کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2431366 1106753 2015 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
A potential Kazal-type serine protease inhibitor involves in kinetics of protease inhibition and bacteriostatic activity
ترجمه فارسی عنوان
یک مهار کننده پروتئاز سرین پروتئاز با ظرفیت کازال، شامل سینتیک مهار پروتئاز و فعالیت باکتری است
کلمات کلیدی
مورل، مهار کننده پروتئاز، پروتئین ضد میکروبی بیان ژن، فعالیت جنبشی
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم کشاورزی و بیولوژیک علوم آبزیان
چکیده انگلیسی


• A Kazal-type serine protease inhibitor was characterized from striped murrel.
• CsKSPI was an extracellular protein based on cellular location analysis.
• CsKSPI gene expression was inducted upon fungus, bacteria and poly I:C.
• Recombinant CsKSPI strongly inhibited trypsin.
• CsKSPI showed antimicrobial activity against selected Gram negative and positive bacteria.

Kazal-type serine protease inhibitor (KSPI) is a pancreatic secretary trypsin inhibitor which involves in various cellular component regulations including development and defense process. In this study, we have characterized a KSPI cDNA sequence of freshwater striped murrel fish Channa striatus (Cs) at molecular level. Cellular location analysis predicted that the CsKSPI was an extracellular protein. The domain analysis showed that the CsKSPI contains a Kazal domain at 47–103 along with its family signature between 61 and 83. Phylogenetically, CsKSPI is closely related to KSPI from Maylandia zebra and formed a sister group with mammals. The 2D structure of CsKSPI showed three α-helical regions which are connected with random coils, one helix at signal sequence and two at the Kazal domain region. The relative gene expression showed that the CsKSPI was highly expressed in gills and its expression was induced upon fungus (Aphanomyces invadans), bacteria (Aeromonas hydrophila) and poly I:C (a viral analogue) challenge. The CsKSPI recombinant protein was produced to characterize and study the CsKSPI gene specific functions. The recombinant CsKSPI strongly inhibited trypsin compared to other tested proteases. The results of the kinetic activity of CsKSPI against trypsin was Vmaxs = 1.62 nmol/min, KMs = 0.21 mM and Kis = 15.37 nM. Moreover, the recombinant CsKSPI inhibited the growth of Gram-negative bacteria A. hydrophila at 20 μM and Gram-positive bacteria Bacillus subtilis at the MIC50 of 15 μM. Overall, the study indicated that the CsKSPI was a potential trypsin inhibitor which involves in antimicrobial activity.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Fish & Shellfish Immunology - Volume 42, Issue 2, February 2015, Pages 430–438
نویسندگان
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