In-situ characterization and DNA profiling of selected genotypes of tamarind (Tamarindus indica L.) (Record no. 308610)

000 -LEADER
fixed length control field 06639nam a22002177a 4500
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 630.28
Item number MRI/IN PG
100 ## - MAIN ENTRY--PERSONAL NAME
Personal name Mrithyunjay Nandakumar
245 ## - TITLE STATEMENT
Title In-situ characterization and DNA profiling of selected genotypes of tamarind (Tamarindus indica L.)
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Place of publication, distribution, etc Vellanikkara
Name of publisher, distributor, etc Department of Plant Breeding and Genetics, College of Agriculture
Date of publication, distribution, etc 2025
300 ## - PHYSICAL DESCRIPTION
Extent 117,ip.
502 ## - DISSERTATION NOTE
Dissertation note MSc
520 3# - SUMMARY, ETC.
Abstract Tamarind (Tamarindus indica L.), belonging to the family Leguminosae, is
widely utilized in food, traditional medicine, cosmetics, and other industries. It is
particularly valued for its acidic pulp as a souring agent. Despite its economic and
ecological significance, research on its genetic variability, remains limited, especially
in Kerala, the region harbouring unique primitive cultivars such as ‘valanpuli’ and
sweet types like ‘madhurapuli’ and ‘thenpuli’. The present study which forms a part
of the ongoing state plan was taken up in this background at COA, Vellanikkara
during 2022-2025 with the objectives of in-situ characterization and DNA profiling of
selected genotypes of tamarind.
Thirty steady bearing tamarind genotypes located from three revenue blocks of
Palakkad district of Kerala formed the material for the study. These genotypes were
subjected to morphological, biochemical and molecular evaluation. The
morphological evaluation based on 11 qualitative and 17 quantitative characters was
done using the descriptors from established studies (Patil, 2004; Singh, 2010) and
Protection of Plant Varieties and Farmer's Rights Authority (PPVFRA,2017)
guidelines. TSS, total sugar, titratable acidity, vitamin C, total antioxidant capacity
and seed protein were estimated following standard procedures for biochemical
characterization.
Wide variability was observed among the accessions for all the quantitative
traits. Variations expressed by the genotypes in terms of both pod and seed
quantitative traits was also high. Among the genotypes, KTJ 166 was having the
highest pod weight and pod length. The highest pulp percentage was observed in KTJ
162, while the highest real pulp value (RPV) was recorded in KTJ 164 (10.83). The
biochemical characters viz., TSS, total sugar, titratable acidity, vitamin C, total
antioxidant capacity and seed protein ranged from 46.35 to 85.97°B, 13.96-41 per
cent, 7.59 - 13.27 per cent, 5.12 - 20.93 mg/100 g, 26.50 to 58.36 mg AAE/g and14.43
g/100 g to 19.87 g/100 g, respectively. The sugar-to-acid ratio in tamarind is a good
way to differentiate between sweet and sour types. Two genotypes, KTJ 60 and KTJ
48, exhibiting acidity levels below 8 per cent, with total sugar content varying
between 36.30-41.00 per cent showed a high sugar acid ratio representing sweet
types. Based on organoleptic evaluation, the maximum score for overall acceptability
was also obtained for KTJ 48 followed by KTJ 88 and KTJ 66.
Agglomerative hierarchical clustering based on quantitative and biochemical
characters resulted in five clusters. Clustering clearly separated KTJ 77 and KTJ 162
from other genotypes by placing them in cluster II and III, respectively. High
heritability coupled with high genetic gain was observed for pod weight, pod length,
pulp percentage, fibre percentage, seed weight, number of seeds per pod, TSS,
titratable acidity, ascorbic acid, total antioxidant capacity and total sugar. Pod weight,
a crucial determinant of yield, demonstrated significant positive correlation with pod
length (r = 0.94), RPV (r= 0.90) seed weight per pod (r = 0.94), and number of seeds
per pod (r = 0.71). RPV demonstrated positive correlations with pod weight, pod
length, pulp percentage, seed weight per pod and number of seeds per pod. TSS
demonstrated a strong positive correlation with total antioxidant capacity. Conversely,
titratable acidity exhibited a significant negative correlation with antioxidant capacity
(r = -0.735). Principal Component Analysis (PCA), done for the purpose of clustering
the accessions, revealed that the first three components explained 88.93 per cent of
total variation. From the comprehensive evaluation of PCA analysis and clustering,
four genotypes—KTJ 84, KTJ 164, KTJ 166, and KTJ 174—were identified as plus
trees with high RPV, while KTJ 48 (41%), KTJ 60 (36.3%), KTJ 77 (39.52%), and
KTJ 172 (36.5%) stood out for notable total sugar content.
All 30 genotypes were initially screened with 39 random primers, of which all
produced reproducible bands except ISSR-835, ISSR-815, (CT)₈T, and (GT)₈GC. The
number of bands per primer ranged from 3 to 13, averaging 6.32. ISSR-29 generated
the highest number of amplicons (368), while ISSR-22 produced the least (80). The
highest polymorphism was observed in ISSR-22 (62.5%), followed by ISSR-18
(56.83%), and ISSR-2 (47.98%), whereas ISSR-30 had the lowest (4.11%). The
UPGMA dendrogram generated via NTSYS-pc software using Jaccard similarity
coefficients indicated high genetic similarity among accessions. At 60 per cent
similarity, 30 genotypes clustered into five groups. KTJ 169 exhibited the greatest
genetic distinction, forming an independent branch, indicating some genetic
divergence. Among 18 shortlisted DNA markers, seven (ISSR-1(800bp) ISSR-2
(1000bp), ISSR-17 (600bp), ISSR-18 (525bp), ISSR-25 (625bp, 725bp), ISSR-26
(900bp), ISSR-34 (325bp)) effectively detected polymorphism, producing unique
bands in KTJ 174, KTJ 51, KTJ 162, KTJ 172, KTJ 169, KTJ 164, and KTJ 89. ISSR
1 (550bp) differentiated KTJ 72 and KTJ 77, while ISSR-1 (700bp) and ISSR-6
(675bp) uniquely identified KTJ 48 and KTJ 60. ISSR-18 (625bp) separated KTJ 48,
KTJ 60, and KTJ 170, and ISSR-24 distinguished KTJ 48, KTJ 60, and KTJ 174.
ISSR-25 (525bp) effectively differentiated KTJ 48, KTJ 84, KTJ 164, and KTJ 168.
The study provides a comprehensive assessment of tamarind genetic diversity
through morphological, biochemical, and molecular characterization. Molecular
markers identified in this study can facilitate further genetic studies and marker
assisted selection in tamarind improvement programs. The findings of this research
are expected to contribute to the conservation and improvement of tamarind
germplasm for future breeding programs.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Plant Breeding and Genetics
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element DNA
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Tamarind
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Tamarindus indica L.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Genotype
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Asna, A C (Guide)
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier https://krishikosh.egranth.ac.in/handle/1/5810226417
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Item type Theses
Holdings
Not for loan Collection code Permanent location Current location Shelving location Date acquired Full call number Barcode Date last seen Koha item type
Not For Loan Thesis KAU Central Library, Thrissur KAU Central Library, Thrissur Technical Processing Division 2025-08-02 630.28 MRI/IN PG 176510 2025-08-02 Theses
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