Role of Transgenic Technology

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    Role of transgenic technology invegetable improvement

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    WHY WE NEED NEW TECHNOLOGIES?

    Global food demand is forecast to at least double by the year

    2050. In India, the population has already exceeded 1.0 billion and

    our country is projected to be the most populous in the world with

    1.5 billion by 2050.

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    The arable land is diminishing every year. Other

    resources like water, fertilizers and labour are also

    becoming scarce and costly.

    About 1.2 billion people in the world are afflicted by

    severe poverty and suffer from malnutrition.

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    1.4 billion women (22% of world population of which 55%

    in the developing countries) suffer from iron deficiency

    anemia.

    About 140 million children suffer from vitamin A deficiency.

    More than 30% of our crop yields are lost to biotic factors.

    Similarly, crop losses due to abiotic stresses.

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    What are transgenic plants?

    TRANSGENIC PLANTS: Refers to plants in which

    functional foreign genes have been inserted.

    Gene(s) for desirable traits from anyorganism

    can be functionally introduced into the crop of interest

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    BASIC STEPS INVOLVED IN THEDEVELOPMENT OF TRANSGENICS.

    1. Isolation of the desired gene

    2. Selection and isolation of a vector

    3. Construction of recombinant vectors

    4. Introduction of recombinant vector into the host cell

    5. Selection and multiplication of the host cells carrying the

    recombinant DNA molecule

    6. Expression of the desired gene.PRE-REQUISITES OF THIS TECHNIQUE To genetically modify a plant, a genetic construct must be

    designed.

    The multiple copies of the gene of our interest.

    A vector for transmission.

    A reliable protocol for the regeneration of whole plants from tissueculture.

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    Plant Transformation Methods

    Physical Chemical Biological

    Microinjection

    Pressure

    Biolistics - gene gun/

    particle bombardment

    Electroporation

    Microinjection

    Silica/carbon fibers

    Lazer mediated

    SAT

    PEG

    DEAE-dextran

    Calcium phosphate

    Artificial lipids

    Proteins

    Dendrimers

    A. Tumefaciens

    A. Rhizogenes

    Virus-mediated

    In planta

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    INTERNATIONAL STATUS OF TRANSGENIC CROPS

    No. of countries 23

    Area in the world=114.3MH

    Area in India = 6. 8 MH

    I transgenic plants 1983Tobacco, Tomato ( Horsch et al., USA)

    I commercial release 1994Herbicide tolerant Soybean, USA

    58

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    S.No Crop Lab stage Greenhouse stage

    Fieldtrialstage

    MLT

    1 Brinjal * * * *

    2 Cabbage * * *3 Cassava *

    4 Cauliflower * * * *

    5 Okra * * * *

    6 Onion *7 Potato * * *

    8 Tomato * * *

    9 Watermelon *

    Status of GM Vegetables in India,2008

    Renuswarup,2008 57

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    Why transgenics ?

    Traits can be combined beyond species border( viruses,

    bacteria, fungi, insects, animals, human beings and

    genes synthesized in the laboratory)

    Quicker & more targeted development of new varieties

    with desired traits

    Gene pyramiding

    Removal of certain specific defects in crops

    60

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    TRADITIONAL PLANT BREEDING

    Desired Gene

    X

    Many genes aretransferred

    DonorPlant

    CommercialPlant Variety

    New PlantVariety

    PLANT BIOTECHNOLOGY

    +

    A single gene istransferred

    Desired Gene

    CommercialPlant

    Variety

    ImprovedCommercial

    PlantVariety

    Desired

    Gene

    Donor

    Plant genetic engineering

    12 59

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    We need transgenic for

    To meet the worlds need of food

    To increase yield

    To improve quality

    To cope better with climatic change

    Nutritional improvement

    Increased shelf life

    Improved taste and texture

    Stress resistance: drought, heat, cold, salt tolerance To reduce loss during transportation and storage

    Herbicide resistance

    Insect resistance

    Virus resistance

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    11

    AVENUES OF

    TRANSGENIC

    TRAITS

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    Flavr-Savr tomato - 1st FDA approval for a food

    1995 Monsanto's Roundup Ready soybeans

    approved for sale in the United States.

