Refine your search
Co-Authors
- K. Rajagopal
- Venkat Gopalan
- Dinkar Sahal
- Kaustuv Sanyal
- R. Uma Shaanker
- N. Thirunavukkarasu
- Ben Jahnes
- Arthur Broadstock
- M. B. Govinda Rajulu
- T. S. Murali
- P. T. Devarajan
- K. P. Girivasan
- M. B. Govindarajulu
- V. Kumaresan
- T. Rajamani
- G. Venkatesan
- S. Tangjang
- M. Sudhakara Reddy
- Tapi Taka
- D. L. Hawksworth
- Karaba N. Nataraja
- J. P. Ravishankar
- V. Muruganandam
- Dairick Minj
Journals
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z All
Suryanarayanan, T. S.
- Fungal Endophytes (Phellophytes) of some Tropical Forest Trees
Abstract Views :329 |
PDF Views:0
Authors
Source
Indian Forester, Vol 126, No 2 (2000), Pagination: 165-170Abstract
The periderm tissue of ten tree species growing in a dry deciduous forest and a montane evergreen forest of the Western Ghats was sampled for the presence of filamentous fungi (phellophytes). These trees, belonging to six families, yielded a total of 963 phellophyte isolates that could be grouped in to 36 species. Of these, four were Ascomycetes, one belonged to Coelomycetes, and eleven were Hyphomycetes. The rest were sterile mycelial forms. Alternaria alternata and a Fusarium sp. (49) could be isolated from more number of tree species. Some phellophytes were unique to certain tree species. The mean density of colonisation was maximum for the bark of Rhododendron arboreum. Twenty three isolates of phellophytes occurred as endophytes in living leaf tissues of the trees.- Establishing a national fungal genetic resource to build a major cog for the bioeconomy
Abstract Views :414 |
PDF Views:177
Authors
Affiliations
1 Vivekananda Institute of Tropical Mycology, Ramakrishna Mission Vidyapith, Chennai 600 004,, IN
2 Department of Chemistry and Biochemistry and Center for RNA Biology, The Ohio State University, Columbus, OH 43210, US
3 Malaria Research Laboratory, International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi 110 067, IN
4 Molecular Mycology Laboratory, Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur, Bengaluru 560 064, IN
1 Vivekananda Institute of Tropical Mycology, Ramakrishna Mission Vidyapith, Chennai 600 004,, IN
2 Department of Chemistry and Biochemistry and Center for RNA Biology, The Ohio State University, Columbus, OH 43210, US
3 Malaria Research Laboratory, International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi 110 067, IN
4 Molecular Mycology Laboratory, Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur, Bengaluru 560 064, IN
Source
Current Science, Vol 109, No 6 (2015), Pagination: 1033-1037Abstract
Global conservation activities of animals and plants to protect endangered species are laudable. Similarly, various national and international bodies have recognized the value of preserving different types of microbes, the ‘hidden-constituents’ that are present in all habitats. However, conservation of microbial biodiversity has generally not been a priority in the world. We present a roadmap for creating a national genetic resource for fungi, whose diversity reflects their remarkable fitness for the rich and varied habitats and environments in India. In addition to offering fine prospects for research-based higher education, this national asset will accelerate technology development and the bioeconomy.References
- Smith, D., McCluskey, K. and Stackebrandt, E., Investment into thefuture of microbial resources: culture collection funding models andBRC business plans for biological resource centres.SpringerPlus, 2014, 3, 81–92.
- Griffith, G. W., Do we need a global strategy for microbial conservation? TrendsEcol. Evol., 2012, 2, 1–2.
- Heilmann-Clausen, J. et al., A fungal perspective on conservation biology. Conserv. Biol., 2015, 29, 61–68.
- Blackwell, M., The fungi: 1, 2, 3 … 5.1 million species?. Am. J.Bot., 2011, 98, 426–438.
- Heilmann-Clausen, J. et al., Communities of wood-inhabiting bryophytesand fungi on dead beech logs in Europe – reflecting substratequality or shaped by climate and forest conditions? J. Biogeogr., 2014, 41, 2269–2282.
- Pringle, A., Barron, E., Sartor, K. and Wares, J., Fungi and the Anthropocene: biodiversity discovery in an epoch of loss. Fungal Ecol., 2011, 4, 121–123.
- Heckman, D. S., Geiser, D. M., Eidell, B. R., Stauffer, R. L., Kardos, N. L. and Hedges, S. B., Molecular evidence for the early colonizationof land by fungi and plants. Science, 2001, 293,1129–1133.
- Angelard, C., Tanner, C. J., Fontanillas, P., Niculita-Hirzel, H., Masclaux, F. and Sanders, I. R., Rapid genotypic change and plasticity inarbuscular mycorrhizal fungi is caused by a host shift and enhancedby segregation. Int. Soc. Microb. Ecol. J., 2014, 8, 284–294.
- Wenzl, P., Wong, L., Kwang-Won, K. and Jefferson, R. A., A functionalscreen identifies lateral transfer of b-glucuronidase (gus) from bacteria to fungi. Mol. Biol. Evol., 2005, 22, 308–316.
- Scazzocchio, C., Fungal biology in the post-genomic era. Fungal Biol. Biotechnol., 2014, 1, 7.
- Suryanarayanan, T. S., Thirumalai, E., Prakash, C. P., Govindarajulu, M. B. and Thirunavukkarasu, N., Fungi from two forests of southernIndia: a comparative study of endophytes, phellophytes andleaf litter fungi. Can. J. Microbiol., 2009, 55, 419–426.
- Kaushik, N. K., Murali, T. S., Sahal, D. and Suryanarayanan, T. S., A search for antiplasmodial metabolites among fungal endophytes ofterrestrial and marine plants of southern India. Acta Parasitol., 2014, 59, 745–757.
