1、BSI Standards Publication PD CEN/TS 15634-4:2016 Foodstuffs Detection of food allergens by molecular biological methods Part 4: Peanut (Arachis hypogaea) Qualitative detection of a specific DNA sequence in chocolate by real-time PCRPD CEN/TS 15634-4:2016 PUBLISHED DOCUMENT National foreword This Pub
2、lished Document is the UK implementation of CEN/TS 15634-4:2016. The UK participation in its preparation was entrusted to Technical Committee AW/275, Food analysis - Horizontal methods. A list of organizations represented on this committee can be obtained on request to its secretary. This publicatio
3、n does not purport to include all the necessary provisions of a contract. Users are responsible for its correct application. The British Standards Institution 2016. Published by BSI Standards Limited 2016 ISBN 978 0 580 90304 5 ICS 07.100.30; 67.190 Compliance with a British Standard cannot confer i
4、mmunity from legal obligations. This Published Document was published under the authority of the Standards Policy and Strategy Committee on 30 April 2016. Amendments issued since publication Date Text affectedPD CEN/TS 15634-4:2016TECHNICAL SPECIFICATION SPCIFICATION TECHNIQUE TECHNISCHE SPEZIFIKATI
5、ON CEN/TS 15634-4 March 2016 ICS 07.100.30; 67.190 English Version Foodstuffs - Detection of food allergens by molecular biological methods - Part 4: Peanut (Arachis hypogaea) - Qualitative detection of a specific DNA sequence in chocolate by real-time PCR Produits alimentaires - Dtection dallergnes
6、 alimentaires par des mthodes de biologie molculaire - Partie 4 : Arachide (Arachis hypogaea) - Dtection qualitative dune squence dADN spcifique dans du chocolat, par PCR en temps rel Lebensmittel - Nachweis von Lebensmittelallergenen mit molekularbiologischen Verfahren - Teil 4: Erdnuss (Arachis hy
7、pogaea) - Qualitativer Nachweis einer spezifischen DNA-Sequenz in Schokolade mittels Real- time PCR This Technical Specification (CEN/TS) was approved by CEN on 11 February 2016 for provisional application. The period of validity of this CEN/TS is limited initially to three years. After two years th
8、e members of CEN will be requested to submit their comments, particularly on the question whether the CEN/TS can be converted into a European Standard. CEN members are required to announce the existence of this CEN/TS in the same way as for an EN and to make the CEN/TS available promptly at national
9、 level in an appropriate form. It is permissible to keep conflicting national standards in force (in parallel to the CEN/TS) until the final decision about the possible conversion of the CEN/TS into an EN is reached. CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croati
10、a, Cyprus, Czech Republic, Denmark, Estonia, Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and Uni
11、ted Kingdom. EUROPEAN COMMITTEE FOR STANDARDIZATION COMIT EUROPEN DE NORMALISATION EUROPISCHES KOMITEE FR NORMUNG CEN-CENELEC Management Centre: Avenue Marnix 17, B-1000 Brussels 2016 CEN All rights of exploitation in any form and by any means reserved worldwide for CEN national Members. Ref. No. CE
12、N/TS 15634-4:2016 EPD CEN/TS 15634-4:2016 CEN/TS 15634-4:2016 (E) 2 Contents Page European foreword . 3 1 Scope 4 2 Principle . 4 3 Reagents . 4 3.1 DNA extraction with CTAB . 4 3.2 DNA purification by means of solid phase extraction 5 3.3 Real-time PCR reagents . 5 4 Apparatus and equipment . 5 4.1
13、 DNA extraction . 6 4.2 PCR 6 5 Procedure. 6 5.1 General 6 5.2 Sample preparation 6 5.3 DNA extraction with CTAB . 6 5.4 DNA purification by means of solid phase extraction 7 5.5 Measuring the mass concentration and purity of the extracted DNA 7 5.6 Real-time PCR . 8 6 Validation status and performa
14、nce criteria 9 6.1 General 9 6.2 Detection . 10 6.3 Reliability of the method . 10 6.3.1 Setup of the interlaboratory study 10 6.3.2 Results 10 6.3.3 Specificity 11 7 Test report 11 Bibliography . 13 PD CEN/TS 15634-4:2016 CEN/TS 15634-4:2016 (E) 3 European foreword This document (CEN/TS 15634-4:201
15、6) has been prepared by Technical Committee CEN/TC 275 “Food analysis - Horizontal methods”, the secretariat of which is held by DIN. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. CEN and/or CENELEC shall not be held responsible
16、 for identifying any or all such patent rights. EN 15634, Foodstuffs Detection of food allergens by molecular biological methods, is currently composed with the following parts: Part 1: General considerations; Part 2: Celery (Apium graveolens) Qualitative determination of a specific DNA sequence in
17、cooked sausages by real-time PCR Technical Specification; Part 3: Hazelnut (Corylus avellana) Qualitative detection of a specific DNA sequence in chocolate by real-time PCR Technical Specification; Part 4: Peanut (Arachis hypogaea) Qualitative detection of a specific DNA sequence in chocolate by rea
