Marine Fungi. II. Ascomycetes and Deuteromycetes from submerged wood and drift Spartina

1964 ◽  
Vol 11 (6) ◽  
pp. 948
Keyword(s):  
Mycologia ◽  
1956 ◽  
Vol 48 (6) ◽  
pp. 841 ◽  
Author(s):  
T. W. Johnson
Keyword(s):  

1991 ◽  
Vol 69 (4) ◽  
pp. 883-886 ◽  
Author(s):  
W. F. Leong ◽  
T. K. Tan ◽  
K. D. Hyde ◽  
E. B. Gareth Jones

Halosarpheia minuta sp.nov. on submerged wood of Avicennia alba, A. lanata, Bruguiera cylindrica, and Rhizophora apiculata, from Singapore, Malaysia, and Brunei, is described and illustrated. Key words: Ascomycotina, taxonomy, marine fungi, mangrove, tropical.


Science ◽  
1959 ◽  
Vol 129 (3341) ◽  
pp. 93-94 ◽  
Author(s):  
D. L. RAY ◽  
D. E. STUNTZ
Keyword(s):  

1989 ◽  
Vol 67 (9) ◽  
pp. 2686-2691 ◽  
Author(s):  
T. K. Tan ◽  
W. F. Leong ◽  
E. B. G. Jones

Randomly collected mangrove wood and wood blocks of Avicennia alba and Avicennia lanata submerged for 60 weeks in Mandai mangrove, Singapore, were investigated for marine fungi. Very frequent species on the random samples were Halosarpheia retorquens and Lignincola laevis and on the submerged wood blocks were Didymosphaeria enalia, Lignincola laevis, Lulworthia sp. 1, Aigialus parvus, Aniptodera marina, Halocyphina villosa, and Ascomycete No. 25. The fungi growing on the wood blocks showed a pattern of succession, with L. laevis as an early colonizer, D. enalia and Lulworthia sp. 1 intermediate colonizers, and A. parvus a late colonizer. The variations in the results obtained from the two sampling methods are also discussed.


Planta Medica ◽  
2016 ◽  
Vol 81 (S 01) ◽  
pp. S1-S381
Author(s):  
K Israel Notarte ◽  
Y Nakao ◽  
T Yaguchi ◽  
K Suganuma ◽  
T Edison dela Cruz

2020 ◽  
Vol 24 (4) ◽  
pp. 354-401 ◽  
Author(s):  
Keisham S. Singh

Marine natural products (MNPs) containing pyrone rings have been isolated from numerous marine organisms, and also produced by marine fungi and bacteria, particularly, actinomycetes. They constitute a versatile structure unit of bioactive natural products that exhibit various biological activities such as antibiotic, antifungal, cytotoxic, neurotoxic, phytotoxic and anti-tyrosinase. The two structure isomers of pyrone ring are γ- pyrone and α-pyrone. In terms of chemical motif, γ-pyrone is the vinologous form of α- pyrone which possesses a lactone ring. Actinomycete bacteria are responsible for the production of several α-pyrone compounds such as elijopyrones A-D, salinipyrones and violapyrones etc. to name a few. A class of pyrone metabolites, polypropionates which have fascinating carbon skeleton, is primarily produced by marine molluscs. Interestingly, some of the pyrone polytketides which are found in cone snails are actually synthesized by actinomycete bacteria. Several pyrone derivatives have been obtained from marine fungi such as Aspergillums flavus, Altenaria sp., etc. The γ-pyrone derivative namely, kojic acid obtained from Aspergillus fungus has high commercial demand and finds various applications. Kojic acid and its derivative displayed inhibition of tyrosinase activity and, it is also extensively used as a ligand in coordination chemistry. Owing to their commercial and biological significance, the synthesis of pyrone containing compounds has been given attention over the past years. Few reviews on the total synthesis of pyrone containing natural products namely, polypropionate metabolites have been reported. However, these reviews skipped other marine pyrone metabolites and also omitted discussion on isolation and detailed biological activities. This review presents a brief account of the isolation of marine metabolites containing a pyrone ring and their reported bio-activities. Further, the review covers the synthesis of marine pyrone metabolites such as cyercene-A, placidenes, onchitriol-I, onchitriol-II, crispatene, photodeoxytrichidione, (-) membrenone-C, lihualide-B, macrocyclic enol ethers and auripyrones-A & B.


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