Database on commercialized genetically modified foods[*]
Jakob Lindenmeyer[†], Wolfram
Hemmer[‡], Lillian
Auberson†, Martin Schrott[§], Andreas Wurz[**], Matthias Foth[††], Hermann
Rüggeberg††, Peter Singer[‡‡], Hermann Broll[§§]
The goal of work package 4
(WP4) of the DMIF-GEN project was the development of a database on detection
methods for genetically modified foods. The data themselves is mainly based on
publicly available information compiled in a pre-existing database [Hemmer].
The structure of this database was developed in an iterative approach of 8
steps. The developed conceptual schema is independent of a specific database
management system (DBMS) and globally normalized (no redundancy). Two logic
structures were extracted thereof: an Internet version based on Inprise
InterBase and Java (by the German Federal Institute for Health Protection of
Consumers and Veterinary Medicine) and a local version based on the latest
version of MS Access (by the Agency BATS and the Swiss Federal Office of Public
Health). Using these two approaches as a basis, this document shows the
detailed process of the structure and schema development of the database as
well as the characterization of data types and domains.
The information for every
data set includes the country in which the GMO has been approved, contact
persons, literature about the GMO, the genetic construct and the DNA sequence
as far as available and detection methods to identify the genetic alteration in
foodstuffs. By choosing the query forms in the independent windows it will be
possible to search for specific items like organisms, genetic elements, etc.
The online version will be accessible from everywhere, independent which hard-
and software is used. Moreover different access levels could be set up to
control data distribution.
Within the last 7 years US authorities have
approved 50 genetically modified (GM) plants. Half of the approvals concerned
corn (13) and tomato (11), followed by soybean and cotton (each 5), potato and rapeseed (each 4). Two approvals
concerned beet and squash and only a single approval has been given for
chicory, flax, papaya and rice, respectively (table 1). For almost all of these
products, the US authorities were the first to approve them for food use.
Whereas none of the products approved so far needs to be labeled as GMO product
in the US, regulations of other countries require labeling. Switzerland in
contrast, requires labeling of GMO products on the basis of detectability using
DNA-based detection methods if the product contains more than 1 per cent GMO.
The limit of one per cent is based on experiences in the detection of GMOs and
was the result of a consensus between the industry, farmers, authorities and
consumers [Schrott]. Within the EU, labeling is also required for certain
products as regulated by the Novel Food Directive [Regulation (EC) No 258/97]
and related directives. A detection limit of probably one per cent is likely to
be introduced in the near future. Under these circumstances, the increasing
globalization of trade represents an extensive challenge to our food control
authorities with respect to the control of compliance with national
requirements (labeling and compulsory premarket approval).
The goal of
work package 4 of the DMIF-GEN project SMT4-CT96-2072 was to set up a database,
which would comprise important information for the development of detection
methods for commercialized genetically modified foods. This includes
information on the genetic elements introduced, modified DNA sequences,
detection methods (including DNA-extraction procedures, primer and probe
sequences) and literature about the foodstuffs. During the first phase of the
project a concept had been established defining the format of the data, sources
of data, filters and controls for data entry, concepts about maintenance,
access and distribution (according to the technical annex of the DMIF-GEN
project in [Schreiber]). The following chapters focus on the data format, the
types and domains, as well as the structure of the database.
The major
goal of a database is the correct, safe, efficient and permanent management of
the data. The data themselves stay much longer in use, than all the application
programs that use them. Therefore it is more important for a good database to
have a long-term structure for the data, than to have a good-looking
implementation in a specific database. This long-term structure is called a
conceptual schema. With the upcoming of new DBMS it can be taken as a long-term
basis to develop new DBMS-specific logical schemata (figure 1).
Figure 1: The conceptual
schema is the basis for a long-term data structure. Thereof different logical
schemata can be extracted. (Adapted according to [Zehnder]).
Table 1: Genetically
modified crops approved for food use in the USA. Sorted by crop and date of
approval (Date according to ISO 8601:1988: "Representation of dates and
times". Form: CCYY-MM-DD/hh:mm:ss with leading zeros. In case of reduced
precision, parts are omitted starting from the right-hand side [ISO]). Status:
September 20th, 1999. Two examples (Maximizerâ Maize Bt176 and Flavr Savr™ Tomato) are further
discussed in figures 5, 9 and 12 and table 5.
Crop |
Company |
Altered Trait |
Approval date |
Beet |
AgrEvo |
Herbicide tolerant (Phosphinothricin) |
1998-04-28 |
|
Novartis Seeds |
Herbicide tolerant (Glyphosate) |
1998-12-23 |
Chicory |
Bejo |
Male sterile |
1997-11-07 |
Corn |
Ciba Seeds (Novartis) |
Insect resistant (Lepidopteran) Example Maximizerâ
Maize Bt 176[***] |
1995-05-17 |
|
AgrEvo |
Herbicide tolerant (Phosphinothricin) |
1995-06-22 |
|
Monsanto |
Insect resistant (Lepidopteran) |
1995-08-22 |
|
DeKalb |
Herbicide tolerant (Phosphinothricin) |
1995-12-19 |
|
Northrup King |
Insect resistant (European Corn Borer) |
1996-01-18 |
|
Plant Genetic Systems |
Male sterile |
1996-02-22 |
|
Monsanto |
Insect resistant (European Corn Borer) |
1996-03-15 |
|
DeKalb |
Insect resistant (European Corn Borer) |
1997-03-28 |
|
Monsanto |
Insect resistant (European Corn Borer) and Herbicide tolerant
(Glyphosate) |
1997-05-27 |
|
Monsanto |
Herbicide tolerant (Glyphosate) |
1997-11-18 |
|
AgrEvo |
Insect resistant (Lepidopteran) and Herbicide
tolerant (Phosphinothricin) |
1998-05-08 |
|
Pioneer |
Herbicide tolerant (Phosphinothricin) and Male
sterile |
1998-05-14 |
|
AgrEvo |
Herbicide tolerant (Phosphinothricin) and Male
sterile |
1999-04-22 |
Cotton |
Calgene |
Herbicide tolerant (Bromoxynil) |
1994-02-15 |
|
Monsanto |
Insect resistant (Lepidopteran) |
