Soil quality - Direct extraction of soil DNA (ISO 11063:2020)

The present document specifies a method for direct extraction of DNA from soil samples to analyse the abundance and composition of microbial communities by various techniques of molecular biology including real-time quantitative PCR (qPCR). This method is mainly dedicated to agricultural and forest soils. This method can possibly not be suitable for soils rich in organic matter (e.g. peat soils) or soils heavily polluted with organic pollutants or heavy metals.
The direct extraction of DNA from soil samples provides unique insight into the α- and β-diversity of microbial communities. Next-generation sequencing of amplicons obtained by PCR (polymerase chain reaction) amplification of soil DNA constitutes a promising domain which will in the near future contribute to the development of routine tools to monitor microbial communities in soil environments.

Bodenbeschaffenheit - Direkte Extraktion von DNA aus Bodenproben (ISO 11063:2020)

Dieses Dokument legt ein Verfahren zur direkten Extraktion von DNA aus Bodenproben für die Analyse der Abundanz und Zusammensetzung von mikrobiellen Lebensgemeinschaften mit verschiedenen Methoden der Molekularbiologie einschließlich quantitative Echtzeit PCR (real-time qPCR) fest. Dieses Verfahren ist vorwiegend für landwirtschaftlich genutzte Böden und Waldboden anzuwenden. Es ist möglicherweise nicht anzuwenden für Böden mit hohem organischen Anteil (z. B. Torfböden) oder Böden, die stark mit organischen Verunreinigungen oder Schwermetallen belastet sind.
Die direkte Extraktion von DNA aus Bodenproben bietet einen einzigartigen Einblick in die α  und β Diversität von mikrobiellen Lebensgemeinschaften. Next-Generation Sequencing von Amplikons, die durch PCR Amplifikation von Boden-DNA erhalten wurden, stellen einen vielversprechenden Ansatz dar und können in naher Zukunft zur Entwicklung von Routinewerkzeugen beitragen, die die Abschätzung der mikrobiellen Gemeinschaften im Boden ermöglichen.

Qualité du sol - Extraction directe de l'ADN du sol (ISO 11063:2020)

Le présent document spécifie une méthode pour l'extraction directe de l'ADN des échantillons de sol afin d'analyser l'abondance et la composition des communautés microbiennes au moyen de différentes techniques de biologie moléculaire, y compris la PCR quantitative en temps réel (qPCR). Cette méthode est principalement destinée aux sols agricoles et forestiers. Cette méthode peut ne pas être appropriée aux sols riches en matières organiques (par exemple sols de tourbières) ou aux sols très pollués par des polluants organiques ou des métaux lourds.
L'extraction directe de l'ADN des échantillons de sol fournit des informations précieuses sur la diversité α et β des communautés microbiennes. Le séquençage de dernière génération des amplicons obtenus par amplification PCR (amplification en chaîne par polymérase) de l'ADN extrait du sol offre des perspectives prometteuses et pourra contribuer, dans un avenir proche, au développement d'outils de routine permettant de surveiller les communautés microbiennes des sols.

Kakovost tal - Neposredna ekstrakcija DNK iz vzorcev tal (ISO 11063:2020)

General Information

Status
Published
Public Enquiry End Date
03-Nov-2019
Publication Date
04-Nov-2020
Technical Committee
KAT - Soil quality
Current Stage
6060 - National Implementation/Publication (Adopted Project)
Start Date
28-Oct-2020
Due Date
02-Jan-2021
Completion Date
05-Nov-2020

Relations

Effective Date
01-Dec-2020

Overview

EN ISO 11063:2020 - Soil quality: Direct extraction of soil DNA specifies a standardized laboratory method for the direct extraction of DNA from soil to analyse the abundance and composition of microbial communities. Designed primarily for agricultural and forest soils, the method supports downstream molecular biology techniques including real-time quantitative PCR (qPCR) and next‑generation sequencing (NGS) of PCR amplicons. The standard replaces EN ISO 11063:2013 and refines steps to improve DNA recovery and representativeness of bacterial, archaeal and fungal communities. Note: the procedure may be unsuitable for soils very rich in organic matter (peat) or heavily polluted with organic contaminants or heavy metals.

