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1.
Appl Microbiol Biotechnol ; 100(2): 743-55, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26476643

ABSTRACT

Light is an essential factor for pigment formation and fruit body development in Cordyceps militaris, a well-known edible and medicinal fungus. Cmwc-1, a homolog of the blue-light receptor gene white collar-1 (wc-1) in Neurospora crassa, was cloned from the C. militaris genome in our previous study. Here, Cmwc-1 gene inactivation results in thicker aerial hyphae, disordered fruit body development, a significant reduction in conidial formation, and carotenoid and cordycepin production. These characteristics were restored when the ΔCmwc-1 strains were hybridized with wild-type strains of the opposite mating type. A genome-wide expression analysis revealed that there were 1042 light-responsive genes in the wild-type strain and only 458 in the ΔCmwc-1 strain. Among five putative photoreceptors identified, Vivid, cryptochrome-1, and cyclobutane pyrimidine dimer photolyase are strongly induced by light in a Cmwc-1-dependent manner, while phytochrome and cryptochrome-2 were not induced. The transcription factors involved in the fungal light reaction were mainly of the Zn2Cys6 type. CmWC-1 regulates adenylosuccinate synthase, an important enzyme for adenosine de novo synthesis, which could explain the reduction in cordycepin production. Some G protein-coupled receptors that control fungal fruit body formation and the sexual cycle were regulated by CmWC-1, and the cAMP pathway involved in light signal transduction in N. crassa was not critical for the photoreaction in the fungus here. A transcriptional analysis indicated that steroid biosynthesis was more active in the ΔCmwc-1 strain, suggesting that CmWC-1 might switch the vegetative growth state to primordia differentiation by suppressing the expression of related genes.


Subject(s)
Cordyceps/growth & development , Cordyceps/metabolism , Fruiting Bodies, Fungal/growth & development , Genes, Fungal , Photoreceptors, Microbial/genetics , Photoreceptors, Microbial/metabolism , Carotenoids/metabolism , Cordyceps/genetics , Deoxyadenosines/metabolism , Fruiting Bodies, Fungal/genetics , Fruiting Bodies, Fungal/metabolism , Gene Expression Profiling , Genome, Fungal , Light , Neurospora crassa/genetics , Secondary Metabolism , Steroids/biosynthesis , Transcription Factors/metabolism
2.
J Microbiol ; 52(8): 659-66, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24996897

ABSTRACT

Cordyceps militaris, the type species of genus Cordyceps, is one of the most popular mushrooms and a nutraceutical in eastern Asia. It is considered a model organism for the study of Cordyceps species because it can complete its life cycle when cultured in vitro. In the present study, the occurrence and sequence variation of SSU rDNA group I introns, Cmi.S943 and Cmi.S1199, among different isolates of C. militaris were analyzed. Based on the secondary structure predictions, the Cmi.S943 intron has been placed in subgroup IC1, and the Cmi.S1199 intron has been placed in subgroup IE. No significant similarity between Cmi.S943 and Cmi.S1199 suggested different origins. Three genotypes, based on the frequency and distribution of introns, were described to discriminate the 57 surveyed C. militaris strains. It was found that the genotype was related to the stroma characteristics. The stromata of all of the genotype II strains, which possessed only Cmi.S943, could produce perithecium. In contrast, the stromata of all genotype III strains, which had both Cmi.S943 and Cmi.S1199, could not produce perithecium. Cmi.S1199 showed the lowest level of intra-specific variation among the tested strains. Group I introns can be lost during strain cross-mating. Therefore, we presumed that during cross-mating and recombination, intron loss could be driven by positive Darwinian selection due to the energetic cost of transcribing long introns.


Subject(s)
Cordyceps/genetics , DNA, Fungal/genetics , DNA, Ribosomal/genetics , Genetic Variation , Introns , Recombination, Genetic , Base Sequence , Cordyceps/growth & development , Fruiting Bodies, Fungal/ultrastructure , Genes, rRNA , Genotype , Phylogeny , Polymerase Chain Reaction , Reverse Transcription , Sequence Analysis, DNA
3.
Bioresour Technol ; 144: 100-6, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23867530

ABSTRACT

Aerobic biodegradation of crude oil and its pathways were investigated via in vitro culture and GC-MS analysis in water flooding wells of Dagang oil field. The in vitro aerobic culture lasted 90 days when 99.0% of n-alkanes and 43.03-99.9% of PAHs were degraded and the biomarkers and their ratios were changed. The spectra of components in the residual oil showed the similar biodegradation between aerobic process of 90 days and degradation in reservoir which may last for some millions years, and the potential of serious aerobic biodegradation of petroleum in reservoir. 24 Metabolites compounds were separated and identified from aerobic culture, including fatty acid, naphthenic acid, aromatic carboxylic acid, unsaturated acid, alcohols, ketones and aldehydes. The pathways of alkanes and aromatics were proposed, which suggests that oxidation of hydrocarbon to organic acid is an important process in the aerobic biodegradation of petroleum.


Subject(s)
Environmental Restoration and Remediation/methods , Oil and Gas Fields/microbiology , Petroleum/metabolism , Water/chemistry , Aerobiosis , Alkanes/metabolism , Biodegradation, Environmental , Biomarkers/metabolism , China , Gas Chromatography-Mass Spectrometry , Polycyclic Aromatic Hydrocarbons
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