Search Results
Oriental melon (Cucumis melo var. makuwa Makino) is a fruit with distinctive characteristics that is grown in Fuzhou, China. Fusarium wilt disease management remains a major challenge in the production of this fruit. Here, we performed seven field trials at four locations in Fuzhou, Fujian Province, China, to evaluate the control of fusarium wilt and yield of Oriental melons grafted on two Cucurbita rootstocks [Shengyan Tianzhen (SYTZ) and Nanzhen No. 1 (NZ1)]. During the growing seasons of 2008 to 2011, Oriental melons grafted on SYTZ and NZ1 exhibited dramatically reduced incidences of fusarium wilt disease and increased yields compared with nongrafted Oriental melons. Disease was only recorded in Trial 3 at Hongwei (2009), where plants grafted on SYTZ and NZ1 exhibited 1.05% and 1.1% infection, respectively. In the other six field trials, wilting was not observed at all. In comparison, the incidence of the disease in nongrafted Oriental melons ranged from 45.0% to 100.0%. The use of Cucurbita rootstocks improved the qualitative and quantitative carotenoid profiles, increasing lutein levels (12.7 and 10.8 μg·g−1 of fresh weight, respectively) and ζ-carotene and phytofluene amounts in fruit samples from SYTZ- and NZ1-grafted plants. In particular, the Liyu/NZ1 combination significantly increased β-carotene content ≈4-fold compared with nongrafted samples. In conclusion, Cucurbita rootstocks provided acceptable protection of Oriental melon cv. Liyu against fusarium wilt and improved the productivity and quality of fruits.
Soil salinity influences plant growth and crop yield significantly. Former studies indicated that uneven salt distribution in the root zone could relieve salt stress. But, how uneven salt distribution influences Na+ and Ca2+ concentration in the stem, leaf, and fruit and whether this influence would bring effects on fruit blossom-end rot (BER) still needs to be further studied. Under consideration of this, pot experiment with four treatments, T1:1, T1:5, T2:4, and T3:3, was conducted by setting the upper soil layer salinity at 1‰, 1‰, 2‰, and 3‰ and the lower soil layer at salinities of 1‰, 5‰, 4‰, and 3‰, respectively. Compared with the uniform salt concentration in the root zone (T3:3 treatment), the incidence of BER in the T1:5 and T2:4 treatments decreased by 60% and 35%, respectively. The fruit Na+ concentration and Na+/Ca2+ ratio were positively correlated with the incidence of BER. The value of the upper-root selective absorption Ca2+ over Na+ (SCa/Na(upper root)) for T1:5 was 0.8 times more than that of T1:1. The results showed that the incidence of BER was positively correlated with root dry matter and SCa/Na(root) weighted mean salinity. The overall results suggested that uneven salt distribution in the root zone could promote the Ca2+ absorption, Ca2+/Na+ ratio, and selective absorption Ca2+ over Na+ and consequently decrease the incidence of BER in tomato fruit.
Chinese cymbidiums are important flowering ornamental plants. Traditional propagation via seed or division cannot satisfy growers’ demand for commercialization of new cultivars, and in vitro propagation has a low micropropagation efficiency due to the browning of rhizomes. In this study, rhizomes of Cymbidium ‘14-16-13’ and ‘14-16-5’ were cultured on half-strength Murashige and Skoog (MS) medium supplemented with 6-benzyl aminopurine (BAP), NAA (α-napthaleneacetic acid), or BAP with NAA under either the dark or light. The degree of browning was read, and rhizome proliferation or sprouting (sprout numbers) was evaluated. Results showed that there was significant difference in browning grade of rhizomes between ‘14-16-13’ and ‘14-16-5’ regardless of dark and light culture. Dark culture induced rhizome proliferation but failed to induce sprouts. Light culture slightly elevated the degree of browning but induced sprouting. Among the growth regulators evaluated, BAP was more effective for sprout induction. As rhizome browning appeared to be inevitable in micropropagation of the cymbidiums, a compromise between browning and sprout production could be a realistic approach. Our study showed that rhizomes cultured on half-strength MS medium supplemented with 1.5 mg·L−1 BAP were able to produce more than 16 sprouts per vessel even though browning occurred in the rhizomes. Thus, culturing rhizomes in this medium could be a practical solution for in vitro propagation of Chinese cymbidiums.
Sulforaphane is an anticarcinogenic isothiocyanate derived from 4-methylsulfinylbutyl glucosinolate (glucoraphanin), which is abundant in broccoli (Brassica oleracea var. italica) florets. However, some breakdown products from alkenyl glucosinolates present in many broccoli cultivars, particularly oxazolidine-2-thione hydrolyzed from 2-(R)-hydroxy-3-butenyl glucosinolate (progoitrin), have potentially harmful effects on human and animal health. The main objective of this study was to improve the glucoraphanin concentration in F1 hybrids by cross-breeding with inbred lines and doubled haploids. Glucoraphanin concentrations in 31 of the 61 F1 hybrids were significantly higher (P = 0.05) than that of the commercial cultivar (Youxiu) with the highest concentration of glucoraphanin (4.18 μmol·g−1 dry weight) among eight reference cultivars. Sixteen of the F1 hybrids had glucoraphanin concentrations 3-fold higher than that of ‘Youxiu’. Alkenyl glucosinolates were not detected in the new hybrids as a result of the parents having few of these compounds but were found in five reference cultivars. Most F1 hybrids showed moderate indole glucosinolate concentrations and acceptable commercial traits. IL609 and IL702.2 were determined to be promising parental lines as a result of the high glucoraphanin concentration that they and their offspring contained. The findings also indicated that some F1 hybrids do not show the high-glucoraphanin character of their parents; consequently, evaluation of these F1 hybrids for their glucosinolate content is required for breeding high-glucoraphanin broccoli.