- Govinda Rajulu, M. B., Thirunavukkarasu, N., Suryanarayanan, T. S., Ravishankar, J. P., El Gueddari, N. E. and Moerschbacher, B. M., Chitinolytic enzymes from endophytic fungi. Fungal Divers.,2011, 47, 43–53.
- Govinda Rajulu, M. B., Lai, L. B., Murali, T. S., Gopalan, V. and Suryanarayanan, T. S., Several fungi from fire-prone forests of southernIndia can utilize furaldehydes. Mycol. Prog., 2014, 13,1049–1056.
- Nagarajan, A., Thirunavukkarasu, N., Suryanarayanan, T. S. and Gummadi, S. N., Screening and isolation of novel glutaminase freeL-asparaginase from fungal endophytes. Res. J. Microbiol.,2014, 9, 163–176.
- Suryanarayanan, T. S., Thirunavukkarasu, N., Govindarajulu, M. B. and Gopalan, V., Fungal endophytes: an untapped source of biocatalysts. Fungal Divers., 2012, 54, 19–30.
- Nagaraju, D., Govinda Rajulu, M. B., El Gueddari N. E., Suryanarayanan, T. S. and Moerschbacher, B. M., Identification and characterization ofchitinolytic enzymes from endophytic fungi. Sugars inNorwich–Royal Soc. Chemistry, Carbohydrate Meeting, London,2009.
- Preface
Abstract Views :374 |
PDF Views:146
Authors
Source
Current Science, Vol 109, No 1 (2015), Pagination: 37-38Abstract
No Abstract.- Screening Marine-Derived Endophytic Fungi for Xylan-Degrading Enzymes
Abstract Views :429 |
PDF Views:178
Authors
N. Thirunavukkarasu
1,
Ben Jahnes
2,
Arthur Broadstock
3,
M. B. Govinda Rajulu
4,
T. S. Murali
5,
Venkat Gopalan
2,
T. S. Suryanarayanan
4
Affiliations
1 Department of Botany, Ramakrishna Mission Vivekananda College, Chennai 600 004, IN
2 Department of Microbiology, The Ohio State University, Columbus, OH 43210, US
3 Department of Chemistry and Biochemistry, The Ohio State University, Columbus, OH 43210, US
4 Vivekananda Institute of Tropical Mycology, Ramakrishna Mission Vidyapith, Chennai 600 004, IN
5 Department of Biotechnology, School of Life Sciences, Manipal University, Manipal 576 104, IN
1 Department of Botany, Ramakrishna Mission Vivekananda College, Chennai 600 004, IN
2 Department of Microbiology, The Ohio State University, Columbus, OH 43210, US
3 Department of Chemistry and Biochemistry, The Ohio State University, Columbus, OH 43210, US
4 Vivekananda Institute of Tropical Mycology, Ramakrishna Mission Vidyapith, Chennai 600 004, IN
5 Department of Biotechnology, School of Life Sciences, Manipal University, Manipal 576 104, IN
Source
Current Science, Vol 109, No 1 (2015), Pagination: 112-120Abstract
Marine-derived fungi surviving as symptomless endophytes in seaweeds and seagrasses were screened for production of xylan-degrading enzymes. Of the eight endophyte isolates obtained from five different seagrasses and another eight from six different marine algae, half of them exhibited xylanase activity in an agar plate assay. Further examination of these lead candidates using spectrophotometric assays revealed that Trichoderma harzianum, endophytic in the brown alga Sargassum wightii, had the maximum secreted xylanase and xylosidase activity. Moreover, this fungus could grow in NaCl-containing media (up to 1.2 M NaCl), and inclusion of 0.26 M NaCl in the media elicited a two- and three-fold increase in extracellular xylanase and xylosidase activity respectively. These findings highlight the potential of prospecting marine derived fungal endophytes to identify novel cell-wall degrading enzymes of value to the biofuel industry.Keywords
Biomass Deconstruction, Marine-Derived Fungi, Trichoderma harzianum, Xylan-Degrading Enzymes.- Crowdsourcing to Create National Repositories of Microbial Genetic Resources: Fungi as a Model
Abstract Views :378 |
PDF Views:133
Authors
Affiliations
1 Vivekananda Institute of Tropical Mycology, Ramakrishna Mission Vidyapith, Chennai 600 004, IN
2 Department of Chemistry and Biochemistry and Center for RNA Biology, The Ohio State University, Columbus, OH 43210, US
1 Vivekananda Institute of Tropical Mycology, Ramakrishna Mission Vidyapith, Chennai 600 004, IN
2 Department of Chemistry and Biochemistry and Center for RNA Biology, The Ohio State University, Columbus, OH 43210, US
Source
Current Science, Vol 106, No 9 (2014), Pagination: 1196-1200Abstract
To address the challenging task of identifying, obtaining and cataloging the different microbes in a country with wide-ranging environments and habitats, we present a crowdsourcing model. With fungi as the prototype, we discuss approaches for rapid collection and identification of strains from environments and habitats that might lead to novel genes of industrial importance. Also, we expect the use of easy culture preservation methods to promote colleges as mini culture-collection centres and serve as the initial focal point in a national research initiative. Our model envisions the concerted involvement of undergraduate students, faculty, industries, national laboratories and culture- collection repositories to rapidly build a large assemblage of rare fungal strains and enhance the biodiversity resource of a country.Keywords
Biodiversity, Crowdsourcing Model, Fungi, Microbial Culture.- A historic perspective of Bordeaux mixture: the first commercial scale fungicide
