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PROTEGES-Kartikey Vikram Singh
And
Vineet Dubey
MENTOR-Santosh Kr. Mishra




Recently there has been a perceptible revival of
interest in the use of medicinal plants
throughout the world culminating into a
manifold increase of medicinal plant based
products.
At present there are about 130 clinically useful
prescription drugs of known chemical
structures, solely derived from higher plants
and used in modern system of medicines.


In view of the spectacular increase in the
demand of plant based compounds, the
concerned medicinal plants have been
indiscriminately exploited leading to scarcity
or extinction of many valuable plant species.

plant species

product

Cost($/kg)

Cath. roseus

Ajmalicine

37,000

P. somniferum

Codeine

17,000

Cath. roseus

Vincristine

20,00,000

Cath. roseus

Vinblastine

10,00,000

Colchium autumnale

colchicine

35,000

Panax ginseng

Ginsenosides

50,000






This project deals with the production of highvalue secondary metabolites including
pharmaceuticals and food additives through
root cultures and transgenic roots obtained
through biotechnological means.
Recent developments in transgenic research
have opened up the possibility of the metabolic
engineering of biosynthetic pathways to
produce high-value secondary metabolites.
Definition
 It is the culture produced after the infection of
explants or cultures by the gram negative soil
bacterium Agrobacterium rhizogenes.


This processes take advantage of the naturally
occurring hairy root disease in Dicotyledons.




Agrobacterium
recognizes
some
signal
molecules exuded by wounded plant cells and
becomes attached to it.
The bacteria contain the Root inducing plasmid
(Ri-plasmid) The bacteria genetically transfer
part of the Ri-plasmid called the transfer DNA
(T-DNA) to the plant genome.




where it gets expressed and make the plant cell
to proliferate by increasing the rate of cell
division (cytokine expression) and cell
elongation ( auxin expression) to produce the
hairy roots.
Produce the opines which is a type of unusual
amino acids (octopine, agropine, nopaline,
mannopine, and cucumopine) which is used by
the bacterium as a carbon, nitrogen and energy
source.








The hairy root system is genetically and
biosynthetically stable.
High production of secondary metabolites.

The culture can grow under phyto-hormonefree conditions.
The culture shows fast growth which reduces
the culture time and easy the handling
1.
2.
3.
4.
5.

The main aim of this project is to synthesize secondary
metabolites from hairy root culture of medicinal plants
this process will comprise of following stages:
Selecting a plant species appropriate for the desired
product.
Through Micropropagation obtaining an infection free
sample.
By means of genetic transformation induce the hairy
root culture.
Obtaining the product and analysing the final product
for quality.
Observing effect of different chemicals on the culture.
Time

Objective

two month

Literature and Review

two month

Micro propagation of the Selected
Plant

two month

Biotransformation

two month

Optimisation of different parameters
of culture

two month

effect of different types of chemical
factor on hairy root culture

two month

Analysis of secondary metabolites
produced by hairy roots








To grow the culture of A. rhizogenes we can
prepare media either LB or YEB.
To grow the hairy root we are preparing MS
media and enzyme supplement stock solutions.
Establishment of culture room is in progress.

Selection of the plant species for micro
propagation.
References:







S. Ramachandra Rao and G.A. Ravishankar;
Biotechnology advances 20 (2002) 101 – 153; Plant cell
cultures: Chemical factories of secondary metabolites.
Suchitra Banerjee, Sailendra Singh, Laiq Ur Rahman;
Biotechnology advances 30 (2012) 461–468;
Biotransformation studies using hairy root cultures.
Flores HE, Dai YR, Freyer AJ, Michaels PJ.
Biotransformation of menthol and geraniol by hairy
root cultures. Plant Physiol Biochem 1994;32:511–9.
Jung G, Tepfer D. Use of genetic transformation by the
T-DNA of Agrobacterium rhizogenesto stimulate
biomass and tropane alkaloid production in Atropa
belladonna and Calystegiasepium roots grown in vitro.
Plant Sci1987;50:145 – 51.








Ambros PF, Matzke AJM, Matzyke MA.
Localization of Agrobacterium rhizogenes T-DNA
in plant chromosomes by in situ hybridization.
EMBO J 1986;5:2073 – 7
Newman DJ, Cragg GM. Natural products as
sources of new drugs over the last 25 years.J Nat
Prod 2007;70:461–77
Subroto MA, Kwok K, Hamill JD, Doran PM.
Coculture of genetically transformed roots and
shoots for synthesis, translocation and
biotransformation of secondary metabolites.
Biotechnol Bioeng 1996;49:481 – 94.
Banerjee S, Shang TQ, Wilson AM, Moore AL,
Strand SE, Gordon MP, et al. Expression of
functional mammalian P450 2E1 in hairy root
cultures. Biotechnol Bioeng 2002;77:462–6.

