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    plant tissue culture of aloe vera plant tissue culture of aloe vera Presentation Transcript

    • Plant tissue culture of Aloe vera
      By-
      GarimaShrivastava
      Pratibha Singh
    • INTRODUCTION
      Aloe verasynbarbadensisMill. belongs to the family Liliaceae.
      Commonly called as 'Burn plant'. It is a xerophyte and can be grown even in dry lands under rain fed conditions.
      Aloe is a coarse looking perennial plant with a short stem.
      Found in the semi-wild state in many parts of the country.
    • Leaves 30-60 cm long, erect, crowded in a basal rosette, full of juice, glaucous-green, narrow –lanceolate, long-acuminate, smooth except for the spiny teeth on the margins.
      Commercial Aloes are obtained from wild as well as cultivated plants.
    • PROPAGATION
      Propagation is primarily by means of suckers (or) offshoots, which are separated carefully from mature plants.
      Medium sized suckers are chosen and carefully dugout without damaging the parent plant at the base and can be directly planted in the field and transplanted.
    • Elite Plant Material of Aloe vera
    • Key Constituents
      Anthraquinones (aloin, Aloe - emodin), Resins, Tannins, Polysaccharides etc.
      The principal constituent of aloin is a water-soluble crystalline glycoside barbaloin.
      Leaves exude a bitter liquid, which is dried and known as "bitter Aloes." They also contain a clear gel, which is a soothing skin remedy.
      Leaves are broken off and the clear gel is applied to the skin as a first aid for burns.
    • Aloe containscathartic anthra-glycosides and its active principle ranging from 4.5 to 25% of Aloin.
      These are extensively used as active ingredients in laxative, anti-obesity preparation, as a moisturizer, emollient, wound healer, in various cosmetic and pharmaceutical formulations. It is a drug as well as a cosmetic.
    • MATERIALS AND METHODS USED FOR CULTURING
      Plant material-
      • Elite plants were healthy and free of symptoms of disease, pest problems and showed good biomass yield.
      • Shoot with young leaves was collected from the elite plants.
    • Explant sterilization-
      • Explants first were washed thoroughly in running tap water for 30 minutes.
      • Washed with liquid detergent and Tween 20 for 10min with vigorous shaking. After washing with detergent explants were again washed with running tap water to remove any traces of detergent for 30 minutes.
      • Explant taken in laminar hood where 2-3 sterile washing is done and then explant kept in 70% alcohol for 30 seconds.
      • After alcohol dip, explants were surface sterilized with freshly prepared 0.1% w/v aqueous solution of Mercuric chloride for 5 minutes.
      • After Mercuric chloride treatment, explants were thoroughly washed for 3-4 times with sterile water to remove any traces of Mercuric chloride.
    • Culture media-
      • The basal medium used for the culture is Murashige and Skoog medium with sucrose 3% and 0.8% agar.
      • Growth hormones, 6-benzylaminopurine (BA), 3-Indolebutyric acid (IBA), kinetin (Kn), Adenine sulphate were added to the basal medium either singly or in various combinations.
      • Autoclaved the media when taken all material in fixed amount.
    • Inoculation of explants
      The explants were further trimmed and extra outer leaves were removed to make them in suitable sizes.
      After cutting explants into suitable size (2-3cm),explants are transferred to culture bottles containing MS medium with 0.2mg/L BA and 0.2 mg/L IBA.
      Inoculated plants then transfered to growth room.
      • Shoot proliferation- In this the explantis being scratched from the parent plant by means of scalpel and then is being proliferated in the MS solid and liquid medias. Then preserved for 28 days.
      • Rooting of microshoots- 3-4 cm of shoots were being exuaded from the parent plant and then placed in 2 types of rooting MS media onw with hormone and the other without. 15days culture is being done.
    • Fig.1 fig. 2
      microshoot inoculated in MS medium shoot proliferation
      • Culture conditions: All cultures were incubated under 16 hr photoperiod with light intensity of 2000-2500 lux.
      • Acclimatization: After 15 days of culture on rooting media, the plantlets were shifted to plastic pots for their hardening prior to final transfer to soil to natural conditions.
      After planting the plantswerethoroughly watered and kept under polyhouse having 80% humidity and31oC temperature for ten days.
      In-between the ten days plants were thoroughly watered .
      Then the plants were shifted to shade house with less humidity level and indirect sunlight.
    • fig 3 fig 4
      • DNA isolation-
      For the DNA isolation of the new generated plant, we use CTAB plant DNA extraction kit.
      Agarose. gel electrophoresis is being done to identify the bands of DNA.
    • fig 5
      normal plant genomic DNA
    • Uses
      • Edible uses
      Aloes have been used worldwide for more than 3,500 years.
      Leaves - cooked.
      A gel in the leaves is sometimes used as an ingredient of commercial jellies.
      Juice is also taken from the aloe vera leaves. The bitter juice is often prepared as a flavored drink and is used to help with digestive problems.
    • MEDICINAL USES
      • Aloe vera is a fairly well known herbal preparation with a long history of use. It is widely used in modern herbal practice and is often available in proprietary herbal preparations.
      • It has two distinct types of medicinal use.
      The clear gel contained within the leaf makes an excellent treatment for wounds, burns and other skin disorders, placing a protective coat over the affected area. This action is in part due to the presence of aloectin B, which stimulates the immune system
      • The second use comes from the yellow sap at the base of the leaf. The leaves are cut transversally at their base and the liquid that exudes from this cut is dried. It is called bitter aloes and contains anthraquinones which are a useful digestive stimulant .
      • Aloe is used in many skin care products because of its ability to stimulate healthy cell growth and repair damaged tissues. Most people think of using Aloe only on their skin because that is all they know about
      • Used for the treatment of chronic contipation.
      • Aloe extract may be useful in the treatment of diabetes.
      • Contains numerous vitamins and enzymes which have anti-microbial activities.
    • USES IN COSMETICS
      • It is beneficial for the cosmetic products such as make up, anti-wrinkle creams, facial masks, skin conditioners and lipsticks.
      • The leaf extracts are used in skin-care cosmetic products.
    • CONCLUSION
      • Aloe verasynbarbadensis Mill. is a xerophytic medicinal plant of considerable importance.
      • Widely used in cosmetic and drug industry and its demand is increasing day by day.
      • Due to widespread male sterility it propagates only through vegetative mode of reproduction.
      • But its propagation rate is very slow to meet commercial demand of high quality planting material for its commercial cultivation. So, micropropagationis done on this plant.
      • Hundred percent shoot showed rooting response on hormone –free medium.
      • Regenerated plantlets, 85% survival during polyhouse conditions and 82% during shade house stage of hardening.
      • All the plants produced were morphologically similar to the mother/control plants.
    • BIBLIOGRAPHY
      • Plant tissue culture by Bhojwani and Razdan.
      • Dissertation by Mr.DiwakarAggarwal.
      • www.google.com
      • www.pubmed.com
      • www.wikipedia.com