Biochemical characterization of C4 protein of Cotton Leaf Curl Kokhran Virus-Dabawali

2013 ◽  
Vol 1830 (6) ◽  
pp. 3734-3744 ◽  
Author(s):  
Debojit Guha ◽  
C.G. Poornima Priyadarshini ◽  
Arunima Purakayastha ◽  
R. Thippeswamy ◽  
M. Lakshmikanth ◽  
...  
2015 ◽  
Vol 13 (4) ◽  
pp. 3-9
Author(s):  
Muhammad Azmat Ullah Khan ◽  
Ahmad Ali Shahid ◽  
Abdul Qayyum Rao ◽  
Kamran Shehzad Bajwa ◽  
Tahir Rehman Samiullah ◽  
...  

Virus Genes ◽  
2012 ◽  
Vol 46 (1) ◽  
pp. 111-119 ◽  
Author(s):  
Neha Tiwari ◽  
P. K. Sharma ◽  
V. G. Malathi

Viruses ◽  
2014 ◽  
Vol 6 (1) ◽  
pp. 223-242 ◽  
Author(s):  
Muhammad Ashraf ◽  
Ahmad Shahid ◽  
Abdul Rao ◽  
Kamran Bajwa ◽  
Tayyab Husnain

PLoS ONE ◽  
2011 ◽  
Vol 6 (11) ◽  
pp. e26929 ◽  
Author(s):  
C. G. Poornima Priyadarshini ◽  
M. V. Ambika ◽  
R. Tippeswamy ◽  
H. S. Savithri

2021 ◽  
Vol 3 (1) ◽  
pp. 28-34
Author(s):  
Fizza Akhter ◽  
Muhammad Tahir

Begomoviruses are a serious threat to cotton production throughout the world. In Pakistan, enormous crop losses occur as a result of cotton leaf curl disease (CLCuD) caused by begomoviruses. Molecular characterization of begomoviruses has made possible the identification and analysis of begomoviruses prevalent in a host plant. Infected cotton leaf sample (C-59) was obtained from area around Khanewal during 2011. The total DNA was isolated from the infected sample by Cetyl trimethyl ammonium bromide (CTAB) method. An expected size band of approximately 1100bp, covering coat protein region of the virus, was amplified using universal primers. The amplified product was T/A cloned and sequenced to its entirety. DNA sequence showed 99% nucleotide sequence identity to each of Cotton leaf curl Burewala virus ((CLCuBuV; Accession No HF549Begomoviruses are a serious threat to cotton production throughout the world. In Pakistan, enormous crop losses occur as a result of cotton leaf curl disease (CLCuD) caused by begomoviruses. Molecular characterization of begomoviruses has made possible the identification and analysis of begomoviruses prevalent in a host plant. Infected cotton leaf sample (C-59) was obtained from area around Khanewal during 2011. The total DNA was isolated from the infected sample by Cetyl trimethyl ammonium bromide (CTAB) method. An expected size band of approximately 1100bp, covering coat protein region of the virus, was amplified using universal primers. The amplified product was T/A cloned and sequenced to its entirety. DNA sequence showed 99% nucleotide sequence identity to each of Cotton leaf curl Burewala virus ((CLCuBuV; Accession No HF549184)) and Cotton leaf curl Kokhran virus (CLCuKV; Accession No AJ002449)). Since CLCuBuV is a recombinant of CLCuKV and Cotton leaf curl Multan virus and the coat protein region of CLCuBuV was derived from CLCuKV that is most probable reason that the available sequence showed identity with CLCuBuV as well as CLCuKV. A complete characterization of full length virus will determine whether isolate C-59 is CLCuBuV or CLCuKV. Literature indicates that there is no existence of CLCuKV within the region and CLCuBuV is dominating within Indo-Pak184)) and Cotton leaf curl Kokhran virus (CLCuKV; Accession No AJ002449)). Since CLCuBuV is a recombinant of CLCuKV and Cotton leaf curl Multan virus and the coat protein region of CLCuBuV was derived from CLCuKV that is most probable reason that the available sequence showed identity with CLCuBuV as well as CLCuKV. A complete characterization of full length virus will determine whether isolate C-59 is CLCuBuV or CLCuKV. Literature indicates that there is no existence of CLCuKV within the region and CLCuBuV is dominating within Indo-Pak


Phyton ◽  
2021 ◽  
Vol 90 (6) ◽  
pp. 1613-1632
Author(s):  
Zunaira Sher ◽  
Muhammad Umair Majid ◽  
Sameera Hassan ◽  
Fatima Batool ◽  
Beenish Aftab ◽  
...  

Author(s):  
J. H. Resau ◽  
N. Howell ◽  
S. H. Chang

Spinach grown in Texas developed “yellow spotting” on the peripheral portions of the leaves. The exact cause of the discoloration could not be determined as there was no evidence of viral or parasitic infestation of the plants and biochemical characterization of the plants did not indicate any significant differences between the yellow and green leaf portions of the spinach. The present study was undertaken using electron microscopy (EM) to determine if a micro-nutrient deficiency was the cause for the discoloration.Green leaf spinach was collected from the field and sent by express mail to the EM laboratory. The yellow and equivalent green portions of the leaves were isolated and dried in a Denton evaporator at 10-5 Torr for 24 hrs. The leaf specimens were then examined using a JEOL 100 CX analytical microscope. TEM specimens were prepared according to the methods of Trump et al.


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