Abstract Views :52 |
Authors
Affiliations
1 Vivekananda Institute of Tropical Mycology (VINSTROM), Ramakrishna Mission Vidyapith, Chennai 600 004, IN
1 Vivekananda Institute of Tropical Mycology (VINSTROM), Ramakrishna Mission Vidyapith, Chennai 600 004, IN
Source
Current Science, Vol 127, No 8 (2024), Pagination: 990-991Abstract
No Abstract.Keywords
No Keywords.Full Text
- The Host Range of Multi-Host Endophytic Fungi
Abstract Views :303 |
PDF Views:132
Authors
T. S. Suryanarayanan
1,
P. T. Devarajan
2,
K. P. Girivasan
3,
M. B. Govindarajulu
1,
V. Kumaresan
4,
T. S. Murali
5,
T. Rajamani
6,
N. Thirunavukkarasu
6,
G. Venkatesan
7
Affiliations
1 Vivekananda Institute of Tropical Mycology, RKM Vidyapith, Chennai 600 004, IN
2 Department of Plant Biology and Plant Biotechnology, Presidency College, Chennai 600 005, IN
3 Department of Botany, Government Arts College for Men, Nandanam, Chennai 600 035, IN
4 Department of Botany, Kanchi Mamunivar Centre for Post Graduate Studies, Puducherry 605 008, IN
5 Department of Biotechnology, School of Life Sciences, Manipal Academy of Higher Education, Manipal 576 104, IN
6 PG & Research Department of Botany, RKM Vivekananda College, Chennai 600 004, IN
7 Department of Botany, Mannai Rajagopalaswamy Government Arts College, Thanjavur 614 001, IN
1 Vivekananda Institute of Tropical Mycology, RKM Vidyapith, Chennai 600 004, IN
2 Department of Plant Biology and Plant Biotechnology, Presidency College, Chennai 600 005, IN
3 Department of Botany, Government Arts College for Men, Nandanam, Chennai 600 035, IN
4 Department of Botany, Kanchi Mamunivar Centre for Post Graduate Studies, Puducherry 605 008, IN
5 Department of Biotechnology, School of Life Sciences, Manipal Academy of Higher Education, Manipal 576 104, IN
6 PG & Research Department of Botany, RKM Vivekananda College, Chennai 600 004, IN
7 Department of Botany, Mannai Rajagopalaswamy Government Arts College, Thanjavur 614 001, IN
Source
Current Science, Vol 115, No 10 (2018), Pagination: 1963-1969Abstract
Mature leaves of 224 angiosperm plant species belonging to 60 families and growing in Andaman Islands, and the states of Arunachal Pradesh, Kerala and Tamil Nadu were sampled for the presence of endophytic fungi. Fungal genera such as Alternaria, Arthrinium, Aureobasidium, Chaetomium, Cladosporium, Glomerella/ Colletotrichum, Drechslera, Fusarium, Fusicoccum, Lasiodiplodia, Paecilomyces, Pestalotiopsis, Phoma, Diaporthe/Phomopsis, Guignardia/Phyllosticta, Sporormiella and Xylaria showed an isolation frequency of 5% or more. Species of Colletotrichum, Phyllosticta, Phomopsis and Xylaria occurred as endophytes in the leaves of many plant hosts including those that were taxonomically not closely related. The need to address the broad host range of some genera of fungal endophytes is discussed.Keywords
Diversity, Foliar Endophytes, Fungal Endophytes, Mutualism.References
- Zhang, T. and Yao, Y. F., Endophytic fungal communities associated with vascular plants in the high arctic zone are highly diverse and host plant specific. PLoS ONE, 2015, 10, e0130051.
- Rosa, L. H., Vaz, A. B. M., Caligiorne, R. B., Campolina, S. and Rosa, C. A., Endophytic fungi associated with the Antarctic grass Deschampsia Antarctica Desv. (Poaceae). Polar Biol., 2009, 32, 161–167.
- Suryanarayanan, T. S. and Murali, T. S., Incidence of Leptosphaerulina crassiasca in symptomless leaves of peanut in southern India. J. Basic Microbiol., 2006, 46, 305–309.
- Davis, E. C. and Shaw, A. J., Biogeographic and phylogenetic patterns in diversity of liverwort-associated endophytes. Am. J. Bot., 2008, 95, 914–924.
- Sudhakara Reddy, M., Murali, T. S., Suryanarayanan, T. S., Govinda Rajulu, M. B. and Thirunavukkarasu, N., Pestalotiopsis species occur as generalist endophytes in trees of Western Ghats forests of southern India. Fungal Ecol., 2016, 24, 70–75.
- Suryanarayanan, T. S., Endophyte research: going beyond isolation and metabolite documentation. Fungal Ecol., 2013, 6, 561–568.
- Suryanarayanan, T. S., Murali, T. S., Thirunavukkarasu, N., Govinda Rajulu, M. B., Venkatesan, G. and Sukumar, R., Endophytic fungal communities in woody perennials of three tropical forest types of the Western Ghats, southern India. Biodiver. Conserv., 2011, 20, 913–928.
- Pandey, A. K., Reddy, M. S. and Suryanarayanan, T. S., ITSRFLP and ITS sequence analysis of a foliar endophytic Phyllosticta from different tropical trees. Mycol. Res., 2003, 107, 439–444.
- Jeewon, R., Liew, E. C. Y. and Hyde, K. D., Phylogenetic evaluation of species nomenclature of Pestalotiopsis in relation to host association. Fungal Divers., 2004, 17, 39–55.
- Murali, T. S., Suryanarayanan, T. S. and Geeta, R., Endophytic Phomopsis species: host range and implications for diversity estimates. Can. J. Microbiol., 2006, 52, 673–680.
- Wei, J. G., Xu, T., Guo, L.D., Liu A. R., Zhang, Y. and Pan, X. H., Endophytic Pestalotiopsis species associated with plants of Podocarpaceae, Theaceae and Taxaceae in southern China. Fungal Divers., 2007, 24, 55–74.