1995-06-22 |
|
Monsanto |
Herbicide tolerant (Glyphosate) |
1995-07-11 |
|
DuPont |
Herbicide tolerant (Sulfonylurea) |
1996-01-25 |
|
Calgene |
Herbicide tolerant (Bromoxynil) and Insect resistant
(Lepidopteran) |
1997-04-30 |
Flax |
U of Saskatchewan |
Tolerant to soil residues of sulfonylurea |
1999-05-19 |
Papaya |
Cornell Univ. |
Virus resistant (PRSV) |
1996-07-31 |
Potato |
Monsanto |
Insect resistant (Coleopteran) |
1995-03-02 |
|
Monsanto |
Insect resistant (Colorado potato beetle) |
1996-05-03 |
|
Monsanto |
Insect resistant (Colorado potato beetle) and Virus resistant (PLRV) |
1998-01-29 |
|
Monsanto |
Insect resistant (Colorado potato beetle) and Virus
resistant (PVY) |
1999-02-25 |
Rapeseed |
Calgene |
Oil profile altered |
1994-10-31 |
|
AgrEvo |
Herbicide tolerant (Phosphinothricin) |
1998-01-29 |
|
Monsanto |
Herbicide tolerant (Glyphosate) |
1999-01-27 |
|
AgrEvo |
Herbicide tolerant (Phosphinothricin) and Male
sterile |
1999-03-22 |
Rice |
AgrEvo |
Herbicide tolerant (Phosphinothricin) |
1999-04-15 |
Soybean |
Monsanto |
Herbicide tolerant (Glyphosate) |
1994-05-19 |
|
AgrEvo |
Herbicide tolerant (Phosphinothricin)
1996-07-31, 1998-04-30 and 1998-10-14 |
|
|
DuPont |
Oil profile altered |
1997-05-07 |
Squash |
Upjohn) |
Virus resistant (WMV2 and ZYMV) |
1994-12-07 |
|
Asgrow |
Virus resistant (CMV, WMV2 and ZYMV) |
1996-06-14 |
Tomato |
Calgene |
Fruit ripening altered Example Flavr Savr™ Tomato[†††] 1992-10-19, 1994-10-03, 1994-11-18, |
|
|
DNA Plant Techn. |
Fruit ripening altered |
1995-01-17 |
|
Zeneca & Petoseed |
Fruit Polygalacturonase level |
1995-06-06 |
|
Monsanto |
Fruit ripening altered |
1995-09-27 |
|
Agritope |
Fruit ripening altered |
1996-03-27 |
|
Monsanto |
Insect resistant (Lepidopteran) |
1998-03-26 |
Data source: The Federal Register, product approvals by USDA/APHIS (US
regulatory agency), current status of petitions under:
http://www.aphis.usda.gov/biotech/petday.html
The
development of the DMIF-GEN database followed the 8 iterative steps of database
development according to [Zehnder] (figure 2). Some adaptations to that process
have been made, when information from a number of existing databases from partners
has been integrated into the new prototype. The advantage gained, was to have a
conceptual schema, that could be implemented in different DBMS (e.g. Inprise
InterBase or MS Access, see figure 1) with all redundancies eliminated: every
fact should only be integrated once. The disadvantage of such a systematic
development was that the structure of the database became very complex and
contained many more tables than all the individual databases combined.
The
development of the structure is not a unique process, because there is often
more than one way to model the real world. To improve a resulted model, it is
often necessary to go back to the first two steps and iterate through the
following processes. The first 5 steps of the systematic development method are
independent of a specific DBMS and result in the conceptual schema. The last 3
steps depend on a specific DBMS and result in a logical schema necessary for
the implementation of a ready-to-use database.
1.
Analysis of the problem
2.
Creation of entity-sets
3.
Definition of relationships
4.
Definition of identification keys
5.
Normalization of the whole model
Iteration
Conceptual schema
6.
Definition of local attributes
7.
Implementation of further consistency
constraints
8.
Definition of transactions
Logical schema
Figure 2: The
8 iterative steps of database development adapted according to [Zehnder]
The
conceptual schema is an independent data description. It is not designed
according to a specific computer-infrastructure but to the real world. It is
independent from a specific DBMS or computer-system. The conceptual schema is
an orientation tool for coordinating the collaborative interaction between
computer experts and other scientists, to support for changes in the system logic
and to improve the long-term data planning. It is a master plan for all applications
based on the schema. As happened in the DMIF-GEN database development, it's
possible to extract several logical schemata for different DBMS (e.g. InterBase
5.5 or Access 2000) from the same conceptual schema (see figure 1).
The
conceptual schema can either be developed manually or supported by tools. A
manual development means more detail work but gives a better overview. On the
other side tools overtake the work of all the details, but they seduce to
involve too many details so that the overview gets lost. The conceptual schema
of the DMIF-GEN database was partly developed with the help of ERWin, an entity
relationship modeling software for Windows operating systems.
The goal of
work package 4 of the DMIF-GEN project SMT4-CT96-2072 was to set up a database,
which would comprise important information for the development of detection
methods for commercialized genetically modified foodstuffs. This included
information on the genetic elements introduced, modified DNA sequences,
detection methods and literature (for details see project description in
[Schreiber]). The basis for the database-development was the existing
BATS-database of Wolfram Hemmed as described in the BATS-report 2/97 [Hemmer].
Through questionnaires the project
partners were involved in the evaluation of the goals. In the second DMIF-GEN
questionnaire all project partners were asked to analyze the importance of 13
topics of the database. This resulted in a ranking of the main goals and
showed, that information about the genetic elements comprised the most
important data (3,89 out of 4). This was followed by detection and
PCR-Information (3,78) and approval details (3,67). The full results are
available on the web under http://www.bats.ch/dmif-gen/results/.
Figure 3: The importance of 13
topics of the database according to a questionnaire to all DMIF-GEN project
partners [Lindenmeyer]. For a detailed description of the topics see table 2.
An entity
is an individual element in the real world (e.g. an author name). Entities with
similar properties (e.g. authors, title, date and journal of a publication) are
summarized in entity sets (e.g. "Literature"). An entity set is a
group of entities with the same or similar properties but different values. The
attributes of the entity sets are not explored in detail until in step 6. Table
2 shows the entity sets used to describe the data of the detection methods for
genetically engineered foods and the surrounding information:
Table 2: DMIF-GEN entity sets and description.
