Planta - Cotton S-adenosylmethionine decarboxylase-, rather than spermine synthase-, mediated spermine biosynthesis is required for salicylic acid- and leucine-correlated signaling in the defense... 相似文献
Body size in insects is coupled with numerous physiological, life-history and ecological traits. Its variation along temperature gradient is widely studied. However, information regarding variations in body size of insects along altitudinal gradient is limited. Present study was designed considering hypothesis that there would be an increase in body size of Parthenium beetle, Zygogramma bicolorata Pallister (Coleoptera: Chrysomelidae) with increasing altitude and decreasing in temperature. To achieve the objectives, beetles were collected from three eco-climatic zones of NEPAL [Kathmandu (1400 mts, 24 °C; warm temperate zone), Chitwan (415 mts, 25 °C; upper tropical/sub-tropical zone), and Mahendranagar (229 mts, 34 °C; humid subtropical zone)], and one of INDIA [Varanasi (81 mts, 36 °C; humid subtropical zone)] for their morphometric analysis (body length and body biomass). Results revealed that the size of beetles in all eco-climatic zones increased with increasing altitude and decreasing temperature. While adults of Kathmandu were largest, followed by Chitwan and Mahendranagar, but those of Varanasi were smallest in size. The sex ratio was female-biased in Kathmandu and Varanasi, but was male-biased in Chitwan and Mahendranagar. Irrespective of temperature and altitude, females were larger than males in all eco-climatic zones. Our results affirmed our hypothesis and were in compliance with Bergmann’s rule. The findings may be helpful in understanding phenotypic plasticity and distribution pattern of Z. bicolorata adults in Indian sub-continent under global climate change scenario. 相似文献
A bacterial strain, designated AETb3-4T was isolated from the rhizosphere of lily. Comparison of 16S rRNA gene sequences showed that the sequence from strain AETb3-4T exhibits high sequence similarity with those of Arthrobacter silviterrae KIS14-16T (97.9%), Arthrobacter livingstonensis LI2T (97.2%) and Arthrobacter stackebrandtii CCM 2783T (97.0%). Whole genome average nucleotide identity (ANI) and the digital DNA-DNA hybridization (dDDH) values between strain AETb3-4T and the reference strains A. silviterrae DSM 27180T, A. livingstonensis L12T and A. stackebrandtii DSM 16005T were below 83.6% and 27.7%, respectively, values which are considerably below the proposed thresholds for the species delineation, consistent with the proposal that strain AETb3-4T represents a novel species. The genome size of strain AETb3-4T is 4.33 Mb and the genomic DNA G?+?C content is 67.3%. The main polar lipids were identified as phosphatidylglycerol, diphosphatidylglycero, phosphatidylinositol and an unidentified glycolipid. The major fatty acids (>?10%) were identified as anteiso-C15: 0 and anteiso-C17: 0. The predominant menaquinone was found to be menaquinone 9 (MK-9) (H2) (82.2%). Phenotypic tests allowed the strain to be differentiated from its close phylogenetic neighbors. Based on the results obtained, it is proposed that the strain AETb3-4T (=?CFCC 16390T?=?LMG 31708T) represents a novel species in the genus Arthrobacter, for which the names Arthrobacter wenxiniae sp. nov. is proposed. In addition, the novel strain AETb3-4T has multiple plant growth-promoting characters including ACC-deaminase activity and production of IAA. Furthermore, the genome contains secondary metabolite biosynthesis gene clusters, including a carotenoid biosynthetic gene cluster, suggesting potential capacities for secondary metabolite synthesis. These data suggest that strain AETb3-4T may have potential applications both in medicine and sustainable agriculture.
10–23 DNAzyme is an artificially selected catalytic DNA molecule. Its great potential as genetic therapeutics promoted chemical modifications for more efficient DNAzymes. Here, 10–23 DNAzyme was modified on its six deoxyadenosine residues (A5, A9, A11, A12, A15 in the catalytic domain and A0 of the recognition arm next to the cleavage site) with compound 1, an adenosine analogue with 2′-O-[N-(aminoethyl)carbamoyl]methyl group. A positive effect of compound 1 at A15 was observed (HJDS-05, kobs = 0.0111 min−1). Compared to the effect of 2′-H and 2′-OMe at A15, this result provided an approach for more efficient DNAzyme by combining 2′-substituted amino group of adenosine with A15 as the lead structure. 相似文献