A Bowman–Birk protease inhibitor purified, cloned, sequenced and characterized from the seeds of <i>Maclura pomifera</i> (Raf.) Schneid
- Autores
- Indarte, Martín; Lazza, Cristian Martín; Assis, Diego M.; Caffini, Néstor Oscar; Juliano, María A.; Avilés, Francesc X.; Daura, Xavier; López, Laura María Isabel; Trejo, Sebastián Alejandro
- Año de publicación
- 2017
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- A new BBI-type protease inhibitor with remarkable structural characteristics was purified, cloned, and sequenced from seeds of Maclura pomifera, a dicotyledonous plant belonging to the Moraceae family. In this work, we report a Bowman–Birk inhibitor (BBI) isolated, purified, cloned, and characterized from Maclura pomifera seeds (MpBBI), the first of this type from a species belonging to Moraceae family. MpBBI was purified to homogeneity by RP-HPLC, total RNA was extracted from seeds of M. pomifera, and the 3′RACE-PCR method was applied to obtain the cDNA, which was cloned and sequenced. Peptide mass fingerprinting (PMF) analysis showed correspondence between the in silico-translated protein and MpBBI, confirming that it corresponds to a new plant protease inhibitor. The obtained cDNA encoded a polypeptide of 65 residues and possesses 10 cysteine residues, with molecular mass of 7379.27, pI 6.10, and extinction molar coefficient of 9105 M⁻¹ cm⁻¹. MpBBI inhibits strongly trypsin with Kᵢ in the 10⁻¹⁰ M range and was stable in a wide array of pH and extreme temperatures. MpBBI comparative modeling was applied to gain insight into its 3D structure and highlighted some distinguishing features: (1) two non-identical loops, (2) loop 1 (CEEESRC) is completely different from any known BBI, and (3) the amount of disulphide bonds is also different from any reported BBI from dicot plants.
Centro de Investigación de Proteínas Vegetales
Instituto Multidisciplinario de Biología Celular - Materia
-
Ciencias Exactas
Biología
BBI-type protease inhibitor
Cloning
Homology modeling
Loop
Three-dimensional structure
Trypsin inhibition - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by/4.0/
- Repositorio
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/144454
Ver los metadatos del registro completo
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A Bowman–Birk protease inhibitor purified, cloned, sequenced and characterized from the seeds of <i>Maclura pomifera</i> (Raf.) SchneidIndarte, MartínLazza, Cristian MartínAssis, Diego M.Caffini, Néstor OscarJuliano, María A.Avilés, Francesc X.Daura, XavierLópez, Laura María IsabelTrejo, Sebastián AlejandroCiencias ExactasBiologíaBBI-type protease inhibitorCloningHomology modelingLoopThree-dimensional structureTrypsin inhibitionA new BBI-type protease inhibitor with remarkable structural characteristics was purified, cloned, and sequenced from seeds of <i>Maclura pomifera</i>, a dicotyledonous plant belonging to the Moraceae family. In this work, we report a Bowman–Birk inhibitor (BBI) isolated, purified, cloned, and characterized from <i>Maclura pomifera</i> seeds (MpBBI), the first of this type from a species belonging to Moraceae family. MpBBI was purified to homogeneity by RP-HPLC, total RNA was extracted from seeds of <i>M. pomifera</i>, and the 3′RACE-PCR method was applied to obtain the cDNA, which was cloned and sequenced. Peptide mass fingerprinting (PMF) analysis showed correspondence between the in silico-translated protein and MpBBI, confirming that it corresponds to a new plant protease inhibitor. The obtained cDNA encoded a polypeptide of 65 residues and possesses 10 cysteine residues, with molecular mass of 7379.27, pI 6.10, and extinction molar coefficient of 9105 M⁻¹ cm⁻¹. MpBBI inhibits strongly trypsin with Kᵢ in the 10⁻¹⁰ M range and was stable in a wide array of pH and extreme temperatures. MpBBI comparative modeling was applied to gain insight into its 3D structure and highlighted some distinguishing features: (1) two non-identical loops, (2) loop 1 (CEEESRC) is completely different from any known BBI, and (3) the amount of disulphide bonds is also different from any reported BBI from dicot plants.Centro de Investigación de Proteínas VegetalesInstituto Multidisciplinario de Biología Celular2017-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf343-353http://sedici.unlp.edu.ar/handle/10915/144454enginfo:eu-repo/semantics/altIdentifier/issn/1432-2048info:eu-repo/semantics/altIdentifier/issn/0032-0935info:eu-repo/semantics/altIdentifier/doi/10.1007/s00425-016-2611-6info:eu-repo/semantics/altIdentifier/pmid/27778107info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-10T12:34:58Zoai:sedici.unlp.edu.ar:10915/144454Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-10 12:34:58.799SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
A Bowman–Birk protease inhibitor purified, cloned, sequenced and characterized from the seeds of <i>Maclura pomifera</i> (Raf.) Schneid |
title |
A Bowman–Birk protease inhibitor purified, cloned, sequenced and characterized from the seeds of <i>Maclura pomifera</i> (Raf.) Schneid |
spellingShingle |
A Bowman–Birk protease inhibitor purified, cloned, sequenced and characterized from the seeds of <i>Maclura pomifera</i> (Raf.) Schneid Indarte, Martín Ciencias Exactas Biología BBI-type protease inhibitor Cloning Homology modeling Loop Three-dimensional structure Trypsin inhibition |
title_short |
A Bowman–Birk protease inhibitor purified, cloned, sequenced and characterized from the seeds of <i>Maclura pomifera</i> (Raf.) Schneid |
title_full |
A Bowman–Birk protease inhibitor purified, cloned, sequenced and characterized from the seeds of <i>Maclura pomifera</i> (Raf.) Schneid |
