+ All Categories
Home > Documents > Final Presentation-group 2

Final Presentation-group 2

Date post: 05-Apr-2018
Category:
Upload: hayati-atiqah-salleh
View: 216 times
Download: 0 times
Share this document with a friend

of 13

Transcript
  • 8/2/2019 Final Presentation-group 2

    1/13

    GROUP 3

    Mazlina Ismail

    Wahurun Iin Mohd Taha

    Hayati Atiqah Salleh

  • 8/2/2019 Final Presentation-group 2

    2/13

    Boesenbergia rotunda (L.) Mansf. Kulturpfl. known as kra-chai & temu kunci.

    Characteristics: small herbaceous plant

    short, fleshy or slight rhizomes with a few leaves. unique scent and also slightly sharp taste.

    (Amy Yap Li Ching et al., 2007).

    Scientific Classification

    Kingdom : PlantaeOrder : Zingiberales

    Family : Zingiberaceae

    Genus : Boesenbergia

    Species : B. rotunda

    INTRODUCTION

  • 8/2/2019 Final Presentation-group 2

    3/13

    Oftenly used as food ingredient and in folkmedicine treatment

    Rhizome (enzymes) as tonics & lotionIngredients

    Commercially use in pharmaceuticals products

    Pharmacological importance - presence offlavanoids, essential oil and chalcones

    (pinostrobin, pinocembrin, cardamonin,alpinetin and boesenbergin molecules)

  • 8/2/2019 Final Presentation-group 2

    4/13

    Primary health care project of Thailand- rhizome

    part to treat dyspepsia

    Potential values (biological activities)

    antipyretic, analgesic, anti-mutagenic, anti-inflammatory, antioxidant enzymes, anti-humanimmunodeficiency virus 1 (anti-HIV-1) proteaseinhibition, anti-tumour, antibacterial, antifungal,

    antispasmodic, and insecticidal activities.

    Enhanced the acceleration of wound healing

    area

  • 8/2/2019 Final Presentation-group 2

    5/13

    a) To observe the effect of plant medium supplemented

    with different level hormones concentration on

    growth ofB. rotunda in vitro culture.

    b) To determine the best level different hormones and

    hormone combinations on growth ofB. rotunda in

    vitro culture.

    OBJECTIVES

  • 8/2/2019 Final Presentation-group 2

    6/13

    Freq of shoot formation in the

    explants is different for

    different MS salt strength

    Supplementation of the PGR -

    BAP and NAA (BN) is better for

    shoot regeneration in BR

    HYPOTHESIS

  • 8/2/2019 Final Presentation-group 2

    7/13

    MATERIALS

    B. rotunda

    Use B.rotundas stem

    (explants) obtained from in

    vitro culture

    Hormones

    1. Benzyl aminopurine (BAP)

    2. 1-naphtalenacetic acid (NAA).3. Indole acetic acid (IAA)

  • 8/2/2019 Final Presentation-group 2

    8/13

    TREATMENTS

    I MSO

    II

    III

    IV

    V

    VI

    MS + BAPa) 0.5mg/L

    b)1.0mg/L

    c) 2.0mg/L3/4MS

    3/4MS + BAPa) 0.5mg/L

    b)1.0mg/L

    c) 2.0mg/L3/4MS + BN

    3/4MS + BI

    NAA 0.1mg/L 0.5mg/L

    BAP

    0.5mg/L a b

    2.0mg/L c d

    IAA 0.1mg/L 0.5mg/L

    BAP

    0.5mg/L a b

    2.0mg/L c d

  • 8/2/2019 Final Presentation-group 2

    9/13

    RESULT

    MS basalsupplemented

    with:

    (a)0.5mg/L BAP

    (b)1.0 mg/L BAP

    (c) 2.0 mg/L BAP

    Media

    Response Frequency(%)

    week 2 week 4I 16.67% 16.67%

    II 0.00% 16.67%

    III (a) 22.22% 33.33%

    III (b) 0.00% 0.00%III (c) 0.00% 0.00%

    IV (a) 83.33% 83.33%

    IV (b) 50.00% 50.00%

    IV (c) 33.33% 66.66%

  • 8/2/2019 Final Presentation-group 2

    10/13

    MS supp with

    + 0.1mg/L NAA

    + 2.0 mg/L BAP

    MS supp with

    + 0.5mg/L IAA

    + 2.0 mg/L BAP

    Media

    Response freq (%)

    week 2 week 4

    I 16.67% 16.67%II 0.00% 16.67%

    III (a) 22.22% 33.33%

    III (b) 0.00% 0.00%

    III (c) 0.00% 0.00%

    IV (a) 83.33% 83.33%IV (b) 50.00% 50.00%

    IV (c) 33.33% 66.66%

    V (a) 0.00% 33.33%

    V (b) 0.00% 50.00%

    V (c) 50.00% 100.00%

    V (d) 25.00% 58.30%

    VI (a) 0.00% 0.00%

    VI (b) 0.00% N/A

    VI (c) 66.67% 66.67%VI (d) 100.00% N/A

  • 8/2/2019 Final Presentation-group 2

    11/13

    Media

    % of

    adventitious

    shoot

    generation

    I 11.22II 5.61

    III (a) 5.61

    III (b) N/A

    III N/A

    IV (a) 6.73

    IV (b) 5.61

    IV 8.42

    V (a) 5.61

    V (b) 5.61V 11.22

    V (d) 7.22

    VI (a) N/A

    VI (b) N/A

    VI 8.42

    MEDIA VI (d) - Shoots formation on MSsupplemented with 2mg/L BAP + 0.5 mg/L IAA

    MEDIA V (c) - Shoots formation on MS

  • 8/2/2019 Final Presentation-group 2

    12/13

    MS

    higher shoot production rate agreement with other monocots (K.galanga, Trillium

    erectum and T.grandiflorum) (Shirin et al, 2000) (Pence & Sourkp, 1993)

    Combination of both BAP+NAA & BAP+IAA

    showed multiple shoot formation Previous study by (Geetha, 1993) support this however study

    by (Swapna, 2004) did not show the same reult

    Similarity between the highest shootformation frequency Media V (c) & VI (d): [BAP] 2.0mg/L

    DISCUSSION

  • 8/2/2019 Final Presentation-group 2

    13/13

    CON

    MS produced higher percentage ofmultiple shoot formation than full strength

    MS media

    Supplementation of 2.0mg/L BAP + auxinworks in multiple shoot formation

    Media V (c), V (d), VI (c) and VI (d) showed

    higher number of shoot formationThe best media is MS supplemented with

    2.0mg/L BAP + auxin

    CONCLUSION


Recommended