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1.
Microbiol Res ; 199: 29-39, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28454707

ABSTRACT

In current scenario, crop productivity is being challenged by decreasing soil fertility. To cope up with this problem, different beneficial microbes are explored to increase the crop productivity with value additions. In this study, Brassica napus L., an important agricultural economic oilseed crop with rich source of nutritive qualities, was interacted with Piriformospora indica, a unique root colonizing fungus with wide host range and multifunctional aspects. The fungus-treated plants showed a significant increase in agronomic parameters with plant biomass, lodging-resistance, early bolting and flowering, oil yield and quality. Nutritional analysis revealed that plants treated by P. indica had reduced erucic acid and glucosinolates contents, and increased the accumulation of N, Ca, Mg, P, K, S, B, Fe and Zn elements. Low erucic acid and glucosinolates contents are important parameters for high quality oil, because oils high in erucic acid and glucosinolates are considered undesirable for human nutrition. Furthermore, the expression profiles of two encoding enzyme genes, Bn-FAE1 and BnECR, which are responsible for regulating erucic acid biosynthesis, were down-regulated at mid- and late- life stages during seeds development in colonized plants. These results demonstrated that P. indica played an important role in enhancing plant growth, rapeseed yield and quality improvement of B. napus.


Subject(s)
Basidiomycota/physiology , Brassica napus/growth & development , Brassica napus/microbiology , Seeds/growth & development , Seeds/microbiology , Basidiomycota/genetics , Brassica napus/chemistry , Brassica napus/genetics , Brassica rapa , Coculture Techniques/methods , Crops, Agricultural/microbiology , DNA, Fungal/genetics , Erucic Acids/analysis , Erucic Acids/metabolism , Fatty Acids/biosynthesis , Fatty Acids/metabolism , Flowers/growth & development , Flowers/microbiology , Food , Gene Expression Regulation, Plant , Genes, Plant , Glucosinolates/analysis , Plant Oils/chemistry , Plant Oils/metabolism , Plant Roots/microbiology , Seeds/chemistry , Seeds/genetics , Soil , Soil Microbiology , Transcriptome
2.
BMC Genomics ; 16: 394, 2015 May 19.
Article in English | MEDLINE | ID: mdl-25986380

ABSTRACT

BACKGROUND: Chinese bayberry (Myrica rubra Sieb. & Zucc.) is an important subtropical evergreen fruit tree in southern China. Generally dioecious, the female plants are cultivated for fruit and have been studied extensively, but male plants have received very little attention. Knowledge of males may have a major impact on conservation and genetic improvement as well as on breeding. Using 84 polymorphic SSRs, we genotyped 213 M. rubra individuals (99 male individuals, 113 female varieties and 1 monoecious) and compared the difference in genetic diversity between the female and the male populations. RESULTS: Neighbour-joining cluster analysis separated M. rubra from three related species, and the male from female populations within M. rubra. By structure analysis, 178 M. rubra accessions were assigned to two subpopulations: Male dominated (98) and Female dominated (80). The well-known cultivars 'Biqi' and 'Dongkui', and the landraces 'Fenhong' are derived from three different gene pools. Female population had a slightly higher values of genetic diversity parameters (such as number of alleles and heterozygosity) than the male population, but not significantly different. The SSR loci ZJU062 and ZJU130 showed an empirical Fst value of 0.455 and 0.333, respectively, which are significantly above the 95 % confidence level, indicating that they are outlier loci related to sex separation. CONCLUSION: The male and female populations of Chinese bayberry have similar genetic diversity in terms of average number of alleles and level of heterozygosity, but were clearly separated by genetic structure analysis due to two markers associated with sex type, ZJU062 and ZJU130. Zhejiang Province China could be the centre of diversity of M. rubra in China, with wide genetic diversity coverage; and the two representative cultivars 'Biqi' and 'Dongkui', and one landrace 'Fenhong' in three female subpopulations. This research provides genetic information on male and female Chinese bayberry and will act as a reference for breeding programs.


Subject(s)
Genetic Markers/genetics , Genetic Variation , Genome, Plant , Myrica/genetics , Alleles , Bayes Theorem , Breeding , China , Cluster Analysis , Fruit/genetics , Genetic Loci , Genotype , Heterozygote , Microsatellite Repeats/genetics , Myrica/classification , Phylogeny , Polymorphism, Genetic
3.
Age (Dordr) ; 35(4): 1133-42, 2013 Aug.
Article in English | MEDLINE | ID: mdl-22653297

ABSTRACT

Curcumin is a polyphenolic bioactive compound in turmeric. We examined if antioxidant effects of curcumin are associated with lifespan extension in Drosophila. In this experiment, females and males of Drosophila were fed diets either containing no curcumin (C0) or supplemented with curcumin at 0.5 (C1) and 1.0 (C2) mg/g of diet. The levels of malondialdehyde (MDA), enzyme activity of superoxide dismutase (SOD), and expression of seven age-related genes in females and males were analyzed. We found that C1 and C2 increased mean lifespan by 6.2 % and 25.8 % in females, and by 15.5 % and 12.6 % in males, respectively. Meanwhile, C1 and C2 significantly decreased MDA levels and increased SOD activity in both genders. Diets C1 in females and C2 in males are effective in extending mean lifespan and improving levels of two physiological and biochemical measures related to aging in Drosophila. Lifespan extension of curcumin in Drosophila was associated with the up-regulation of Mn-SOD and CuZn-SOD genes, and the down-regulation of dInR, ATTD, Def, CecB, and DptB genes. The present results suggest that curcumin increases mean lifespan of Drosophila via regulating gene expression of the key enzyme SOD and reducing accumulation of MDA and lipid peroxidation. This study provided new insights for understanding the anti-aging mechanism of curcumin in Drosophila.


