Extracellular protease of Natrialba magadii : purification and biochemical characterization

Extremophiles ◽  
2000 ◽  
Vol 4 (3) ◽  
pp. 181-188 ◽  
Author(s):  
María I. Giménez ◽  
Claudia A. Studdert ◽  
Jorge J. Sánchez ◽  
R. E. De Castro
Keyword(s):  
Biochemical Characterization ◽  
Extracellular Protease ◽  
Natrialba Magadii

scholarly journals Functional roles of C-terminal extension (CTE) of salt-dependent peptidase activity of the Natrialba magadii extracellular protease (NEP)

2018 ◽  
Vol 113 ◽  
pp. 1134-1141 ◽  
Author(s):  
Alyne Marem ◽  
Debora N. Okamoto ◽  
Lilian C.G. Oliveira ◽  
Diego M. Ruiz ◽  
Roberto A. Paggi ◽  
...  
Keyword(s):  
Extracellular Protease ◽  
Peptidase Activity ◽  
Functional Roles ◽  
Natrialba Magadii

scholarly journals Gene cloning and heterologous synthesis of a haloalkaliphilic extracellular protease of Natrialba magadii (Nep)

Extremophiles ◽  
2008 ◽  
Vol 12 (5) ◽  
pp. 677-687 ◽  
Author(s):  
Rosana E. De Castro ◽  
Diego M. Ruiz ◽  
María I. Giménez ◽  
María X. Silveyra ◽  
Roberto A. Paggi ◽  
...  
Keyword(s):  
Gene Cloning ◽  
Extracellular Protease ◽  
Natrialba Magadii

Plant Pathology Diagnosed by X-Ray Microanalysis

1987 ◽  
Vol 45 ◽  
pp. 974-975
Author(s):  
J. H. Resau ◽  
N. Howell ◽  
S. H. Chang
Keyword(s):  
Electron Microscopy ◽  
Plant Pathology ◽  
Biochemical Characterization ◽  
Nutrient Deficiency ◽  
Green Leaf ◽  
Parasitic Infestation ◽  
X Ray

Spinach grown in Texas developed “yellow spotting” on the peripheral portions of the leaves. The exact cause of the discoloration could not be determined as there was no evidence of viral or parasitic infestation of the plants and biochemical characterization of the plants did not indicate any significant differences between the yellow and green leaf portions of the spinach. The present study was undertaken using electron microscopy (EM) to determine if a micro-nutrient deficiency was the cause for the discoloration.Green leaf spinach was collected from the field and sent by express mail to the EM laboratory. The yellow and equivalent green portions of the leaves were isolated and dried in a Denton evaporator at 10-5 Torr for 24 hrs. The leaf specimens were then examined using a JEOL 100 CX analytical microscope. TEM specimens were prepared according to the methods of Trump et al.

The in vivo distribution and dynamics of DNA topoisomerase II in Drosophila embryonic nuclei and chromosomes

1993 ◽  
Vol 51 ◽  
pp. 74-75
Author(s):  
Jason R. Swedlow ◽  
Neil Osheroff ◽  
Tim Karr ◽  
John W. Sedat ◽  
David A. Agard
Keyword(s):  
Topoisomerase Ii ◽  
Biochemical Characterization ◽  
Developmental Cycle ◽  
Dna Topoisomerase Ii ◽  
Chromosomal Distribution ◽  
Dna Topoisomerase ◽  
Ideal System ◽  
Dnase Treatment

DNA topoisomerase II is an ATP-dependent double-stranded DNA strand-passing enzyme that is necessary for full condensation of chromosomes and for complete segregation of sister chromatids at mitosis in vivo and in vitro. Biochemical characterization of chromosomes or nuclei after extraction with high-salt or detergents and DNAse treatment showed that topoisomerase II was a major component of this remnant, termed the chromosome scaffold. The scaffold has been hypothesized to be the structural backbone of the chromosome, so the localization of topoisomerase II to die scaffold suggested that the enzyme might play a structural role in the chromosome. However, topoisomerase II has not been studied in nuclei or chromosomes in vivo. We have monitored the chromosomal distribution of topoisomerase II in vivo during mitosis in the Drosophila embryo. This embryo forms a multi-nucleated syncytial blastoderm early in its developmental cycle. During this time, the embryonic nuclei synchronously progress through 13 mitotic cycles, so this is an ideal system to follow nuclear and chromosomal dynamics.

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