Entity set |
Description of the entity |
Altered trait |
Describes the altered characteristic in the phenotype of the GMO as
compared to the parent organism. |
Contact |
Specifies organizations, institutions, companies or authorities where
information about the GMO is available. |
Contact person |
Specifies the coordinates of individual persons who can provide
information concerning the GMO. |
Country |
Defines the country where an approval or a request for an approval has
been made. |
Detection |
Properties of the methods to identify genetically modified foods. |
Extraction |
Describes the method, the costs and the quality of the procedure for
the extraction of DNA (RNA) during the analysis of GMO products. |
Genetic Element |
Information about the type of the introduced genetic element (promoter
etc.), the altered characteristic after expression of the genetic element in
the GMO as compared to the parent organism, and where and when this trait is
expressed. |
Legal decision |
Describes the regulation and the status of any legal decision (e.g.
Approval, Petition, Notification) for the GMO in the countries concerned.
Historically the relation “Legal decision” was first named “Approval”. In
order to include more general entries it was then changed into “Legal
decision”. Therefore, some attribute names still start with the name
approval. |
Literature |
Provides bibliographical information of various publication types
(literature references, databases, software, Internet addresses) concerning
the GMO, giving information about relevant data such as production, quality,
performance, safety issues etc. |
Oligo |
Describes DNA/RNA- or amino acid-sequences typical for a particular
GMO; only primers and oligos; mostly synthetic. Whole genomes or genes or
longer parts of genes, see entity set "Sequence". |
Organism |
Classifies the GMO according to taxonomic nomenclature. |
PCR |
Specifies materials and methods for the analysis of DNA or RNA of the
GMO product. |
Position |
Describes the position relative to known genes of the parent organism
and the copy number of the introduced gene. |
Product |
Information about the product type, the state, shape or form, as well
as about the treatment and preservation of the product. |
Production |
Attributes about the process of development of a specific product. |
Transformation line |
The centerpiece of the database; according to which a GMO can be
identified. This relation describes the GMO as a descendant of the parent
organism, the genetic elements introduced, the production method and the
resulting altered trait. |
Sequence |
Known DNA- or amino acid-sequences of the GMO. Mostly natural, not
synthetic. Contains sequences of whole genomes or genes or longer parts of
genes, but not primers and oligos. For primers and oligos, see entity set
"Oligo". |
In step 3
every entity set out of step 2 was linked to other entity sets, if there was a
relationship between the two. A relationship is the combination of an
association with its counterpart between two entity sets. An association
defines how many entities out of an entity set A can be matched to a specific
entity in another entity set B. Roughly the associations can be grouped into 4
types:
· Single association ("1"): One entity out of entity set A
matches to exactly one entity out of entity set B.
· Conditional association ("c"): One entity out of A matches to
one or zero entities out of B.
· Multiple association ("m"): One entity out of A matches to one
or several entities out of B.
· Multiple-conditional association ("mc"): One entity out of A
matches to zero, one or several entities out of B.
The
overview over the relationships between the entity sets can be improved, if the
relationships are characterized with an describing expression and the
associations of the relationship. Figure 3 shows a simplified version of the
entity-relationship model with the relationships between the most important entity
sets of the DMIF-GEN database.
Figure 4: A simplified structure
of the relationships between the main entity sets. Details and attributes in
figure 6.
In step 4
every entity set out of step 2 acquires an identification key. The
identification key can either be naturally (existing, unique attribute) or
artificially designed (special designed attribute, mainly a continuous number).
The DMIF-GEN database used artificially designed identification keys. Their
names are built of the entity sets name combined with the extension
"_id" for identification key. E.g.: contact_id, contact-person_id,
decision_id, detection_id, element_id, extraction_id, line_id, literature_id,
oligo_id, organism_id, pcr_id, position_id, sequence_id, trait_id.
In step 5
non-hierarchical and recursive relationships are replaced by 2 hierarchical
relationships (1-1, 1-c, 1-m and 1-mc) and a relationship-entity set. The names
of the new relationship-entity sets are built up from the names of the two
connected entity sets divided by a hyphen "-". E.g.:
TF_LINE-GENETIC_ELEMENT contains the names of the transformation line and its
corresponding genetic element (see figure 5). The new relationship-entity set
contains the two identification keys of the connected entity sets as foreign
keys. The relationship is built by the connection of these two foreign keys to
the corresponding entity sets.
Figure
5: The relationship-entity set
"TF_LINE-GENETIC_ELEMENT" with its 378 data sets matching each
genetic element to the corresponding transformation line(s), e.g. as shown in
figure 5 the genetic elements pCGN 1436, PG antisense gene, nptII, P-35, tml
3', mas 5' (mannopine synthase), mas 3' and LacZ of the Flavr Savr™ Tomato line
501-1436-1001 (for details see table 5).
The result
of step 5 was a globally normalized entity-relationship model called the
conceptual schema (see figures 2 and 4). With step 5 the conceptual development
of the database was finished. The conceptual schema contains the entity
relationship model (entity sets and relationships) and a set of identification
keys out of step 4. Until now most work was done by pencil and paper and not on
the computer. After step 5 started the logical development with a focus on
Access and InterBase as specific DBMS as development tools (on the computer).
The logic
schema describes the data in the data description language of a specific
database management system (DBMS). It is not DBMS-independent as is the
conceptual schema. DBMS as MS Access deliver many development-tools to design a
database structure and the transactions. The result of this second part of the
database-development is a logical schema for a specific application and a
specific DBMS. The implementation of the database is the transformation of the
logical schema into commands for the DBMS by its development-tool. The logical
schema imports the entity sets, the relationships and the identification keys
from the conceptual schema. The development-tool of the DBMS does especially
support the development of the logical schema in describing the local
attributes (6th step in figure 2) and in the consistency checks (7th step):
e.g. MS Access offers detailed descriptions of most aspects of the attributes
and the description of the data types (9 different ones as shown in figure 8)
and limited domains for a specific attribute. To offer an optimal selection in
these domains (table 3) was one of the major work of step 6 in the development
of the logical schema of the MS Access version of the DMIF-GEN database.
Since the
development of the logical scheme is dependent on a specific DBMS, the members
of the work package had to choose the best candidate. To evaluate the technical
background of all project members, 2 questionnaires were sent to the partners
of the DMIF-GEN project: The first one in spring 1997 (presentation at the 2nd
DMIF-GEN meeting in Gent in October 1997) and the second one in spring 1998
(presentation at the 3rd DMIF-GEN meeting in Rome in October 1998). The
questionnaires can be accessed under: http://www.bats.ch/dmif-gen/questionnaire/.
Some results have been published in the Internet [Lindenmeyer].