- Tejesvi, M. V., Tamhankar, S. A., Kini, K. R., Rao, V. S. and Prakash, H. S., Phylogenetic analysis of endophytic Pestalotiopsis species from ethnopharmaceutically important medicinal trees. Fungal Divers., 2009, 38, 167–183.
- Govindarajulu, M. B., Thirunavukkarasu, N., Babu, A. G., Aggarwal, A., Suryanarayanan, T. S. and Reddy, M. S., Endophytic Xylariaceae from the forests of Western Ghats, Southern India: distribution and biological activities. Mycology, 2013, 4, 29–37.
- Woolhouse, M. E., Taylor, L. H. and Haydon, D. T., Population biology of multihost pathogens. Science, 2001, 292, 1109–1112.
- Cord-Landwehr, S., Melcher, R. L. J., Kolkenbrock, S. and Moerschbacher, B., A chitin deacetylase from the endophytic fungus Pestalotiopsis sp. efficiently inactivates the elicitor activity of chitin oligomers in rice cells. Sci. Rep., 2016, 6, Article number: 38018.
- Webb, C. O., Ackerly, D. D. and Kembel, S. W., Phylocom: software for the analysis of phylogenetic community structure and trait evolution. Bioinformatics, 2008, 24, 2098–2100.
- Sieber, T. N., Endophytic fungi in forest trees: are they mutualists? Fungal Biol. Rev., 2007, 21, 75–89.
- Gilbert, G. S. and Webb, C. O., Phylogenetic signal in plant pathogenhost range. Proc. Natl. Acad. Sci. USA, 2007, 104, 4979–4983.
- Saunders, M. and Kohn, L. M., Evidence for alteration of fungal endophyte community assembly by host defense compounds. New Phytol., 2009, 182, 229–238.
- Larkin, B. G., Hunt, L. S. and Ramsey, P. W., Foliar nutrients shape fungal endophyte communities in Western white pine (Pinus monticola) with implications for white-tailed deer herbivory. Fungal Ecol., 2012, 5, 252–260.
- Van Bael, S., Estrada, C. and Arnold, A. E., Foliar endophyte communities and leaf traits in tropical trees. In The Fungal Community: Its Organisation and Role in the Ecosystem (eds Dighton, J. and White, J. F.), CRC Press, Taylor and Francis, Boca Raton, FL, 2017, pp. 79–94.
- May, R. M., How many species are there on earth? Science, 1988, 241, 1441–1449.
- May, R. M., A fondness for fungi. Nature, 1991, 352, 475–476.
- Suryanarayanan, T. S., Govinda Rajulu, M. B., Thirumalai, E., Reddy, M. S. and Money, N. P., Agni’s fungi: heat-resistant spores from the Western Ghats, southern India. Fungal Biol., 2011, 115, 833–838.
- Govinda Rajulu, M. B., Lai, L. B., Murali, T. S., Gopalan, V. and Suryanarayanan, T. S., Several fungi from fire-prone forests of southern India can utilize furaldehydes. Mycol. Prog., 2014, 13, 1049–1056.
- Shipunov, A., Newcombe, G., Raghavendra, A. and Anderson, C., Hidden diversity of endophytic fungi in an invasive plant. Am. J. Bot., 2008, 95, 1096–1108.
- Navaud, O., Barbacci, A., Taylor, A., Clarkson, J. P. and Raffaele, S., Shifts in diversification rates and host jump frequencies shaped the diversity of host range among Sclerotiniaceae fungal plant pathogens. Mol. Ecol., 2018, 27, 1309–1323.
- Redman, R. S., Dunigan, D. D. and Rodriguez, R. J., Fungal symbiosis from mutualism to parasitism: who controls the outcome, host or invader? New Phytol., 2001, 151, 705–716.
- Krings, M., Taylor, T. N., Hass, H., Kerp, H., Dotzler, N., Hermsen, E. J., Fungal endophytes in a 400-million-yr-old land plant: infection pathways, spatial distribution and host responses. New Phytol., 2007, 174, 648–657.
- Mejía, L. C. et al., Pervasive effects of a dominant foliar endophytic fungus on host genetic and phenotypic expression in a tropical tree. Front. Microbiol., 2014, 5, 479.
- Jacott, C. N., Murray, J. D. and Ridout, C. J., Trade-offs in arbuscular mycorrhizal symbiosis: Disease resistance, growth responses and perspectives for crop breeding. Agronomy, 2017, 75, 4–18.
- Gomes, R. R., Glienke, C., Videira, S. I. R., Lombard, L., Groenewald, J. Z. and Crous, P. W., Diaporthe: a genus of endophytic, saprobic and plant pathogenic fungi. Persoonia: Mol. Phyl. Evol. Fungi, 2013, 31, 1–41.
- O’Connell, R. J. et al., Lifestyle transitions in plant pathogenic Colletotrichum fungi deciphered by genome and transcriptome analyses. Nat. Genet., 2012, 44, 1060–1065.
- Stereostratum corticioides (Berk. & Broome) H. Magn. rust on Phyllostachys bambusoides Siebold & Zucc. from Arunachal Pradesh, India
Abstract Views :435 |
PDF Views:164
Authors
Affiliations
1 Department of Botany, Rajiv Gandhi University, Rono Hills 791 112, IN
2 Department of Biotechnology, Thapar University, Patiala 147 004, IN
3 Vivekananda Institute of Tropical Mycology, Ramakrishna Mission Vidyapith, Chennai 600 004,, IN
1 Department of Botany, Rajiv Gandhi University, Rono Hills 791 112, IN
2 Department of Biotechnology, Thapar University, Patiala 147 004, IN
3 Vivekananda Institute of Tropical Mycology, Ramakrishna Mission Vidyapith, Chennai 600 004,, IN
Source
Current Science, Vol 115, No 11 (2018), Pagination: 2011-2012Abstract
Arunachal Pradesh, the largest of the northeastern states of India, with its many forest types1 and large forest cover (80.43%)2 supports a rich biodiversity of plants and animals. It is considered as one of the 200 biologically valuable ecoregions of the world3. However, the phytopathogenic fungal diversity of this eastern Himalayan state has not been explored to any extent. Here we report the occurrence of the culm rust fungus on a bamboo species from Ziro valley of Arunachal Pradesh.References
- Kaul, R. N. and Haridasan, K., J. Econ. Tax. Bot., 1987, 9, 378–389.
