method specified in this International Standard. A recommended sampling method is given in ISO 707 IDF 50 2 .Test samples may be stored at a temperature of 5 C or lower for 2 mon

40、ths. In case of a long storage period, store the test samples frozen, e.g. at 18 C, as that will significantly improve the stability of the lipase powder. 7 Procedure 7.1 Substrate Disperse 600 mg of sodium caseinate (4.2) in 95 g water in the blender vessel. Add 0,5 ml lecithin solution (4.3) and 1

41、,0 ml tributyrin (4.1). Blend for 60 s at low speed. Pour the substrate into a flask or beaker and keep it at room temperature on a magnetic stirrer using slow speed. Use the substrate within 4 h. 7.2 Preparation of lipase test solution 7.2.1 Liquid lipase sample Accurately pipette the required amou

42、nt of the liquid lipase sample or control into a 100 ml one-mark volumetric flask (5.2) to obtain a 100 ml lipase solution with a concentration of (4 1) ILU/ml. Make up to the mark with water. NOTE Volumetric flasks of different capacities can be used or the sample can be analysed undiluted if the l

43、ipase activity is 5 ILU or below. ISO 13082:2011(E) IDF 218:2011(E) 4 ISO and IDF 2011 All rights reserved7.2.2 Powder lipase sample Lipase powder may be inhomogeneous. Therefore, mix the powder gently in order to take a representative sample. Weigh the required amount of each powder lipase sample o

44、r control into a beaker to obtain a 100 ml lipase solution with a concentration of (4 1) ILU/ml. Dissolve or suspend the lipase test sample or the control sample in approximately 90 ml water with constant and efficient stirring. Check the pH and adjust, if needed, to 8,50 0,1 at suitable intervals w

45、ith a sodium hydroxide solution of appropriate concentration, i.e. 0,1 mol/l NaOH solution. After a total dissolution time of 20 min, transfer the content to a 100 ml one-mark volumetric flask (5.2). Make up to the mark with water. Transfer the lipase solution back into a dry beaker and stir continu

46、ously. Analyse the solution as soon as possible, but no later than 2 h after preparation of the lipase sample. Note the dilution factor d ( total volume in millilitres per gram or millilitres per millilitre sample). Lipase powder often has a poor solubility, which varies with pH. The high pH facilit

47、ates the dissolution and it is critical for the reproducibility that the same pH is always used during dissolving of lipase powder. NOTE Volumetric flasks of different capacities can be used, if necessary. 7.3 Rennet paste samples Mix the rennet paste to obtain a homogeneous paste. Dissolve 15 g 1 g

48、 of rennet paste in a stomacher bag (5.6) in 40 ml of water. Adjust the pH of the solution obtained to 8,5 0,1 using a 0,1 mol/l NaOH solution. Using a stomacher (5.6), homogenize the solution at a recommended speed of 230 r/min for 60 s. Readjust its pH to 8,5 and analyse the rennet paste sample ob

49、tained as soon as possible but not later than 2 h after its preparation. Alternatively, the paste dissolution in the plastic bag can also be done manually in the stomacher bag during 60 s. Record the exact amount of sample taken and the total amount of diluted sample, in grams, to three significant digits. Set the dilution factor d (8.1) of the rennet paste to: the total mass of the diluted sample (including the mass of the paste) divided by the mass of paste. Typical rennet paste has a low activity. If the