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1.
Ajaz Ahmad Naqvi Subhendu Adhikari Bindu R Pillai & Niranjan Sarangi 《Aquaculture Research》2007,38(8):847-851
Survival rate, growth and feed intake were determined for late juveniles (4.31 ± 0.18 g) of river prawn Macrobrachium rosenbergii in freshwater with total ammonia‐N (NH3‐N+NH4‐N) concentrations of 0.015 (control), 0.5, 1.0 and 1.5 mg L−1 for 60 days at pH 7.53 ± 0.04 and temperature 24.0 ± 2.5°C. Survival rate was significantly (P<0.05) lower (54 ± 4.2–70 ± 5.4%) for total ammonia concentrations from 0.5 to 1.5 mg L−1 [0.0139–0.0419 mg L−1 of unionized ammonia (NH3)]. Growth (0.026–0.030 g day−1 range) of the prawns did not differ for the different NH3 levels but were significantly (P<0.05) lower compared with control (0.056 g day−1). Feed intake rates also diminished significantly (P<0.05) from 77.60 ± 2.45% at control (0.015 mg L−1 NH3‐N) to 48.69 ± 2.13% at 1.5 mg L−1 NH3‐N (0.0419 mg L−1 of unionized NH3). 相似文献
2.
Pramoda Kumar Sahoo Mudagandur S Shekhar Abhilipsa Das Manickam Dilli Kumar Bindu R Pillai A S Sahul Hameed 《Aquaculture Research》2012,43(8):1096-1106
The present study evaluated the role of recombinant RNA‐dependent RNA polymerase (RdRp) protein of Macrobrachium rosenbergii nodavirus (MrNV) in modulating the immune response and in reducing MrNV load in infected prawn. In the first experiment, prawns (25–30 g) were injected with recombinant RdRp protein (RP) at a concentration of 0, 1.0 and 10 μg, and immune parameters and expression of some immune‐related genes were measured up to 14 days post injection (p.i.). In the second experiment, early juveniles were injected with a similar dose of RdRp and animals were challenged by immersion with MrNV. The infection status was detected in muscles by nested RT‐PCR up to 21 days post challenge. Prawn injected with higher concentration of RP showed significantly higher total haemocyte count at different period post injection. Significant up‐regulation of immune‐related genes was observed within 24 h in prawn treated with lower dose of RP and after 7 days p.i. at higher level of RP injection compared with adult control. Most of the tested samples (63%) were found to be RT‐PCR positive for MrNV at 48 h of post‐immersion challenge. After 14 days, MrNV was detected only in control prawn, while both RP‐injected groups were MrNV negative. This study elucidated the potential viral load reduction role played by RdRP in MrNV‐infected prawn. 相似文献
3.
Purification and characterization of a β–glucan binding protein from the haemolymph of freshwater prawn Macrobrachium rosenbergii 
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下载免费PDF全文 Jyotirmaya Mohanty Pramoda Kumar Sahoo Bindu R. Pillai Swagatika Mohanty Sushil Kumar Garnayak Shailesh Kumar 《Aquaculture Research》2015,46(1):95-104
β‐glucan binding protein (βGBP), a pattern recognition protein was purified from the haemolymph of freshwater prawn Macrobrachium rosenbergii by heparin affinity chromatography that showed a single band in native gradient PAGE. The β‐glucan binding property of the purified protein was confirmed in a phenoloxidase (PO) assay, where addition of βGBP along with β‐glucan increased the specific PO activity compared with that of β‐glucan alone. The molecular weight of the βGBP was found to be ~316 kDa on gel filtration chromatography. In SDS‐PAGE, βGBP molecule was reduced to one polypeptide chain of molecular weight ~113 kDa. Thus the βGBP in M. rosenbergii is possibly a homotrimeric molecule. The purified sample run on unreduced condition in SDS‐PAGE also revealed a similar size band (~113 kDa) and hence, the polypeptide chains of βGBP are held by non‐covalent interactions. The purified βGBP samples run in native PAGE was stained positively with alcian blue for carbohydrates and Sudan black for lipids indicating the βGBP to be a glycolipoprotein. With rabbit polyclonal anti‐βGBP serum developed, an indirect ELISA was standardized and the normal βGBP concentration in adult M. rosenbergii serum was quantified to be ~2 mg mL?1. Furthermore, the applicability of the developed ELISA is discussed. 相似文献
4.