- Bharali, S. and Khan, M. L., Curr. Sci., 2011, 101, 855–860.
- Olson, D. M. and Dinerstein, E., Conserv. Biol., 1998, 12, 502–515.
- Melkanina, N. P., Indian For., 2008, 134, 344–350.
- Cummins, G. B., The Rust of Cereals, Grasses and Bamboos, Springer-Verlag, New York, 1971.
- Chen, X., Line, R. F. and Leung, H., Genetics, 1993, 83, 1489–1497.
- White, T. J., Bruns, T., Lee, S. and Taylor, J., In PCR Protocols: A Guide to Methods and Application (eds Innis, M. A. et al.), Academic Press, San Diego, 1990, pp. 315–322.
- Tamura, K., Stecher, G., Peterson, D., Filipski, A. and Kumar, S., Mol. Biol. Evol., 2013, 30, 2725–2729.
- Thirumalachar, M. J., Mycologia, 1947, 39, 231–248.
- Mundukur, B. B and Kheswalla, K. F., Mycologia, 1943, 35, 201–206.
- Mohanan, C., Diseases of Bamboos in Asia: An Illustrated Manual. International Network for Bamboo and Rattan, International Development Research Centre, New Delhi, 1997, pp. 79–80.
- Kuai, S. Y., J. Forest Sci. Technol., 1996, 4, 64–71.
- Tangjang, S. and Nair, P. K. R., Int. J. Environ. Agric. Res., 2016, 2, 25–34.
- Hyde, K. D., Zhou, D. Q. and Dalisay, T., Fungal Divers., 2002, 9, 1–14.
- The War against MDR Pathogens:Move Fungi to the Frontline
Abstract Views :371 |
PDF Views:128
Authors
Affiliations
1 Vivekananda Institute of Tropical Mycology, RKM Vidyapith, Chennai 600 004, IN
2 Department of Comparative Plant and Fungal Biology, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3DS, GB
1 Vivekananda Institute of Tropical Mycology, RKM Vidyapith, Chennai 600 004, IN
2 Department of Comparative Plant and Fungal Biology, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3DS, GB
Source
Current Science, Vol 115, No 12 (2018), Pagination: 2201-2205Abstract
The evolution and spread of resistance among pathogenic microbes to different antibiotics currently in use is a global health problem. Attempts are being made to tackle this major health burden by involving policy makers, scientists, healthcare professionals, the general public and industry. Several strategies, including improvement of prescribing practices, use of combination therapies and synthetic antibiotics, and development of species-specific antibiotics have been suggested to retard the evolution of drug resistance. However, most of the new antibiotic molecules which are being prepared to be marketed are only modifications of existing ones, thus lacking novelty in their mechanism of action or target sites. It is reasonable to expect that the introduction of totally new antibiotics would delay the evolution of drug resistance. In this context, the filamentous fungi are a promising source of novel antibiotics. Their diverse biochemical pathways, the range of ecological niches they occupy, and that 8% or less of the 2.2–3.8 million estimated fungal species are known, underscore the now urgent need to screen them for novel antibiotics.Keywords
Drug Resistance, Filamentous Fungi, Novel Antibiotics, Pathogenic Microbes.References
- Kumarasamy, K. K. et al., Emergence of a new antibiotic resistance mechanism in India, Pakistan, and the UK: a molecular, biological, and epidemiological study. Lancet Infect. Dis., 2010, 10, 597–602.
- Ventola, C. L., The antibiotic resistance crisis. Part 1: causes and threats. Pharm. Ther., 2015, 40, 277–283.
- The Review on Antimicrobial Resistance. Antimicrobial resistance: tackling a crisis for the health and wealth of nations. 2014, pp. 1–20; https://maerreview.org/sites/default/files/AMR%20Review20Review%20Paper%20%20Tackling%20a%20crisis%20for%20the%20health%20and%20wealth%20of%20nations_1.pdf
- Sharma, A. et al., Estimating the future burden of multidrugresistant and extensively drug-resistant tuberculosis in India, the Philippines, Russia, and South Africa: a mathematical modelling study. Lancet Infect. Dis., 2017, 17, 707–715.
- Martens, E. and Demain, A. L., The antibiotic resistance crisis, with a focus on the United States. J. Antibiot., 2017, 70, 520–526.
- Fair, R. J. and Tor, Y., Antibiotics and bacterial resistance in the 21st century. Perspect. Med. Chem., 2014, 6, 25–64.
- Fischbach, M. A. and Walsh, C. T., Antibiotics for emerging pathogens. Science, 2009, 325, 1089–1093.
- Hawksworth, D. L. and Dentinger, B. T. M., Antibiotics: relax UK import rule on fungi. Nature, 2013, 496, 169.
- Davies, J., What are antibiotics? Archaic functions for modern activities. Mol. Microbiol., 1990, 4, 1227–1232.
- Hibbing, M. E., Fuqua, C., Parsek, M. R. and Peterson, S. B., Bacterial competition: surviving and thriving in the microbial jungle. Nature Rev. Microbiol., 2010, 8, 15–25.
- Wiener, P., Experimental studies on the ecological role of antibiotic production in bacteria. Evol. Ecol., 1996, 10, 405–421.
- Aminov, R. I. and Mackie, R. I., Evolution and ecology of antibiotic resistance genes. FEMS Microbiol. Lett., 2007, 271, 147– 161.
