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131.
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Choi Jae Hee; Chung Gap Chae; Suh Sang Ryong; Yu Jung Ah; Sung Je Hoon; Choi Kyung Ju 《Plant & cell physiology》1997,38(4):495-498
Restriction of tomato roots by growth in small containers stronglysuppressed transport of 45Ca2+ ions to new leaves and apices.Water transport, expressed on a leaf area basis, was marginallyreduced by root restriction, an indication that calcium transportwas more severely limited than water transport. (Received October 11, 1996; Accepted January 27, 1997) 相似文献
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Accelerated solvent extraction (ASE) is an alternative sample extraction procedure for ochratoxin A in roasted coffee. ASE results are comparable to that of the modified Koch method, but required less sample preparation time. Furthermore, ASE gave higher quantitative values than other methods reported for extraction of ochratoxin A. In the end less harmful water could be used for extraction. 相似文献
135.
Je‐Nie Phue Santosh B. Noronha Ritabrata Bhattacharyya Alan J. Wolfe Joseph Shiloach 《Biotechnology and bioengineering》2005,91(5):649-649
The original article to which this Erratum refers was published in Biotechnol Bioeng 2005;90:805–820 相似文献
136.
The freshwater bryozoan Pectinatella magnifica (Leidy, 1851) is an invasive species in many countries all over the world. Although native to North America, it has been found in many countries of Europe and Asia. Pectinatella magnifica forms the largest colonial masses from all recently known bryozoan species. Culturing this organism in an aquarium has never been achieved for more than few days so far. Colonies from laboratory culture are important for various studies on its biology and life cycle of this species in experimental conditions. Young colonies successfully hatched from germinating statoblasts of P. magnifica in the laboratory and were maintained over eight weeks. Moreover, this was the first time when the compound colonies of this species were carried from its natural habitat to the laboratory, into a special aquarium system, and kept alive for more than three weeks. In both experiments the physicochemical parameters of the water (temperature, concentration of dissolved oxygen, electrolytic conductivity and pH) and changes in weight of compound colonies of P. magnifica in laboratory conditions were checked. The results found in this study are essential for understanding the invasiveness of this species and identifying methods for elimination of its ecological risks because these are closely resembling those of other invasive species. 相似文献
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Andrea Gloria‐Soria Diego Ayala Ambicadutt Bheecarry Olger Calderon‐Arguedas Dave D. Chadee Marina Chiappero Maureen Coetzee Khouaildi Bin Elahee Ildefonso Fernandez‐Salas Hany A. Kamal Basile Kamgang Emad I. M. Khater Laura D. Kramer Vicki Kramer Alma Lopez‐Solis Joel Lutomiah Ademir Martins Jr Maria Victoria Micieli Christophe Paupy Alongkot Ponlawat Nil Rahola Syed Basit Rasheed Joshua B. Richardson Amag A. Saleh Rosa Maria Sanchez‐Casas Gonçalo Seixas Carla A. Sousa Walter J. Tabachnick Adriana Troyo Jeffrey R. Powell 《Molecular ecology》2016,25(21):5377-5395
Mosquitoes, especially Aedes aegypti, are becoming important models for studying invasion biology. We characterized genetic variation at 12 microsatellite loci in 79 populations of Ae. aegypti from 30 countries in six continents, and used them to infer historical and modern patterns of invasion. Our results support the two subspecies Ae. aegypti formosus and Ae. aegypti aegypti as genetically distinct units. Ae. aegypti aegypti populations outside Africa are derived from ancestral African populations and are monophyletic. The two subspecies co‐occur in both East Africa (Kenya) and West Africa (Senegal). In rural/forest settings (Rabai District of Kenya), the two subspecies remain genetically distinct, whereas in urban settings, they introgress freely. Populations outside Africa are highly genetically structured likely due to a combination of recent founder effects, discrete discontinuous habitats and low migration rates. Ancestral populations in sub‐Saharan Africa are less genetically structured, as are the populations in Asia. Introduction of Ae. aegypti to the New World coinciding with trans‐Atlantic shipping in the 16th to 18th centuries was followed by its introduction to Asia in the late 19th century from the New World or from now extinct populations in the Mediterranean Basin. Aedes mascarensis is a genetically distinct sister species to Ae. aegypti s.l. This study provides a reference database of genetic diversity that can be used to determine the likely origin of new introductions that occur regularly for this invasive species. The genetic uniqueness of many populations and regions has important implications for attempts to control Ae. aegypti, especially for the methods using genetic modification of populations. 相似文献
139.
Young Chul Kwon Sinil Kim Yong Seok Lee Je Chul Lee Myung-Je Cho Woo-Kon Lee Hyung-Lyun Kang Jae-Young Song Seung Chul Baik Hyeon Su Ro 《Journal of microbiology (Seoul, Korea)》2016,54(5):387-395
HP0059, an uncharacterized gene of Helicobacter pylori, encodes a 284-aa-long protein containing a nuclear localization sequence (NLS) and multiple leucine-rich heptad repeats. Effects of HP0059 proteins in human stomach cells were assessed by incubation of recombinant HP0059 proteins with the AGS human gastric carcinoma cell line. Wild-type HP0059 proteins showed cytotoxicity in AGS cells in a concentration-dependent manner, whereas NLS mutant protein showed no effect, suggesting that the cytotoxicity is attributed to host nuclear localization. AGS cells transfected with pEGFP-HP0059 plasmid showed strong GFP signal merged to the chromosomal DNA region. The chromosome was fragmented into multiple distinct dots merged with the GFP signal after 12 h of incubation. The chromosome fragmentation was further explored by incubation of AGS chromosomal DNA with recombinant HP0059 proteins, which leaded to complete degradation of the chromosomal DNA. HP0059 protein also degraded circular plasmid DNA without consensus, being an indication of DNase I activity. The DNase was activated by MgCl2, but not by CaCl2. The activity was completely blocked by EDTA. The optimal pH and temperature for DNase activity were 7.0–8.0 and 55°C, respectively. These results indicate that HP0059 possesses a novel DNase I activity along with a role in the genomic instability of human gastric cells, which may result in the transformation of gastric cells. 相似文献
140.