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The cyanobacterial CCM as a source of genes for improving photosynthetic CO2 fixation in crop species

dc.contributor.authorPrice, G. D
dc.contributor.authorPengelly, J. J. L
dc.contributor.authorForster, B
dc.contributor.authorDu, J
dc.contributor.authorWhitney, S. M
dc.contributor.authorvon Caemmerer, Susanne
dc.contributor.authorBadger, Murray
dc.contributor.authorHowitt, S. M
dc.contributor.authorEvans, J. R
dc.date.accessioned2015-08-12T04:42:02Z
dc.date.available2015-08-12T04:42:02Z
dc.date.issued2012-10-01
dc.description.abstractCrop yields need to nearly double over the next 35 years to keep pace with projected population growth. Improving photosynthesis, via a range of genetic engineering strategies, has been identified as a promising target for crop improvement with regard to increased photosynthetic yield and better water-use efficiency (WUE). One approach is based on integrating components of the highly efficient CO(2)-concentrating mechanism (CCM) present in cyanobacteria (blue-green algae) into the chloroplasts of key C(3) crop plants, particularly wheat and rice. Four progressive phases towards engineering components of the cyanobacterial CCM into C(3) species can be envisaged. The first phase (1a), and simplest, is to consider the transplantation of cyanobacterial bicarbonate transporters to C(3) chloroplasts, by host genomic expression and chloroplast targeting, to raise CO(2) levels in the chloroplast and provide a significant improvement in photosynthetic performance. Mathematical modelling indicates that improvements in photosynthesis as high as 28% could be achieved by introducing both of the single-gene, cyanobacterial bicarbonate transporters, known as BicA and SbtA, into C(3) plant chloroplasts. Part of the first phase (1b) includes the more challenging integration of a functional cyanobacterial carboxysome into the chloroplast by chloroplast genome transformation. The later three phases would be progressively more elaborate, taking longer to engineer other functional components of the cyanobacterial CCM into the chloroplast, and targeting photosynthetic and WUE efficiencies typical of C(4) photosynthesis. These later stages would include the addition of NDH-1-type CO(2) pumps and suppression of carbonic anhydrase and C(3) Rubisco in the chloroplast stroma. We include a score card for assessing the success of physiological modifications gained in phase 1a.en_AU
dc.identifier.issn0022-0957en_AU
dc.identifier.urihttp://hdl.handle.net/1885/14691
dc.publisherOxford University Pressen_AU
dc.relationhttp://purl.org/au-research/grants/arc/DP120101013en_AU
dc.rights© The Author [2012]. Published by Oxford University Press [on behalf of the Society for Experimental Biology.en_AU
dc.sourceJournal of Experimental Botanyen_AU
dc.subjectbacterial proteinsen_AU
dc.subjectcarbon dioxideen_AU
dc.subjectchloroplastsen_AU
dc.subjectcrops, agriculturalen_AU
dc.subjectcyanobacteriaen_AU
dc.subjectmetabolic engineeringen_AU
dc.subjectphotosynthesisen_AU
dc.titleThe cyanobacterial CCM as a source of genes for improving photosynthetic CO2 fixation in crop speciesen_AU
dc.typeJournal articleen_AU
dcterms.dateAccepted2012-08-22
local.bibliographicCitation.issue3en_AU
local.bibliographicCitation.lastpage768en_AU
local.bibliographicCitation.startpage753en_AU
local.contributor.affiliationPrice, D., Research School of Biology, The Australian National Universityen_AU
local.contributor.authoruidu8201788en_AU
local.identifier.citationvolume64en_AU
local.identifier.doi10.1093/jxb/ers257en_AU
local.identifier.essn1460-2431en_AU
local.publisher.urlhttp://www.oxfordjournals.org/en/en_AU
local.type.statusPublished Versionen_AU

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