- Wang, R. et al., The global distribution and spread of the mobilized colistin resistance gene mcr-1. Nature Commun., 2018, 9, 1179; doi:10.1038/s41467-018-03205-z
- Hiltunen, T., Virta, M. and Laine, A.-L., Antibiotic resistance in the wild: an eco-evolutionary perspective. Philos. Trans. R. Soc. London, Ser. B, 2017, 372, 20160039; http://dx.doi.org/10.1098/rstb.2016.0039
- Munita, J. M. and Arias, C. A., Mechanisms of antibiotic resistance. Microbiol. Spectr., 2016, 4; doi:10.1128/microboilspec.VMBF-0016-2015.
- Belousoff, M. J. et al., Structural basis for linezolid binding site rearrangement in the Staphylococcus aureus ribosome. mBio, 2017, 8, e00395-17; https://doi.org/10.1128/mBio.00395-17.
- Ventola, C. L., The antibiotic resistance crisis: Part 2: management strategies and new agents. Pharm. Ther., 2015, 40, 344–352.
- Chiang, C-Y., Uzoma, I., Moore, R. T., Gilbert, M., Duplantier, A. J. and Panchal, R. G., Mitigating the impact of antibacterial drug resistance through host-directed therapies: current progress, outlook, and challenges. mBio, 2018, 9, e01932-17; https://doi.org/ 10.1128/mBio.01932-17.
- Seiple, I. B. et al., A platform for the discovery of new macrolide antibiotics. Nature, 2016, 533, 338–345.
- Onaka, H., Novel antibiotic screening methods to awaken silent or cryptic secondary metabolic pathways in actinomycetes. J. Antibiot., 2017, 70, 865–870.
- Wilson, D. N. et al., Species-specific antibiotic–ribosome interactions: implications for drug development. Biol. Chem., 2005, 386, 1239–1252.
- Lewis, K., Platforms for antibiotic discovery. Nature Rev. Drug Discov., 2013, 12, 371–387.
- Rossolini, G. M. and Thaller, M. C., Coping with antibiotic resistance: contributions from genomics. Genome Med., 2010, 2, 15.
- Hover, B. M. et al., Culture-independent discovery of the malacidins as calcium-dependent antibiotics with activity against multidrugresistant Gram-positive pathogens. Nature Microbiol., 2018, 3, 415–422.
- Simpkin, V. L., Renwick, M. J., Kelly, R. and Mossialos, E., Incentivising innovation in antibiotic drug discovery and development: progress, challenges and next steps. J. Antibiot., 2017, 70, 1087–1096.
- Moskvitch, K., How to solve the problem of antibiotic resistance. Sci. Am., 2015, 28; https://www.scientificamerican.com/article/how-to-solve-the-problem-of-antibiotic-resistance/
- Stern, S., Chorzelski, S., Franken, L., Völler, S., Rentmeister, H. and Grosch, B., Breaking through the wall: A call for concerted action on antibiotics research and development, The Boston Consulting, Group, Berlin, 2017, pp. 1–80.
- Renwick, M. J., Simpkin, V. and Mossialos, E., Targeting innovation in antibiotic drug discovery and development: the need for a one health, one Europe, one world framework. European Observatory on Health Systems and Policies, Copenhagen, Denmark, Health Policy Series No. 45, 2016, pp. 1–133.
- Ling, L. L. et al., A new antibiotic kills pathogens without detectable resistance. Nature, 2015, 517, 455–459.
- Wright, G. D., Solving the antibiotic crisis. ACS Infect. Dis., 2015, 1, 80–84.
- Ho, W. H., To, P. C. and Hyde, K. D., Induction of antibiotic production of freshwater fungi using mix-culture fermentation. Fungal Divers., 2003, 12, 45–51.
- Hyde, K. D., Increasing the likelihood of novel compound discovery from filamentous fungi. In Bio-exploitation of Filamentous Fungi (eds Pointing, S. B. and Hyde, K. D.), Fungal Diversity Research Series 6, Fungal Diversity Press, Hong Kong, 2001, pp. 77–91.
- Macheleidt, J. et al., Regulation and role of fungal secondary metabolites. Annu. Rev. Genet., 2016, 50, 371–392.
- Kück, U., Bloemendal, S. and Teichert, I., Putting fungi to work: harvesting a cornucopia of drugs, toxins, and antibiotics. PLoS Pathog., 2014, 10, e1003950; https://doi.org/10.1371/journal.ppat.1003950.
- Hawksworth, D. L. and Lücking, R., Fungal diversity revisited: 2.2 to 3.8 million species. In The Fungal Kingdom (eds Heitman, J. et al.), ASM Press, Washington, USA, 2018, pp. 79–95.
- Bugni, T. S. and Ireland, C. M., Marine-derived fungi: a chemically and biologically diverse group of microorganisms. Nat. Prod. Rep., 2004, 21, 143–163.
- Sugie, Y. et al., CJ-15,801, a novel antibiotic from a fungus, Seimatosporium sp. J. Antibiot., 2001, 54, 1060–1065.
- Kaushik, N. K., Murali, T. S., Sahal, D. and Suryanarayanan, T. S., A search for antiplasmodial metabolites among fungal endophytes of terrestrial and marine plants of southern India. Acta Parasitol., 2014, 59, 745–757.
- Chang, W., Zhang, M., Li, Y., Li, X., Gao, Y., Xie, Z. and Lou, H., Lichen endophyte derived pyridoxatin inactivates Candida growth by interfering with ergosterol biosynthesis. Biochim. Biophys. Acta, 2015, 1850, 1762–1771.
- Yedukondalu, N. et al., Diapolic acid A–B from an endophytic fungus, Diaporthe terebinthifolii depicting antimicrobial and cytotoxic activity. J. Antibiot., 2017, 70, 212–215.
