Nitric oxide donor sodium nitroprusside-induced transcriptional changes and hypocrellin biosynthesis of Shiraia sp. S9.


Journal

Microbial cell factories
ISSN: 1475-2859
Titre abrégé: Microb Cell Fact
Pays: England
ID NLM: 101139812

Informations de publication

Date de publication:
28 Apr 2021
Historique:
received: 15 12 2020
accepted: 17 04 2021
entrez: 29 4 2021
pubmed: 30 4 2021
medline: 15 10 2021
Statut: epublish

Résumé

Nitric oxide (NO) is a ubiquitous signaling mediator in various physiological processes. However, there are less reports concerning the effects of NO on fungal secondary metabolites. Hypocrellins are effective anticancer photodynamic therapy (PDT) agents from fungal perylenequinone pigments of Shiraia. NO donor sodium nitroprusside (SNP) was used as a chemical elicitor to promote hypocrellin biosynthesis in Shiraia mycelium cultures. SNP application at 0.01-0.20 mM was found to stimulate significantly fungal production of perylenequinones including hypocrellin A (HA) and elsinochrome A (EA). SNP application could not only enhance HA content by 178.96% in mycelia, but also stimulate its efflux to the medium. After 4 days of SNP application at 0.02 mM, the highest total production (110.34 mg/L) of HA was achieved without any growth suppression. SNP released NO in mycelia and acted as a pro-oxidant, thereby up-regulating the gene expression and activity of reactive oxygen species (ROS) generating NADPH oxidase (NOX) and antioxidant enzymes, leading to the increased levels of superoxide anion (O The results of this study provide a valuable strategy for large-scale hypocrellin production and can facilitate further understanding and exploration of NO signaling in the biosynthesis of the important fungal metabolites.

Sections du résumé

BACKGROUND BACKGROUND
Nitric oxide (NO) is a ubiquitous signaling mediator in various physiological processes. However, there are less reports concerning the effects of NO on fungal secondary metabolites. Hypocrellins are effective anticancer photodynamic therapy (PDT) agents from fungal perylenequinone pigments of Shiraia. NO donor sodium nitroprusside (SNP) was used as a chemical elicitor to promote hypocrellin biosynthesis in Shiraia mycelium cultures.
RESULTS RESULTS
SNP application at 0.01-0.20 mM was found to stimulate significantly fungal production of perylenequinones including hypocrellin A (HA) and elsinochrome A (EA). SNP application could not only enhance HA content by 178.96% in mycelia, but also stimulate its efflux to the medium. After 4 days of SNP application at 0.02 mM, the highest total production (110.34 mg/L) of HA was achieved without any growth suppression. SNP released NO in mycelia and acted as a pro-oxidant, thereby up-regulating the gene expression and activity of reactive oxygen species (ROS) generating NADPH oxidase (NOX) and antioxidant enzymes, leading to the increased levels of superoxide anion (O
CONCLUSIONS CONCLUSIONS
The results of this study provide a valuable strategy for large-scale hypocrellin production and can facilitate further understanding and exploration of NO signaling in the biosynthesis of the important fungal metabolites.

Identifiants

pubmed: 33910564
doi: 10.1186/s12934-021-01581-8
pii: 10.1186/s12934-021-01581-8
pmc: PMC8082767
doi:

Substances chimiques

Nitric Oxide Donors 0
Quinones 0
Reactive Oxygen Species 0
Nitroprusside 169D1260KM
Phenol 339NCG44TV
Perylene 5QD5427UN7
hypocrellin A V86371B0XS

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

92

Subventions

Organisme : National Natural Science Foundation of China
ID : 82073955
Organisme : National Natural Science Foundation of China
ID : 81773695
Organisme : Priority Academic Program Development of the Jiangsu Higher Education Institutes
ID : PAPD

