The effectiveness of power ultrasound for the microbial decontamination of minimally processed fruits and vegetables was studied. Reductions in Salmonella typhimurium attached to iceberg lettuce obtained by cleaning with water, chlorinated water, ultrasound with water and ultrasound with chlorinated water were 0.7, 1.7, 1.5 and 2.7 logs, respectively, for small‐scale (2 L) trials. The cleaning action of cavitation appears to remove cells attached to the surface of fresh produce, rendering the pathogens more susceptible to the sanitizer. For large‐scale (40 L) trials, the addition of chlorine to water in the tank gave a systematic difference in Escherichia coli decontamination efficiency. However, the frequency of ultrasound treatment (25, 32–40, 62–70 kHz) had no significant effect on decontamination efficiency (P > 0.69). With the potentially high capital expenditure together with the expensive process of optimization and water treatment, it is unlikely that the fresh produce industry would be willing to take up this technology. Furthermore, the additional one log reduction achieved by applying ultrasound to a chlorinated water wash does not completely eliminate the risk of pathogens on fresh produce.

No abstract

Restriction fragment length polymorphisms (RFLP) were assessed among accessions within six peanut species of the Arachis section: tetraploid cultivated species, A. hypogaea; tetraploid wild species, A. monticola; and four diploid wild species, A. batizocoi,A. cardenasii, A. duranensis and A. glandulifera. While the two tetraploid species did not show polymorphism with 16 PstI-generated random genomic probes, two of seven seed cDNA probes detected polymorphisms. The RFLP variation detected by two seed cDNA probes appeared to be related to structural changes occurring within tetraploid species. The botanical var. 'fastigiata' (Valencia market type) of A. hypogaea subspecies fastigiata was shown to be the most variable. Arachis monticola was found to be more closely related to A. hypogaea subspecies hypogaea than to subspecies fastigiata. Diploid species A. cardenasii, A. duranensis, and A. glandulifera showed considerable intraspecific genetic diversity, but A. batizocoi showed little polymorphism. The genetic distance between the cultivated peanut and wild diploid species was found to be closest for A. duranensis.

Crop improvement in bahiagrass (Paspalum notatum Flüggé) is limited by apomixis in most natural tetraploids, however, diploid sexual types occur. Production of sexual tetraploids by chromosome doubling will allow hybridization with apomictic tetraploids. Diploid bahiagrass (Paspalum notatum Flüggé) embryogenic callus tissue was exposed to three concentrations of three antimitotic chemical agents, colchicine, oryzalin and trifluralin. Callus was generated to plants and ploidy was evaluated by stomata size, mitotic chromosome counts, and flow cytometry. A total of 310 plants were verified as tetraploid of 1,432 plants that reached transplanting size. All treatments yielded 4x plants. The mean percentage success over all treatments was 22%, with means of 31% for oryzalin, 24% for colchicine and 16% for trifluralin. The high rates of success indicate that all agents can be successfully used to double chromosome numbers in bahiagrass. The percentage of 4x plants ranged from 9% (20 lM trifluralin) to 43% (20 lM oryzalin). Several treatments adversely affected regeneration. Mitotic chromosome counts are difficult and labor intensive in bahiagrass. Therefore, leaf stomata measurements were used as a preliminary screen. Data gave a bimodal distribution with overlapping tails and based on chromosome counts would have given an error rate of 12%. Flow cytometry analysis of regenerated plants resulted in mean nucleus fluorescence distributions consistent with control diploid or tetraploid values. These values agreed with chromosome counts, and this method is recommended for determining bahiagrass ploidy level. Research goals and available resources should be taken into consideration when selecting a treatment for chromosome doubling in bahiagrass.

Lignin is a complex, aromatic polymer that limits plant cell wall degradation by ruminants and reduces the nutritional value of forages. Genetic engineering, using an antisense strategy, offers the potential to modulate enzymes in the lignin biosynthetic pathway as a way to reduce lignin, thereby improving forage quality and animal performance. We investigated the effectiveness of expressing antisense sorghum O‐methyltransferase gene (omt) to downregulate maize OMT and reduce lignin. Constructs contained a sorghum omt coding region in the antisense orientation driven by the maize ubiquitin‐1 (Ubi) promoter (with the first intron and exon) along with bar, that confers glufosinate herbicide resistance, driven by the CaMV 35S promoter. Twenty‐eight T0 plants regenerated from 17 herbicide‐resistant callus lines from 13 independent bombardments expressed the brown midrib phenotype. O‐methyltransferase activity was significantly lower in T1 transgenics compared with controls, with some plants showing a 60% reduction. Those T1 transgenics with downregulated OMT averaged 20% less lignin in stems and 12% less lignin in leaves compared with controls. On a whole‐plant basis, lignin was reduced by an average of 17% with the greatest reduction being 31%. Digestibility was significantly improved in transgenic plants by 2% in leaves and 7% in stems. Mean whole‐plant digestibility increased from 72 to 76%. This research demonstrates that genetic engineering has the potential to improve forage grass digestibility. This could be important, especially in tropical forage species, which generally have lower quality than temperate species.