Key topics and technical requirements

  • Sample size and handling
    • Direct extraction from 1 g (dry weight equivalent) of soil.
    • Follow standard sampling/handling practices (see referenced ISO 18400-206) to preserve microbiological integrity.
  • Lysis strategy
    • Combined mechanical (bead-beating) and chemical lysis to release DNA from diverse and hard-to-lyse microbes.
    • Mechanical lysis duration increased in this edition to improve yield.
  • Bead composition and quantities
    • Specific bead types and amounts are defined to optimise cell disruption across taxa (changes from the previous edition noted).
  • Chemical processing
    • Thermal incubation (e.g., 70 °C for 30 min) for chemical lysis.
    • Potassium acetate used to precipitate proteins.
    • DNA precipitation with ice‑cold isopropanol, wash with 70% ethanol, and final resuspension in sterile water or TE buffer.
  • Quality control and quantification
    • DNA integrity assessed by agarose gel electrophoresis.
    • DNA quantity measured with a fluorometer.
  • Validation, storage and reporting
    • Procedures for validating extraction performance, storing nucleic acids, and preparing a compliant test report are specified.

Applications and users

  • Practical applications
    • Microbial community profiling (α- and β-diversity), ecological and agronomic soil health monitoring, impact assessment, and research involving soil microbiomes.
    • Supports qPCR, amplicon-based NGS workflows and other molecular assays used for soil monitoring, biodiversity studies and environmental diagnostics.
  • Who should use it
    • Soil scientists, environmental microbiologists, contract testing laboratories, agricultural and forestry researchers, environmental consultants, and regulatory agencies implementing routine soil microbial monitoring.

Related standards

  • ISO 18400-206: Sampling, handling and storage of soil for microbiological assessment (normative reference).
  • EN ISO 11063:2020 supersedes EN ISO 11063:2013 - consult Annex A of the standard for detailed differences.

Keywords: EN ISO 11063:2020, soil DNA extraction, soil quality, direct extraction of soil DNA, qPCR, next-generation sequencing, microbial community, soil monitoring.

Standard

SIST EN ISO 11063:2020

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Frequently Asked Questions

SIST EN ISO 11063:2020 is a standard published by the Slovenian Institute for Standardization (SIST). Its full title is "Soil quality - Direct extraction of soil DNA (ISO 11063:2020)". This standard covers: The present document specifies a method for direct extraction of DNA from soil samples to analyse the abundance and composition of microbial communities by various techniques of molecular biology including real-time quantitative PCR (qPCR). This method is mainly dedicated to agricultural and forest soils. This method can possibly not be suitable for soils rich in organic matter (e.g. peat soils) or soils heavily polluted with organic pollutants or heavy metals. The direct extraction of DNA from soil samples provides unique insight into the α- and β-diversity of microbial communities. Next-generation sequencing of amplicons obtained by PCR (polymerase chain reaction) amplification of soil DNA constitutes a promising domain which will in the near future contribute to the development of routine tools to monitor microbial communities in soil environments.

The present document specifies a method for direct extraction of DNA from soil samples to analyse the abundance and composition of microbial communities by various techniques of molecular biology including real-time quantitative PCR (qPCR). This method is mainly dedicated to agricultural and forest soils. This method can possibly not be suitable for soils rich in organic matter (e.g. peat soils) or soils heavily polluted with organic pollutants or heavy metals. The direct extraction of DNA from soil samples provides unique insight into the α- and β-diversity of microbial communities. Next-generation sequencing of amplicons obtained by PCR (polymerase chain reaction) amplification of soil DNA constitutes a promising domain which will in the near future contribute to the development of routine tools to monitor microbial communities in soil environments.

SIST EN ISO 11063:2020 is classified under the following ICS (International Classification for Standards) categories: 13.080.30 - Biological properties of soils. The ICS classification helps identify the subject area and facilitates finding related standards.

SIST EN ISO 11063:2020 has the following relationships with other standards: It is inter standard links to SIST EN ISO 11063:2013. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.

You can purchase SIST EN ISO 11063:2020 directly from iTeh Standards. The document is available in PDF format and is delivered instantly after payment. Add the standard to your cart and complete the secure checkout process. iTeh Standards is an authorized distributor of SIST standards.