18、l-time PCR Technical Specification; Part 5: Mustard (Sinapis alba) and soya (Glycine max) Qualitative dectection of a specific DNA sequence in cooked sausages by real-time PCR Technical Specification. According to the CEN-CENELEC Internal Regulations, the national standards organizations of the foll
19、owing countries are bound to announce this Technical Specification: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherla
20、nds, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the United Kingdom. PD CEN/TS 15634-4:2016 CEN/TS 15634-4:2016 (E) 4 1 Scope This Technical Specification describes a procedure for the qualitative detection of peanut (Arachis hypogaea) in chocolate u
21、sing real-time PCR based on the gene for the peanut allergen Ara h 2 4, 5. 2 Principle The total DNA is extracted from the sample and the DNA content estimated. A sequence specific to peanut from the gene for Ara h 2 is multiplicated using real-time PCR. The amplicon with a length of 86 base pairs (
22、bp) formed in this way is detected by annealing a sequence-specific probe and generating a fluorescence signal 4. 3 Reagents As a rule, analytical grade chemical reagents suitable for molecular biology shall be used. The water used shall be double distilled or equivalent quality. Solutions should be
23、 prepared by dissolving the appropriate reagents in water and autoclaving, unless indicated differently. 3.1 DNA extraction with CTAB 3.1.1 Chloroform. 3.1.2 Ethanol, volume fraction = 96 %. 3.1.3 Ethylenediaminetetraacetic acid disodium salt (Na 2EDTA). 3.1.4 Cetyltrimethylammoniumbromide (CTAB). 3
24、.1.5 Hydrochloric acid, mass fraction w = 37 %. 3.1.6 Isoamyl alcohol. 3.1.7 Isopropanol. 3.1.8 Proteinase K. 3.1.9 Sodium chloride. 3.1.10 Sodium hydroxide. 3.1.11 Tris(hydroxymethyl)aminomethane (TRIS). 3.1.12 Chloroform isoamyl alcohol mixture. Mix 24 parts by volume of chloroform (3.1.1) with on
25、e part by volume of isoamyl alcohol (3.1.6). Commercially available and comparable mixtures can be used. 3.1.13 CTAB extraction buffer solution, containing CTAB (mass concentration = 20 g/l), sodium chloride (substance concentration c = 1,4 mol/l), TRIS (c = 0,1 mol/l), Na 2EDTA (c = 0,02 mol/l). Ad
26、just the pH value with hydrochloric acid to pH = 8,0. 3.1.14 Ethanol solution, = 70 %. 3.1.15 Proteinase K solution, = 20 mg/ml. PD CEN/TS 15634-4:2016 CEN/TS 15634-4:2016 (E) 5 The freshly produced Proteinase K solution should be stored in the form of aliquots at -20 C. 3.1.16 TE buffer solution, c
27、ontaining TRIS (c = 0,001 mol/l) and Na 2-EDTA (c = 0,000 1 mol/l). Adjust the pH value with hydrochloric acid or sodium hydroxide solution to pH = 8,0. 3.2 DNA purification by means of solid phase extraction Various systems are commercially available for DNA purification by means of solid phase ext
28、raction, including spin filter columns or plates or also with vacuum operated systems. Commercially available kits can also be used. Observe the manufacturers data for this. 3.3 Real-time PCR reagents 3.3.1 PCR master mix 1 ) , containing reaction buffers, dNTPs, MgCl 2 and Hotstart Taq polymerase.
29、3.3.2 Oligonucleotides, 10 mol each. 3.3.2.1 Peanut (AR-58 F), gCA gCA gTg ggA ACT CCA Agg AgA CA. 3.3.2.2 Peanut (AR-143 R), gCA TgA gAT gTT gCT CgC Ag. 3.3.2.3 Peanut probe (AR-103 T), FAM CgA gAg ggC gAA CCT gAg gCC TAMRA or BHQ1. 3.3.3 Negative PCR control, conducted with DNA-free water instead
30、of the DNA extract from the sample. 3.3.4 Negative extraction control, performing all steps of the DNA extraction procedure, except addition of the test portion, e.g. by substitution of a corresponding amount of water for the test portion. 3.3.5 Negative process control, sample of the food matrix wi
31、thout target sequence, which passes through all steps of the analytical process (blank sample). 3.3.6 Positive PCR control 2 )reaction containing the target DNA in a specified quantity or number of copies. 3.3.7 Positive process control, sample of the food matrix with known quantity of peanut, which
32、 passes through all steps of the analytical process. 3.3.8 External amplification control (inhibition control), control DNA that is added to an aliquot of the extracted nucleic acid in a specified quantity or number of copies and used in a separate reaction to check the influence of co-extracted sub
33、stances from the sample matrix on the amplification. 4 Apparatus and equipment General aspects are described in EN ISO 24276 3. 1)Ready-to-use reagents or single components may be used as a PCR master mix, insofar as they provide comparable or better results. 2) DNA for the positive PCR control is e
34、xtracted from phenotypically identified pure peanuts as described in 5.3 and 5.4. DNA mass concentration is determined as described in 5.5. PD CEN/TS 15634-4:2016 CEN/TS 15634-4:2016 (E) 6 Plastic and glass materials shall be sterilised and free of DNA before use. In addition, the use of aerosol pro
