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N. MATHAN, M. PARANI, A. PARIDA AND S. NAIR. 1996. Strains of root-nodulating bacteria isolated from Arachis hypogaea showed physiological characteristics of both fast and slow growers. Random amplified polymorphic DNA (RAPD) markers showed most of the genotypes could be identified using one or two primers; however, cluster analysis based on the number of bands shared by the genotypes showed a homogenous cluster. These strains were halotolerant in nature and have potential for use in saline soil. 相似文献
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The Auxin-Regulated CrRLK1L Kinase ERULUS Controls Cell Wall Composition during Root Hair Tip Growth 总被引:1,自引:0,他引:1
Sébastjen Schoenaers Daria Balcerowicz Gordon Breen Kristine Hill Malgorzata Zdanio Grégory Mouille Tara J. Holman Jaesung Oh Michael H. Wilson Natalia Nikonorova Lam Dai Vu Ive De Smet Ranjan Swarup Winnok H. De Vos Isabel Pintelon Dirk Adriaensen Claire Grierson Malcolm J. Bennett Kris Vissenberg 《Current biology : CB》2018,28(5):722-732.e6
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D. K. Yadava Swarup K. Parida V. K. Dwivedi A. Varshney Irfan A. Ghazi V. Sujata T. Mohapatra 《Journal of plant biochemistry and biotechnology.》2009,18(1):29-36
The present study was carried out with the objective of evaluating genomic STMS markers developed earlier in Brassica napus, B. oleracea, B. rapa and B. nigra for their use in Brassica juncea and B. carinata. Ninety-six of the 100 STMS markers used under standardized annealing temperatures and gel concentrations produced clear reproducible amplification pattern. For majority of the markers 60 °C annealing temperature and 3.5% metaphor agarose gel were found suitable. High cross-transferability of STMS markers to related Brassica species including B. carinata (91.6%) and B. juncea (87.5%) suggested the possibility of utilizing these markers for genome analysis in the species where no such markers are available. The ‘B’ genome derived markers showed lower level of transferability to the ‘A’ and ‘C’ genome Brassica species. The potential of STMS markers to detect polymorphism among Brassica species and genera was 98.9%. The level of inter-specific polymorphism was much higher than the intea-specific polymorphism. The markers capable of revealing polymorphism among Brassica species and genera would be useful in Brassica introgression breeding programme. The polymorphic markers were found efficient in establishing the expected evolutionary relationships among the six different Brassica species and two related genera. Low level of intra-specific polymorphism revealed by these markers suggested use of a large set of such markers for various applications in Brassica genetics, genomics and breeding. 相似文献
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Asish?Kumar?Parida A.?B.?DasEmail author B.?Mittra 《Trees - Structure and Function》2004,18(2):167-174
The effects of a range of salinity (0, 100, 200 and 400 mM NaCl) on growth, ion accumulation, photosynthesis and anatomical changes of leaves were studied in the mangrove, Bruguiera parviflora of the family Rhizophoraceae under hydroponically cultured conditions. The growth rates measured in terms of plant height, fresh and dry weight and leaf area were maximal in culture treated with 100 mM NaCl and decreased at higher concentrations. A significant increase of Na+ content of leaves from 46.01 mmol m-2 in the absence of NaCl to 140.55 mmol m-2 in plants treated with 400 mM NaCl was recorded. The corresponding Cl- contents were 26.92 mmol m-2 and 97.89 mmol m-2. There was no significant alteration of the endogenous level of K+ and Fe2+ in leaves. A drop of Ca2+ and Mg2+ content of leaves upon salt accumulation suggests increasing membrane stability and decreased chlorophyll content respectively. Total chlorophyll content decreased from 83.44 g cm-2 in untreated plants to 46.56 g cm-2 in plants treated with 400 mM NaCl, suggesting that NaCl has a limiting effect on photochemistry that ultimately affects photosynthesis by inhibiting chlorophyll synthesis (ca. 50% loss in chlorophyll). Light-saturated rates of photosynthesis decreased by 22% in plants treated with 400 mM NaCl compared with untreated plants. Both mesophyll and stomatal conductance by CO2 diffusion decreased linearly in leaves with increasing salt concentration. Stomatal and mesophyll conductance decreased by 49% and 52% respectively after 45 days in 400 mM NaCl compared with conductance in the absence of NaCl. Scanning electron microscope study revealed a decreased stomatal pore area (63%) in plants treated with 400 mM NaCl compared with untreated plants, which might be responsible for decreased stomatal conductance. Epidermal and mesophyll thickness and intercellular spaces decreased significantly in leaves after treatment with 400 mM NaCl compared with untreated leaves. These changes in mesophyll anatomy might have accounted for the decreased mesophyll conductance. We conclude that high salinity reduces photosynthesis in leaves of B. parviflora, primarily by reducing diffusion of CO2 to the chloroplast, both by stomatal closure and by changes in mesophyll structure, which decreased the conductance to CO2 within the leaf, as well as by affecting the photochemistry of the leaves. 相似文献
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Ko-ichiro Miyamoto Parida Yamada Ryo-taro Yamaguchi Takami Muto Ayumi Hirano Yasuo Kimura Michio Niwano Hiroko Isoda 《Cytotechnology》2007,55(2-3):143-149
In this study, we report on an in situ monitoring system of living cultured cells using infrared absorption spectroscopy in
the geometry of multiple internal reflections (MIR-IRAS). In order to observe living cultured cells, the temperature in the
sample chamber of a FT-IR spectrometer was maintained at 37 °C and a humidified gas mixture containing 5% CO2 was introduced into the sample chamber. Human breast cell line MCF-7 cultured on Si MIR prisms were placed in the sample
chamber and infrared spectra of MCF-7 cells were collected for 5 h. It was found that the adhesion and metabolism of MCF-7
cells could be monitored by the absorption intensity of amide-II protein band (1,545 cm−1) and also by the absorption intensities of CH
x
bands (2,700–3,100 cm−1). These results suggest that our system is useful for a nondestructive and non-label monitoring of cell viability. Our method
based on infrared absorption spectroscopy has a potential for bioscreening application. 相似文献