Standards Content (Sample)


SLOVENSKI STANDARD
01-december-2020
Nadomešča:
SIST EN ISO 11063:2013
Kakovost tal - Neposredna ekstrakcija DNK iz vzorcev tal (ISO 11063:2020)
Soil quality - Direct extraction of soil DNA (ISO 11063:2020)
Bodenbeschaffenheit - Direkte Extraktion von DNA aus Bodenproben (ISO 11063:2020)
Qualité du sol - Extraction directe de l'ADN du sol (ISO 11063:2020)
Ta slovenski standard je istoveten z: EN ISO 11063:2020
ICS:
13.080.30 Biološke lastnosti tal Biological properties of soils
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

EN ISO 11063
EUROPEAN STANDARD
NORME EUROPÉENNE
October 2020
EUROPÄISCHE NORM
ICS 13.080.30 Supersedes EN ISO 11063:2013
English Version
Soil quality - Direct extraction of soil DNA (ISO
11063:2020)
Qualité du sol - Extraction directe de l'ADN du sol (ISO Bodenbeschaffenheit - Direkte Extraktion von DNA aus
11063:2020) Bodenproben (ISO 11063:2020)
This European Standard was approved by CEN on 18 September 2020.

CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this
European Standard the status of a national standard without any alteration. Up-to-date lists and bibliographical references
concerning such national standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN
member.
This European Standard exists in three official versions (English, French, German). A version in any other language made by
translation under the responsibility of a CEN member into its own language and notified to the CEN-CENELEC Management
Centre has the same status as the official versions.

CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia,
Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway,
Poland, Portugal, Republic of North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and
United Kingdom.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION

EUROPÄISCHES KOMITEE FÜR NORMUNG

CEN-CENELEC Management Centre: Rue de la Science 23, B-1040 Brussels
© 2020 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 11063:2020 E
worldwide for CEN national Members.

Contents Page
European foreword . 3

European foreword
This document (EN ISO 11063:2020) has been prepared by Technical Committee ISO/TC 190 "Soil
quality" in collaboration with Technical Committee CEN/TC 444 “Environmental characterization of
solid matrices” the secretariat of which is held by NEN.
This European Standard shall be given the status of a national standard, either by publication of an
identical text or by endorsement, at the latest by April 2021, and conflicting national standards shall be
withdrawn at the latest by April 2021.
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. CEN shall not be held responsible for identifying any or all such patent rights.
This document supersedes EN ISO 11063:2013.
According to the CEN-CENELEC Internal Regulations, the national standards organizations of the
following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria,
Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland,
Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Republic of
North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the
United Kingdom.
Endorsement notice
The text of ISO 11063:2020 has been approved by CEN as EN ISO 11063:2020 without any modification.

INTERNATIONAL ISO
STANDARD 11063
Second edition
2020-09
Soil quality — Direct extraction of
soil DNA
Qualité du sol — Extraction directe de l'ADN du sol
Reference number
ISO 11063:2020(E)
©
ISO 2020
ISO 11063:2020(E)
© ISO 2020
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting
on the internet or an intranet, without prior written permission. Permission can be requested from either ISO at the address
below or ISO’s member body in the country of the requester.
ISO copyright office
CP 401 • Ch. de Blandonnet 8
CH-1214 Vernier, Geneva
Phone: +41 22 749 01 11
Email: copyright@iso.org
Website: www.iso.org
Published in Switzerland
ii © ISO 2020 – All rights reserved

ISO 11063:2020(E)
Contents Page
Foreword .iv
Introduction .v
1 Scope . 1
2 Normative references . 1
3 Terms and definitions . 1
4 Principle . 1
5 Test materials . 2
5.1 Soil . 2
5.2 Chemicals . 2
5.3 Buffers and reagents . 3
6 Apparatus . 4
7 Procedures . 4
7.1 Preparation of soil samples . 4
7.2 Mechanical and chemical lyses . 4
7.3 Protein precipitation . 4
7.4 Nucleic acid precipitation and washing . 4
7.5 Nucleic acid storage . 5
8 Estimation of soil DNA quality and quantity . 5
8.1 Soil DNA quality and purity . 5
8.2 Soil DNA quantity . 5
9 Validation of the extraction procedure . 5
10 Test report . 6
Annex A (informative) Differences between ISO 11063:2012 and the revised document for
direct extraction of DNA from soil samples . 7
Annex B (informative) Possible methods to purify soil DNA extracts . 8
Bibliography . 9
ISO 11063:2020(E)
Foreword
ISO (the International Organization for 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 right 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.
The procedures used to develop this document and those intended for its further maintenance are
described in the ISO/IEC Directives, Part 1. In particular the different approval criteria needed for the
different types of ISO documents should be noted. This document was drafted in accordance with the
editorial rules of the ISO/IEC Directives, Part 2 (see www .iso .org/ directives).
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. Details of
any patent rights identified during the development of the document will be in the Introduction and/or
on the ISO list of patent declarations received (see www .iso .org/ patents).
Any trade name used in this document is information given for the convenience of users and does not
constitute an endorsement.
For an explanation on the voluntary nature of standards, the meaning of ISO specific terms and
expressions related to conformity assessment, as well as information about ISO's adherence to the
World Trade Organization (WTO) principles in the Technical Barriers to Trade (TBT) see the following
URL: www .iso .org/ iso/ foreword .html.
This document was prepared by Technical committee ISO/TC 190/SC 4, Soil quality, Subcommittee SC 4
Biological characterization
This second edition cancels and replaces the first edition (ISO 11063:2012), which has been technically
revised. The main changes compared to the previous edition are as follows (see details in Annex A):
— the amount of soil used (1 g instead of 0,25 g dry mass equivalent);
— the nature and amount of beads (2,5 g of ceramic beads, 2 g of 0,1 mm silica beads and 4 glass beads
instead of 0,5 g of 106 µm glass beads and 2 glass beads);
— the duration of the mechanical lysis (90 s instead of 30 s);
— the salt used to precipitate the proteins (potassium acetate instead of sodium acetate).
Any feedback or questions on this document should be directed to the user’s national standards body. A
complete listing of these bodies can be found at www .iso .org/ members .html.
iv © ISO 2020 – All rights reserved

