Anther culture of Capsicum L. for doubled haploid production (Record no. 289754)

MARC details
000 -LEADER
fixed length control field 04751nam a22002177a 4500
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 660.6
Item number NIN/AN PG
100 ## - MAIN ENTRY--PERSONAL NAME
Personal name Ninitha Vijayan
245 ## - TITLE STATEMENT
Title Anther culture of Capsicum L. for doubled haploid production
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Place of publication, distribution, etc Vellayani
Name of publisher, distributor, etc Department of Plant Biotechnology, College of Agriculture
Date of publication, distribution, etc 2022
300 ## - PHYSICAL DESCRIPTION
Extent 64p.
502 ## - DISSERTATION NOTE
Dissertation note MSc
520 3# - SUMMARY, ETC.
Abstract The study entitled “Anther culture of Capsicum annuum L. for doubled haploid <br/>production” was carried out at the Department of Plant Biotechnology, College of <br/>Agriculture, Vellayani, Thiruvananthapuram during 2019 - 2021. The objective of the study <br/>was to develop haploids of Capsicum annuum var. Arka Meghana by anther culture.<br/>Standardisation of the suitable stage of bud of Capsicum annuum var. Arka Meghana <br/>for anther culture was carried out by staining the anthers of different bud stages with 1% <br/>aceto-orcein and calculating the percentage of microspores at late uninucleate and early <br/>binucleate stages. Buds collected at six days after bud initiation had 57% of microspores in <br/>the late uninucleate stage and 34% in the early binucleate stage. Buds collected at nine days <br/>after bud initiation had 21% of microspores in the late uninucleate stage and 49% in the early <br/>binucleate stage. Hence the buds collected at six and nine days after bud initiation were found <br/>to be most suitable for anther culture.<br/>The optimum surface sterilization condition for buds was standardised by treating the <br/>buds with 70% of ethanol and 4% of sodium hypochlorite for different time intervals. Surface <br/>sterilization with 70% ethanol for 30 seconds followed by 4% sodium hypochlorite for 15 <br/>minutes was found to be most effective.<br/>Anther culture was carried out in nine media compositions for optimization. Anthers <br/>were inoculated onto full strength Murashige and Skoog (1962) medium (MS) and Dumas de <br/>Vaulx (1981) medium (CP) with different concentrations of plant growth regulators Kinetin, <br/>BA, NAA, IAA and 2,4-D with AgNO3 and activated charcoal as additives. The anthers were <br/>incubated at 25°C for two and eight days in darkness. The treatment T5 - MS + 4.00 mg/L <br/>NAA + 0.10 mg/L BA + 0.25% activated charcoal + 10 mg/L AgNO3 incubated at 25°C for <br/>two days in darkness showed callogenesis (3.17%) at six weeks after inoculation. All the <br/>treatments incubated at 25°C for eight days in darkness showed response at sixth week of <br/>inoculation with callogenesis varying from 3.75% to 15.38%. Among the nine treatments, <br/>highest callogenesis of 15.38% was observed in the treatment T5 at sixth week of inoculation. <br/>Globular embryo initiation (1.25%) was observed in the treatment T4 - MS + 4.00 mg/L NAA <br/>+ 1.00 mg/L BA at sixth week of inoculation.<br/>The six treatments that showed good response at 25°C incubation temperature and <br/>eight days darkness were incubated at 35°C in two days darkness. All the treatments showed <br/>response varying from 4% to 15.54% of callogenesis at second week of inoculation. <br/>Callogenesis varying from 10.66% to 34.48% and embryonic calli induction varying from <br/>3.17% to 17.24% was observed in the fourth week of inoculation. At sixth week of <br/>inoculation callogenesis varied from 11.11% to 37.93% and embryonic callus induction <br/>varied from 3.17% to 19.54%. Among the six treatments, the maximum callogenesis of <br/>37.93% and embryonic calli induction of 19.54% was observed in the treatment T5 at fourth <br/>week of inoculation. <br/>Embryogenesis was observed in the treatment T7 – MS + 4.00 mg/L NAA + 0.50 <br/>mg/L BA+ 0.25% activated charcoal + 15 mg/L AgNO3 (1.82%) and treatment T6 - MS + <br/>4.00 mg/L NAA + 0.10 mg/L BA + 0.25% activated charcoal + 15mg/L AgNO3 (1.33%) at <br/>fourth week of inoculation. <br/>At sixth week of inoculation, embryo induction (1.15%) was observed in the <br/>treatment T5 – MS + 4.00 mg/L NAA + 0.10 mg/L BA + 0.25% activated charcoal + 10mg/L <br/>AgNO3. Highest embryogenesis of 2.72% was observed in the treatment T7 – MS + 4.00 <br/>mg/L NAA + 0.50 mg/L BA+ 0.25% activated charcoal + 15 mg/L AgNO3. <br/>To conclude, among the treatments tested in Capsicum annuum var. Arka Meghana <br/>the best treatment for indirect embryogenesis and direct embryogenesis was MS + 4.00 mg/L <br/>NAA + 0.10 mg/L BA + 0.25% activated charcoal + 10 mg/L AgNO3 and MS + 4.00 mg/L <br/>NAA + 0.50 mg/L BA + 0.25% activated charcoal + 15 mg/L AgNO3 respectively at culture <br/>conditions of 35°C initial incubation temperature and two days darkness.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Plant Biotechnology
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Capsicum
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Anther culture
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Arka Meghana
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Embryogenesis
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Swapna Alex (Guide)
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier https://krishikosh.egranth.ac.in/handle/1/5810225389
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Dewey Decimal Classification
Item type Theses
Holdings
Not for loan Collection code Home library Current library Shelving location Date acquired Full call number Barcode Date last seen Koha item type
Not For Loan Reference Book KAU Central Library, Thrissur KAU Central Library, Thrissur Theses 25/07/2022 660.6 NIN/AN PG 175425 25/07/2022 Theses
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