    1994

    First successful field trial ofGM cotton crop1990

    GM plants resistant to insects, viruses, and

    bacteria are field tested for the first time -

    USEFUL TRAITS

    1985

    1st transgenic plant: antibiotic resistant tobacco

    engineered with a yeast gene1983

    Researchers develop the ability to isolate genes1973

    First regeneration of entire plants from an in vitro culture1950

    Development of GM foods

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    Potential of GM crops in low input, sustainable

    agriculture

    TraditionalGM crop with pest resistance

    plus post-harvest qualities

    4 tonnes/ha produced 5 tonnes/ha

    25% losses

    post-harvest

    = 1 tonne/ha

    3 tonnes/ha to eat

    10% losses

    post-harvest

    = 0.5 tonne/ha

    4.5 tonnes/ha to eat

    O OG O O O

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    Tomato was one of the first plants to be transformed

    Agrobacterium tumefaciens and regenerated into fertile,

    productive plants (Fillaetttial., 1987).

    The success of early work to obtain transgenic plants

    allowed for the first commercial release of a transgenic

    food product, the Flavr Savr tomato, with extended shelflife of the ripe fruit.

    A major goal of tomato genetic engineering has been to

    manipulate the ripening process in order to delay fruitsenescence and deterioration.

    HNOLOGY OF TOMATO

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    Pectin: Cell rigidity

    PG

    Polygalacturonase

    GE FOR CELL WALL MODIFICATION

    31

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    The FlavrSavr tomato (introduced in 1994by

    Calgene Inc.) is designed to ripen on the vine, with

    minimal softening.

    Ripe tomatoes produces the enzyme

    polyglacturonase(PG).

    The PG enzyme is responsible for the breakdown

    pectin, a building block in cell walls, which gives

    tomatoes their firmness.

    To slow down the softening process, the Flavr

    Savr employs antisense technology to block PG

    enzyme production.

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    ANTISENSE TECHNOLOGY

    Antisense technology is a method of gene silencing.

    The first step in this process involved the isolation ofthe PG gene from the tomato.

    Then clone the antisense DNA with the PG gene andinsert this DNA into the plasmid of an agrobacterium.

    The bacterium is introduced to plant cells whichtransfers the gene of interest into plant cells.

    The cells with the plasmid are grown by addingspecific hormones.

    The re-generated plants will express the antisense

    DNA and when the mRNA is made through the

    process of transcription the sense mRNA will bind to

    the anti-sense mRNA. This interferes with protein

    production (PG enzyme in tomato).

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    How enzyme is made?

    DNA

    PRODUCED

    Summary of Antisense

    mechanism:

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    What Happens When A

    Cloned Antisense DNA Is

    Added To The Original

    DNA?

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    When A ClonedAntisense DNA Is Added

    To The Original DNA:

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    Formation of antisense RNA blocks

    translation

    F avr Savr Tra t ona

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    F avr Savr Tra t ona

    The Flavr Savr tomato ripens

    on the vine resulting in fuller

    flavour. It is modified so that it

    remains firm after harvesting.

    Ripe and Increased Flavour.

    The traditional tomato must be

    harvested while it is still green

    and firm so that it is not crushed

    on the way to the supermarket.

    The traditional tomato is

    sprayed with ethylene

    after shipping to induce

    ripening.

    Ripe but decreased Flavour.

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    PG antisense AC102

    PG antisense AC105

    Response to cracking after transport

    Schuch et al., 1991

    27

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    Wild type tomato

    Transplastomic tomato ErwiniacrtY

    Transplastomic tomato Narcissus Lyc

    Apel and Bock,2009 45

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    2.1 HPLC analysis of pigment accumulation in fruits

    Apel and Bock, 2009 44

    *P

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    2.2 HPLC analysis of pigment accumulation in leaves