ISO 11063:2020(E)
Introduction
DNA (deoxyribonucleic acid) is an essential component of any living organism coding for enzymes
responsible for any biological activities. The study of DNA sequences from DNA sources extracted from
different matrices, by means of numerous molecular approaches, provides molecular markers that can
be used to sharply distinguish and identify different organisms (bacteria, archaea and eucaryotes).
Up to now, most of the studies aiming to develop microbial soil quality indicators applicable to complex
environments, such as soil, were biased by the unculturability of many microorganisms and the lack of
[1]
sensitivity of traditional microbiological methods. The recent development of numerous molecular
biology methods based primarily on amplification of soil-extracted nucleic acids have provided a
pertinent alternative to classical culture-based microbiological methods, providing unique insight into
[2],[3],[4],[5],[6]
the composition, richness, and structure of microbial communities. DNA-based approaches
are now well-established in soil ecology and serve as genotypic (molecular genetic) markers for
determining microbial diversity.
The results of molecular analyses of soil microbial communities and/or populations rely on two main
parameters:
a) the extraction of DNA representative of the indigenous bacterial community composition;
b) PCR bias, such as the choice of primers, the concentration of amplified DNA, errors in the PCR, or
[4],[7],[8],[9]
even the method chosen for analysis. Recently, numerous studies have investigated new
[10]
methods to improve extraction, purification, amplification, and quantification of DNA from soils .
The first edition (ISO 11063:2012) described the procedure used to extract DNA directly from soil
samples suitable for the study of the composition of microbial community by both quantitative (q-PCR)
[11]
and qualitative (A-RISA) approaches .
[12]
The aim of this document is to describe a new method recently reported derived from the first
edition procedure to analyse the diversity of soil microorganisms by next-generation sequencing of
ribosomal amplicons generated by polymerase chain reactions (PCR) using soil DNA as template. This
new method was shown to increase the DNA recovery and to better represents the abundance and the
[12]
structure of archaeal and fungal communities as compared to the original method .
INTERNATIONAL STANDARD ISO 11063:2020(E)
Soil quality — Direct extraction of soil DNA
1 Scope
The present document specifies a method for direct extraction of DNA from soil samples to analyse
the abundance and composition of microbial communities by various techniques of molecular biology
including real-time quantitative PCR (qPCR). This method is mainly dedicated to agricultural and forest
soils. This method can possibly not be suitable for soils rich in organic matter (e.g. peat soils) or soils
heavily polluted with organic pollutants or heavy metals.
The direct extraction of DNA from soil samples provides unique insight into the α- and β-diversity
of microbial communities. Next-generation sequencing of amplicons obtained by PCR (polymerase
chain reaction) amplification of soil DNA constitutes a promising domain which will in the near future
contribute to the development of routine tools to monitor microbial communities in soil environments.
2 Normative references
The following documents are referred to in the text in such a way that some or all of their content
constitutes requirements of this document. For dated references, only the edition cited applies. For
undated references, the latest edition of the referenced document (including any amendments) applies.
ISO 18400-206, Soil quality — Sampling — Part 206: Collection, handling and storage of soil under aerobic
conditions for the assessment of microbiological processes, biomass and diversity in the laboratory
3 Terms and definitions
For the purposes of this document, the following terms and definitions apply.
ISO and IEC maintain terminological databases for use in standardization at the following addresses:
— ISO Online browsing platform: avai
...

