2013
DOI: 10.1590/s0100-54052013000400002
|View full text |Cite
|
Sign up to set email alerts
|

Espécies de Phytophthora associadas à gomose em pomares de citros no Estado do Paraná, Brasil

Abstract: RESUMOPalavras-chave adicionais: Phytophthora nicotianae, Phytophthora citrophthora, etiologia, Citrus spp.A gomose dos citros é considerada uma doença de grande importância para a citricultura no Brasil e em nível mundial. A etiologia desta doença compreende um complexo de espécies de Phytophthora. Embora importante, pouco se conhece sobre a gomose nas regiões produtoras de citros no Estado do Paraná. Por isso, este trabalho teve como objetivo identificar espécies de Phytophthora associadas à gomose em pomare… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2016
2016
2022
2022

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(1 citation statement)
references
References 9 publications
0
1
0
Order By: Relevance
“…The PCR was performed in a thermal cycler MyCycler (Bio-Rad Laboratories, Inc). For amplification of the ITS region, PCR was performed with a master mix containing 2 ll of DNA (50 ng ll À1 ); 5 ll of 109 buffer (100 mmol l À1 Tris-HCL, 500 mmol l À1 KCl, pH8Á3), 1Á5 ll of MgCl 2 (50 mmol l À1 ), 1 ll of each primer (10 mmol l À1 ); 1Á0 ll of dNTPs (10 mmol l À1 ); 0Á25 ll of Taq DNA polymerase (5 U ll À1 ) and 38Á25 ll of ultrapure water (Milli-Q) with a final reaction volume of 50 ll (Caixeta et al 2013). The PCR cycle consisted of initial denaturation at 94°C for 5 min; 35 cycles of denaturation at 94°C for 30 s, annealing at 52°C for 45 s, extension at 72°C for 2 min and a final extension cycle at 72°C for 7 min.…”
Section: Molecular Characterization Of the Isolatesmentioning
confidence: 99%
“…The PCR was performed in a thermal cycler MyCycler (Bio-Rad Laboratories, Inc). For amplification of the ITS region, PCR was performed with a master mix containing 2 ll of DNA (50 ng ll À1 ); 5 ll of 109 buffer (100 mmol l À1 Tris-HCL, 500 mmol l À1 KCl, pH8Á3), 1Á5 ll of MgCl 2 (50 mmol l À1 ), 1 ll of each primer (10 mmol l À1 ); 1Á0 ll of dNTPs (10 mmol l À1 ); 0Á25 ll of Taq DNA polymerase (5 U ll À1 ) and 38Á25 ll of ultrapure water (Milli-Q) with a final reaction volume of 50 ll (Caixeta et al 2013). The PCR cycle consisted of initial denaturation at 94°C for 5 min; 35 cycles of denaturation at 94°C for 30 s, annealing at 52°C for 45 s, extension at 72°C for 2 min and a final extension cycle at 72°C for 7 min.…”
Section: Molecular Characterization Of the Isolatesmentioning
confidence: 99%