Literature DB >> 28282252

Tobacco phytaspase: Successful expression in a heterologous system.

Sharmila Narayanan1, Pallab Sanpui2, Lingaraj Sahoo1, Siddhartha Sankar Ghosh1,2.   

Abstract

Phytaspase, a plant serine protease, has been demonstrated to play an important role in the programmed cell death of various plants. Phytaspase is synthesized as an inactive proenzyme containing an N-terminal signal peptide followed by a pro-domain and a mature protease catalytic domain. Pre-prophytaspase autocatalytically processes itself into a pro-domain and an active mature phytaspase enzyme. We have recently demonstrated the successful expression of mature phytaspase from tobacco in a bacterial system. Herein, we focus on the expression of pre-prophytaspase as a GST-tag fusion and on its purification by affinity chromatography.

Entities:  

Keywords:  affinity chromatography; caspases; heterologous expression; phytaspase; programmed cell death; serine protease; subtilases

Mesh:

Substances:

Year:  2017        PMID: 28282252      PMCID: PMC5639862          DOI: 10.1080/21655979.2017.1292187

Source DB:  PubMed          Journal:  Bioengineered        ISSN: 2165-5979            Impact factor:   3.269


  21 in total

Review 1.  Plant phytaspases and animal caspases: structurally unrelated death proteases with a common role and specificity.

Authors:  Nina V Chichkova; Alexander I Tuzhikov; Michael Taliansky; Andrey B Vartapetian
Journal:  Physiol Plant       Date:  2012-01-28       Impact factor: 4.500

2.  Phytaspase, a relocalisable cell death promoting plant protease with caspase specificity.

Authors:  Nina V Chichkova; Jane Shaw; Raisa A Galiullina; Georgina E Drury; Alexander I Tuzhikov; Sang Hyon Kim; Markus Kalkum; Teresa B Hong; Elena N Gorshkova; Lesley Torrance; Andrey B Vartapetian; Michael Taliansky
Journal:  EMBO J       Date:  2010-01-28       Impact factor: 11.598

3.  Ca2+-dependent maturation of subtilisin from a hyperthermophilic archaeon, Thermococcus kodakaraensis: the propeptide is a potent inhibitor of the mature domain but is not required for its folding.

Authors:  Marian Pulido; Kenji Saito; Shun-Ichi Tanaka; Yuichi Koga; Masaaki Morikawa; Kazufumi Takano; Shigenori Kanaya
Journal:  Appl Environ Microbiol       Date:  2006-06       Impact factor: 4.792

Review 4.  Subtilases: the superfamily of subtilisin-like serine proteases.

Authors:  R J Siezen; J A Leunissen
Journal:  Protein Sci       Date:  1997-03       Impact factor: 6.725

Review 5.  [Phytaspases: aspartate-specific proteases involved in plant cell death].

Authors:  N V Chichkova; R A Galiullina; R E Beloshistov; A V Balakireva; A B Vartapetian
Journal:  Bioorg Khim       Date:  2014 Nov-Dec

6.  N-terminal deletion of Tk1689, a subtilisin-like serine protease from Thermococcus kodakaraensis, copes with its cytotoxicity in Escherichia coli.

Authors:  Nouman Rasool; Naeem Rashid; Saima Iftikhar; Muhammad Akhtar
Journal:  J Biosci Bioeng       Date:  2010-05-08       Impact factor: 2.894

7.  Heterologous expression and functional characterization of phytaspase, a caspase-like plant protease.

Authors:  Sharmila Narayanan; Pallab Sanpui; Lingaraj Sahoo; Siddhartha Sankar Ghosh
Journal:  Int J Biol Macromol       Date:  2016-11-17       Impact factor: 6.953

8.  Substrate Specificity and Possible Heterologous Targets of Phytaspase, a Plant Cell Death Protease.

Authors:  Raisa A Galiullina; Paulina Kasperkiewicz; Nina V Chichkova; Aleksandra Szalek; Marina V Serebryakova; Marcin Poreba; Marcin Drag; Andrey B Vartapetian
Journal:  J Biol Chem       Date:  2015-08-17       Impact factor: 5.157

9.  Self-processing of a barley subtilase expressed in E. coli.

Authors:  Stephan Plattner; Clemens Gruber; Friedrich Altmann; Holger Bohlmann
Journal:  Protein Expr Purif       Date:  2014-06-11       Impact factor: 1.650

10.  Proteolytic processing of a precursor protein for a growth-promoting peptide by a subtilisin serine protease in Arabidopsis.

Authors:  Renu Srivastava; Jian-Xiang Liu; Stephen H Howell
Journal:  Plant J       Date:  2008-07-04       Impact factor: 6.417

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