    Apel and Bock, 200943

    *P

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    Fruit specific expression of yeast gene

    ySAMdc

    Tomatoes with 300% more Lycopene

    Increases total polyamines & shelf life

    Transgenic tomato line 579HO

    Mehta et al., 2002

    42

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    Mehta et al., 2002

    3.1 Quality of transgenic tomato processed juice

    41

    Parameter Wildtype

    Azygous Homozygous

    566HO 579HO

    Soluble solids (Brix) 4.40.4 3.70.1 4.1 0.2 4.3 0.0

    Acidity (% citric acid) 3.10.2 3.00.2 3.0 0.1 3.3 0.2

    pH 4.40.0 4.40.0 4.4 0.1 4.3 0.0

    Precipitate weight ratio 9.12.7 9.82.0 13.0 1.5* 14.5 0.3*

    Viscosity 80.911.2 94.94.8 106 4.4* 119.2 9.8**P

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    3.2 Quality attributes of transgenic tomato (SAMdc)

    Mehta et al., 2002

    40

    **P

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    3.3 Lycopene content transgenic tomato (SAMdc

    Mehta et al., 2002

    39

    *P

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    4.1 Fruit specific phenotypes of tomato

    Wild type

    Del/Ros1C

    Del/Ros1N

    37Butelli et al., 2008

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    36

    Butelli et al., 2008

    4.2 Anthocyanin levels in tomato lines

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    Powell et al.,2003

    7.1 Firmness of transgenic tomato fruit

    control AC (white bar)AC-Exp1 (light stipple)AC-PG (heavystipple)H ACPG-EXP1(black bar)AC + Exp1 (hatched bar)

    24

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    Parthenocarpy

    Rotino et al., 2005

    7

    Control F1 transgenic

    DefH9-RI-iaaM

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    Rotino et al., 2005

    6

    Genotype Marketable yield Unmarketable yield

    Green fruits Rotten

    fruits

    Yield Pl-1

    (g)

    No.of

    fruits

    Fr wt

    (g)

    Yield Pl-1

    (g)

    No.of

    fruits

    Yield Pl-1

    (g)Allflesh(F1) 1906362 32.36.1 60.53.4 9822 3.40.5 3.80.6

    UC82(control) 1380301 21.64.3 65.52.5 19665 6.21.9 5.21.2

    Ri4(trans) 1538159 43.25.0 37.01.1 12315 5.60.6 6.91.4

    Ri5(trans) 1227147 33.73.6 38.01.5 14944 6.71.5 5.20.9

    13.1 Performance of transgenic tomato lines

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    5

    Genotype Shape

    index

    seed (%) No. of

    seeds fruit-1Brix (o) -Carotene

    (g g-1 dw)

    Allflesh 1.270.02 86.75.4 68.86.2 5.30.18 491.119.7

    UC82 1.250.02 85.08.8 36.56.5 3.80.14 566.68.6

    Ri4 1.240.03 26.75.4 18.43.8 4.50.12 698.910.1

    Ri5 1.270.03 20.04.7 11.43.8 4.20.23 643.615.1

    Rotino et al., 2005

    13.2 Performance of transgenic tomato lines

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    Purple Tomatoes, Rich In Health-Protecting

    Anthocyanins, Developed With Help Of

    Snapdragons

    Cancer susceptible Trp53-/- mice

    fed a diet supplemented with thehigh anthocyanin tomatoesshowed a significant extension oflife span

    Butelliet al., 200

    GENETIC MANIPULATION OF ETHYLENE

    http://www.sciencedaily.com/images/2008/10/081026150149-large.jpg
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    GENETIC MANIPULATION OF ETHYLENE

    BIOSYNTHESIS:

    Second transgenic approach have been used to reduce

    endogenous ethylene production in ripening fruit inorder to delay the onset and rate of fruit ripening.

    The pathway of ethylene biosynthesis is now well known

    and the final two steps in the pathway, conversion of S-

    adenosyl methionine (SAM) to 1-aminocyclopropane-1-carboxylic acid (ACC) and its oxidization to ethylene have

    been targeted for modification in transgenic plants.

    One approach has been to metabolize eitherSAM or ACC

    to an inactive product and the second approach has beento specifically suppress the expression of the two ethylene

    biosynthetic enzymes required to catalyze the final steps in

    the pathway.