Already the
first questionnaire showed that nearly all DMIF-GEN partners possessed an Intel
Pentium PC. Three partners using mainly Apple Macintosh hardware also had
access to a PC. On the other hand, the first questionnaire revealed that 13 of
the 23 partners or inter laboratory study participants were using a 32-bit
operating system such as Windows NT 4.0 or Windows 95. However, most of the
partners having Windows 3.X as operating system were planning to update to one
of the 32-bit operating systems within the near future. 4 out of 5 DMIF-GEN
partners already had MS Access as database management system. Although most
partners had older versions, the present know-how in working with MS Access
will be applicable for the work with any Access version. One year later, in
October 1998, already 90% had version 8 of the DBMS Access. Filemaker was
available to only 2 partners.
From the
beginning it was a discussion in the WP4 whether to develop a local or a
web-based database. Since only few partner had Internet access in 1997, the
first questionnaire didn't favor an Internet version. This changed in the
second questionnaire in 1998 when 95% of the partners had Internet access and
56% wanted a web-based database (see figure 6), which has several advantages
compared to a local database, especially concerning access and distribution:
e.g. updated data, access controls, online submission or hard- and software
independent accessibility).
Figure
6: Results of the 2nd DMIF-GEN questionnaire
under http://www.bats.ch/dmif-gen/results/ concerning preferred future
database and infrastructure (Internet connection).
Microsoft's
Access is a flexible database-tool for personal computers with Intel processors
and a Windows operating system. It contains a relational DBMS and a development
tool with a shared data basis. The switch between development- and
operation-mode is very easy. The main advantage of MS Access compared to its major
competitor, Claris Filemaker Pro, was the wider distribution of software and
knowledge among the partners of the DMIF-GEN project. Another major point were
the already existing MS Access databases of some partners (BATS, SFOPH and
Gene-Scan) of the DMIF-GEN project. It is also important to note, that the
simplicity of Filemaker leads to several restrictions in the data structure,
especially in a network structure. Moreover there are more restrictions in the
design of queries in Filemaker than in Access.
The results
of the first DMIF-GEN questionnaire showed that already in 1997 all DMIF-GEN
partners had access to PC's with an Intel Pentium processor, more than 50% were
employing a 32-bit operating system (the rest planned to upgrade) and around
80% already had MS as database management system [Lindenmeyer]. On a work
package 4 (database development-group) meeting in the German Federal Institute
for Health Protection of Consumers and Veterinary Medicine (BgVV) in Berlin in
May 1997 it was therefore decided unanimously to use MS Access as the database
management system for the development of a local version of the DMIF-GEN
database.
Before
starting with step 6, the conceptual schema was imported into the chosen DBMS,
Access. The import procedure contained the definition of tables and
identification keys and in a second step the drawing of the relationships
between the tables. The result in the "Relationship-Window" of MS
Access (figure 7) looked similar to the entity relationship model, with the
difference, that in the Access-model all local attributes are included as well.
The import of the pencil-drawn conceptual schema (figure 4) into the DBMS
Access (figure 7) was a system change and therefore contained several restrictions.
E.g. the data types in MS Access are restricted to 9 types: text, number, memo,
automatic value, date/time, currency, boolean, hyperlink and OLE-object.
Special data types like for example the domain "A, C, G, T" for
DNA-sequences are not possible. But Access offers tools to define an own domain
of values in a given data type (mainly text). Dozens of such domains defined in
step 6 (table 3) made it a lot easier to make transactions with the DMIF-GEN
database.
Figure
7: The "Relationship-Window" of MS
Access: simplified entity relationship model from figure 4 together with all
local attributes and the relationship entity-sets (e.g. figure 5).
The input
of the local attributes started after the input of entity relationship model
and identification keys into the new DBMS Access. Local or describing
attributes are called local, because they are only used in one entity set, not
like the key attributes (or global attributes).
As the
development window of the table "Legal decision" shows in figure 8,
each local attribute consists of a field name, one out of 9 data types and a
description about the attribute. For each attribute it is possible to define if
it is necessary to include data or if it is possible to leave it empty. Mostly
it is necessary to include an identification key, a name and the author of the
data set.
Figure
8: The MS Access development window of the table
"Legal decision". For the corresponding view in a web-form in
Internet Explorer 5 see figure 9.
To restrict the choice of possible entries, it
is recommended to design special "domains" for the data to be
entered. A domain is a set of different data values of the same scalar data
type. Example: Petition, Notification, Deregulation are values of the attribute
"Procedure" of the relation "Legal decision". They are all
from the data type "text". Such domains allow the formatted
presentation of attributes. This means, that the description of an attribute
allows only a value out of a given domain, but no other values. Attributes with
domains are similar to the 9 data types of MS Access. A domain can be tight or
tolerant, if it contains only a few or many selectable values.
Table 3: 6
Examples of domains of formatted attributes of the DMIF-GEN database.
Entity set |
Genetic element |
Transformation_Line |
Altered_Trait |
Attribute |
Element_type |
transfection_method |
altered_trait type |
Selectable
values of the domain |
Chromosome |
Biological: |
Fungal
resistance |
Expression
Cassette |
Agrobacterium tumefaciens |
Insect resistance: |
|
Intron |
Lepidoptera |
||
Genome |
Agrobacterium |
Coleoptera |
|
Integrated
Sequence |
Diptera |
||
Leader Sequence |
Cell
competence |
Nematode resistance |
|
Oligo |
Physical: |
Virus resistance |
|
Plasmid |
Microinjection |
Bacterial resistance |
|
Promotor |
Electroporation |
Antibiotic resistance |
|
Terminator |
Particle gun |
Herbicide tolerance: |
|
Structural Gene
(=SG): |
Chemical: |
Bromoxinyl |
|
altered |
Calcium phosphate precipitation |
Glufosinate; |
|
antisense |
Phosphoinotricin |
||
altered codon usage |
Polyethyleneglycol |
Glyphosate |
|
chimeric |
Liposomes |
Sulfonyl urea |
|
truncated |
Other |
Altered profiles |
|
deletion / insertion |
Unknown |
Stress resistance |
Entity set |
Detection |
Legal decision |
Legal decision |
Attribute |
Detection method |
LegalDecisionPurpose |
LegalDecisionStatus |
Selectable
values of the domain |
Nucleotide based: |
food |
received |
PCR |
feed |
complete |
|
LCR
(ligase chain reaction) |
seed production |
pending |
|
RAPD(random amplified
polymorphic DNA)-typing |
field release |
approved |
|
technical |
rejected |
||
RFLP(restriction fragment length polymorphism)-analysis |
pharmacological |
expired |
|
research |
withdrawn |
||
AFLP(amplified fragment length polymorphism)-analysis |
production under containment |
suspended |
|
extended |
|||
probe
hybridisation screening |
production for extraction |
End comment |
|
Protein based: |
FRnotice |
||
Immunological |
enzyme
production |
Other |
|
ELISA |
Other |
Unknown |
|
Protein Activity |
Unknown |
To describe the entity set "Product"
it would be nice to use attributes with defined domains of international
standards, such as (e.g.) the internationally standardized food description language
LanguaL [Hendricks], [Ireland-Ripert] under http://www.bats.ch/langual/.
