2018
DOI: 10.1186/s12896-018-0464-8
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Overexpression of a rice BAHD acyltransferase gene in switchgrass (Panicum virgatum L.) enhances saccharification

Abstract: BackgroundSwitchgrass (Panicum virgatum L.) is a promising bioenergy feedstock because it can be grown on marginal land and produces abundant biomass. Recalcitrance of the lignocellulosic components of the switchgrass cell wall to enzymatic degradation into simple sugars impedes efficient biofuel production. We previously demonstrated that overexpression of OsAT10, a BAHD acyltransferase gene, enhances saccharification efficiency in rice.ResultsHere we show that overexpression of the rice OsAT10 gene in switch… Show more

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Cited by 42 publications
(55 citation statements)
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References 60 publications
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“…Some engineering efforts have focused on reducing the presence of these otherwise naturally occurring inhibitors, such as cell wall-bound ferulic acid. 17 Feedstock engineering can deliver biomass tailored to the end use, which can in turn have a dramatic impact on product yields, costs, and net environmental impacts. This requires a detailed knowledge of plant cell wall biosynthesis and carbon metabolism.…”
Section: Plant Engineering For Cell Wall Optimization and In-planta Pmentioning
confidence: 99%
“…Some engineering efforts have focused on reducing the presence of these otherwise naturally occurring inhibitors, such as cell wall-bound ferulic acid. 17 Feedstock engineering can deliver biomass tailored to the end use, which can in turn have a dramatic impact on product yields, costs, and net environmental impacts. This requires a detailed knowledge of plant cell wall biosynthesis and carbon metabolism.…”
Section: Plant Engineering For Cell Wall Optimization and In-planta Pmentioning
confidence: 99%
“…The BAHD superfamily has members in various ester synthetic pathways. The functions of several BAHD genes have been reported [43][44][45]. Here, by detecting their HXXXD and DFGWG motifs using a HMMER search, we identified 717 BAHD genes from seven Rosaceae species.…”
Section: Discussionmentioning
confidence: 99%
“…The real time PCR amplification mixture (20 μL) contained 1 μg of cDNA, 10 μL of 2× TransStart® Top Green qPCR Super Mix Kit, 0.4 μL of 50× Dye II and 4 μL of 5 μM forward and reverse primers. The relative quantification of each transcript of different genes was calculated using the 2 -ΔΔCT method, normalized to the internal control actin gene (LOC_Os03g50885) (Li et al 2018).…”
Section: Methodsmentioning
confidence: 99%