Coat protein of potyviruses. I. Comparison of the four Australian strains of sugarcane mosaic virus

Virology ◽  
1981 ◽  
Vol 111 (2) ◽  
pp. 455-462 ◽  
Author(s):  
Keith H. Gough ◽  
Dharma D. Shukla
2018 ◽  
Vol 45 (6) ◽  
pp. 2749-2758 ◽  
Author(s):  
Retnosari Apriasti ◽  
Suvia Widyaningrum ◽  
Weny N. Hidayati ◽  
Widhi D. Sawitri ◽  
Nurmalasari Darsono ◽  
...  

1995 ◽  
Vol 140 (10) ◽  
pp. 1817-1831 ◽  
Author(s):  
G. R. Smith ◽  
R. Ford ◽  
J. D. Bryant ◽  
R. L. Gambley ◽  
T. K. McGhie ◽  
...  

2005 ◽  
Vol 151 (2) ◽  
pp. 409-412 ◽  
Author(s):  
F. Espejel ◽  
D. Jeffers ◽  
J. C. Noa-Carrazana ◽  
S. Ruiz-Castro ◽  
L. Silva-Rosales

2005 ◽  
Vol 151 (1) ◽  
pp. 167-172 ◽  
Author(s):  
A. L. Gemechu ◽  
P. Chiemsombat ◽  
S. Attathom ◽  
K. Reanwarakorn ◽  
R. Lersrutaiyotin

2019 ◽  
Vol 24 (1) ◽  
pp. 57
Author(s):  
Natalia Tri Astuti ◽  
Nurmalasari Darsono ◽  
Suvia Widyaningrum ◽  
Widhi Dyah Sawitri ◽  
Sri Puji Astuti ◽  
...  

Sugarcane mosaic virus (SCMV, genus Potyvirus, family Potyviridae) is a prominent pathogen of sugarcane (Saccharum sp. hybrids). It can cause losses in susceptible varieties, in crop as well as sugar production, economically. Although it has been studied in major sugar-producing countries, research on the definement of SCMV from Indonesian isolates based on molecular study has been very limited. This study aimed to obtain a proper recombinant antigens emanating from coat protein of SCMV from Indonesian isolate in order to produce polyclonal antibodies that cann be used for immunodiagnosis assays in a subsequent study. A gene-encoding coat protein of SCMV (CP-SCMV) was amplified using RT-PCR and cloned into vector pJET1.2. The cDNA was inserted into 6X His-tag expression plasmid of pET28a(+) and over-expressed in Escherichia coli BL21(DE3) to produce a recombinant protein. The highest expression was found in 0.1M IPTG induction media for 5 h at 37oC. SDS-PAGE analysis clarified that the recombinant CP-SCMV remained as an insoluble fraction. Purifications was carried out by the affinity Ni-NTA resin, followed by electroelution to obtain a highly purified protein. To meet the quality requirements of a proper antigen, the highly purified protein was concentrated. A molecular weight of the rCP-SCMV (approximately 40 kDa) was clearly observed by 10% SDS-PAGE at the concentration of 16.184 mg/mL. 


Agronomy ◽  
2018 ◽  
Vol 8 (6) ◽  
pp. 93 ◽  
Author(s):  
Nurmalasari Darsono ◽  
Novita Azizah ◽  
Kiky Putranty ◽  
Natalia Astuti ◽  
Hardian Addy ◽  
...  

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