35、tected filter tips is obligatory due to the high sensitivity of the PCR analytics and the resultant risk of DNA contamination. In addition to the usual laboratory facilities, the following equipment is required. 4.1 DNA extraction 4.1.1 Suitable reaction vials, 1,5 ml and 2 ml, DNA-free. 4.1.2 50 ml
36、 centrifuge tubes, sterile. 4.1.3 Thermostat or water bath, preferably with shaker function. 4.1.4 Centrifuge, suitable for centrifuging 50 ml centrifuge tubes at 8 000 g 3 ) . 4.1.5 Centrifuge, suitable for centrifuging 1,5 ml and 2 ml reaction vials at 14 500 g. 4.1.6 Apparatus and/or material for
37、 grinding the sample, e.g. blender or mill. 4.1.7 UV spectrometer or other detection instruments, suitable for estimating the amount of DNA. 4.2 PCR 4.2.1 Suitable PCR tubes. 4.2.2 Microcentrifuge for PCR tubes. 4.2.3 Real-time PCR equipment, suitable for excitation and for emission measurement of f
38、luorescence-marked oligonucleotides. NOTE Laboratories participating in the interlaboratory trial used the following real-time PCR equipment: Rotor Gene 6000, Stratagene Mx 3005P, ABI PRISM 7500, ABI PRISM 7900HT and Roche LightCycler 1,5.4)5 Procedure 5.1 General General aspects are described in EN
39、 ISO 24276 3. 5.2 Sample preparation Ensure e.g. by milling or homogenizing, that the test sample is representative of the laboratory sample. 5.3 DNA extraction with CTAB Measures and work steps to be considered for the DNA extraction are described in EN ISO 21571 2. 3)g = 9,81 m s 24 ) Rotor Gene 6
40、000, Stratagene Mx 3005P, ABI PRISM 7500, ABI PRISM 7900HT and Roche LightCycler 1.5 are examples of suitable products available commercially. This information is given for the convenience of users of this Technical Specification and does not constitute an endorsement by CEN of these products. Equiv
41、alent products may be used if they can be shown to lead to the same results. PD CEN/TS 15634-4:2016 CEN/TS 15634-4:2016 (E) 7 It is acceptable to use a commercially available kit instead of the DNA extraction procedure described below, if it is ensured that comparable or better results are obtained.
42、 In parallel to the test samples, carry out the controls listed in 3.3.4, 3.3.5 and 3.3.7 adequately. Prepare every sample twice in accordance with the following scheme: Weigh 2 g of the sample into 50 ml centrifuge tubes; Add 10 ml of CTAB extraction buffer solution (3.1.13); Add 30 l of Proteinase
43、 K solution (3.1.15) and mix; Incubate and shake for 90 min at 65 C; Centrifuge for 5 min at 6 000 g to 8 000 g; Place 500 l of chloroform isoamyl alcohol mixture (3.1.12) in a 2 ml reaction vial; Add 700 l of supernatant and mix thoroughly for 30 s; Centrifuge for 15 min at about 14 500 g; Place 50
44、0 l of cold isopropanol (3.1.7) in a 1,5 ml reaction vial; Add 500 l of supernatant (aqueous phase) and mix carefully; Incubate for 30 min at room temperature; Centrifuge for 15 min at about 14 500 g; Carefully remove and discard the supernatant; Fill the reaction vial with 500 l of ethanol (3.1.2)
45、and swirl the reaction vial several times; Centrifuge for 5 min at about 14 500 g; Carefully remove and discard the supernatant; Dry the extracted DNA; Dissolve the dried DNA extract in 100 l of TE buffer solution (3.1.16). 5.4 DNA purification by means of solid phase extraction Purify the DNA extra
46、ct according to the instructions given by the respective kit manufacturer. The DNA extract can be stored cooled (approximately 4 C) for a short period. If storage times exceed more than one week, the DNA extracts should be stored at temperatures of 18 C. 5.5 Measuring the mass concentration and puri
47、ty of the extracted DNA The mass concentration of a DNA aliquot can be determined by means of a UV spectrometer at 260 nm. Calculate the DNA mass concentration as follows: (DNA) in ng/l = 50 optical density dilution factor of the measured aliquot PD CEN/TS 15634-4:2016 CEN/TS 15634-4:2016 (E) 8 In o
48、rder to check its purity, the sample can in addition be measured at 280 nm. The ratio of the values for optical density at wavelengths of 260 nm and 280 nm should be approximately 1,8. The DNA mass concentration may also be estimated using other suitable procedures. 5.6 Real-time PCR PCR NOTE 1 In o
49、rder to exclude false-negative results occurring due to PCR inhibition or highly degraded DNA, the PCR suitability of the isolated DNA can be checked by, e.g. an amplification of universal sequences from plants 6. Alternatively, a possible inhibition of the PCR can be detected by spiking the sample DNA with a positive control in a separate reaction (see 3.3.8). NOTE 2 The method description for peanut detection applies for a total volume per P