LanguaL is an open international framework for food description, based on the
principle of a faceted thesaurus, where each food indexed is described by a set
of standard terms grouped in facets characteristic of the nutritional and/or
hygienic quality of a food. Examples are the biological origin, the methods of
cooking and conservation, and technological treatments. Proposed integration:
14 attributes of the relation "Product" for the 14 LanguaL-facets.
Each of the attributes has to be filled in by selecting the best matching name
and number out of the Windows compatible "Thesaurus Manager".
Table 4: The 14 attributes
of the LanguaL-Thesaurus for the entity set product (adapted according to
[Hendricks], [Ireland-Ripert]).
Attribute |
Description |
A. Product type |
Food group having common consumption,
functional or manufacturing characteristics. |
B. Food source |
Individual plant or animal from which the
food product or its major ingredient is derived; also a chemical food source. |
C. Part of plant or animal |
Anatomical part of the plant or animal from
which the food product or its major ingredient is derived. |
E. Physical state, shape or form |
The physical state of the food product. Solid
food products are further subdivided by shape or form. |
F. Extent of heat treatment |
Heat treatment causes chemical changes and/or
reduction of enzyme and of microbial activity and thus affects food safety
and shelf life. |
G. Cooking method |
Cooking means raising the temperature of a
food by heat or microwaves for a time sufficient to convert it from a raw or
partially cooked state to a partially or fully cooked state. The physical and
biochemical changes in the food and its components which affect the safety,
palatability or nutritional characteristics of the food. |
H. Treatment applied |
Treatment or processes applied to the product
or any indexed ingredient. |
J. Preservation method |
The methods contributing to the prevention or
retardation of microbial or enzymatic spoilage and thus to the extension of
shelf life. |
K. Packing medium |
The medium in which the food is packed for
preservation and handling or the medium surrounding homemade foods. |
M. Container or wrapping |
The main container material, the container
form, and the material of the liner lids or ends. |
N. Food contact surface |
The specific container or coating materials
in direct contact with the food. |
P. Consumer group, dietary use or label claim |
Consumer group, human or animal, for which
the food product is produced and marketed; dietary use, where the food has
special characteristics, claims or uses or is intended for individuals with
particular dietary needs; and label or labeling claims, used when special
dietary use factor terms were derived from actual food labels. |
R. Geographic places and regions |
Country codes according to ISO 3166-1:1997
"Codes for the representation of names of countries and their
subdivisions" [ISO] or regions and places as in the thesaurus. |
Z. Adjunct characteristics of food |
Additional groups of factor terms of a
miscellaneous nature. |
There are
always unformatted attributes that cannot be restricted through a given domain,
e.g. a comment field or a description field. Unfortunately long text or
sequences are not easy to search by queries such as QBE- or SQL-queries. But
big and powerful DBMS, such as Oracle, support the search for unformatted
attributes through full-text search. Also the Internet version of the DMIF-GEN
database based upon InterBase 5.5 and Java plans to provide a full-text search
on its data.
Consistency
constraints are fulfilled, if the data follow some predefined restrictions,
e.g. if the data correspond to their data type, if the data are a selection of
the corresponding domain as specified in step 6 and if there aren't expressions
that oppose each other. Step 7 checks these consistency constraints and - if
necessary - adds new ones or removes some, to give more tolerance and
flexibility for the operation of the database. It is also possible to make a
tighter restriction for the domains and data types than specified in a first
approach in step 6. MS Access supports the consistency checks through tools
like reference integrity (no connections to empty data sets) and identification
keys in the design process of the relationships.
Transactions include operations like
data-mutation through forms or tables and data-extraction through queries or
forms. Several members of the WP4 subgroup contributed exemplary questions
concerning detection of genetically engineered foods. A collection of these
questions has been provided as queries in the distributed version 1.0 (e.g.:
"Which transformation-lines contain the promoter P-35S?"). By
adjusting such queries new questions can easily be created. Adjusting QBE- or
selection-queries is harmless to the
content of the database (in contrary to the action queries). In MS Access 2000
most of the proposed questions can be implemented as QBE-queries. More complex
queries are implemented with the SQL-view in MS Access 2000. A manual for MS
Access and the design of QBE- and SQL-queries provided by one of the authors is
available for free on the Internet under: [Fessler et al.]. The project
partners proposals of typical questions that should be implemented as queries
in the DMIF-GEN database contained examples like:
· Which genetic
elements are common to all approved species in a specific country?
· How can you
differentiate between the different lines?
· List all lines
where organism = "tomato" and promoter = "P35S".
· List the lines that
do not contain the genetic elements "P35S", "NOS" and
"NPT II".
· List all primers
detecting "P35S", "NOS" or "NPT II".
· List the genetic
elements differing between BT-11 and BT-176.
· List all legal
decisions after a certain date of approval.
· List all attributes
of the products which are approved, but not in the EU.
· Which approvals are
covered by applying a specific PCR-system?
· Is the
"P35S"-promotor in a specific line the same as the one used in
another line?
· What is the copy
number of a certain element in a specific transgenic line?
· Which other plant
lines do have the same arrangement of genetic elements?
· Which plants do
have notification/application of the EU according to the Novel Foods ordinance?
· In which countries
are which GMO-plants grown at a specific point in time?
· What are the
regulatory accepted methods for detection of GMOs in a particular country?
In 1997 the DMIF-GEN database development group of work package 4 (WP4
subgroup) designed a conceptual schema of a comprehensive relational database
providing information relevant for the development of methods for detecting
genetically modified organisms (GMOs). Based on this model and based on an
already existing database [Hemmer], a prototype for the DMIF-GEN database had
been implemented by the Agency BATS and the Swiss Federal Office of Public
Health (SFOPH), with technical support provided by the Institute of Scientific
Computing of the Swiss Federal Institute of Technology (schedule see figure 1).
