2017
DOI: 10.2135/cropsci2016.06.0513
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Metabolic Engineering to Increase the Corn Seed Storage Lipid Quantity and Change Its Compositional Quality

Abstract: Given limited global food supplies and the fact that the global population is expected to double by 2050, there is an urgent need for the development of high‐calorie foods, including culinary oils. The seeds of oil crops contain high‐energy density oil composed of triacylglycerides (TAGs) at up to 80% by dry mass. However, maize (Zea mays L.) seeds are relatively poor in calorie and nutritional values. Therefore, in this report, we address this constraint via metabolic engineering to improve maize seed lipids … Show more

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Cited by 13 publications
(6 citation statements)
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“…Rooting took place on the MS media containing 1 mg/L IBA (Figure 2C). We followed all details according to our previous studies 26,33,34 …”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Rooting took place on the MS media containing 1 mg/L IBA (Figure 2C). We followed all details according to our previous studies 26,33,34 …”
Section: Resultsmentioning
confidence: 99%
“…For root induction, 1 mg/L indole‐3‐butyric acid (IBA) was used. Hardening regenerated plants was performed based on our previous work 33,34 …”
Section: Methodsmentioning
confidence: 99%
“…The overexpression of T. majus DGAT1 in Arabidopsis, high‐erucic‐acid rapeseed, and canola‐type B. napus also led to enhanced seed oil content (Xu et al, ). Following these aforementioned studies, many groups have further used DGAT1 from different species to boost seed content in various crops such as G. max (Hatanaka et al, ; Roesler et al, ), B. juncea (Savadi et al, ), Z. mays (Alameldin et al, ), C. sativa (Kim et al, ), and Jatropa curcas (Maravi et al, ). Moreover, overexpression of DGAT1 from microalgae, such as Chlorella ellipsoidea and Nannochloropsis oceanica , also led to increased oil content in Arabidopsis and B. napus (Guo et al, ; Zienkiewicz et al, ).…”
Section: Introductionmentioning
confidence: 99%
“…In microalgae, on the other hand, one or two copies of DGAT1 and several copies of DGAT2 were found to likely contribute to the complexity of TAG formation, although their physiological roles remain ambiguous (Turchetto‐Zolet et al , ; Chen and Smith, ; Gong et al , ; Liu and Benning, ; Liu et al , ; Xu et al , ; Mao et al , ). Given the importance of the enzyme in governing the flux of substrates into TAG, over‐expression of DGAT cDNAs has been used to manipulate oil production in the seeds of Arabidopsis thaliana and oilseed crops such as soybean ( Glycine max ), B. napus , corn ( Zea mays ) and Camelina sativa (Jako et al , ; Lardizabal et al , ; Weselake et al , ; Oakes et al , ; Li et al , ; Roesler et al , ; Kim et al , ), in the leaves of Nicotiana tabacum , N. benthamiana and Z. mays (Bouvier‐Navé et al , ; Alameldin et al , ; Chen et al , ; Vanhercke et al , ), and in oleaginous yeast (Greer et al , ; Chen et al , ) and several microalgae including Chlamydomonas reinhardtii , Phaeodactylum tricornutum and Nannochloropsis oceanica (Iwai et al , ; Xin et al , , ; Zulu et al , ; Mao et al , ).…”
Section: Introductionmentioning
confidence: 99%