Acetosyringone treatment duration affects large T-DNA molecule transfer to rice callus

Abstract Background Large T-DNA fragment transfer has long been a problem for Agrobacterium-mediated transformation. Although vector systems, such as the BIBAC series, were successfully developed for the purpose, low transformation efficiencies were consistently observed. Results To gain insights of this problem in monocot transformation, we investigated the T-strand accumulation of various size of T-DNA in two kinds of binary vectors (one copy vs. multi-copy) upon acetosyringone (AS) induction and explored ways to improve the efficiency of the large T-DNA fragment transfer in Agrobacterium-mediated rice transformation. By performing immuno-precipitation of VirD2-T-strands and quantitative real-time PCR assays, we monitored the accumulation of the T-strands in Agrobacterium tumeficiens after AS induction. We further demonstrated that extension of AS induction time highly significantly improved large-size T-DNA transfer to rice cells. Conclusions Our data provide valuable information of the T-strand dynamics and its impact on large T-DNA transfer in monocots, and likely dicots as well

Selective elimination of perennial ryegrass by activation of a pro-herbicide through engineering E. coli argE gene

Perennial ryegrass is widely used for overseeding dormant bermudagrass on golf courses and sports fields in Southeastern United States to provide green color and improved playability. Late spring and summer persistence of perennial ryegrass may decrease the quality of the bermudagrass turf and reduce its winter hardiness. To help solve this problem, we developed a strategy to activate a pro-herbicide within the transgenic perennial ryegrass plants and to cause self elimination of the plants. An E. coli argE gene was introduced into perennial ryegrass by the biolistic method, which resulted in four independently transformed green plants. The mRNA of argE gene was detected in three of the plants by RT-PCR. Perennial ryegrass plants expressing the argE transgene were selectively controlled upon application of a pro-herbicide, N-acetyl-l-phosphinothricin (or N-acetyl-PPT), since the N-acetylornithinase encoded by argE gene is able to convert N-acetyl-PPT to the herbicide phosphinothricin (PPT). The non-transgenic bermudagrass plants were unaffected by the treatment. This approach provides a means to selectively remove a group of transgenic plants without affecting other plants growing with them

Accumulation of medium-chain, saturated fatty acyl moieties in seed oils of transgenic Camelina sativa.

With its high seed oil content, the mustard family plant Camelina sativa has gained attention as a potential biofuel source. As a bioenergy crop, camelina has many advantages. It grows on marginal land with low demand for water and fertilizer, has a relatively short life cycle, and is stress tolerant. As most other crop seed oils, camelina seed triacylglycerols (TAGs) consist of mostly long, unsaturated fatty acyl moieties, which is not desirable for biofuel processing. In our efforts to produce shorter, saturated chain fatty acyl moieties in camelina seed oil for conversion to jet fuel, a 12:0-acyl-carrier thioesterase gene, UcFATB1, from California bay (Umbellularia californica Nutt.) was expressed in camelina seeds. Up to 40% of short chain laurate (C12:0) and myristate (C14:0) were present in TAGs of the seed oil of the transgenics. The total oil content and germination rate of the transgenic seeds were not affected. Analysis of positions of these two fatty acyl moieties in TAGs indicated that they were present at the sn-1 and sn-3 positions, but not sn-2, on the TAGs. Suppression of the camelina KASII genes by RNAi constructs led to higher accumulation of palmitate (C16:0), from 7.5% up to 28.5%, and further reduction of longer, unsaturated fatty acids in seed TAGs. Co-transformation of camelina with both constructs resulted in enhanced accumulation of all three medium-chain, saturated fatty acids in camelina seed oils. Our results show that a California bay gene can be successfully used to modify the oil composition in camelina seed and present a new biological alternative for jet fuel production

Evaluation of parameters affecting switchgrass tissue culture: toward a consolidated procedure for Agrobacterium-mediated transformation of switchgrass (Panicum virgatum)

