Synthesis of glycinamides using protease immobilized magnetic nanoparticles

In the present investigation, Bacillus subtilis was isolated from slaughterhouse waste and screened for the production of protease enzyme. The purified protease was successfully immobilized on magnetic nanoparticles (MNPs) and used for the synthesis of series of glycinamides. The binding and thermal...

Full description

Bibliographic Details
Main Authors: Abha Sahu, Pallavi Sharad Badhe, Ravindra Adivarekar, Mayur Ramrao Ladole, Aniruddha Bhalchandra Pandit
Format: Article
Language:English
Published: Elsevier 2016-12-01
Series:Biotechnology Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2215017X16300297
id doaj-32d7e764f4e44f8da810071d3d8f0b5f
record_format Article
spelling doaj-32d7e764f4e44f8da810071d3d8f0b5f2020-11-24T22:51:52ZengElsevierBiotechnology Reports2215-017X2016-12-0112C132510.1016/j.btre.2016.07.002Synthesis of glycinamides using protease immobilized magnetic nanoparticlesAbha SahuPallavi Sharad BadheRavindra AdivarekarMayur Ramrao LadoleAniruddha Bhalchandra PanditIn the present investigation, Bacillus subtilis was isolated from slaughterhouse waste and screened for the production of protease enzyme. The purified protease was successfully immobilized on magnetic nanoparticles (MNPs) and used for the synthesis of series of glycinamides. The binding and thermal stability of protease on MNPs was confirmed by FTIR spectroscopy and TGA analysis. The surface morphology of MNPs before and after protease immobilization was carried out using SEM analysis. XRD pattern revealed no phase change in MNPs after enzyme immobilization. The processing parameters for glycinamides synthesis viz. temperature, pH, and time were optimized using Response Surface Methodology (RSM) by using Design Expert (9.0.6.2). The maximum yield of various amides 2 butyramidoacetic acid (AMD-1,83.4%), 2-benzamidoacetic acid (AMD-2,80.5%) and 2,2′((carboxymethyl) amino)-2-oxoethyl)-2-hydroxysuccinyl)bis(azanediyl))diacetic acid (AMD-3,80.8%) formed was observed at pH-8, 50 °C and 30 min. The synthesized immobilized protease retained 70% of the initial activity even after 8 cycles of reuse.http://www.sciencedirect.com/science/article/pii/S2215017X16300297ProteaseMagnetic nanoparticlesImmobilizationGlycinamidesResponse surface methodology
collection DOAJ
language English
format Article
sources DOAJ
author Abha Sahu
Pallavi Sharad Badhe
Ravindra Adivarekar
Mayur Ramrao Ladole
Aniruddha Bhalchandra Pandit
spellingShingle Abha Sahu
Pallavi Sharad Badhe
Ravindra Adivarekar
Mayur Ramrao Ladole
Aniruddha Bhalchandra Pandit
Synthesis of glycinamides using protease immobilized magnetic nanoparticles
Biotechnology Reports
Protease
Magnetic nanoparticles
Immobilization
Glycinamides
Response surface methodology
author_facet Abha Sahu
Pallavi Sharad Badhe
Ravindra Adivarekar
Mayur Ramrao Ladole
Aniruddha Bhalchandra Pandit
author_sort Abha Sahu
title Synthesis of glycinamides using protease immobilized magnetic nanoparticles
title_short Synthesis of glycinamides using protease immobilized magnetic nanoparticles
title_full Synthesis of glycinamides using protease immobilized magnetic nanoparticles
title_fullStr Synthesis of glycinamides using protease immobilized magnetic nanoparticles
title_full_unstemmed Synthesis of glycinamides using protease immobilized magnetic nanoparticles
title_sort synthesis of glycinamides using protease immobilized magnetic nanoparticles
publisher Elsevier
series Biotechnology Reports
issn 2215-017X
publishDate 2016-12-01
description In the present investigation, Bacillus subtilis was isolated from slaughterhouse waste and screened for the production of protease enzyme. The purified protease was successfully immobilized on magnetic nanoparticles (MNPs) and used for the synthesis of series of glycinamides. The binding and thermal stability of protease on MNPs was confirmed by FTIR spectroscopy and TGA analysis. The surface morphology of MNPs before and after protease immobilization was carried out using SEM analysis. XRD pattern revealed no phase change in MNPs after enzyme immobilization. The processing parameters for glycinamides synthesis viz. temperature, pH, and time were optimized using Response Surface Methodology (RSM) by using Design Expert (9.0.6.2). The maximum yield of various amides 2 butyramidoacetic acid (AMD-1,83.4%), 2-benzamidoacetic acid (AMD-2,80.5%) and 2,2′((carboxymethyl) amino)-2-oxoethyl)-2-hydroxysuccinyl)bis(azanediyl))diacetic acid (AMD-3,80.8%) formed was observed at pH-8, 50 °C and 30 min. The synthesized immobilized protease retained 70% of the initial activity even after 8 cycles of reuse.
topic Protease
Magnetic nanoparticles
Immobilization
Glycinamides
Response surface methodology
url http://www.sciencedirect.com/science/article/pii/S2215017X16300297
work_keys_str_mv AT abhasahu synthesisofglycinamidesusingproteaseimmobilizedmagneticnanoparticles
AT pallavisharadbadhe synthesisofglycinamidesusingproteaseimmobilizedmagneticnanoparticles
AT ravindraadivarekar synthesisofglycinamidesusingproteaseimmobilizedmagneticnanoparticles
AT mayurramraoladole synthesisofglycinamidesusingproteaseimmobilizedmagneticnanoparticles
AT aniruddhabhalchandrapandit synthesisofglycinamidesusingproteaseimmobilizedmagneticnanoparticles
_version_ 1725668416855998464