Expression of soluble recombinant lipoxygenase from Pleurotus sapidus in Pichia pastoris

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Sebastian Kelle
  • Katerina Zelena
  • Ulrich Krings
  • Diana Linke
  • Ralf G. Berger

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Details

OriginalspracheEnglisch
Seiten (von - bis)233-239
Seitenumfang7
FachzeitschriftProtein Expression and Purification
Jahrgang95
PublikationsstatusVeröffentlicht - 15 Jan. 2014

Abstract

The first heterologous expression of an iron-containing lipoxygenase from a basidiomycete in Pichia pastoris is reported. Five different expression constructs of the lipoxygenase gene LOX1 from Pleurotus sapidus were cloned and successfully transferred into P. pastoris SMD1168, but only one pPIC9K vector construct was functionally expressed. In this construct the vector-provided α-factor signal sequence was replaced by insertion of a second Kozak sequence between the signal sequence and the LOX1 gene. His+ transformants were screened for their level of resistance to geneticin (G418). Lox1 was expressed under different culture conditions and purified using the N-terminal His-tag. Relative enzyme activity increased significantly 48 h after methanol induction and was highest with 2 ml l-1 inducer. The recombinant enzyme showed an optimal lipoxygenase activity at pH 7 and 30-35 C and a vmax like the wild-type enzyme.

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Expression of soluble recombinant lipoxygenase from Pleurotus sapidus in Pichia pastoris. / Kelle, Sebastian; Zelena, Katerina; Krings, Ulrich et al.
in: Protein Expression and Purification, Jahrgang 95, 15.01.2014, S. 233-239.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Kelle S, Zelena K, Krings U, Linke D, Berger RG. Expression of soluble recombinant lipoxygenase from Pleurotus sapidus in Pichia pastoris. Protein Expression and Purification. 2014 Jan 15;95:233-239. doi: 10.1016/j.pep.2014.01.004
Kelle, Sebastian ; Zelena, Katerina ; Krings, Ulrich et al. / Expression of soluble recombinant lipoxygenase from Pleurotus sapidus in Pichia pastoris. in: Protein Expression and Purification. 2014 ; Jahrgang 95. S. 233-239.
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abstract = "The first heterologous expression of an iron-containing lipoxygenase from a basidiomycete in Pichia pastoris is reported. Five different expression constructs of the lipoxygenase gene LOX1 from Pleurotus sapidus were cloned and successfully transferred into P. pastoris SMD1168, but only one pPIC9K vector construct was functionally expressed. In this construct the vector-provided α-factor signal sequence was replaced by insertion of a second Kozak sequence between the signal sequence and the LOX1 gene. His+ transformants were screened for their level of resistance to geneticin (G418). Lox1 was expressed under different culture conditions and purified using the N-terminal His-tag. Relative enzyme activity increased significantly 48 h after methanol induction and was highest with 2 ml l-1 inducer. The recombinant enzyme showed an optimal lipoxygenase activity at pH 7 and 30-35 C and a vmax like the wild-type enzyme.",
keywords = "Functional expression, Kozak sequence, Lipoxygenase, Pichia pastoris, Pleurotus sapidus",
author = "Sebastian Kelle and Katerina Zelena and Ulrich Krings and Diana Linke and Berger, {Ralf G.}",
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AU - Kelle, Sebastian

AU - Zelena, Katerina

AU - Krings, Ulrich

AU - Linke, Diana

AU - Berger, Ralf G.

N1 - Funding information: Support of the work by the BMBF cluster Biokatalyse2021 ( FKZ0315172B ) is gratefully acknowledged.

PY - 2014/1/15

Y1 - 2014/1/15

N2 - The first heterologous expression of an iron-containing lipoxygenase from a basidiomycete in Pichia pastoris is reported. Five different expression constructs of the lipoxygenase gene LOX1 from Pleurotus sapidus were cloned and successfully transferred into P. pastoris SMD1168, but only one pPIC9K vector construct was functionally expressed. In this construct the vector-provided α-factor signal sequence was replaced by insertion of a second Kozak sequence between the signal sequence and the LOX1 gene. His+ transformants were screened for their level of resistance to geneticin (G418). Lox1 was expressed under different culture conditions and purified using the N-terminal His-tag. Relative enzyme activity increased significantly 48 h after methanol induction and was highest with 2 ml l-1 inducer. The recombinant enzyme showed an optimal lipoxygenase activity at pH 7 and 30-35 C and a vmax like the wild-type enzyme.

AB - The first heterologous expression of an iron-containing lipoxygenase from a basidiomycete in Pichia pastoris is reported. Five different expression constructs of the lipoxygenase gene LOX1 from Pleurotus sapidus were cloned and successfully transferred into P. pastoris SMD1168, but only one pPIC9K vector construct was functionally expressed. In this construct the vector-provided α-factor signal sequence was replaced by insertion of a second Kozak sequence between the signal sequence and the LOX1 gene. His+ transformants were screened for their level of resistance to geneticin (G418). Lox1 was expressed under different culture conditions and purified using the N-terminal His-tag. Relative enzyme activity increased significantly 48 h after methanol induction and was highest with 2 ml l-1 inducer. The recombinant enzyme showed an optimal lipoxygenase activity at pH 7 and 30-35 C and a vmax like the wild-type enzyme.

KW - Functional expression

KW - Kozak sequence

KW - Lipoxygenase

KW - Pichia pastoris

KW - Pleurotus sapidus

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U2 - 10.1016/j.pep.2014.01.004

DO - 10.1016/j.pep.2014.01.004

M3 - Article

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JO - Protein Expression and Purification

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