Abstract Background Switchgrass (Panicum virgatum), a robust perennial C4-type grass, has been evaluated and designated as a model bioenergy crop by the U.S. DOE and USDA. Conventional breeding of switchgrass biomass is difficult because it displays self-incompatible hindrance. Therefore, direct genetic modifications of switchgrass have been considered the more effective approach to tailor switchgrass with traits of interest. Successful transformations have demonstrated increased biomass yields, reduction in the recalcitrance of cell walls and enhanced saccharification efficiency. Several tissue culture protocols have been previously described to produce transgenic switchgrass lines using different nutrient-based media, co-cultivation approaches, and antibiotic strengths for selection. Results After evaluating the published protocols, we consolidated these approaches and optimized the process to develop a more efficient protocol for producing transgenic switchgrass. First, seed sterilization was optimized, which led to a 20% increase in yield of induced calluses. Second, we have selected a N6 macronutrient/B5 micronutrient (NB)-based medium for callus induction from mature seeds of the Alamo cultivar, and chose a Murashige and Skoog-based medium to regenerate both Type I and Type II calluses. Third, Agrobacterium-mediated transformation was adopted that resulted in 50–100% positive regenerated transformants after three rounds (2 weeks/round) of selection with antibiotic. Genomic DNA PCR, RT-PCR, Southern blot, visualization of the red fluorescent protein and histochemical β-glucuronidase (GUS) staining were conducted to confirm the positive switchgrass transformants. The optimized methods developed here provide an improved strategy to promote the production and selection of callus and generation of transgenic switchgrass lines. Conclusion The process for switchgrass transformation has been evaluated and consolidated to devise an improved approach for transgenic switchgrass production. With the optimization of seed sterilization, callus induction, and regeneration steps, a reliable and effective protocol is established to facilitate switchgrass engineering

Medium-chain, saturated FA compositions in seed oil of two camelina lines co-transformed with <i>UcFATB1</i> and <i>CsKASII</i> RNAi-2.

<p>Thirty T₂ seeds of Line 15, and 26 seeds of Line 18, and four wild type seeds were analyzed by gas chromatography.</p

Accumulation of medium-chain, saturated fatty acyl moieties in seed oils of transgenic <i>Camelina sativa</i>

<div><p>With its high seed oil content, the mustard family plant <i>Camelina sativa</i> has gained attention as a potential biofuel source. As a bioenergy crop, camelina has many advantages. It grows on marginal land with low demand for water and fertilizer, has a relatively short life cycle, and is stress tolerant. As most other crop seed oils, camelina seed triacylglycerols (TAGs) consist of mostly long, unsaturated fatty acyl moieties, which is not desirable for biofuel processing. In our efforts to produce shorter, saturated chain fatty acyl moieties in camelina seed oil for conversion to jet fuel, a 12:0-acyl-carrier thioesterase gene, <i>UcFATB1</i>, from California bay (<i>Umbellularia californica</i> Nutt.) was expressed in camelina seeds. Up to 40% of short chain laurate (C12:0) and myristate (C14:0) were present in TAGs of the seed oil of the transgenics. The total oil content and germination rate of the transgenic seeds were not affected. Analysis of positions of these two fatty acyl moieties in TAGs indicated that they were present at the <i>sn-1</i> and <i>sn-3</i> positions, but not <i>sn-2</i>, on the TAGs. Suppression of the camelina <i>KASII</i> genes by RNAi constructs led to higher accumulation of palmitate (C16:0), from 7.5% up to 28.5%, and further reduction of longer, unsaturated fatty acids in seed TAGs. Co-transformation of camelina with both constructs resulted in enhanced accumulation of all three medium-chain, saturated fatty acids in camelina seed oils. Our results show that a California bay gene can be successfully used to modify the oil composition in camelina seed and present a new biological alternative for jet fuel production.</p></div

Seed oil content analysis of four T₄ <i>UcFATB1</i> transgenic lines and WT as measured with gas chromatography (30 mCherry positive or WT seeds per sample, 5 replicates).

<p>* indicates significant difference compared to other samples (P<0.05).</p

Transgene <i>UcFATB1</i> expression was detected in T₃ immature seeds.

<p>There is no <i>UcFATB1</i> transgene expression detected in Wt. The <i>UcFATB1</i> expression level of Line 80 was used as a calibrator (expression level was arbitrarily set at 1), other lines’ expression levels were expressed as the fold of the expression level of line 80.</p