The relationship between soil texture and the degree of apple replant disease (ARD) was analyzed from the perspective of the microbial community structure and diversity within the rhizosphere soil of Malus hupehensis Rehd. seedlings. Three different textured soils were taken from different apple orchards in Laizhou, Yantai. The soils were divided into two parts, one was kept in replanted conditions, and the other was fumigated with methyl bromide to act as a high standard control. The strength of ARD occurrence was examined by measuring fresh and dry weight suppression (%) of the M. hupehensis seedlings. Differences in the fungal community structure (especially in Fusarium) among the three soil texture types were analyzed using high-throughput sequencing. The results showed that replanted loam clay soil had the highest fungal diversity, followed by sandy loam soil and finally loam soil. The richness of fungi between soil textures, however, was not significantly different. At the genus level, the relative abundance of Fusarium was 1.96%, 0.78%, and 10.89% in replanted sandy loam, replanted loam soil, and replanted loam clay soil, respectively. Moreover, the gene copy number of Fusarium oxysporum, Fusarium solani, and the inhibition rate of fresh weight of M. hupehensis seedlings were the same in the three soil textures. The plant height, photosynthesis (net) (Pn), and stomatal conductance (g S) of the M. hupehensis seedlings were significantly less in the replanted soil compared with the control treatments, with the overall difference being greatest in replanted loam clay soil, followed by replanted sandy loam and then replanted loam soil.
Dendrobium officinale Kimura et Migo is a famous traditional Chinese medicinal plant. It produces various phytochemicals, particularly polysaccharides, which have nutraceutical and pharmaceutical values. To increase its biomass production and polysaccharide content, our breeding program has generated a series of polyploid cultivars through colchicine treatment of protocorm-like bodies (PLBs). The present study compared two tetraploid cultivars, 201-1-T1 and 201-1-T2, with their diploid parental cultivar, 201-1, in an established in vitro culture system. Tetraploid ‘201-1-T1’ and ‘201-1-T2’ had shorter leaves and shorter and thicker stems and roots, and they produced higher biomass compared with the diploid cultivar. The length and width of stomata significantly increased, but stomatal density decreased in tetraploid cultivars. The PLB induction rates from the stem node explants of the tetraploid cultivars were significantly higher than those of diploid. However, the PLB proliferation of tetraploids was lower than that of the diploid. The mean number of plantlets regenerated from tetraploid PLBs was also lower than that of the diploid after 4 months of culture. Polysaccharide contents in stems, leaves, and roots of 6-month-old tetraploid plantlets were significantly higher than those of diploids. The polysaccharide content in the stem of ‘201-1-T1’ was 12.70%, which was a 2-fold increase compared with the diploid cultivar. Our results showed that chromosome doubling could be a viable way of improving D. officinale in biomass and polysaccharide production.
Pear (Pyrus spp.) is the third-largest economic crop in China after apples (Malus pumila Mill.) and citrus (Citrus reticulata Blanco), and it is mainly cultivated by smallholders. Currently, the yield of Chinese pear ranks midlevel globally, with only 17.9 t⋅ha−1⋅year−1, which is lower than that of the United States (36.0 t⋅ha−1⋅year−1). However, the factors limiting pear production dominated by smallholders are unclear. We interviewed 75 smallholders about 18 yield-related indicators for pear-typical planting areas. The boundary line model was used to analyze the contribution of internal factors and dominant external factors affecting yield and to simulate strategies for increasing yield through the scenario analysis. The results showed that the average gap between the average and highest attainable yields for smallholders was 10.5 t⋅ha−1⋅year−1 in Luniao County. Among individual yield-limiting factors, chemical fertilizer nitrogen (N) input (13.3%) was the most significant, followed by the soil-available N content (12.0%) and leaf magnesium content (12.0%). Overall, the contribution of all soil factors (42.7%) was the largest compared with the other factor categories. However, the contribution of internal factors could not be ignored and accounted for 25.3% of the total. A scenario analysis showed that comprehensive strategies considering soil, management, and internal factors achieved the largest yield improvement (14%), as did reducing the fertilizer application rate (66%) compared with only using soil or leaf diagnosis methods. Therefore, integrated methods should be considered when developing pear orchard management measures and include soil, management, and internal factors.
The chloroplast genome of an albino mutant isolated from tissue culture of the bamboo Bambusa edulis Munro was examined to identify aberrations. A number of the chloroplast genes encoding ATP synthases, photosystem II subunits, NADH dehydrogenase, and ribosomal proteins had been deleted, at least partially, in the albino mutant. Comparison of the two-dimensional electrophoresis profiles of albino and green bamboos revealed three spots of reduced intensity, indicating repression of these proteins in the albino mutants. Mass spectroscopic analysis subsequently revealed that two of these proteins are 33-kDa subunits of the photosystem II oxygen-evolving protein complex (PsbO) and one is a 23-kDa subunit of photosystem II oxygen-evolving protein complex (PsbP). The genes encoding these two proteins were cloned from B. edulis, and were denoted BePsbO (accession no. EF669513) and BePsbP (accession no. EF669512). Reverse transcription polymerase chain reaction and two-dimensional gel analyses of BePsbO and BePsbP in green and albino bamboos grown in the light or dark revealed that the albino mutant, similar to its green counterpart, sensed the light signal, resulting in the induction of BePsbO and BePsbP transcription, but it did not accumulate the protein products. We conclude that the repression of protein-expressing BePsbO and BePsbP is because of a defect in post-transcriptional regulation in the albino mutant.