2006
DOI: 10.1128/aem.72.1.760-768.2006
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Involvement of Quinolinate Phosphoribosyl Transferase in Promotion of Potato Growth by a Burkholderia Strain

Abstract: Burkholderia sp. strain PsJN stimulates root growth of potato explants compared to uninoculated controls under gnotobiotic conditions. In order to determine the mechanism by which this growth stimulation occurs, we used Tn5 mutagenesis to produce a mutant, H41, which exhibited no growth-promoting activity but was able to colonize potato plants as well as the wild-type strain. The gene associated with the loss of growth promotion in H41 was shown to exhibit 65% identity at the amino acid level to the nadC gene … Show more

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Cited by 27 publications
(24 citation statements)
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“…Burkholderia phytofirmans PsJN T is a prominent and efficient plant growth-promoting endophyte (2,5,9), which was isolated from Glomus vesiculiferum-infected onion roots (4,7).…”
Section: Burkholderia Phytofirmans Psjnmentioning
confidence: 99%
“…Burkholderia phytofirmans PsJN T is a prominent and efficient plant growth-promoting endophyte (2,5,9), which was isolated from Glomus vesiculiferum-infected onion roots (4,7).…”
Section: Burkholderia Phytofirmans Psjnmentioning
confidence: 99%
“…Nicotinamidase activity was determined as described by Wang and Pichersky (2007). QPRT was assayed as described by Wang et al (2006). NAD synthase was assayed as described by Wagner and Wagner (1985), with the exception that the NAD produced was determined enzymatically as described by Gibon and Larher (1997).…”
Section: Nad Biosynthesis Enzyme Activity Assaymentioning
confidence: 99%
“…These growth conditions were used for all experiments unless specified otherwise. The leaf buds generated were dipped into PsJN bacterial suspension for 1 min (Wang et al 2006). They were then dried in a sterile petri dish and transferred into test tubes containing growth media at pH 6.…”
Section: Generation and Maintenance Of Plant Materials And Plant Inocmentioning
confidence: 99%
“…The bacteria were streaked onto nutrient broth agar medium and incubated at 30°C for 48 h. A single colony was then transferred into a test tube (height 15 cm × width 1.5 cm, VWR) containing 5 mL of nutrient broth culture and was incubated overnight at 30°C on a shaker. The PsJN bacterial culture was used to inoculate newly grown leaf buds under sterile conditions (Wang et al 2006).…”
Section: Bacterium Strain and Growth Conditionsmentioning
confidence: 99%
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