Literature DB >> 30634078

Purification and characterization of Bowman-Birk and Kunitz isoinhibitors from the seeds of Rhynchosia sublobata (Schumach.) Meikle, a wild relative of pigeonpea.

Soundappan S Mohanraj1, Mariyamma Gujjarlapudi2, Vadthya Lokya2, Nalini Mallikarjuna3, Aparna Dutta-Gupta4, Kollipara Padmasree5.   

Abstract

Rhynchosia sublobata, a wild relative of pigeonpea, possesses defensive proteinase/protease inhibitors (PIs). Characterization of trypsin specific PIs (RsPI) separated from seeds by column chromatography using 2-D gel electrophoresis and Edman degradation method identified R. sublobata possessed both Bowman-Birk isoinhibitors (RsBBI) and Kunitz isoinhibitors (RsKI). A quick method was developed to separate RsBBI and RsKI from RsPI based on their differential solubility in TCA and acetate buffer. N-terminus sequencing of RsBBI and RsKI by MALDI-ISD ascertained the presence of Bowman Birk and Kunitz type isoinhibitors in R. sublobata. RsBBI (9216 Da) and RsKI (19,412 Da) exhibited self-association pattern as revealed by western blotting with anti-BBI antibody and MALDI-TOF peptide mass fingerprint analysis, respectively. RsBBI and RsKI varied significantly in their biochemical, biophysical and insecticidal properties. RsBBI inhibited the activity of trypsin (Ki = 128.5 ± 4.5 nM) and chymotrypsin (Ki = 807.8 ± 23.7 nM) while RsKI (Ki = 172.0 ± 9.2 nM) inhibited the activity of trypsin alone, by non-competitive mode. The trypsin inhibitor (TI) and chymotrypsin inhibitor (CI) activities of RsBBI were stable up to 100 °C. But, RsBBI completely lost its TI and CI activities on reduction with 3 mM DTT. Conversely, RsKI lost its TI activity on heating at 100 °C and retained >60% of its TI activity in presence of 3 mM DTT. CD spectroscopic studies on RsBBI and RsKI showed their secondary structural elements in the following order: random coils > β-sheets/β-turns > α-helix. However, RsKI showed reversible denaturation midpoint (Tm) of 75 °C. Further, the significant inhibitory activity of RsBBI (IC50 = 24 ng) and RsKI (IC50 = 59 ng) against trypsin-like gut proteases of Achaea janata (AjGPs) and Helicoverpa armigera (HaGPs) suggest them as potential biomolecules in the management of A. janata and H. armigera, respectively.
Copyright © 2019 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Achaea janata (Noctuidae); Helicoverpa armigera (Noctuidae); Protease inhibitor; Rhynchosia sublobata (Fabaceae); Sodium acetate; Trichloroacetic acid; Trypsin-like midgut proteases

Mesh:

Substances:

Year:  2019        PMID: 30634078     DOI: 10.1016/j.phytochem.2018.12.018

Source DB:  PubMed          Journal:  Phytochemistry        ISSN: 0031-9422            Impact factor:   4.072


  5 in total

Review 1.  Plant Kunitz Inhibitors and Their Interaction with Proteases: Current and Potential Pharmacological Targets.

Authors:  Camila Ramalho Bonturi; Ana Beatriz Silva Teixeira; Vitória Morais Rocha; Penélope Ferreira Valente; Juliana Rodrigues Oliveira; Clovis Macêdo Bezerra Filho; Isabel Fátima Correia Batista; Maria Luiza Vilela Oliva
Journal:  Int J Mol Sci       Date:  2022-04-25       Impact factor: 6.208

2.  Protein purification from Arachis hypogaea in one step: stability studies and anticarcinogenic analysis.

Authors:  Afaque Ahmad; Hirday N Verma; Prahalad Bharti; Kamlesh Pandey; Shahbaz Khan; Kapil Dev
Journal:  Food Sci Biotechnol       Date:  2019-08-08       Impact factor: 2.391

Review 3.  Bowman-Birk Inhibitors: Insights into Family of Multifunctional Proteins and Peptides with Potential Therapeutical Applications.

Authors:  Agata Gitlin-Domagalska; Aleksandra Maciejewska; Dawid Dębowski
Journal:  Pharmaceuticals (Basel)       Date:  2020-11-25

4.  Characterization of a Bowman-Birk type trypsin inhibitor purified from seeds of Solanum surattense.

Authors:  Abhijeet P Herwade; Sainath S Kasar; Niraj R Rane; Shadab Ahmed; Jaswinder Singh Maras; Pankaj K Pawar
Journal:  Sci Rep       Date:  2021-04-21       Impact factor: 4.379

5.  Response of Midgut Trypsin- and Chymotrypsin-Like Proteases of Helicoverpa armigera Larvae Upon Feeding With Peanut BBI: Biochemical and Biophysical Characterization of PnBBI.

Authors:  Vadthya Lokya; Marri Swathi; Nalini Mallikarjuna; Kollipara Padmasree
Journal:  Front Plant Sci       Date:  2020-03-24       Impact factor: 5.753

  5 in total

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