F. Niepold, “A Simple and Fast Extraction Procedure to Obtain Amplifyable DNA from Ralstonia (Pseudomonas) solanacearum and Clavibacter michiganensis ssp Sepedonicus Inoculated Potato Tuber Extracts and Naturally Infected Tubers to Conduct a Polymerase Chain Reaction (PCR),” Journal of Phytopathology, Vol. 147, 1999, pp. 249-256. doi:10.1046/j.1439-0434.1999.147004249.x

has been cited by the following article:

• TITLE: Rapid Method for Isolation of PCR Amplifiable Genomic DNA of Ralstonia solanacearum Infested in Potato Tubers

  AUTHORS: Alka Grover, Swarup K. Chakrabarti, Wamik Azmi, S. M. P. Khurana

  KEYWORDS: Ralstonia solanacearum; PCR; Detection; Potato; DNA

  JOURNAL NAME: Advances in Microbiology, Vol.2 No.4, December 25, 2012

  ABSTRACT: The aim of the present study was to develop a very fast and simple genomic DNA isolation method for Ralstonia solanacearum which infest potato tubers. One hundred potato tubers were collected and ten composite samples were prepared having 10 tubers each. Four different DNA isolation methods were used for bacterial genomic DNA isolation present in tubers. PCR with R. solanacearum specific primers and pathogenicity tests were performed. Out of four methods two gave PCR amplifiable DNA. The simplest method was boiling the cell lysate for 5 min, vortexing for 2 min then extraction with phenol chloroform method. This method provides significant amount of DNA which is free from contaminants thus rendering the DNA amicable to PCR amplification. The developed method would be useful for quick and sensitive detection of this pathogen in seed potatoes and would be beneficial to stop the further spread of pathogen.