Subject(s)
Aging/genetics , Curcumin/pharmacology , Drosophila melanogaster/genetics , Gene Expression Regulation , Longevity/genetics , RNA/genetics , Superoxide Dismutase/genetics , Aging/drug effects , Animals , Chromatography, High Pressure Liquid , Dietary Supplements , Drosophila melanogaster/drug effects , Drosophila melanogaster/enzymology , Female , Lipid Peroxidation/drug effects , Lipid Peroxidation/genetics , Longevity/drug effects , Male , Real-Time Polymerase Chain Reaction , Superoxide Dismutase/biosynthesis
4.
Biosci Rep ; 29(2): 121-9, 2009 Apr.
Article in English | MEDLINE | ID: mdl-18715222

ABSTRACT

Although the ecdysteroid of the silkworm had been studied for decades, the proteome of the prothoracic gland, the primary source of ecdysteroid hormones, has not been studied previously. In the present paper, we utilized a proteomic approach to investigate the fifth instar prothoracic gland during the growth and development of the silkworm, Bombyx mori L. The two-dimensional electrophoresis results showed that the majority of proteins were acidic proteins, especially concentrated in the area of 25-65 kDa, with pI values of between 4 and 7, and the difference was not distinct. When compared with Qiufeng (Japanese strain), the interspecific distinction was larger than the intraspecific distinction, and 19 particular spots, excized from the third, fifth and ninth days of p50 (Chinese strain) and Qiufeng were subjected to MALDI-TOF-MS (matrix-assisted laser-desorption ionization-time-of-flight MS) analysis. We sorted them into seven catagories: energetics and/or metabolism, storage proteins, protection, lipid metabolism, signal transduction, cell function and unknown function proteins. Of these proteins, arginine methyltransferase is discussed as playing an important role in regulating the activation of ecdysteroidogenesis via transcription or translation.


Subject(s)
Bombyx/growth & development , Corpora Allata/growth & development , Insect Proteins/analysis , Proteome/analysis , Amino Acid Sequence , Animals , Bombyx/metabolism , Corpora Allata/metabolism , Ecdysteroids/genetics , Ecdysteroids/metabolism , Larva/growth & development , Molecular Sequence Data , Proteomics , Silk/biosynthesis
5.
J Chem Ecol ; 34(12): 1593-601, 2008 Dec.
Article in English | MEDLINE | ID: mdl-19023627

ABSTRACT

An odorant-binding protein cDNA (Acer-ASP2) was cloned and characterized from antennae of adult workers of an Asian honey bee, Apis cerana cerana F. (Hymenoptera: Apidae). The full-length open reading frame of Acer-ASP2 cDNA was 429 bp, encoding 142 amino acids. Protein signature analyses revealed that it contained six conserved cysteines with an N-terminal signal sequence of 19 amino acids. The deduced protein sequence shares high homology with Amel-ASP2 from the honey bee, Apis mellifera L., and low similarity with odorant-binding proteins from other species of insects. Immunocytochemical localization showed that Acer-ASP2 was concentrated in the lymph of olfactory sensilla, such as sensilla placodea and sensilla trichodea A. Real-time polymerase chain reaction of Acer-ASP2 transcripts showed that Acer-ASP2 was expressed on antennae but not in other general anatomical regions of the body. Temporally, Acer-ASP2 was expressed at a relatively high level in adults during two periods (9 and 27 vs. 1, 15, and 30 days). This timing is correlated with the production of beeswax and searching behavior for nectar/pollen, respectively. Thus, Acer-ASP2 is a species-specific gene that we propose to be involved in the acquisition of odorant molecules from nectar, pollen, and other general odorant sources.


Subject(s)
Bees/genetics , Bees/metabolism , Insect Proteins/analysis , Insect Proteins/genetics , Receptors, Odorant/analysis , Receptors, Odorant/genetics , Amino Acid Sequence , Animals , Base Sequence , Bees/immunology , Cloning, Molecular , DNA, Complementary/genetics , Escherichia coli/genetics , Gene Expression , Gene Expression Profiling , Immune Sera/immunology , Immunohistochemistry , Insect Proteins/chemistry , Insect Proteins/immunology , Molecular Sequence Data , Polymerase Chain Reaction , Receptors, Odorant/chemistry , Receptors, Odorant/immunology
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