scholarly journals Molecular fingerprinting of lal teer chili variety “morich super f1”

2019 ◽  
Author(s):  
Hossain Sohrawardy ◽  
Salina Sultana

Abstract Background : Molecular markers do not influence the environment and age of the plant species. DNA fingerprinting is a useful tool for varietal protection for the seed industry. Molecular fingerprinting helps to maintain the genetic purity of parent lines and hybrids. Result: Primer PP 24 and PP 53 showed polymorphic band to Morich Super F 1 and its parents. Conclusion: Morich Super hybridity test conducts at the Lal Teer Biotech Laboratory using these primers.

Planta Medica ◽  
2006 ◽  
Vol 72 (11) ◽  
Author(s):  
S Sukrong ◽  
T Phadungcharoen ◽  
N Ruangrungsi

2020 ◽  
Vol 103 (2) ◽  
pp. 325-334 ◽  
Author(s):  
Solène Pruvot-Woehl ◽  
Sarada Krishnan ◽  
William Solano ◽  
Tim Schilling ◽  
Lucile Toniutti ◽  
...  

Abstract Background Locating the optimal varieties for coffee cultivation is increasingly considered a key condition for sustainable production and marketing. Variety performance varies when it comes to susceptibility to coffee leaf rust and other diseases, adaptation to climate change and high cup quality for specialty markets. But because of poor organization and the lack of a professional coffee seed sector, most existing coffee farms (and even seed lots and nurseries) do not know which varieties they are using. DNA fingerprinting of coffee planting material will contribute to professionalize the coffee seed sector. Objective The objective of this paper is i) to check in a large scale the robustness of the existing coffee DNA fingerprinting method based on eight Single Sequence Repeats markers (SRR) and ii) to describe how it can help in moving the needle towards a more professional seed sector. Method 2533 samples representing all possible genetic background of Arabica varieties were DNA fingerprinted with 8 SRR markers. The genetic diversity was analyzed and the genetic conformity to varietal references was assessed. Results The DNA fingerprinting method proved to be robust in authenticating varieties and trace back the history of C. arabica breeding and of the movement of C. arabica varieties. The genetic conformity of two important coffee varieties, Marseillesa and Gesha, proved to be 91% and 39% respectively. Conclusions DNA fingerprinting provides different actors in the coffee sector with a powerful new tool—farmers can verify the identity of their cultivated varieties, coffee roasters can be assured that marketing claims related to varieties are correct, and most of all, those looking to establish the a more professional and reliable coffee seed sector have a reliable new monitoring tool to establish and check genetic purity of seed stock and nursery plants. Highlights While C. arabica is primarily self-pollinating, even fixed line varieties appear to be drifting away from their original genetic reference due to uncontrolled cross pollination. A set of 8 SSR markers applied to the largest possible genetically diverse set of samples prove to discriminate between a wide range of varieties Figures confirm that genetic non conformity of coffee varieties can represent up to 61% of checked samples.


2018 ◽  
Vol 7 (4) ◽  
pp. 379-390 ◽  
Author(s):  
Vanisri Satturu ◽  
Durga Rani ◽  
Swathi Gattu ◽  
Jamal Md ◽  
Sreedhar Mulinti ◽  
...  

2007 ◽  
Vol 115 (1) ◽  
pp. 7-12 ◽  
Author(s):  
Li-Wang Liu ◽  
Yan Wang ◽  
Yi-Qin Gong ◽  
Tong-Min Zhao ◽  
Guang Liu ◽  
...  

2013 ◽  
Vol 41 (3) ◽  
pp. 464-468
Author(s):  
H.F. Yu ◽  
J.S. Wang ◽  
Z.Q. Zhao ◽  
X.G. Sheng ◽  
H.H. Gu

Author(s):  
Dilek Tekdal

Vuralia turcica is endemic to Turkey and currently endangered. Little molecular information is available for this plant. Previous characterization and classification of V. turcica have been based on the DNA sequences of the ITS region. Molecular markers are essential for studying of genotyping and biogeography, but any of each marker is not enough to characterize a plant species in its use alone. In this study, the chloroplast rbcL and trnL regions were amplified in V. turcica using the primers that have been published in the previous studies. Successfully amplified DNA fragments were extracted and commercially sequenced. The partial rbcL and trnL sequences were submitted to the NCBI database (accession number KX164510, KX164511, respectively). Amplified both DNA of two regions of rbcL and trnL were used to construct a phylogenetic tree.


Sign in / Sign up

Export Citation Format

Share Document