- Adelin, E., Le Goff, G., Retailleau, P., Bonfill, M. and Ouazzani, J., Isolation of the antibiotic methyl (R,E)-3-(1-hydroxy-4oxocyclopent-2-en-1-yl)-acrylate EA-2801 from Trichoderma atroviridae. J. Antibiot., 2017, 70, 1053–1056.
- Takahashi, K. et al., Cladomarine, a new anti-saprolegniasis compound isolated from the deep-sea fungus, Penicillium coralligerum YK-247. J. Antibiot., 2017, 70, 911–914.
- Wang, Y.-T., Xue, Y.-R. and Liu, C.-H., A brief review of bioactive metabolites derived from deep-sea fungi. Mar. Drugs, 2015, 13, 4594–4616.
- Wang, J. et al., Screening of anti-biofilm compounds from marinederived fungi and the effects of secalonic acid D on Staphylococcus aureus biofilm. J. Microbiol. Biotechnol., 2017, 27, 1078–1089.
- Gao, X.-W., Liu, H.-X., Sun, Z.-H., Che, Y.-C., Tan, Y.-Z. and Zhang, W.-M., Secondary metabolites from the deep-sea derived fungus Acaromyces ingoldii FS121. Molecules, 2016, 21, 371.
- He, K.-Y. et al., New chlorinated xanthone and anthraquinone produced by a mangrove-derived fungus Penicillium citrinum HL5126. J. Antibiot., 2017, 70, 823–827.
- Suryanarayanan, T. S., Venkatachalam, A., Thirunavukkarasu, N., Ravishankar, J. P., Doble, M. and Geetha, V., Internal mycobiota of marine macroalgae from the Tamilnadu coast: distribution, diversity and biotechnological potential. Bot. Mar., 2010, 53, 456– 468.
- Suryanarayanan, T. S., The diversity and importance of fungi associated with marine sponges. Bot. Mar., 2012, 55, 553–564.
- Thirunavukkarasu, N., Suryanarayanan, T. S., Girivasan, K. P., Venkatachalam, A., Geetha, V., Ravishankar, J. P. and Doble, M., Fungal symbionts of marine sponges from Rameswaram, southern India: species composition and bioactive metabolites. Fungal Divers., 2012, 55, 37–46.
- Ookura, R., Kito, K., Ooi, T., Namikoshi, M. and Kusumi, T., Structure revision of circumdatins A and B, benzodiazepine alkaloids produced by marine fungus Aspergillus ostianus by X-ray crystallography. J. Org. Chem., 2008, 73, 4245–4247.
- Wiese, J. et al., Phylogenetic identification of fungi isolated from the marine sponge Tethya aurantium and identification of their secondary metabolites. Mar. Drugs, 2011, 9, 561–585.
- Karwehl, S. and Stadler, M., Exploitation of fungal biodiversity for discovery of novel antibiotics. In How to Overcome the Antibiotic Crisis (eds Stadler, M. and Dersch, P.), Curr. Top. Microbiol. Immunol., 2016, 398, 303–338.
- Suryanarayanan, T. S. and Hawksworth, D. L., Fungi from littleexplored and extreme habitats. In Bio-Diversity of Fungi: Their Role in Human Life (eds Deshmukh, S. K. and Rai, M. K.), Oxford & IBH Publishing, 2005, pp. 33–48.
- Liu, T. et al., Two new amides from a halotolerant fungus, Myrothecium sp. GS-17. J. Antibiot., 2015, 68, 267–270.
- Lu, X.-L. et al., Pimarane diterpenes from the arctic fungus Eutypella sp. D-1. J. Antibiot., 2014, 67, 171–174.
- Chávez, R., Fierro, F., García-Rico, R. O. and Vaca, I., Filamentous fungi from extreme environments as a promising source of novel bioactive secondary metabolites. Front. Microbiol., 2015, 6, 903.
- Blackwell, M., Made for each other: ascomycete yeasts and insects. In The Fungal Kingdom (eds Heitman, J. et al.), ASM Press, Washington, USA, 2018, pp. 945–962.
- Bao, J. et al., Antifouling and antibacterial polyketides from marine gorgonian coral-associated fungus Penicillium sp. SCSGAF 0023. J. Antibiot., 2013, 66, 219–223.
- He, H., Bigelis, R., Yang, H. Y., Chang, L.-P. and Singh, M. P., Lichenicolins A and B, new bisnaphthopyrones from an unidentified lichenicolous fungus, strain LL-RB0668. J. Antibiot., 2005, 58, 731–736.
- Suryanarayanan, T. S., Govindarajulu, M. B., Rajamani, T., Tripathi, M. and Joshi, Y., Endolichenic fungi in lichens of Champawat district, Uttarakhand, northern India. Mycol. Prog., 2017, 16, 205–211.
- Chepkirui, C. and Stadler, M., The genus Diaporthe: a rich source of diverse and bioactive metabolites. Mycol. Prog., 2017, 16, 477– 494.
- Andersen, M. R. et al., Accurate prediction of secondary metabolite gene clusters in filamentous fungi. Proc. Natl. Acad. Sci. USA, 2013, 110, E99–E107.
- Hemphill, C. F. P., Sureechatchaiyan, P., Kassack, M. U., Orfali, R. S., Lin, W., Daletos, G. and Proksch, P., OSMAC approach leads to new fusarielin metabolites from Fusarium tricinctum. J. Antibiot., 2017, 70, 726–732.
- Brakhage, A. A. and Schroeckh, V., Fungal secondary metabolites – Strategies to activate silent gene clusters. Fungal Genet. Biol., 2011, 48, 15–22.
- Connolly, L. R., Smith, K. M. and Freitag, M., The Fusarium graminearum histone H3 K27 methyltransferase KMT6 regulates development and expression of secondary metabolite gene clusters. PLoS Genet., 2013, 9, e1003916.