C. Bindu Roy Zoe-Joy Newby Jacob Mathew David Ian Guest 《European journal of plant pathology / European Foundation for Plant Pathology》2017,147(1):129-139
In 2010, symptoms of cobweb disease were observed on cultivated Pleurotus eryngii crops in Spain. Based on morphological and genetic analyses, the causal agent of cobweb was identified as Cladobotryum mycophilum. Pathogenicity tests on fruit bodies were performed using conidial suspensions of three C. mycophilum isolates. The causal agent was re-isolated in 80–85 % of the fruit bodies inoculated internally and 15–40 % of those fruit bodies inoculated on the cap surface. The results pointed to a certain resistance of the P. eryngii cap surface to the mycelium of C. mycophilum. Two cropping trials inoculated with C. mycophilum were set up to evaluate the pathogenicity of the causal agent of cobweb in two casings. At the end of the growth cycle, 50–60 % of the inoculated blocks cased with mineral soil, and 20–33 % of the inoculated blocks cased with black peat showed cobweb symptoms. This difference in the appearance of the disease and its aggressiveness may be partly explained by different electrical conductivity values of the casing materials used. In vitro sensitivity of the C. mycophilum isolates and P. eryngii strains against four fungicides (chlorothalonil, prochloraz-Mn, thiabendazole and thiophanate-methyl) was assessed in radial growth experiments on fungicide-amended media. The most effective fungicides for inhibiting the in vitro growth of C. mycophilum were prochloraz-Mn and chlorothalonil, while prochloraz-Mn was also the most selective fungicide between P. eryngii and C. mycophilum, and chlorothalonil was the most toxic fungicide against the P. eryngii mycelium. 相似文献
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本研究利用巴西橡胶树（Hevea brasiliensis）这一重要产胶植物的基因组文库进行了简单重复序列（SSRs）,也即微卫星序列的分离鉴定。对来自无性系GTl的小插入基因组文库进行SSRs（AC／TG及CT／GA基序）筛选鉴定共获得154个克隆。采用载体通用引物及重复序列进行PCR扩增发现,其中114个为阳性克隆。限制性酶切分析结果显示,这些阳性克隆中有6个为重复拷贝,故予以剔除。之后,对剩余108个克隆中的50个进行了序列分析。此外,试验中对来自优良无性系RRII105的大插入基因组文库也进行了筛选。所获24个阳性克隆的测序结果也证实了橡胶基因组中微卫星序列的存在。经过最终的序列分析,本研究共鉴定出67个具有不同特点的简单及复合型微卫星序列,其中59个来自GT1,其余8个来自RRII105。所检测到的重复基序包括二核苷酸（TG／AC,AG／TC,TA,AT）,三核苷酸（AAG,AGG,A1T）,四核苷酸（GAAA,AAGG,ATCC,TAAA,AAAT）,以及一个五核苷酸（GAAAT）。与其它作物的报道结果类似,在橡胶基因组中也观察到大量的CT／GA重复。 相似文献
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P. Thomas Bindu Panicker T. Janakiram B. N. Sathyanarayana 《The Journal of Horticultural Science and Biotechnology》2013,88(6):653-659
SummaryTo develop a micropropagation protocol for the elite chrysanthemum cultivar, ‘Arka Ravi’, in vitro cultures were established using surface-sterilised nodal microcuttings (1.0 – 1.2 cm) on semi-solid MS medium. Microbial contamination was observed in 22% of cultures during the initiation phase. Cultures that were devoid of obvious contamination were transferred to culture bottles containing MS medium supplemented with 30 g l–1 sucrose, 2.5 g l–1 Phytagel® and either benzyl adenine (BA) or kinetin (KIN) supplied at 0, 1, 5, 10, or 20 µM, and were monitored, over eight in vitro passages, for their growth and microbial association. Shoot-tip and nodal microcuttings yielded a single shoot, coupled with rooting, in medium devoid of BA or KIN which was the best medium for continuous micropropagation. Rooting was inhibited with increasing concentrations of BA or KIN, and one or more shorter shoots with condensed internodes were induced, resulting in low rates of propagation. Culture indexing (i.e., testing the medium and tissue from visibly clean cultures using enriched bacteriological media) revealed quiescent endophytic bacteria associated with 80 – 100% of such cultures. Three distinct colony morphotypes were isolated and were identified as Ralstonia, Enterobacter, and Methylobacterium spp., based on their 16S rRNA gene sequences. These endophytes did not interfere with normal micropropagation, but tended to grow actively and outgrow older cultures, especially at higher cytokinin concentrations. Stable micropropagation of ‘Arka Ravi’ chrysanthemum for ≥ 2 years, with their resident endophytic bacteria in a covert form, was achieved on basal MS medium with > 90% shoot growth and rooting, a four-to-five-fold propagation rate at each 2 – 3 week sub-culture cycle, and with > 90% establishment of rooted plantlets ex vitro. These results suggest that in vitro cultures of chrysanthemum often harbour endophytes with no obvious indications of their presence or with possible hidden effects during micropropagation. 相似文献
7.