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    TRANSGENICS FOR PARTHENOCARPY

    Parthenocarpic mutants have been identified inseveral plant species, but their use for

    generating parthenocarpic varieties is limited by

    the reduction of fruit set and fruit size.

    The parthenocarpic trait is polygenic and it

    proves cumbersome in breeding programmes.

    For these reasons biotechnology may prove to

    be an interesting alternative method. Transgeniceggplants expressing the coding region of the

    iaaM gene from Pseudomonas syringae drivenby an ovule-specific promoter show

    parthenocarpic development.

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    The iaaM gene codes for an indolacetamide

    monoxygenase that converts tryptophan to

    indolacetamide, a precursor of the plant hormoneauxin.

    Transgenic plants produced seedless fruit of

    marketable size when the flowers were

    emasculated or in adverse conditions when

    untransformed lines where unable to set fruit.

    iaaM gene is a powerful biotechnological tool forgenerating parthenocarpic eggplants that proves to

    be superior to the use of both agricultural practices

    and traditional genetic methods

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    POTATO

    Potato breeding started around the beginning of the 19th

    century but its complex tetraploid genetics means that

    targeted breeding is a time-consuming exercise.

    Comparatively speaking, potato has a narrow genetic base,

    which, at least in part, contributes to slower progress in crop

    improvement than with other major crop species. Attemptsto introgress genes from wild relatives has met with some

    success for disease resistance traits but undesirable side

    effects from hybridization minimizes the crop improvement

    through conventional methods. Since back-crossing to remove undesirable effects is not an

    easy option for potato, the approach of improving existing

    cultivars using gene transfer or genetic engineering

    technology has been an attractive proposition.

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    INSECT-RESISTANT POTATO Nature Mark potato lines named NewLeaf confer

    resistance to Colorado potato beetle.

    The potatoes were transformed with a gene, whichencodes for the Cry3A protein from the bacteria Bacillusthuringiensis (var. tenebrionis) using the constitutive 35S

    CaMV promoter.

    The product has been endorsed by the World HealthOrganization (WHO) and other regulatory agenciesthroughout the world. The protein affects directly only the

    target pest, Colorado potato beetle (CPB) and has noeffect on other insects, mammals or wildlife.

    Mammalian toxicology and digestive fate studies, whichhave been conducted and confirmed that these Cryproteins are non-toxic to humans and pose no significant

    concern for allergicity.

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    GENETIC ENGINEERING OF CUCURBITS FOR DISEASE RESISTANCE

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    PEPPER

    Transgenic hot peppers showing resistance to bialaphos, a non-selective

    Herbicide have been generated by transfer of the bar gene via A.tumefaciens.

    Transgenic plants were capable of withstanding 5000 mg/L of bialaphosapplied to the leaves. Sweet peppers expressing (phosphinothricin N -

    acetyl transferase) gene introduced via A.tumefaciens exhibitedtolerance to applications of 0.44% of the commercial preparation of Basta

    containing 20% phosphinothricin.

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    LEGUMES

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    BIOTECHNOLOGY OF BULKY ORGANS( CARROTS, SWEET POTATOES, ALLIUM SPS)

    Roots, bulbs and other bulky organs used as vegetablesbelong to a wide range of horticultural species. Except forthe potato, very few of them have received attention interms of improvement via biotechnology.Resistance to insects and fungi

    The most important pests of sweet potatoes are insects,mainly the sweet potato weevil (Cyclas formicarius, Fab).Losses dues to insect attacks may reach 60 to 100%.The genetics of sweet potatoes is complex due to thehexaploid genome and self-incompatibility. Transfer offoreign genes via biotechnology is therefore of greatinterest.

    Moran et al. obtained several clones of the Jewel sweetpotato cultivar carrying the CryIIIA gene that exhibitedsome resistance to sweet potato weevil infestation undergreenhouse and field conditions as compared to control

    plants although the level of expression of the gene was

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    Quality traits The sugar content of carrots represents an important

    quality trait.

