Ranyere Lucena de Souza

Dr. Ranyere Lucena de Souza

orcid

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 March 2013 in Enzyme and Microbial Technology
Verified
Journal Article
Closed access
RSRanyere Lucena de Souza
Ranyere Lucena de Souza
EFEmanuelle Lima Pache de Faria
Emanuelle Lima Pache de Faria
RFRenan Figueiredo
Renan Figueiredo
LFLisiane dos Santos Freitas
Lisiane dos Santos Freitas
MIMiguel Iglesias
Miguel Iglesias
CSCleide Mara Faria Soares
Cleide Mara Faria Soares

19 March 2015 in Green Chemistry
Verified
Journal Article
Closed access
PDF file
RSRanyere Lucena de Souza
Ranyere Lucena de Souza
SVSonia P. M. Ventura
Sonia P. M. Ventura
CSCleide Mara Faria Soares
Cleide Mara Faria Soares
JCJoao Coutinho
Joao Coutinho
Álvaro Silva LimaÁlvaro Silva Lima
Álvaro Silva Lima
Aqueous two-phase systems (ATPS) are efficient, environmentally friendly, and “biocompatible” separation processes, which allow the recovery of enzymes. The most common systems are based on polymers and salts, and recently, to overcome the low polarity difference between the phases of the polymeric systems, ATPS based on ionic liquids (ILs) were proposed and have been successfully applied in this field. This work discusses the use of imidazolium-based ILs not as phase forming compounds but as adjuvants (5 wt%) in ATPS of polyethylene glycol systems (1500, 4000, 6000 and 8000 g mol−1) with potassium phosphate buffer at pH 7, in the extraction and purification of a lipase produced by submerged fermentation by Bacillus sp. ITP-001. An initial optimization study was carried out with the commercial lipase B from Candida antarctica (CaLB) allowing us to further purify the commercial CaLB (purification factor = 5.2). Using the optimized conditions, a purification factor of 245 for the lipase from Bacillus sp. ITP-001 was achieved with 1-hexyl-3-methyl imidazolium chloride. The high purification factor is a consequence of the favorable interactions between the IL and the contaminant proteins that migrate for the PEG-rich phase, where the IL also concentrates preferentially, while the enzyme remains in the salt-rich phase.

1 August 2014 in Fluid Phase Equilibria
Verified
Journal Article
Closed access
RSRanyere Lucena de Souza
Ranyere Lucena de Souza
VCVictor C. Campos
Victor C. Campos
SVSonia P. M. Ventura
Sonia P. M. Ventura
CSCleide Mara Faria Soares
Cleide Mara Faria Soares
JCJoao Coutinho
Joao Coutinho
Álvaro Silva LimaÁlvaro Silva Lima
Álvaro Silva Lima

17 June 2019 in Biotechnology and Applied Biochemistry
Verified
Journal Article
Closed access
PDF file
MBMilson S. Barbosa
Milson S. Barbosa
CFCintia C. C. Freire
Cintia C. C. Freire
LALays C. Almeida
Lays C. Almeida
LFLisiane S. Freitas
Lisiane S. Freitas
RSRanyere Lucena de Souza
Ranyere Lucena de Souza
CSCleide Mara Faria Soares
Cleide Mara Faria Soares

1 November 2015 in Separation and Purification Technology
Verified
Journal Article
Closed access
RSRanyere Lucena de Souza
Ranyere Lucena de Souza
RLRafaella A. Lima
Rafaella A. Lima
JCJoao Coutinho
Joao Coutinho
CSCleide Mara Faria Soares
Cleide Mara Faria Soares
Álvaro Silva LimaÁlvaro Silva Lima
Álvaro Silva Lima

1 December 2011 in Journal of Chromatography B
Verified
Journal Article
Closed access
JBJosé Murillo P. Barbosa
José Murillo P. Barbosa
RSRanyere Lucena de Souza
Ranyere Lucena de Souza
AFAlini Tinoco Fricks
Alini Tinoco Fricks
GZGisella Maria Zanin
Gisella Maria Zanin
CSCleide Mara Faria Soares
Cleide Mara Faria Soares
Álvaro Silva LimaÁlvaro Silva Lima
Álvaro Silva Lima