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The SIST EN ISO 11063:2020 standard outlines a precise methodology for the direct extraction of soil DNA, enhancing the understanding of soil quality through the analysis of microbial communities. The scope of this standard is particularly relevant to agricultural and forest soils, emphasizing its application in assessing the abundance and composition of these communities via advanced molecular biology techniques, notably real-time quantitative PCR (qPCR). One of the primary strengths of this standard is its focus on providing a robust and standardized methodology that can yield reliable results for researchers and practitioners. By optimizing the extraction process, it facilitates a more comprehensive understanding of α- and β-diversity within microbial ecosystems. This is crucial for monitoring soil health, fertility, and the ecological impacts of land management practices. Moreover, the standard acknowledges potential limitations by indicating that it may not be applicable to soils rich in organic matter, such as peat soils, or those that are significantly polluted with organic pollutants or heavy metals. This transparency regarding the method's applicability enhances the credibility of the standard and guides users in selecting appropriate soils for study. The incorporation of next-generation sequencing techniques, as highlighted in the document, positions SIST EN ISO 11063:2020 at the forefront of innovative soil analysis methodologies. The potential for routine monitoring of microbial communities through the application of PCR amplicons aligns with current trends in environmental science and biotechnology, ensuring that this standard remains relevant in the evolving landscape of soil quality assessment. In summary, the SIST EN ISO 11063:2020 standard serves as a critical resource for enhancing soil quality analysis through direct extraction of DNA, providing methodological rigor and facilitating insights into microbial biodiversity that are essential for sustainable agricultural and forestry practices.

La norme SIST EN ISO 11063:2020, intitulée "Qualité des sols - Extraction directe de l'ADN du sol", est d'une grande importance dans le domaine de l'analyse de la qualité des sols. Son champ d'application est clair et spécifique ; elle établit une méthode pour l'extraction directe de l'ADN à partir d'échantillons de sol, permettant ainsi l'analyse de l'abondance et de la composition des communautés microbiennes à l'aide de techniques de biologie moléculaire, comme la PCR quantitative en temps réel (qPCR). L'une des forces majeures de cette norme réside dans sa capacité à dévoiler des informations précieuses sur la diversité α et β des communautés microbiennes présentes dans les sols agricoles et forestiers. Grâce à cette méthode, les chercheurs peuvent obtenir des données significatives qui étaient auparavant difficiles à recueillir. L'utilisation du séquençage de nouvelle génération sur les amplicons issus de l'amplification de l'ADN du sol par PCR ouvre de nouvelles perspectives pour l'étude des écosystèmes du sol, rendant possible le suivi régulier des communautés microbiennes. De plus, la norme met en exergue certaines limitations, en précisant que la méthode peut ne pas convenir aux sols riches en matière organique, tels que les tourbières, ou aux sols fortement pollués par des polluants organiques ou des métaux lourds. Cette clarification renforce la pertinence de la norme, car elle aide les utilisateurs à évaluer si l’application de cette méthode est appropriée dans leurs contextes spécifiques. En somme, la SIST EN ISO 11063:2020 se révèle être un outil stratégique pour la compréhension et la gestion des écosystèmes des sols, particulièrement dans les secteurs agricoles et forestiers. Son adoption pourrait bien favoriser le développement d'outils de surveillance de routine, contribuant ainsi à l'avancement des pratiques de gestion durable des sols.

SIST EN ISO 11063:2020 표준 문서는 토양 시료에서 DNA를 직접 추출하는 방법을 명확히 규정하고 있으며, 이를 통해 미생물 군집의 풍부함 및 구성 분석에 활용할 수 있습니다. 이 표준은 농업 및 산림 토양에 주로 적용되며, 다양한 분子 생물학 기술, 특히 실시간 정량적 PCR(qPCR)을 이용한 분석을 지원합니다. 그러나 유기물 함량이 높은 토양(예: 이탄 토양)이나 유기 오염물 또는 중금속으로 심각하게 오염된 토양에는 적합하지 않을 수 있다는 점에서 사용 범위가 제한적입니다. 이 표준의 강점은 토양 샘플에서 DNA를 직접 추출하는 방법이 미생물 군집의 α-다양성과 β-다양성에 대한 독특한 통찰력을 제공한다는 것입니다. PCR 증폭을 통한 증폭체의 차세대 시퀀싱은 미생물 군집을 모니터링하는 도구 개발에 기여할 가능성이 높으며, 이는 토양 환경 내에서의 생태계 건강 평가 및 관리를 위한 중요한 수단으로 자리잡을 것입니다. 따라서 SIST EN ISO 11063:2020은 토양 품질 분석 및 생물다양성 연구에서 중요한 역할을 하는 표준으로, 특히 농업 및 산림 분야의 미생물 생태학적 연구에 있어서의 유용성이 높습니다.