title_fullStr |
A Bowman–Birk protease inhibitor purified, cloned, sequenced and characterized from the seeds of <i>Maclura pomifera</i> (Raf.) Schneid |
title_full_unstemmed |
A Bowman–Birk protease inhibitor purified, cloned, sequenced and characterized from the seeds of <i>Maclura pomifera</i> (Raf.) Schneid |
title_sort |
A Bowman–Birk protease inhibitor purified, cloned, sequenced and characterized from the seeds of <i>Maclura pomifera</i> (Raf.) Schneid |
dc.creator.none.fl_str_mv |
Indarte, Martín Lazza, Cristian Martín Assis, Diego M. Caffini, Néstor Oscar Juliano, María A. Avilés, Francesc X. Daura, Xavier López, Laura María Isabel Trejo, Sebastián Alejandro |
author |
Indarte, Martín |
author_facet |
Indarte, Martín Lazza, Cristian Martín Assis, Diego M. Caffini, Néstor Oscar Juliano, María A. Avilés, Francesc X. Daura, Xavier López, Laura María Isabel Trejo, Sebastián Alejandro |
author_role |
author |
author2 |
Lazza, Cristian Martín Assis, Diego M. Caffini, Néstor Oscar Juliano, María A. Avilés, Francesc X. Daura, Xavier López, Laura María Isabel Trejo, Sebastián Alejandro |
author2_role |
author author author author author author author author |
dc.subject.none.fl_str_mv |
Ciencias Exactas Biología BBI-type protease inhibitor Cloning Homology modeling Loop Three-dimensional structure Trypsin inhibition |
topic |
Ciencias Exactas Biología BBI-type protease inhibitor Cloning Homology modeling Loop Three-dimensional structure Trypsin inhibition |
dc.description.none.fl_txt_mv |
A new BBI-type protease inhibitor with remarkable structural characteristics was purified, cloned, and sequenced from seeds of <i>Maclura pomifera</i>, a dicotyledonous plant belonging to the Moraceae family. In this work, we report a Bowman–Birk inhibitor (BBI) isolated, purified, cloned, and characterized from <i>Maclura pomifera</i> seeds (MpBBI), the first of this type from a species belonging to Moraceae family. MpBBI was purified to homogeneity by RP-HPLC, total RNA was extracted from seeds of <i>M. pomifera</i>, and the 3′RACE-PCR method was applied to obtain the cDNA, which was cloned and sequenced. Peptide mass fingerprinting (PMF) analysis showed correspondence between the in silico-translated protein and MpBBI, confirming that it corresponds to a new plant protease inhibitor. The obtained cDNA encoded a polypeptide of 65 residues and possesses 10 cysteine residues, with molecular mass of 7379.27, pI 6.10, and extinction molar coefficient of 9105 M⁻¹ cm⁻¹. MpBBI inhibits strongly trypsin with Kᵢ in the 10⁻¹⁰ M range and was stable in a wide array of pH and extreme temperatures. MpBBI comparative modeling was applied to gain insight into its 3D structure and highlighted some distinguishing features: (1) two non-identical loops, (2) loop 1 (CEEESRC) is completely different from any known BBI, and (3) the amount of disulphide bonds is also different from any reported BBI from dicot plants. Centro de Investigación de Proteínas Vegetales Instituto Multidisciplinario de Biología Celular |
description |
A new BBI-type protease inhibitor with remarkable structural characteristics was purified, cloned, and sequenced from seeds of <i>Maclura pomifera</i>, a dicotyledonous plant belonging to the Moraceae family. In this work, we report a Bowman–Birk inhibitor (BBI) isolated, purified, cloned, and characterized from <i>Maclura pomifera</i> seeds (MpBBI), the first of this type from a species belonging to Moraceae family. MpBBI was purified to homogeneity by RP-HPLC, total RNA was extracted from seeds of <i>M. pomifera</i>, and the 3′RACE-PCR method was applied to obtain the cDNA, which was cloned and sequenced. Peptide mass fingerprinting (PMF) analysis showed correspondence between the in silico-translated protein and MpBBI, confirming that it corresponds to a new plant protease inhibitor. The obtained cDNA encoded a polypeptide of 65 residues and possesses 10 cysteine residues, with molecular mass of 7379.27, pI 6.10, and extinction molar coefficient of 9105 M⁻¹ cm⁻¹. MpBBI inhibits strongly trypsin with Kᵢ in the 10⁻¹⁰ M range and was stable in a wide array of pH and extreme temperatures. MpBBI comparative modeling was applied to gain insight into its 3D structure and highlighted some distinguishing features: (1) two non-identical loops, (2) loop 1 (CEEESRC) is completely different from any known BBI, and (3) the amount of disulphide bonds is also different from any reported BBI from dicot plants. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-02 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Articulo http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://sedici.unlp.edu.ar/handle/10915/144454 |
url |
http://sedici.unlp.edu.ar/handle/10915/144454 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/issn/1432-2048 info:eu-repo/semantics/altIdentifier/issn/0032-0935 info:eu-repo/semantics/altIdentifier/doi/10.1007/s00425-016-2611-6 info:eu-repo/semantics/altIdentifier/pmid/27778107 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International (CC BY 4.0) |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International (CC BY 4.0) |
dc.format.none.fl_str_mv |
application/pdf 343-353 |
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reponame:SEDICI (UNLP) instname:Universidad Nacional de La Plata instacron:UNLP |
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Universidad Nacional de La Plata |
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SEDICI (UNLP) - Universidad Nacional de La Plata |
repository.mail.fl_str_mv |
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