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Establishment of hairy root culture with genetic transformation

  • 1. PROTEGES-Kartikey Vikram Singh And Vineet Dubey MENTOR-Santosh Kr. Mishra
  • 2.   Recently there has been a perceptible revival of interest in the use of medicinal plants throughout the world culminating into a manifold increase of medicinal plant based products. At present there are about 130 clinically useful prescription drugs of known chemical structures, solely derived from higher plants and used in modern system of medicines.
  • 3.  In view of the spectacular increase in the demand of plant based compounds, the concerned medicinal plants have been indiscriminately exploited leading to scarcity or extinction of many valuable plant species. plant species product Cost($/kg) Cath. roseus Ajmalicine 37,000 P. somniferum Codeine 17,000 Cath. roseus Vincristine 20,00,000 Cath. roseus Vinblastine 10,00,000 Colchium autumnale colchicine 35,000 Panax ginseng Ginsenosides 50,000
  • 4.    This project deals with the production of highvalue secondary metabolites including pharmaceuticals and food additives through root cultures and transgenic roots obtained through biotechnological means. Recent developments in transgenic research have opened up the possibility of the metabolic engineering of biosynthetic pathways to produce high-value secondary metabolites.
  • 5. Definition  It is the culture produced after the infection of explants or cultures by the gram negative soil bacterium Agrobacterium rhizogenes.  This processes take advantage of the naturally occurring hairy root disease in Dicotyledons.
  • 6.   Agrobacterium recognizes some signal molecules exuded by wounded plant cells and becomes attached to it. The bacteria contain the Root inducing plasmid (Ri-plasmid) The bacteria genetically transfer part of the Ri-plasmid called the transfer DNA (T-DNA) to the plant genome.
  • 7.   where it gets expressed and make the plant cell to proliferate by increasing the rate of cell division (cytokine expression) and cell elongation ( auxin expression) to produce the hairy roots. Produce the opines which is a type of unusual amino acids (octopine, agropine, nopaline, mannopine, and cucumopine) which is used by the bacterium as a carbon, nitrogen and energy source.
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  • 10.     The hairy root system is genetically and biosynthetically stable. High production of secondary metabolites. The culture can grow under phyto-hormonefree conditions. The culture shows fast growth which reduces the culture time and easy the handling
  • 11. 1. 2. 3. 4. 5. The main aim of this project is to synthesize secondary metabolites from hairy root culture of medicinal plants this process will comprise of following stages: Selecting a plant species appropriate for the desired product. Through Micropropagation obtaining an infection free sample. By means of genetic transformation induce the hairy root culture. Obtaining the product and analysing the final product for quality. Observing effect of different chemicals on the culture.
  • 12. Time Objective two month Literature and Review two month Micro propagation of the Selected Plant two month Biotransformation two month Optimisation of different parameters of culture two month effect of different types of chemical factor on hairy root culture two month Analysis of secondary metabolites produced by hairy roots
  • 13.     To grow the culture of A. rhizogenes we can prepare media either LB or YEB. To grow the hairy root we are preparing MS media and enzyme supplement stock solutions. Establishment of culture room is in progress. Selection of the plant species for micro propagation.
  • 14. References:    S. Ramachandra Rao and G.A. Ravishankar; Biotechnology advances 20 (2002) 101 – 153; Plant cell cultures: Chemical factories of secondary metabolites. Suchitra Banerjee, Sailendra Singh, Laiq Ur Rahman; Biotechnology advances 30 (2012) 461–468; Biotransformation studies using hairy root cultures. Flores HE, Dai YR, Freyer AJ, Michaels PJ. Biotransformation of menthol and geraniol by hairy root cultures. Plant Physiol Biochem 1994;32:511–9. Jung G, Tepfer D. Use of genetic transformation by the T-DNA of Agrobacterium rhizogenesto stimulate biomass and tropane alkaloid production in Atropa belladonna and Calystegiasepium roots grown in vitro. Plant Sci1987;50:145 – 51.
  • 15.     Ambros PF, Matzke AJM, Matzyke MA. Localization of Agrobacterium rhizogenes T-DNA in plant chromosomes by in situ hybridization. EMBO J 1986;5:2073 – 7 Newman DJ, Cragg GM. Natural products as sources of new drugs over the last 25 years.J Nat Prod 2007;70:461–77 Subroto MA, Kwok K, Hamill JD, Doran PM. Coculture of genetically transformed roots and shoots for synthesis, translocation and biotransformation of secondary metabolites. Biotechnol Bioeng 1996;49:481 – 94. Banerjee S, Shang TQ, Wilson AM, Moore AL, Strand SE, Gordon MP, et al. Expression of functional mammalian P450 2E1 in hairy root cultures. Biotechnol Bioeng 2002;77:462–6.

Notes de l'éditeur

  1. Nos=nitric oxide synthase, mcs=multiple cloning site, Osadh 5'-UTR=translation enhancer