Références

Photochem Photobiol. 1995 Jun;61(6):529-39
pubmed: 7568399
Microb Cell Fact. 2019 Jul 5;18(1):121
pubmed: 31277643
Front Microbiol. 2018 Oct 18;9:2508
pubmed: 30405568
Appl Microbiol Biotechnol. 2009 Nov;85(2):285-92
pubmed: 19562334
FEMS Microbiol Lett. 2006 May;258(1):102-7
pubmed: 16630263
Bioresour Technol. 2014 May;159:112-7
pubmed: 24632633
J Agric Food Chem. 2016 Dec 28;64(51):9680-9688
pubmed: 27959549
Environ Pollut. 2002;116(1):37-47
pubmed: 11808554
Nat Methods. 2008 Jul;5(7):621-8
pubmed: 18516045
J Photochem Photobiol B. 2018 May;182:100-107
pubmed: 29656218
Appl Microbiol Biotechnol. 2015 May;99(10):4361-72
pubmed: 25582560
Folia Microbiol (Praha). 2013 Jul;58(4):283-9
pubmed: 23229285
Mol Microbiol. 2020 May;113(5):872-882
pubmed: 31968137
Curr Genet. 2015 Nov;61(4):601-20
pubmed: 25862648
Mol Plant Pathol. 2011 Aug;12(6):606-16
pubmed: 21722298
Ultrason Sonochem. 2017 Sep;38:214-224
pubmed: 28633821
Acta Biol Hung. 2018 Dec;69(4):437-448
pubmed: 30587015
J Integr Plant Biol. 2008 Jan;50(1):49-55
pubmed: 18666951
Genome Announc. 2014 Feb 06;2(1):
pubmed: 24503982
Microbiol Res. 2015 Nov;180:11-22
pubmed: 26505307
Biotechnol Lett. 2015 Jan;37(1):153-9
pubmed: 25214226
Appl Microbiol Biotechnol. 2018 Jan;102(1):153-163
pubmed: 29098415
Photochem Photobiol. 2019 May;95(3):812-822
pubmed: 30338861
Int J Mol Sci. 2020 Jan 30;21(3):
pubmed: 32019072
J Ind Microbiol Biotechnol. 2017 Oct;44(10):1415-1429
pubmed: 28685359
J Biomed Biotechnol. 2004;2004(4):227-237
pubmed: 15467163
Genes (Basel). 2020 Mar 25;11(4):
pubmed: 32218164
AMB Express. 2019 Sep 14;9(1):146
pubmed: 31522304
PLoS One. 2013;8(1):e53616
pubmed: 23326470
Planta Med. 1991 Aug;57(4):376-9
pubmed: 1775581
Fungal Genet Biol. 2007 Dec;44(12):1368-79
pubmed: 17897846
Front Microbiol. 2019 Sep 11;10:2023
pubmed: 31572311
Appl Microbiol Biotechnol. 2012 Sep;95(5):1293-304
pubmed: 22410746
G3 (Bethesda). 2020 Jan 7;10(1):23-35
pubmed: 31712259
J Org Chem. 2010 Jan 1;75(1):57-68
pubmed: 19894741
J Microbiol. 2019 Feb;57(2):154-162
pubmed: 30706344
Front Microbiol. 2020 Apr 09;11:643
pubmed: 32373091
Annu Rev Plant Biol. 2008;59:21-39
pubmed: 18031216
Appl Environ Microbiol. 2011 Aug;77(15):5524-8
pubmed: 21642398
Food Chem. 2012 Dec 1;135(3):1220-5
pubmed: 22953846
FEBS Lett. 2005 Jul 18;579(18):4012-6
pubmed: 16004990
Appl Microbiol Biotechnol. 2012 Jan;93(2):455-66
pubmed: 22089384
Chem Sci. 2018 Nov 22;10(5):1457-1465
pubmed: 30809363
J Biotechnol. 2017 Oct 10;259:228-234
pubmed: 28690135
J Photochem Photobiol B. 2014 Nov;140:292-300
pubmed: 25194528
European J Org Chem. 2012 Jul 1;2012(21):3887-3904
pubmed: 24039544
Appl Environ Microbiol. 1999 Dec;65(12):5451-8
pubmed: 10584003
Fungal Genet Biol. 2005 Apr;42(4):284-92
pubmed: 15749048
Nitric Oxide. 2006 Dec;15(4):351-8
pubmed: 16753316
Eur J Biochem. 1974 Sep 16;47(3):469-74
pubmed: 4215654
Appl Biochem Biotechnol. 2010 Apr;160(8):2275-86
pubmed: 19697160
Int J Mol Sci. 2016 Feb 27;17(3):311
pubmed: 26927096
Methods Enzymol. 1984;105:121-6
pubmed: 6727660

Auteurs

Yan Jun Ma (YJ)

College of Pharmaceutical Sciences, Soochow University, Suzhou, 215123, China.
College of Life Sciences, Northwest Normal University, Lanzhou, 730000, China.

Xin Ping Li (XP)

College of Pharmaceutical Sciences, Soochow University, Suzhou, 215123, China.

Yue Wang (Y)

College of Pharmaceutical Sciences, Soochow University, Suzhou, 215123, China.

Jian Wen Wang (JW)

College of Pharmaceutical Sciences, Soochow University, Suzhou, 215123, China. jwwang@suda.edu.cn.

Articles similaires

Biofilms Candida albicans Quorum Sensing Candida glabrata Menthol
Neoplastic Stem Cells Animals Humans Aldehyde Dehydrogenase Tretinoin

Naturally derived 3-aminoquinuclidine salts as new promising therapeutic agents.

Doris Crnčević, Alma Ramić, Andreja Radman Kastelic et al.
1.00
Humans Microbial Sensitivity Tests Anti-Bacterial Agents Biofilms Quinuclidines

Classifications MeSH