SIST EN ISO 11063:2020は、土壌サンプルからDNAを直接抽出する方法を規定しており、微生物群集の豊富さと構成を分子生物学の様々な技術、特にリアルタイム定量PCR(qPCR)を用いて分析するための重要な基準となっています。この標準の適用範囲は主に農業土壌や森林土壌に関するものであり、具体的な手法を提供することで、微生物群集の研究を促進します。 この標準の強みは、土壌からのDNA直接抽出を通じて得られるユニークな洞察であり、微生物群集のα多様性とβ多様性を明らかにする点です。また、土壌DNAのPCR(ポリメラーゼ連鎖反応)増幅によって得られるアンプリコンの次世代シーケンシングは、今後の土壌環境における微生物群集をモニタリングするための定常的なツールの開発に寄与する可能性があります。 ただし、この標準には適用上の制約もあり、有機物が豊富な土壌(例:泥炭土壌)や有機汚染物質や重金属で強く汚染された土壌には適さない可能性があります。この点を考慮した上で、農業や森林の土壌に焦点を当てたこの手法は、環境や農業の持続可能性を改善するための強力なツールとなります。 SIST EN ISO 11063:2020は、微生物群集分析のための標準化された方法を提供することにより、土壌品質の評価や管理において重要な役割を果たすことでしょう。この標準は、分子生物学的手法の進展を背景に、土壌生物多様性の研究と監視を一層推進することが期待されます。

Die Norm SIST EN ISO 11063:2020 legt eine methodische Grundlage für die direkte Extraktion von DNA aus Bodenproben fest, um die Häufigkeit und Zusammensetzung von Mikrobengemeinschaften mittels verschiedener molekularbiologischer Techniken, einschließlich der Echtzeit-quantitativen PCR (qPCR), zu analysieren. Dieser Standard ist besonders relevant für landwirtschaftliche und forstwirtschaftliche Böden und bietet eine wertvolle Ressource für Fachleute und Forscher in diesen Bereichen. Ein herausragendes Merkmal dieser Norm ist ihre Fähigkeit, einzigartige Einblicke in die α- und β-Diversität von Mikrobengemeinschaften zu gewähren. Durch die direkte Extraktion von DNA aus Bodenproben wird es möglich, eine differenzierte Analyse der mikrobiellen Diversität durchzuführen, was für das Verständnis der Bodenqualität und der ökologischen Dynamik essentiell ist. Die Norm berücksichtigt auch die Herausforderungen, die beim Umgang mit Böden auftreten können, die reich an organischer Materie sind oder stark mit organischen Schadstoffen oder Schwermetallen kontaminiert sind. Es ist wichtig zu beachten, dass die Methode möglicherweise nicht für solche Bedingungen geeignet ist, was eine klare Abgrenzung des Anwendungsbereichs bietet und somit den Nutzern hilft, die richtige Methodik für ihre spezifischen Böden auszuwählen. Ein weiterer bedeutender Aspekt der Norm ist die Förderungen der Next-Generation-Sequencing-Technologien, die auf den durch PCR amplifizierten Amplicons der Boden-DNA basieren. Diese Technologien stellen ein vielversprechendes Gebiet dar, das in naher Zukunft die Entwicklung von Routinewerkzeugen zur Überwachung mikrobieller Gemeinschaften in Böden unterstützen wird. Die Einführung solcher Technologien könnte im Bereich der Bodenqualität zu bedeutenden Fortschritten führen. Insgesamt ist die SIST EN ISO 11063:2020 eine wesentliche Norm für die Untersuchung der Bodenqualität und stellt eine sichere und wissenschaftlich fundierte Methode zur Verfügung, die für die Analyse von Mikrobengemeinschaften von großer Bedeutung ist.