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Agdc1p – a Gallic Acid Decarboxylase Involved in the Degradation of Tannic Acid in the Yeast Blastobotrys (Arxula) adeninivorans

Tannins and hydroxylated aromatic acids, such as gallic acid (3,4,5-trihydroxybenzoic acid), are plant secondary metabolites which protect plants against herbivores and plant-associated microorganisms. Some microbes, such as the yeast Arxula adeninivorans are resistant to these antimicrobial substan...

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Autores principales: Meier, Anna K., Worch, Sebastian, Böer, Erik, Hartmann, Anja, Mascher, Martin, Marzec, Marek, Scholz, Uwe, Riechen, Jan, Baronian, Kim, Schauer, Frieder, Bode, Rüdiger, Kunze, Gotthard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5605622/
https://www.ncbi.nlm.nih.gov/pubmed/28966611
http://dx.doi.org/10.3389/fmicb.2017.01777
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author Meier, Anna K.
Worch, Sebastian
Böer, Erik
Hartmann, Anja
Mascher, Martin
Marzec, Marek
Scholz, Uwe
Riechen, Jan
Baronian, Kim
Schauer, Frieder
Bode, Rüdiger
Kunze, Gotthard
author_facet Meier, Anna K.
Worch, Sebastian
Böer, Erik
Hartmann, Anja
Mascher, Martin
Marzec, Marek
Scholz, Uwe
Riechen, Jan
Baronian, Kim
Schauer, Frieder
Bode, Rüdiger
Kunze, Gotthard
author_sort Meier, Anna K.
collection PubMed
description Tannins and hydroxylated aromatic acids, such as gallic acid (3,4,5-trihydroxybenzoic acid), are plant secondary metabolites which protect plants against herbivores and plant-associated microorganisms. Some microbes, such as the yeast Arxula adeninivorans are resistant to these antimicrobial substances and are able to use tannins and gallic acid as carbon sources. In this study, the Arxula gallic acid decarboxylase (Agdc1p) which degrades gallic acid to pyrogallol was characterized and its function in tannin catabolism analyzed. The enzyme has a higher affinity for gallic acid (K(m) −0.7 ± 0.2 mM, k(cat) −42.0 ± 8.2 s(−1)) than to protocatechuic acid (3,4-dihydroxybenzoic acid) (K(m) −3.2 ± 0.2 mM, k(cat) −44.0 ± 3.2 s(−1)). Other hydroxylated aromatic acids, such as 3-hydroxybenzoic acid, 4-hydroxybenzoic acid, 2,3-dihydroxybenzoic acid, 2,4-dihydroxybenzoic acid and 2,5-dihydroxybenzoic acid are not gallic acid decarboxylase substrates. A. adeninivorans G1212/YRC102-AYNI1-AGDC1, which expresses the AGDC1 gene under the control of the strong nitrate inducible AYNI1 promoter achieved a maximum gallic acid decarboxylase activity of 1064.4 U/l and 97.5 U/g of dry cell weight in yeast grown in minimal medium with nitrate as nitrogen source and glucose as carbon source. In the same medium, gallic acid decarboxylase activity was not detected for the control strain G1212/YRC102 with AGDC1 expression under the control of the endogenous promoter. Gene expression analysis showed that AGDC1 is induced by gallic acid and protocatechuic acid. In contrast to G1212/YRC102-AYNI1-AGDC1 and G1212/YRC102, A. adeninivorans G1234 [Δagdc1] is not able to grow on medium with gallic acid as carbon source but can grow in presence of protocatechuic acid. This confirms that Agdc1p plays an essential role in the tannic acid catabolism and could be useful in the production of catechol and cis,cis-muconic acid. However, the protocatechuic acid catabolism via Agdc1p to catechol seems to be not the only degradation pathway.
