Analysis of al-2 mutations in Neurospora.

The orange pigmentation of the fungus Neurospora crassa is due to the accumulation of the xanthophyll neurosporaxanthin and precursor carotenoids. Two key reactions in the synthesis of these pigments, the formation of phytoene from geranylgeranyl pyrophosphate and the introduction of β cycles in des...

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Main Authors: Violeta Díaz-Sánchez, Alejandro F Estrada, Danika Trautmann, M Carmen Limón, Salim Al-Babili, Javier Avalos
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21818281/?tool=EBI
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spelling doaj-e95bbdeaf1104ed7be1ce6284a1d9c822021-03-04T01:44:46ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0167e2194810.1371/journal.pone.0021948Analysis of al-2 mutations in Neurospora.Violeta Díaz-SánchezAlejandro F EstradaDanika TrautmannM Carmen LimónSalim Al-BabiliJavier AvalosThe orange pigmentation of the fungus Neurospora crassa is due to the accumulation of the xanthophyll neurosporaxanthin and precursor carotenoids. Two key reactions in the synthesis of these pigments, the formation of phytoene from geranylgeranyl pyrophosphate and the introduction of β cycles in desaturated carotenoid products, are catalyzed by two domains of a bifunctional protein, encoded by the gene al-2. We have determined the sequence of nine al-2 mutant alleles and analyzed the carotenoid content in the corresponding strains. One of the mutants is reddish and it is mutated in the cyclase domain of the protein, and the remaining eight mutants are albino and harbor different mutations on the phytoene synthase (PS) domain. Some of the mutations are expected to produce truncated polypeptides. A strain lacking most of the PS domain contained trace amounts of a carotenoid-like pigment, tentatively identified as the squalene desaturation product diapolycopene. In support, trace amounts of this compound were also found in a knock-out mutant for gene al-2, but not in that for gene al-1, coding for the carotene desaturase. The cyclase activity of the AL-2 enzyme from two albino mutants was investigated by heterologous expression in an appropriately engineered E. coli strain. One of the AL-2 enzymes, predictably with only 20% of the PS domain, showed full cyclase activity, suggesting functional independence of both domains. However, the second mutant showed no cyclase activity, indicating that some alterations in the phytoene synthase segment affect the cyclase domain. Expression experiments showed a diminished photoinduction of al-2 transcripts in the al-2 mutants compared to the wild type strain, suggesting a synergic effect between reduced expression and impaired enzymatic activities in the generation of their albino phenotypes.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21818281/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Violeta Díaz-Sánchez
Alejandro F Estrada
Danika Trautmann
M Carmen Limón
Salim Al-Babili
Javier Avalos
spellingShingle Violeta Díaz-Sánchez
Alejandro F Estrada
Danika Trautmann
M Carmen Limón
Salim Al-Babili
Javier Avalos
Analysis of al-2 mutations in Neurospora.
PLoS ONE
author_facet Violeta Díaz-Sánchez
Alejandro F Estrada
Danika Trautmann
M Carmen Limón
Salim Al-Babili
Javier Avalos
author_sort Violeta Díaz-Sánchez
title Analysis of al-2 mutations in Neurospora.
title_short Analysis of al-2 mutations in Neurospora.
title_full Analysis of al-2 mutations in Neurospora.
title_fullStr Analysis of al-2 mutations in Neurospora.
title_full_unstemmed Analysis of al-2 mutations in Neurospora.
title_sort analysis of al-2 mutations in neurospora.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description The orange pigmentation of the fungus Neurospora crassa is due to the accumulation of the xanthophyll neurosporaxanthin and precursor carotenoids. Two key reactions in the synthesis of these pigments, the formation of phytoene from geranylgeranyl pyrophosphate and the introduction of β cycles in desaturated carotenoid products, are catalyzed by two domains of a bifunctional protein, encoded by the gene al-2. We have determined the sequence of nine al-2 mutant alleles and analyzed the carotenoid content in the corresponding strains. One of the mutants is reddish and it is mutated in the cyclase domain of the protein, and the remaining eight mutants are albino and harbor different mutations on the phytoene synthase (PS) domain. Some of the mutations are expected to produce truncated polypeptides. A strain lacking most of the PS domain contained trace amounts of a carotenoid-like pigment, tentatively identified as the squalene desaturation product diapolycopene. In support, trace amounts of this compound were also found in a knock-out mutant for gene al-2, but not in that for gene al-1, coding for the carotene desaturase. The cyclase activity of the AL-2 enzyme from two albino mutants was investigated by heterologous expression in an appropriately engineered E. coli strain. One of the AL-2 enzymes, predictably with only 20% of the PS domain, showed full cyclase activity, suggesting functional independence of both domains. However, the second mutant showed no cyclase activity, indicating that some alterations in the phytoene synthase segment affect the cyclase domain. Expression experiments showed a diminished photoinduction of al-2 transcripts in the al-2 mutants compared to the wild type strain, suggesting a synergic effect between reduced expression and impaired enzymatic activities in the generation of their albino phenotypes.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21818281/?tool=EBI
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