8 th Euro Biotechnoloy Congress, 18 – 20 August, Frankfurt, Germany Production of Rosmarinic Acid from in-vitro culture of Basil (Ocimum bacilicum L.)

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Presentation transcript:

8 th Euro Biotechnoloy Congress, 18 – 20 August, Frankfurt, Germany Production of Rosmarinic Acid from in-vitro culture of Basil (Ocimum bacilicum L.) and Lemon balm (Melissa officinalis L.) Production of Rosmarinic Acid from in-vitro culture of Basil (Ocimum bacilicum L.) and Lemon balm (Melissa officinalis L.) Dr: Raoufa Ahmed Abdel Rahman Associate professor of plant biotechnology City of scientific Research & Technology Applications New Borg ElArab, Alexandria, Egypt

 Intoduction  Rosmarinic acid & its medicinal uses.  Basil & Lemon balm.  Plant tissue culture.  Results.  Conclussions.

Secondary Metabolites  Studies on plant secondary metabolites have been increasing over the last 50 years.  Many higher plants are a major source of natural products used as: Pharmaceuticals and Agrochemicals. Flavor and fragrance ingredients. Food additives and Pesticides.

First isolated from Rosmarinus officinalis by (Scarpati and Oriente, 1958) it is an ester of caffeic acid and (3, 4- dihydroxyphenyl) lactic acid.

Antiviral Antibacterial Anti-inflammatory Anti-allergic activities Antioxidant activities Prevents the proliferation of human cancer cells

Basil Ocimum bacilicum is a member of the Lamiaceae (mint) family. The common name is sweet basil.

 Anti bacterial (gram positive & gram negative bacteria).  Anti-inflammatory  Strong antioxidant activity  Anti proliferative effect  Anti cancer  Antiviral  Antifungal activity medicinal properties of O.bacilicum

Lemon balm Melissa officinalis is a member of the Lamiaceae family. The common name is lemon balm.

medicinal properties of M.officinalis  Antioxidant  Antibacterial  Antifungal agent  Anti cancer  Antiviral properties (against HIV-1 and the influenza virus).  useful in the treatment of Alzheimer’s disease.

Plant Tissue Culture Plant tissue culture is a collection of techniques used to maintain or grow plant cells, tissues or organs (explants) under sterile conditions on a nutrient culture medium of known composition.

Plant tissue culture  Over the past three decades, plant cell cultures techniques have proved to be a valuable tool for study biosynthesis and production of secondary natural products.  One of the plant tissue culture protocols that is considered as an attractive alternative for the production of many valuable natural products is hairy root culture.

Hairy root culture Hairy root is a transgenic phenotype resulted from the infection of suitable plant tissues with the gram-negative soil pathogen Agrobacterium rhizogenes.

Advantages of hairy root cultures Hairy roots high growth rate and genetic stability produce high levels of secondary metabolites produce stable levels of secondary metabolites over long time Enhance secondary metabolites production scaling up in plant bioreactor Elicitation Metabolic Trapping Metabolic engineering

Aim of The work study the efficiency of using plant tissue culture techniques for the production of rosmarinic acid from basil and lemon balm.

Materials and Methods Seed germination Lemon balm seedlings Basil seedlings Callus &shoot &hairy root production Rosmarinic acid extraction &determination Data analysis

Results

Ms medium was used for germination of O.bacilicum and M.officinalis seeds under aseptic condition Seed germination: Ocimum bacilicum Germination percentages 63% Melissa officinalis Germination percentages 84%

Media typeLeafStemRoot MS1( basal MS) MS2( MS + 1mg/l BA+1mg/l NAA) 11.75± ± ±0.85 MS3( MS+3mg/l BA+1mg/l NAA) 8.54± ± ±0.22 MS4( MS+5mg/l BA+1mg/l NAA) 4.35± ± ±0.25 Callus production in lemon balm :

Callus production in basil: Media typeLeafStemRoot MS1 (basal MS) MS2 (MS+1mg/l BA+1mg/l NAA) 6.55± ± ±0.67 MS3 (MS+3mg/l BA+1mg/l NAA) 7.33± ± ±0.42 MS4( MS+5mg/l BA+1mg/l NAA) 10.45± ± ±0.32

B A A- Basil callus culture derived from leaf explants grow on MS+1mg/l BA and 1mg/l NAA (MS2). B- Lemon balm callus cultures derived from leaf explants grow on MS+ 5mg/l BA + 1mg/l NAA (MS4).

Shoot production in lemon balm : Media typeNo. of shoots/explant LeafStemRoot M1 (basal MS) 000 M2 ( MS+1mg/l KIN+1mg/l 2,4-D ) 012±1.50 M3( MS+ 3mg/l KIN+1mg/l 2,4-D) 07±0.80 M4( MS+5mg/l KIN+ 1mg/l 2,4-D) 03±0.40

A B Shoot culture culture of basil and lemon balm. A-Basil shoot culture derived from shoot tip explants grow on MS+ 0.4mg/l thiamine HCl + 1mg/l BA. B-Lemon balm shoot culture derived from stem explants grow on MS+1mg/l of both Kin and 2,4-D (M2).

Leaf discs, stem discs, or seedling segments A. rhizogenes Inoculation 1 2 Co-cultivation (1-5 days ) 3 Selection on antibiotic containing medium 4 Hairy root formation 5 Cultivation in liquid medium Method of transformation. Procedure 1

A B C D E F G H Agrobacterium mediated transformation of basil and hairy root culture production using procedure (1).

Effect of explant type on transformation frequency and hairy root production in basil infected with R 1000 strain. Explant type Incubation period Total number of infected explants Number of explants Producing roots Number of hairy roots per explant Root length (cm) Transformation frequency (%) Leaf1hr143110branched 1.0 ± Stem1hr Data collected after 15 days on selection plates

Effect of explant type on transformation frequency and hairy root production in basil infected with A4 strain. Explant type Incubation period Total number of infected explants Number of explants Producing roots Number of hairy roots per explant Root length (cm) Transformation frequency (%) Leaf1hr ± ± Stem1hr Data collected after 15 days on selection plates

In the method a suspension of Agrobacterium is injected into a plant tissues, where it transfers the desired gene to plant cells.

Agrobacterium mediated transformation of lemon balm and hairy root culture production using procedure (2). Arrows showed hairy roots produced after stem injection with Agrobacterium R1000 strain.

Effect of explant type on transformation frequency and hairy root production in lemon balm infected with R 1000 strain. Explant type Incubation period Total number of infected explants Number of explants Producing roots Number of hairy roots per explant Root length (cm) Transformation frequency (%) Leafinjection Steminjection ± ± Data collected after 30 days after infection

Effect of explant type on transformation frequency and hairy root production in lemon balm infected with A4 strain. Explant type Incubation period Total number of infected explants Number of explants Producing roots Number of hairy roots per explant Root length (cm) Transformation frequency (%) Leafinjection Steminjection ± ± Data collected after 30 days after infection

M +Con Con 308bp PCR amplification bands of WT and transformed hairy roots.

Rosmarinic acid levels (ug/mg DW) in control, callus, shoot and hairy root cultures of basil and lemon balm. BasilLemon balm Control9.42± ±0.83 Callus13.20± ±0.39 Shoot25.30±0.2438±25±0.73 Hairy Root68.52± ±0.98 Each treatment is average of three replicates ± SE

Conclusions Plant tissue culture techniques specially Agrobacterium Mediated transformation can be used successfully to produce natural products such as rosmarinic acid.

City of Scientific Research & Technology Applications

Thank You for Attention