    Transgenic carrots in which sucrose synthase, vacuolarand cell wall invertase and tonoplast H+ATPase have beenrepressed were generated.

    The transgenic plants had an altered phenotype withsmaller roots and the strategy for improving the quality ofthe carrot (e.g. in terms of sugar content) remains to beestablished.

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    Resistance to abiotic stresses The generation of plants resistant to environmental

    stress is of great practical interest.

    Modifications of heat tolerance in carrots have beenachieved by constitutively expressing or down-regulating a small heat shock protein gene, Hsp

    Constitutive expression resulted in an increase ofheat tolerance, while down-regulation resulted inlower tolerance.

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    BIOTECHNOLOGY OF LEAFY VEGETABLES (CABBAGE, BROCCOLI,CAULIFLOWER, LETTUCE, SPINACH) AND ASPARAGUSResistance to viruses

    Cauliflower

    Transgenic cauliflower carrying the capsid gene and

    antisense VIof gene the cauliflower mosaic virus havebeen generated throughA.tumefaciens-mediatetransformation.

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    Resistance to insects and fungi

    Cauliflower

    Insect pests represent a serious problem for cauliflower

    cultivation. A trypsin inhibitorfrom the sweet potato hasbeen transferred to Taiwan cauliflower cultivars that gavetransgenic primary transformants substantial resistance tolocal insects.

    Cabbage & Broccoli Metz et al. have generated a large number of transgenic

    broccoli lines carrying the Bt Cry1A(c) gene, most ofthem causing 100% mortality of firstinstar larvae of thediamond moth.

    More recently, a synthetic Bt Cry1C gene was introduced.In addition, theCry1C-transgenic broccoli were alsoresistant to other lepidopteran pests of crucifers such ascabbage looper and imported cabbageworm.

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    Bt BRINJAL

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    What is Bt BrinjalBt Brinjal is a transgenic brinjal created out ofinserting a gene (Cry 1Ac) from the soil bacterium

    Bacillus thuringiensisinto Brinjal.

    The insertion of the gene into the brinjal cell in youngcotyledons through an Agrobacterium-mediated vector.

    This gives to the brinjal plant resistance againstlepidopteran insects like the brinjal fruit and shootborer (L.orbonalis) and fruit borer (Helicoverpa

    armigera).

    when ingestion of the Bt toxin by the insect, therewould be disruption of digestive processes, ultimatelyresulting in the death of the insect.

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    Primary damage Shoot damage

    Brinjal Shoot and Fruit Borer

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    Brinjal Shoot and Fruit Borer

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    Pesticide Use in Vegetables

    Chillies: 5.13 kg of active ingredient /ha

    Brinjal: 4.6 kg of active ingredient /ha

    =Rs 12,000 ha

    Okra: 3.71 kg of active ingredient/ha

    Indian Chemical Industry, 2007

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    MHB-4 Bt, MHB-9 Bt, MHB-10 Bt, MHB-11 Bt, MHB-39 Bt, MHB-80 Bt and MHBJ-99 Bt

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    Mode of action

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    Considerable reduction in cost of production by saving on

    cost of insecticides and labour

    labor cost as a result of reduced spraying.

    Manifold increase in yield per unit area by saving fruits

    from damage caused by FSB.

    Significant improvement in marketable fruits thereby

    increasing income per unit area.

    Reduction in direct exposure to insecticides leading to

    lesser health problems.

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    Reduction in pesticide residues in soil and water in brinjal

    fields.

    Lesser pollution of air and local environment due to

    decreased use of insecticides.

    Protection of naturally occurring predators and

    parasitoids and other beneficial organisms due to

    reduced use of insecticides.

    Reduction in soil and ground-water contamination.

    Safeguarding soil micro flora and invertebrates from

    damage caused by unintended and excessive use of

    insecticides.

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    Effect of Bt on non-target Pests or beneficial insects

    No direct effect was found on sucking pests and beneficial

    insects.

    (IGMORIS: Chapter 5, p 72 of Vol 1.)

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    Capability to reduce Pesticidal Application

    The number of pesticides sprays in the field isconsiderably less for transgenic compared to non-

    transgenic brinjal.

