SANS 5484-2009 Resistance to fungal attack by mixed fungi《混合霉的抗真菌性》.pdf
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1、 Collection of SANS standards in electronic format (PDF) 1. Copyright This standard is available to staff members of companies that have subscribed to the complete collection of SANS standards in accordance with a formal copyright agreement. This document may reside on a CENTRAL FILE SERVER or INTRA
2、NET SYSTEM only. Unless specific permission has been granted, this document MAY NOT be sent or given to staff members from other companies or organizations. Doing so would constitute a VIOLATION of SABS copyright rules. 2. Indemnity The South African Bureau of Standards accepts no liability for any
3、damage whatsoever than may result from the use of this material or the information contain therein, irrespective of the cause and quantum thereof. ISBN 978-0-626-22930-6 SANS 5484:2009Edition 3SOUTH AFRICAN NATIONAL STANDARD Resistance to fungal attack by mixed fungi Published by SABS Standards Divi
4、sion 1 Dr Lategan Road Groenkloof Private Bag X191 Pretoria 0001Tel: +27 12 428 7911 Fax: +27 12 344 1568 www.sabs.co.za SABS SANS 5484:2009 Edition 3 Table of changes Change No. Date Scope Foreword This South African standard was approved by National Committee SABS SC 1028G, Pesticides Resistance t
5、o fungal attack, in accordance with procedures of the SABS Standards Division, in compliance with annex 3 of the WTO/TBT agreement. This document was published in June 2009. This document supersedes SABS SM 484:1981 (first revision). SANS 5484:2009 Edition 3 1 Contents Page Foreword 1 Scope 3 2 Test
6、 fungi and culture medium 3 3 Maintenance of the test fungi 3 4 Apparatus and materials . 4 5 Preparation of test specimens 4 6 Procedure 4 7 Evaluation 5 SANS 5484:2009 Edition 3 2 This page is intentionally left blank SANS 5484:2009 Edition 3 3 Resistance to fungal attack by mixed fungi 1 Scope Th
7、is standard specifies a method for the determination of the resistance to fungal attack by mixed fungi. 2 Test fungi and culture medium 2.1 Test fungi Aspergillus niger, ATCC 16404, SABS TCC 355. Aureobasidium pullulans, ATCC 9348, SABS TCC 402. Chaetomium globosum, ATCC 16021, SABS TCC 15 or ATCC 3
8、6703, SABS TCC 381. Penicillium brevicompactum, ATCC 9056, SABS TCC 389. Trichoderma sp., ATCC 0043, SABS TCC 406. 2.2 Culture medium 2.2.1 Dissolve the following in enough distilled water to yield 1 L of the solution: Agar 15 g Ammonium nitrate 1,0 g Mono-potassium phosphate . 0,7 g Di-potassium ph
9、osphate . 0,7 g Magnesium sulfate, heptahydrate 0,7 g Sodium chloride 0,005 g Ferrous sulfate, heptahydrate 0,002 g Zinc sulfate, heptahydrate 0,002 g Manganous sulfate, heptahydrate 0,001 g 2.2.2 Add enough 0,1 M sodium hydroxide solution to ensure that after sterilization the pH value of the mediu
10、m is 6,3 0,2 at 25 C. 2.2.3 Sterilize the culture medium in bulk by autoclaving at a temperature of 121 C 2 C for 20 min. 3 Maintenance of the test fungi Subculture the test fungi at intervals of 14 d on strips of filter paper placed on slants of the culture medium in suitable tubes. SANS 5484:2009
11、Edition 3 4 4 Apparatus and materials 4.1 Distilled water, that has been distilled in an all-glass apparatus or de-mineralized water of equivalent purity. 4.2 Sterile distilled water. 4.3 Slant cultures of the test fungi. 4.4 Sterile inoculating wire (platinum or nichrome). 4.5 Sterile flasks. 4.6 P
12、etri dishes, of 150 mm in diameter. 4.7 Strips of sterile filter paper, approximately 10 mm 25 mm in size. 4.8 Sterile forceps. 4.9 Sterile pipettes, of capacity 10 mL and 1 mL (graduated in 0,1 mL divisions). 4.10 Wetting agent solution, 0,5 g/L solution in water of a non-ionic wetting agent of whi
13、ch a 0,1 g/L aqueous solution is non-toxic to the test fungus. 5 Preparation of test specimens 5.1 When relevant, subject the test specimens to the appropriate pre-treatment specified in the relevant standard for the required bacteria. 5.2 The quantity and dimensions of the test specimens shall be a
14、s specified in the relevant standard for the required bacteria. 6 Procedure 6.1 Treatment of test specimens 6.1.1 Place the test specimens in a suitable container and add distilled water that contains 0,05 % of the non-ionic wetting agent until they are completely covered. 6.1.2 Keep the specimens s
15、ubmerged for 1 h and then pour off the water. 6.2 Mixed fungus spore suspension 6.2.1 Prepare a spore suspension of each of the five fungi by adding 10 mL of sterile distilled water that contains 0,05 % of the non-ionic wetting agent to one slant culture of each fungus. Using a sterile inoculating w
16、ire, gently scrape the surface growth from the culture of the test fungus. 6.2.2 Filter the spore suspension through sterile coarse cotton gauze into a sterile flask that contains 50 mL of sterile distilled water, and shake the flask. Repeat this operation for each of the test fungi, filtering into
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