Cross-talk between light and glucose regulation controls toxin production and morphogenesis in Aspergillus nidulans

被引:52
作者
Atoui, A. [1 ]
Kastner, C. [2 ]
Larey, C. M. [1 ]
Thokala, R. [1 ]
Etxebeste, O. [3 ]
Espeso, E. A. [3 ]
Fischer, R. [2 ]
Calvo, A. M. [1 ]
机构
[1] NE Illinois Univ, Dept Biol Sci, De Kalb, IL 60115 USA
[2] Karlsruhe Inst Technol, Dept Microbiol, D-76187 Karlsruhe, Germany
[3] Ctr Invest Biol, Dept Med Mol & Celular, Madrid 28040, Spain
关键词
Aspergillus; Light regulation; Glucose regulation; Mycotoxins; Development; Secondary metabolism; VeA; Cellular damage; CARBON CATABOLITE REPRESSION; G-PROTEIN; SEXUAL DEVELOPMENT; TRANSCRIPTION FACTOR; AFLATOXIN; GENE; VEA; BIOSYNTHESIS; NEUROSPORA; EXPRESSION;
D O I
10.1016/j.fgb.2010.08.007
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
Light is a major environmental stimulus that has a broad effect on organisms triggering a cellular response that results in an optimal adaptation enhancing fitness and survival In fungi light affects growth and causes diverse morphological changes such as those leading to reproduction Light can also affect fungal metabolism including the biosynthesis of natural products In this study we show that in Aspergillus nidulans the effect of light on the production of the sterigmatocystm (ST) toxin depends on the glucose concentration In cultures grown with 1% glucose and exposed to light ST production was lower than when grown in the dark This lower ST production coincided with an elevated rate of cellular damage with partial loss of nuclear integrity and vacuolated cytoplasm However in cultures grown with 2% glucose these effects were reversed and light enhanced ST production Glucose abundance also affected the light-dependent subcellular localization of the VeA (velvet) protein a key regulator necessary for normal light-dependent morphogenesis and secondary metabolism in Aspergilli and other fungal genera The role of other VeA-associated proteins particularly the blue-light-sensing proteins LreA and LreB (WC 1 and WC-2 orthologs) on conidiation could also be modified by the abundance of glucose We also show that LreA and LreB as well as the phytochrome FphA modulate not only the synthesis of sterigmatocystin but also the production of the antibiotic penicillin Published by Elsevier Inc
引用
收藏
页码:962 / 972
页数:11
相关论文
共 67 条
[1]
REGULATION OF AFLATOXIN BIOSYNTHESIS - CHARACTERIZATION OF GLUCOSE AS APPARENT INDUCER OF AFLATOXIN PRODUCTION [J].
ABDOLLAHI, A ;
BUCHANAN, RL .
JOURNAL OF FOOD SCIENCE, 1981, 46 (01) :143-146
[2]
Involvement of protein kinase C in the response of Neurospora crassa to blue light [J].
Arpaia, G ;
Cerri, F ;
Baima, S ;
Macino, G .
MOLECULAR AND GENERAL GENETICS, 1999, 262 (02) :314-322
[3]
GENE CLUSTER IN ASPERGILLUS-NIDULANS WITH AN INTERNALLY LOCATED CIS-ACTING REGULATORY REGION [J].
ARST, HN ;
MACDONALD, DW .
NATURE, 1975, 254 (5495) :26-31
[4]
Aziz NH, 1997, NAHRUNG, V41, P150, DOI 10.1002/food.19970410307
[5]
CARBON CATABOLITE REPRESSION IN ASPERGILLUS-NIDULANS [J].
BAILEY, C ;
ARST, HN .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1975, 51 (02) :573-577
[6]
VelB/VeA/LaeA complex coordinates light signal with fungal development and secondary metabolism [J].
Bayram, Oezguer ;
Krappmann, Sven ;
Ni, Min ;
Bok, Jin Woo ;
Helmstaedt, Kerstin ;
Valerius, Oliver ;
Braus-Stromeyer, Susanna ;
Kwon, Nak-Jung ;
Keller, Nancy P. ;
Yu, Jae-Hyuk ;
Braus, Gerhard H. .
SCIENCE, 2008, 320 (5882) :1504-1506
[7]
BAZAN LA, 2009, FUNGAL GENET BIOL, V46, P506
[8]
Effect of photoperiod and day-night temperatures simulating field conditions on growth and ochratoxin A production of Aspergillus carbonarius strains isolated from grapes [J].
Belli, N. ;
Ramos, A. J. ;
Sanchis, V. ;
Marin, S. .
FOOD MICROBIOLOGY, 2006, 23 (07) :622-627
[9]
The Aspergillus nidulans phytochrome FphA represses sexual development in red light [J].
Blumenstein, A ;
Vienken, K ;
Tasler, R ;
Purschwitz, J ;
Veith, D ;
Frankenberg-Dinkel, N ;
Fischer, R .
CURRENT BIOLOGY, 2005, 15 (20) :1833-1838
[10]
LaeA, a regulator of secondary metabolism in Aspergillus spp. [J].
Bok, JW ;
Keller, NP .
EUKARYOTIC CELL, 2004, 3 (02) :527-535