    The number of sprays were reduced from 8-10 to 3-5sprays.

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    Yield Advantage

    Under high level of FSB infestation in the crop, there

    was 80-100 per cent yield advantage in transgenic brinjal

    over non-transgenic counterpart

    (Chapter 1 p69 of Vol 1)

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    Effect of Bt on soil micro floraNo negative effect on soil micro flora was seen.

    No significant cry protein was detected in soil samples of Bt

    brinjal grown field and there was no harmful effect on the

    microbial population.

    (Chapter 6 p89 of Vol 1. Details are given in Vol 5.)

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    Information on gene transfer to cultivated or related species

    No gene flow has been detected in cultivated or relatedspecies of brinjal

    Pollen flow studies were conducted by Indian Institute of

    Vegetable Research (IVRI

    ICAR), Varanasi.

    (Chapter 5.7, p80 of Vol 1)

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    Information on food safety, Allergenicity and toxicity

    No toxic effect has been found (Chapter 7.2 p111-129 of Vol1).

    The skin allergy test was conducted on white rabbits by the

    accredited lab INTOX Pvt Ltd., Pune.

    No skin irritations were seen.

    Detailed Skin irritation test results are published (vol 2)

    Allergenicity was studied in rats in Rallis India Ltd., Bangalore and

    no adverse effect was seen.

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    Information is available on the level of Bt protein present inBt brinjal (raw) vs., processed or cooked brinjal

    Information is available on the level of Bt protein present

    in Bt brinjal (raw) and cooked samples (Desigen

    Diagnostics, Jalna).

    There is no Bt protein detectable in cooked or

    processed brinjal in any form as it is completely degraded

    on cooking.

    Cry protein was absent in the cooked fruit (roasted,

    shallow fried, deep fried and steamed) suggesting that the

    protein was completely degraded on cooking.

    (Chapter 7 p105 of Vol 1).

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    Long-term effect on human or animal health

    It needs to be ascertained

    Monitoring ofBt brinjal over a long time period will onlybe able to answer this issue.

    Risks associated with Bt brinjal

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    s s assoc ated t t b ja

    1. Safety

    Potential human health implications.

    Out-crossing

    Inevitable out-crossing of transgenic plants with naturally

    occurring ones.

    2.Monophagous pest

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    3. Farmers do not plant refuges to manage resistance.

    4. Resistance development Defects in protease production

    Elevated immune response

    Enhanced esterase production

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    5.Labeling

    Mixing GM crops with non-GM confounds labeling attempts.

    (Human Genome Project Information (2003),http://www.ornl.gov/sci/techresources/Human_Genome/elsi/gmfood.shtml)

    6. POLLEN FLOW

    -Isolation distance

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    -India is considered a centre of diversity.

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    9.Minor pest become major pest

    Sucking pest

    10. seed price regulation

    Bt seed high cost

    Comparative figures from experiences with IPM packages applied in some locations.

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    Bt brinjal

    2005-06

    Non Bt-

    Brinjal

    Two

    checks

    IPM by

    GAU

    2001

    IPM by

    ANGRA

    U

    2000-02

    Non chemical

    IPM by OUAT

    Summer 2004

    Fruit

    damage

    13.5 % 28.7% 29.4% 10.64% 17.72 % 13.07+ 7.54 %

    16.02 % 27.72 % 27.69 %

    Marketabl

    le yield

    231.69

    q/ha

    157.08

    q/ha

    182.15

    q/ha

    266.25

    q/ha

    203.98

    q/ha

    214.5+ 16.3

    223.39

    q/ha

    190.26

    q/ha

    192.86

    q/ha

    Transgenic tomato cv. Pusa Uphar expressing a bacterial mannitol-1-

    phosphate dehydrogenase gene confers abiotic stress tolerance

    http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c1%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c1%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c1%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c1%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c1%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c1%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c1%7c1
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    phosphate dehydrogenase gene confers abiotic stress tolerance.Neeraj Khare Danswrang Goyary Singh, N. K. Pramila Shah Meenal Rathore Sivalingam