The developed prototype
version 1.0 ran under the database
management system Microsoft Access 97 (Version 8). The database consisted of 44
interconnected tables containing 210 attributes. In 1998 a limited number of
data sets were entered into the database in order to allow testing of its applicability
by all members of the DMIF-GEN project. The database was primarily designed to
support the development of nucleotide-based detection methods. At present PCR
is clearly the method of choice for detecting GMOs. However, much of the information
necessary for the development of protein-based detection methods can also be
deduced from the database and more specific data may be added in future
versions. In the first version, the database was restricted to GMOs that have
been approved for commercial use.
The first
prototype was distributed at the 2nd DMIF-GEN meeting in Gent in 1997 and
evaluated 6 month later in the 2nd DMIF-GEN questionnaire [Lindenmeyer]. The
feedback from the questionnaire was used to develop a more user friendly
version 2.0 presented at the third DMIF-GEN meeting in Rome in 1998. Based on
the conceptual schema (figure 4), the German Federal Institute for Health
Protection of Consumers and Veterinary Medicine (BgVV) together with Joker
Concept GmbH developed an Internet version 3 (figure 11) [Singer],
[Jankiewicz], and the Agency BATS and the SFOPH developed an Access 2000
version with slight differences (Interface figure 9, schedule figure 1).
Authorities
have (among other services) the duty of information of the public about new trends
in genetically modified foods. E.g. which GM foods are imported in which
amounts or what will appear on the market in the next time. Therefore the
authorities (e.g. the SFOPH) need to stay up to date about GM foods. Since
especially Switzerland does not receive too many petition documents for an
approval procedure, it was necessary to get the needed information about new GM
foods from outside, mainly from the USA. Normally the information was
gathered in a background report (e.g. [Hemmer] or [Regenass-Klotz]) written
through literature study, scattered publications and personal contacts. But
this often takes more time and leads to more mistakes than a systematic
approach with the support of general instructions and guidelines and an
actualized database.
Figure
9: The Web-Interface of the BATS-BAG Access 2000
database (form "Legal decision") in a web-browser (Internet Explorer
5), presenting the corn Bt 176-data set by using the structure defined in
figure 8 and the selection of the domains out of table 3.
Figure 10: Data source for background reports and detection methods.
Extraction of the relation "Literature": Online databases with
Internet address (URL) and description.
Because of special requirements of
the Swiss Government, the Agency BATS modified together with the Swiss Federal
Office of Public Health (SFOPH) the first conceptual schema according to new
requirements of the authorities (e.g. information about production).
The conceptual schema of the DMIF-GEN database was slightly modified to
support not only the detection of genetically modified foods, but also the
acquisition of the necessary data for such background reports. This can also
contain review-information from the Internet such as e.g. [Regenass-Klotz] in the
case of
corn Bt
176. The
logical schema was thoroughly optimized to support the production of
background-data for reports
. The data source was mainly retrieved from the collected full-length
petitions of the USA (table 1) and several data extracted from online databases
as listed in figure 10.
Many
problems concerning access and distribution of the database led to the
conclusion, that an online database would be a better solution with several
advantages compared to the local version: everybody has access to it from
anywhere, no matter which hard- and software is used, access can be controlled
through passwords for different levels and user-privileges, data-distribution
is very easy because of online submission of the data and the information is
always actualized.
The
disadvantage of using the existing logical schema with MS Access97 as Internet
DBMS was the poor performance and the low security level as an online database.
Access is designed for single machines or small local networks. For the
Internet version of the DMIF-GEN database it was therefore decided to design a
new logical schema for a database server. InterBase 5.5 from Inprise was chosen
as the new DBMS. An advantage of InterBase was the disposability of Java as
fundamental part. The InterClient is a Java-driver, that can be used as applet
on a client without any installations. Figure 11 shows the concept of the
web-connectivity of the DMIF-GEN database using client-server architecture,
Java and Inprise InterBase as DBMS.
Server Internet Clients
Figure 11: Web-connectivity
of the DMIF-GEN database using client-server architecture, Java and Inprise
InterBase as DBMS (adapted after [Singer] and [Jankiewicz]).
To use the
Internet-version of the DMIF-GEN database the client needs the following hard-
and software configurations:
a) Access to the Internet and at least a 56 kbit/second modem
b) JAVA enabled Web-Browser (at least Internet Explorer 4.01 or Netscape
4.5.1)
c) The latest JAVA-VM version (e.g. 1.1.6)
d) At least 64 MB RAM
e) 350 MHz Intel Pentium II CPU or G3 266 MHz Apple Macintosh
By using a
computer with less performance the speed will be reduced. The Internet version
can be accessed under: http://www.bgvv.de/GEN_DMIF_APP.html. The login window
allows several access levels (e.g. as guest, user or administrator). The query
form window in figure 12 allows the selection of one of the queries, basically
corresponding to the entity sets in table 2. It is possible to open more than
one query form at the same time, but not of the same type.
The query form (e.g. Transformation line in figure 12) allows the
presentation of a data set with all its connections to other data sets. The
area of the direct data of the data set is in the middle on the top in figure
12, just under the title of the query form. The direct connections (1:1 and
1:c) to other tables are shown on the right and on the left (e.g. "Tomato,
Lycopersicon esculentum" as organism of the presented transformation line
501-1436-1001 in figure 12). The indirect connections (1:m and 1:mc) are shown
in the middle on the bottom. Because several data sets (e.g. the genetic
elements polygalacturonase (PG), nptII, P-35S, tml 3' and P-mas) can
be linked to the actual data set transformation line 501-1436-1001, all
corresponding data sets are listed in a listbox. An empty listbox means that
there are not yet any connections to other data sets of that table (e.g. PCR,
Detection or Literature).
Figure
12: The query result form "Transformation
line" with its connections. Data source out of table 5.
Partner 7
of Work Package 4 of the DMIF-GEN project developed an external data set on DNA
extraction methods. It is a MS Access97 database, like the first version of the
DMIF-GEN database. The data set on DNA extraction methods contains 36 MS Word
files and also a management system for accessing the files. Each of the 36 MS
Word files corresponds to one DNA extraction method. Information is given on
the involved project partners, steps of the DNA extraction procedure, a list of
samples on which the method was already used and the appraisal of performance,
and references (if available). The data on extraction methods derive from Work
Package 1.1: “Development of DNA extraction methods for raw and processed
foods.” Nearly all the project partners were involved in collecting the data on
DNA extraction methods.