Phenotypic and genetic parameters for body traits in the giant freshwater prawn (Macrobrachium rosenbergii) in India 下载免费PDF全文
下载免费PDF全文 Bindu R Pillai Pa Luan Lalrinsanga Raul W Ponzoni Hooi Ling Khaw Kanta Das Mahapatra Swagatika Mohanty Gunamaya Patra Namita Naik Haramohan Pradhan Pallipuram Jayasankar 《Aquaculture Research》2017,48(12):5741-5750
Phenotypic and genetic parameters were estimated for three body traits (harvest weight, carapace length and standard length) and for adult male morphotypes of the giant freshwater prawn Macrobrachium rosenbergii in a fully pedigreed synthetic population in India. The data set included 9,173 progeny produced over four generations from 162 sires and 234 dams. Variance components and genetic parameters were estimated fitting an animal model using the residual maximum‐likelihood methodology. The heritabilities for harvest body weight (HW), carapace length (CL) and standard length (SL) were moderate (0.22 ± 0.056, 0.22 ± 0.055 and 0.25 ± 0.059 respectively). The common environmental effects for HW, CL and SL were 0.10 ± 0.020, 0.08 ± 0.018 and 0.10 ± 0.021 respectively. As M. rosenbergii is sexually dimorphic, we estimated heritabilities within each sex. Heritability of HW in females (0.27 ± 0.068) was greater than that in males (0.15 ± 0.057). CL and SL followed the same pattern. The occurrence of male morphotypes is a unique characteristic of adult populations of M. rosenbergii. Populations from culture ponds exhibit a wide range of sizes. To examine whether there was a heritable component in male morphotype frequencies, we treated male morphotypes as traits. The additive genetic variance (and hence the heritability) was zero for male morphotype, indicating that selective breeding to increase the proportion of desirable male morphotypes would not be effective. The genetic correlations among body traits were all positive, high and approaching unity. The results are discussed in relation to selection plans for the giant freshwater prawn. 相似文献
8.
Shalini Goyat K. Hima Bindu Devendra Singh R.S. Katiyar S.K. Tewari 《East African Agricultural and Forestry Journal》2017,82(2-4):118-129
Betel vine has been identified as an important cash crop in India. It is a vegetatively propagated plant and more than 100 landraces (cultivars) are cultivated in India. They are often named after the localities where they are grown. To assess the molecular genetic diversity among 10 betel vine cultivars, amplified fragment length polymorphism (AFLP) markers were used. Five AFLP primer combinations produced 323 bands of which 155 were polymorphic, leading to a 47.99% polymorphism. Average polymorphic information content (PIC) was 0.14 over all primer combinations. Genetic similarity was calculated from the Jaccard's similarity coefficient (r) value for all accessions which varied from 0.39 to 0.81, with an average of 0.60 implying a medium level of genetic variation between investigated cultivars. Cluster analysis divided the cultivars into two main clusters where M2 and M3 were closely related but F3 was separate from all others. The cluster analysis based on AFLP data indicated that cultivars were not grouped according to their geographic place of collection but rather by genetic relatedness. The principle coordinate analysis (PCA) of the markers was linked to the dendrograms generated by employing UPGMA. 相似文献
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Pseudomonas sp. 30-3, a toluene degrading microorganism isolated from oil-contaminated Antarctic soils, was shown to form aggregated flocs of cells when exposed to temperatures of 22 and 4 °C, with an increase in aggregation at 4 °C. This was speculated to be due to the secretion of an extracellular polymeric substance (EPS), thus protecting the organism from cold or frost damage. The flocs of cells were stained with the Live/Dead BacLight Bacterial Viability kit and found to be viable cells. The EPS was identified by lectin binding analysis to consist of N-acetyl-d-glucosamine and N-acetylneuraminic acid. An enzyme-linked lectinosorbent assay was also carried out to quantify the amount of EPS produced at 37, 22 and 4 °C. Results showed that at 37 °C the amount of EPS secreted was low, but there was little difference in the amount of EPS secreted at 22 and 4 °C by Pseudomonas sp. 30-3. 相似文献