    Anandhan Dinesh Sharma Mohomad Arif Zakwan Ahmed

    Plant Cell, Tissue and Organ Culture. 2010. 103: 2, 267-277. many ref. A bacterial mannitol-1-phosphate dehydrogenase (mtlD)

    gene driven by the constitutive cauliflower mosaic virus(CaMV) 35S promoter was transferred into tomato plantsusing anAgrobacterium tumefaciens-mediatedtransformation protocol in an attempt to improve abiotic

    stress tolerance in the transformed plants Upon exposure to low temperature stress (4 degrees C) in

    a cold chamber, transgenic plants survived up to 48 h,while non-transformed plants were unable to survive andgradually died.Drought (polyethylene glycol in medium)

    and salinity (sodium chloride in medium) tolerance testsrevealed that transgenic lines exhibited a higher tolerancefor abiotic stresses than non-transformed plants. Thesefindings indicate that the introduction of a bacterial mtlDgene into tomato conferred tolerance to abiotic stresses tothe transformed tomato plants.

    Potato R1resistance gene confers resistance against Phytophthora

    http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c1%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c1%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1
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    Potato R1resistance gene confers resistance against Phytophthorainfestansin transgenic tomato plants.Faino, L. Carli, P. Testa, A. Cristinzio, G. Frusciante, L. Ercolano, M. R.

    European Journal of Plant Pathology. 2010. 128: 2, 233-241. 36 ref.

    R1 potato gene was transferred into tomato

    lines.All the plants containing the R1 gene were

    resistant to the late blight isolate IPO-0 and

    susceptible to isolate 88133.

    These results provide evidence for specific

    activation of the R1 gene during pathogen

    challenge. Furthermore, evidence for

    enhancement ofPR-1 gene expression during P.infestans resistance response was obtained.

    Fruit quality of transgenic tomatoes with suppressed expression of LeETR1

    and LeETR2 genes

    http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.14%7c4%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.17%7c2%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.17%7c2%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.17%7c2%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.17%7c2%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.17%7c2%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.17%7c2%7c1
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    and LeETR2 genes.Bao Bili Ke LeQin Jiang JianMei Ying TieJin

    Asia Pacific Journal of Clinical Nutrition. 2007. 16: supp 1, 122-126. 22 ref.

    The effect of antisense suppression of ethylene

    receptor genes LeETR1 and LeETR2 over the

    quality of tomato fruit was investigated in this

    paper.

    . The data suggest that fruit with suppressed LeETR1and LeETR2 genes expression have stronger ethylene

    response, which accelerate fruit ripening and greatly

    altered tomato variety characteristics

    Production of transgenic eggplant (Solanum melongena

    L ) resistant to Colorado Potato Beetle

    http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.17%7c2%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.17%7c2%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.17%7c2%7c1http://ovidsp.tx.ovid.com/sp-3.2.4a/ovidweb.cgi?&S=CLFOFPMDNCDDIMKNNCCLBAJCEECOAA00&Complete+Reference=S.sh.17%7c2%7c1
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    L.) resistant to Colorado Potato Beetle.

    Arpaia et al.,

    The presence of the CryIIIB toxin in leaf extractswas demonstrated in 57 out of 93transgenicplants tested by DAS-ELISA assay.

    High Bt-expressing plants contained a 74-kDaprotein cross-reacting with serum anti-CryIIIBtoxin.Twenty three out of 44 S. melongena plantstested by insect bioassay showed significantinsecticidial activity on neonate larvae ofColorado Potato Beetle (CPB).

    The Bt transgene and the toxic effect on CPBlarvae were transmitted to progenies derived byselfing. Thus,transgenic Bt eggplants represent avery effective means of CPB pest control.

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    83

    CONCLUSIONGrowth in agriculture is less than 2%. If we have toachieve our ambitions of growing at a rapid pace ofover 8%, we must aim at an agricultural growth rateof over 4%.

    Hope that progress of agriculture through use ofmodern science & technology will spread to everynook and corner of the country.

    Dr. Manmohan SinghHonble Prime Minister

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