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spelling pubmed-56056222017-09-29 Agdc1p – a Gallic Acid Decarboxylase Involved in the Degradation of Tannic Acid in the Yeast Blastobotrys (Arxula) adeninivorans Meier, Anna K. Worch, Sebastian Böer, Erik Hartmann, Anja Mascher, Martin Marzec, Marek Scholz, Uwe Riechen, Jan Baronian, Kim Schauer, Frieder Bode, Rüdiger Kunze, Gotthard Front Microbiol Microbiology Tannins and hydroxylated aromatic acids, such as gallic acid (3,4,5-trihydroxybenzoic acid), are plant secondary metabolites which protect plants against herbivores and plant-associated microorganisms. Some microbes, such as the yeast Arxula adeninivorans are resistant to these antimicrobial substances and are able to use tannins and gallic acid as carbon sources. In this study, the Arxula gallic acid decarboxylase (Agdc1p) which degrades gallic acid to pyrogallol was characterized and its function in tannin catabolism analyzed. The enzyme has a higher affinity for gallic acid (K(m) −0.7 ± 0.2 mM, k(cat) −42.0 ± 8.2 s(−1)) than to protocatechuic acid (3,4-dihydroxybenzoic acid) (K(m) −3.2 ± 0.2 mM, k(cat) −44.0 ± 3.2 s(−1)). Other hydroxylated aromatic acids, such as 3-hydroxybenzoic acid, 4-hydroxybenzoic acid, 2,3-dihydroxybenzoic acid, 2,4-dihydroxybenzoic acid and 2,5-dihydroxybenzoic acid are not gallic acid decarboxylase substrates. A. adeninivorans G1212/YRC102-AYNI1-AGDC1, which expresses the AGDC1 gene under the control of the strong nitrate inducible AYNI1 promoter achieved a maximum gallic acid decarboxylase activity of 1064.4 U/l and 97.5 U/g of dry cell weight in yeast grown in minimal medium with nitrate as nitrogen source and glucose as carbon source. In the same medium, gallic acid decarboxylase activity was not detected for the control strain G1212/YRC102 with AGDC1 expression under the control of the endogenous promoter. Gene expression analysis showed that AGDC1 is induced by gallic acid and protocatechuic acid. In contrast to G1212/YRC102-AYNI1-AGDC1 and G1212/YRC102, A. adeninivorans G1234 [Δagdc1] is not able to grow on medium with gallic acid as carbon source but can grow in presence of protocatechuic acid. This confirms that Agdc1p plays an essential role in the tannic acid catabolism and could be useful in the production of catechol and cis,cis-muconic acid. However, the protocatechuic acid catabolism via Agdc1p to catechol seems to be not the only degradation pathway. Frontiers Media S.A. 2017-09-15 /pmc/articles/PMC5605622/ /pubmed/28966611 http://dx.doi.org/10.3389/fmicb.2017.01777 Text en Copyright © 2017 Meier, Worch, Böer, Hartmann, Mascher, Marzec, Scholz, Riechen, Baronian, Schauer, Bode and Kunze. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Meier, Anna K.
Worch, Sebastian
Böer, Erik
Hartmann, Anja
Mascher, Martin
Marzec, Marek
Scholz, Uwe
Riechen, Jan
Baronian, Kim
Schauer, Frieder
Bode, Rüdiger
Kunze, Gotthard
Agdc1p – a Gallic Acid Decarboxylase Involved in the Degradation of Tannic Acid in the Yeast Blastobotrys (Arxula) adeninivorans
title Agdc1p – a Gallic Acid Decarboxylase Involved in the Degradation of Tannic Acid in the Yeast Blastobotrys (Arxula) adeninivorans
title_full Agdc1p – a Gallic Acid Decarboxylase Involved in the Degradation of Tannic Acid in the Yeast Blastobotrys (Arxula) adeninivorans
title_fullStr Agdc1p – a Gallic Acid Decarboxylase Involved in the Degradation of Tannic Acid in the Yeast Blastobotrys (Arxula) adeninivorans
title_full_unstemmed Agdc1p – a Gallic Acid Decarboxylase Involved in the Degradation of Tannic Acid in the Yeast Blastobotrys (Arxula) adeninivorans
title_short Agdc1p – a Gallic Acid Decarboxylase Involved in the Degradation of Tannic Acid in the Yeast Blastobotrys (Arxula) adeninivorans
title_sort agdc1p – a gallic acid decarboxylase involved in the degradation of tannic acid in the yeast blastobotrys (arxula) adeninivorans
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5605622/
https://www.ncbi.nlm.nih.gov/pubmed/28966611
http://dx.doi.org/10.3389/fmicb.2017.01777
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