The
management system for the data set on DNA extraction methods is based on MS
Access 97 and is designed to facilitate the search for extraction methods
suitable to a particular environment, substrate and condition. Since all the
extraction data is contained in the 36 MS Word files, it is also possible to
access the information without MS Access, although it would not be possible to
carry out search operations such as queries or forms or other database
functions.
The data
set on DNA extraction methods consists of 8 tables, grouped around a primary
table called “tabSubstrat” (see figure 13). The non-connected tables
tabDNAModule, tabHomogenisation and tabQuantifizierung contain hyperlinks to
the 36 MS Word on specific DNA extraction methods.
Figure 13: The relations of
the Data collection on DNA extraction methods.
The
graphical user interface allows access to 81 substrates and 36 possible
extraction methods. The most important substrates such as corn, potato, rape,
rice, soybean or tomato are divided into several subgroups that reflect the
various forms in which these substrates appear in food, such as soya beans,
soya granulated, soya flour, soya tofu, soya oil, soya lecithin, soya sprouts,
soy sauce, soya drink, soya carob, soya chocolate, soya snack or as white bread
with soya as one of the baking ingredients. For each substrate under a specific
processing condition, the DNA extraction data set can find the extraction
method. For example, soybean DNA from soybeans processed in chocolate cream can
be extracted through “Qiagen Dneasy” or through “CTAB/Wizard method for
chocolate samples” (see figure 14).
Figure 14: The Substrate-form
of the data collection on DNA extraction methods.
The size of
the data set on DNA extraction methods is 1.12 MB (36 MS Word sheets plus the
management system); making it easy to distribute on floppy discs. In order to
ensure that the correct path is taken from the management system to the word
files, the data set should be copied from the floppy into a directory labeled
“database” on partition C: of the personal computer. This data set is
available, free of charge, from partner 7. Information on ordering and
conditions is available on the Internet under:
http://www.bats.ch/dmif-gen/extraction/.
The data included in the database should be
useful for the development of detection methods for genetically modified foods.
A literature-review of the existing methods clearly revealed that DNA-based
detection methods, most notably PCR-based ones, are the methods of choice
[Köppel et al.], [Pietsch et al.], [Studer et al.], [Wurz and Willmund],
[Hupfer et al.]. With respect to sensitivity, applicability for processed food
stuffs, specificity and applicability in routine laboratory analysis, DNA-based
methods clearly outperform protein-based methods or other possible techniques
[Hemmer]. Thus, the data are specifically selected to provide genetic
information on the elements that have been introduced into GMOs. The database
will be restricted to GM crops approved for commercial use.
Data specifically relevant for protein-based
detection methods have not yet been included into the database. However, such
information can in part be deduced from the present data (e.g. use of
tissue-specific promoters). Expression levels of proteins in approved genetically
modified crops that have been introduced by genetic engineering have been previously
described [Hemmer]. Such data may be integrated into future versions of the
database. The database is also designed to include descriptions of methods that
have already been employed for detecting GMOs [Köppel et al.], [Pietsch et
al.], [Wurz and Willmund]. In addition, it is planned to include information on
the experience of project partners (e.g. PCR-primers and probes or methods for
DNA-extraction). New detection methods will also be included. [Studer et al.],
[Hupfer et al.].
During the first phases of the database
development, data on the various transformation lines of approved GM crops,
including genetic data, were extracted from an existing database [Hemmer].
These data are exclusively derived from approving authorities, from official
publications of these authorities or from petition documents of applicants,
after the deletion of confidential business information. This ensures maximal
reliability of the information and helps to minimize dead-end approaches caused
by guessing or incomplete information. An example of such information is shown
in table 5, describing the approval of the Flavr Savr™ Tomato by various US
authorities. With respect to detection methods and primer systems the database
was designed to receive its information from various DMIF-GEN partners. An
example for this project internal information transfer is the data collection
on DNA extraction methods (figures 13 and 14). Nearly all project partners
contributed to this data collection.
Table 5: Data
source (Flavr Savr™ Tomato) out of BATS-report 2/97 [Hemmer].
ID 1
References USDA/APHIS; Safety
assessment (Redenbaugh et al., 1992, CRC Press)
PRODUCT INFORMATION
Plant Tomato
Product name Flavr Savr™ Tomato (MacGregor's)
Further specification GM lines from approx. 40 different
transformation events, using 2 slightly different plasmids and crosses with
traditional varieties (501-1436-1001, ............. , 540A-4109a-1823)
Scientific name Lycopersicon esculentum Mill
Host organism L. esculentum, tomato lines 501, 502, 7B, 22B, 28B, N73, 114F,
141F, 105F, 35F, 84F, 88F, 121F, 137F, 138F, 519F, 531A, 532A, 540A and 585A)
Company Calgene Inc.
Contact Calgene Inc.; 1920
Fifth Street; Davis, CA 95616, USA
Altered trait Fruit ripening delayed
Classification PQ
Purpose Enhanced fresh
market value
Safety remarks Data on potential toxins,
tomatine level, acute toxicity tests in rats
Qualities checked Increased fungal resistance, stable
inserted, taste, horticultural traits, Ca, Mg, Fe, Na; vitamins A, B1, B2, B6
and C
GENETIC INFORMATION
Plasmid pCGN1436
(driving nptII by mas 5' and mas 3') or pCGN4019a (driving nptII by P-35S and
tml 3')
Inserted genes Flavr
Savr™ gene (= antisense polygalacturonase) (1-3 copies), nptII (1-3 copies),
partial LB and RB, at a single site (haploid)
Transfection method Agrobacterium tumefaciens
Transgene 1 Flavr Savr™ gene
(polygalacturonase (PG) antisense gene)
Source of tg 1 Tomato
Protein product 1 None
Expression 1 No;
level of native PG mRNA is >90 % reduced; residual enzyme activity of native
PG is < 1 % of control lines
Mechanism 1 Antisense
RNA complexes endogenous sense mRNA for PG (transcription for native mRNA might
also be downregulated), thus reducing the levels of PG which normally degrades
pectin, a major component of the cell wall in tomato fruit
Promoter 1 (double-)
CaMV 35S (d-P-35S)
Terminator 1 tml
3'
Transgene 2 nptII (= kanr,
neor = neomycin phosphotransferase II gene )
Source of tg 2 Transposon
Tn5 (E. coli K12)
Protein product 2 APH(3')II
(Aminoglycoside-3'-phosphotransferase II)
Expression 2 <
0.08 % of total protein
Mechanism 2 Allows
for selection during plant tissue culture. APH(3')II inactivates neomycin,
kanamycin and genticin/G418) by ATP-dependent phosphorylation of the
3'-hydroxyl group of the aminohexose moiety of these aminoglycoside
antibiotics. This phosphorylation interferes with uptake and binding of the
aminoglycoside to the bacterial ribosome
Promoter 2 mas
5' (mannopine synthase) or CaMV35S promoter (different plasmids)
Terminator 2 mas
3' (polyA region from mannopine synthase gene of pTiA6) or tml 3' (see plasmid)
Transgene 3 parts of lacZ
Source of tg 3 E. coli
Protein product 3 None
Expression 3 No
Mechanism 3 -
Promoter 3 -
Terminator 3 -
Detailed sequences pCGN1436
sequence from RB to LB
References for pg,
nptII
REGULATORY INFORMATION
Approved by (authority) APHIS
docket-no 92-087-1, 94-096-1, 94-125-1, 95-015-1, 95-056-1, 96-080-1
Approved for (country) USA
Restrictions none
Requirements -
Labeling not
required
Date 1992-10-19,
1994-10-03, 1994-11-18, 1995-03-23, 1995-07-28, 1996-10-09 (see table 1).
