2010
DOI: 10.1016/j.biortech.2009.12.138
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High level production of adrenic acid in Physcomitrella patens using the algae Pavlova sp. Δ5-elongase gene

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Cited by 11 publications
(16 citation statements)
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“…Engineering another thiolase, Δ5-elongase from alga Pavlova sp. into the moss Physcomitrella patens gave high levels of adrenic acid corresponding to the enzyme’s activity in the alga (Kaewsuwan et al 2010). Taken together, it can be concluded that the ACP-KS interaction is permissive across species, directly following from the phylogenetic relatedness and common ancestry of thiolases.…”
Section: Discussionmentioning
confidence: 99%
“…Engineering another thiolase, Δ5-elongase from alga Pavlova sp. into the moss Physcomitrella patens gave high levels of adrenic acid corresponding to the enzyme’s activity in the alga (Kaewsuwan et al 2010). Taken together, it can be concluded that the ACP-KS interaction is permissive across species, directly following from the phylogenetic relatedness and common ancestry of thiolases.…”
Section: Discussionmentioning
confidence: 99%
“…The information from our study is currently being used for the development of a larger scale cultivation process for A. maritima TISTR 1715 as an alternative source for commercial ARA. Physcomitrella patens 14 0.40 3.06 [33]…”
Section: Discussionmentioning
confidence: 99%
“…Our study is the first to report the optimization of culture conditions for biomass and ARA production by A. maritima TISTR 1715 even its productivity was lower than the fungi, especially M. alpina which is a current available source for industrial production. Nevertheless, ARA productivity of A. maritima TISTR 1715 was much higher than in the antarctic bacterium strain 651 [7], several algae [23], and some lower plants [33,45] (Table 7). Moreover, the higher growth rate and easier handling of the bacterium make A. maritima a better choice for investigating it as a cheap versatile source of ARA.…”
Section: Optimization Of Screened Factors and An Analysis Of Their Inmentioning
confidence: 95%
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“…Protonemata tissue (14 day-old, 1 g) was aseptically blended in 250-mL sterile shake-flasks containing 100 mL of optimized liquid BCD medium [27] with a homogenizer (OMNI TH Q , USA) at a speed of 30,000 rpm for 1 min and cultivated in a growth room at 25°C in an orbital shaker (New Brunswick Scientific Innova 2100, Champaign, IL, USA) set at 125 rpm under continuous light provided by fluorescent tubes (9,000 lux). After 14 days of growth, the cultured tissues were used to inoculate the liquid medium at a 4% (w/v) level for all subsequent experiments.…”
Section: Starter Inoculum Preparationmentioning
confidence: 99%