Comment FDA
approved (1994-05); EPA approval not required
CONCLUSION and OUTLOOK
Surpassing
the goal of a stationary version to be contributed on disk, an Internet version
of the DMIF-GEN database has been realized. The Internet version opens the
opportunity for optimal dissemination of the project’s results. Moreover,
working up and integration of new data sets will be easily possible in the
future. The DMIF-GEN database may present a widely used platform for data input
to collect a comprehensive knowledge about GMO containing foods. The database
above all addresses to laboratories confronted with method development but also
to competent authorities world wide. For the latter a particular access level
with confidential data would be of future interest. (The public version of the
DMIF-GEN database contains no confidential data).
Actually the Internet version is upgraded and checked for bugs before it is made freely accessible. This will probably be the case in February/March 2000 with a website linked with the BgVV homepage (http://www.bgvv.de/). Detailed information about the database project in the scope of the DMIF-GEN project is to be found under http://www.bats.ch/dmif-gen/.
The DMIF-GEN database is a relational database and used the entity relationship model as data schema. Because the relational database approach has some disadvantages (especially in data interchange [Schlotke]), it is a long-term plan to transfer the data structure of the DMIF-GEN database into an XML-application (eXtensible Markup Language [Bray]), when XML has been established as an Internet standard. XML is a meta-language for the design of markup languages such as HTML. It allows the definition of many classes of documents. With a future XML standard the data schema of the DMIF-GEN database can be transferred into a more object-oriented way.
1)
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Composition Database Management and Data Interchange. COST Action 99
Report, European Commission, Luxembourg, To be published.
http://www.bats.ch/schlotke/pub/2000EUROFOODSRecommendations.pdf
21) Schreiber, G. et al. (1995) The Technical Annex. SMT4-CT96-2072. Development of Methods to identify Foods produced by means of Genetic
Engineering (DMIF-GEN). Project description. Bundesinstitut für gesundheitlichen
Verbraucherschutz und Veterinärmedizin (BgVV), Berlin, Germany. 13.11.1995
(Application).
22) Schrott, M., Syfrig, J. (1999) Neue Bestimmungen zur GVO-Deklaration:
Informierter Entscheid beim Lebensmittelkauf. BioTeCH-Forum 3/99 pp. 6-7. Basel,
Switzerland. http://bics.ch/g/forum/1999/3/30.html
23) Singer, P. (1999) Technical documentation and user manual of
the DMIF-GEN database. Joker Concept GmbH, Berlin, Germany. http://www.bgvv.de/GEN_DMIF_APP.html
24) Studer, E., Dahinden, I., Lüthy, J.,
Hübner, P. (1997) Nachweis des
gentechnisch veränderten ‘Maximizer’-Mais mittels der
Polymerase-Kettenreaktion. Mitt. Gebiete Lebensm. Hyg., 88: pp. 515-524.
25) Wurz, A., Willmund, R. (1997) Identification of transgenic
glyphosate-resistant soybeans. in: Foods produced by means of genetic
engineering. 2nd Status Report. Schreiber, G.A., Bögl, K.W. (eds.) Bundesinstitut
für gesundheitlichen Verbraucherschutz und Veterinärmedizin, Berlin, Germany. BgVV-Hefte
1/1997, pp. 115-117. ISBN 3-931675-07-6. http://www.bgvv.de/publik/hefte.htm
26)
Zehnder,
C.A. (1998) Informationssysteme und
Datenbanken. B.G. Teubner Verlag Stuttgart, Germany und vdf
Hochschulverlag, Zürich, Switzerland. 6. Auflage. ISBN 3-7281-2019-7. http://www.vdf.ethz.ch/info/2019.html
* This is an abridged version for the final report of
the DMIF-GEN project. The full version is available under:
http://www.bats.ch/dmif-gen/final/
[†] Agency for
Biosafety Research and Assessment of Technology Impacts of the Priority Program
Biotechnology of the Swiss National Science Foundation (BATS), Clarastr. 13, CH-4058 Basel, Switzerland.
www.bats.ch, E-mail: jakob@lindenmeyer.ch
[‡] GATC GmbH, R & D, Fritz Arnold Str. 23, D-78467 Konstanz, Germany.
www.gatc.de, E-mail: w.hemmer@gatc.de
[§] Swiss Federal
Office of Public Health (SFOPH), Division of Food Science, CH-3003 Bern,
Switzerland. www.admin.ch/bag/, E-mail: martin.schrott@bag.admin.ch
[**] Gene-Scan GmbH, D-79111 Freiburg, Germany.
www.genescan.com, E-mail: wurz@genescan.com
[††] Hanse Analytik, Bremen, Germany.
www.hanse-analytik.de, E-mail: rueggeberg@hanse-analytik.de
[‡‡] Joker Concept GmbH, Berlin, Germany. E-mail: singer@joker-concept.b.uunet.de
[§§] German Federal Institute for Health Protection of
Consumers and Veterinary Medicine (BgVV), D-14195 Berlin, Germany. www.bgvv.de,
E-mail: h.broll@bgvv.de
[***] Example of
Maximizerâ Maize Bt176 from Novartis: data set example in figure
9.
[†††] Example Flavr
Savr™ Tomato (MacGregor's) from Calgene: see table 5 and figures 5 and 12.