- Smith, K. M., Gautschi, J. T. and Freitag, M., Decoding the cryptic genomes of fungi: the promise of novel antibiotics. Future Microbiol., 2014, 9, 265–268.
- Thaker, M. N. and Wright, G. D., Opportunities for synthetic biology in antibiotics: expanding glycopeptide chemical diversity. ACS Synth. Biol., 2015, 20, 195–206.
- Bills, G. F. et al., Enhancement of antibiotic and secondary metabolite detection from filamentous fungi by growth on nutritional arrays. J. Appl. Microbiol., 2008, 104, 1644–1658.
- Scherlach, K. and Hertweck, C., Discovery of aspoquinolones A–D, prenylated quinoline-2-one alkaloids from Aspergillus nidulans, motivated by genome mining. Org. Biomol. Chem., 2006, 4, 3517–3520.
- Stierle, A. A. et al., The berkeleylactones, antibiotic macrolides from fungal coculture. J. Nat. Prod., 2017, 80, 1150–1160.
- Nielsen, J. C. et al., Global analysis of biosynthetic gene clusters reveals vast potential of secondary metabolite production in Penicillium species. Nature Microbiol., 2017, 2, article number: 17044.
- Endophytes in Agriculture
Abstract Views :438 |
PDF Views:134
Authors
Affiliations
1 Vivekananda Institute of Tropical Mycology, Ramakrishna Mission Vidyapith, Chennai 600 004, IN
2 Department of Crop Physiology, University of Agricultural Sciences, GKVK, Bengaluru 560 065, IN
1 Vivekananda Institute of Tropical Mycology, Ramakrishna Mission Vidyapith, Chennai 600 004, IN
2 Department of Crop Physiology, University of Agricultural Sciences, GKVK, Bengaluru 560 065, IN
Source
Current Science, Vol 117, No 9 (2019), Pagination: 1420-1421Abstract
A symposium on endophytes and their applications in agriculture was held recently. The subject of the symposium is of immediate relevance to crop production considering the emerging fact that the performance of plants and their response to abiotic and biotic stresses are controlled not only by the plant genome but also by its microbiome, which includes the endophytes. To the best of our knowledge, a symposium exclusively devoted to the application of endophytes in agriculture has not been organized in the country till now.- Repository of Fungal Endophytes at Vinstrom, Chennai:Waiting to be Harnessed
Abstract Views :478 |
PDF Views:122
Authors
Affiliations
1 Vivekananda Institute of Tropical Mycology, Ramakrishna Mission Vidyapith, Chennai 600 004, IN
1 Vivekananda Institute of Tropical Mycology, Ramakrishna Mission Vidyapith, Chennai 600 004, IN
Source
Current Science, Vol 117, No 9 (2019), Pagination: 1469-1474Abstract
Our thirty years of research at Vivekananda Institute of Tropical Mycology (VINSTROM) on fungal endophytes of terrestrial and aquatic plants have yielded many interesting insights into this ecological group of fungi, a constituent of the plant microbiome. Having pioneered the study of fungal endophytes in India, we have established a culture collection of these fungi in VINSTROM. It now has about 1700 fungal endophyte isolates obtained from plants of different ecosystems in different parts of India. Endophytes produce an extraordinary array of bioactive compounds, novel industrial enzymes and enhance the fitness of the plants they colonize by elevating their tolerance to abiotic and biotic stressors. Considering such desirable traits of fungal endophytes, VINSTROM’s culture collection is a unique repository that needs to be explored for the technological use of endophytes.Keywords
Bioprospecting, Bioactive Compounds, Culture Collection, Industrial Enzymes.References
- Stergiopoulos, I. and Gordon, T. R., Cryptic fungal infections: the hidden agenda of plant pathogens. Front. Plant Sci., 2014, 5, 506.
- Davis, E. C. and Shaw, A. J., Biogeographic and phylogenetic patterns in diversity of liverwort-associated endophytes. Am. J. Bot., 2008, 95, 914–924.
- Hardoim, P. R. et al., The hidden world within plants: ecological and evolutionary considerations for defining functioning of microbial endophytes. Microbiol. Mol. Biol. Rev., 2015, 79, 293– 320.
- Krings, M., Taylor, T. N., Hass, H., Kerp, H., Dotzler, N. and Hermsen, E. J., Fungal endophytes in a 400-million-yr-old land plant: infection pathways, spatial distribution and host responses. New Phytol., 2007, 174, 648–657.
- Gange, A. C., Koricheva, J., Currie, A. F., Jaber, L. R. and Vidal, S., Meta‐analysis of the role of entomopathogenic and unspecialized fungal endophytes as plant bodyguards. New Phytol., 2019; doi:10.1111/nph.15859
- Harrison, J. G., Beltran, L. P., Buerkle, C. A., Cook, D., Gardner, D. R., Parchman, T. L. and Forister, M. L., A suite of rare microbes interacts with a dominant, heritable, fungal endophyte to influence plant trait expression. bioRxiv, 2019, p.608729.
- Khan, A. L., Hamayun, M., Kang, S. M., Kim, Y. H., Jung, H. Y., Lee, J. H. and Lee, I. J., Endophytic fungal association via gibberellins and indole acetic acid can improve plant growth under abiotic stress: an example of Paecilomyces formosus LHL10. BMC Microbiol., 2012, 12, 1–14.
- Toghueo, R. M. K., Kemgne, E. A. M., Eke, P., Kanko, M. I. M., Dize, D., Sahal, D. and Boyom, F. F., Antiplasmodial potential and GC-MS fingerprint of endophytic fungal extracts derived from Cameroonian Annona muricata. J. Ethnopharmacol., 2019, 235, 111–121.
- Hyde, K. D. et al., The amazing potential of fungi, 50 ways we can exploit fungi industrially. Fungal Divers., 2019, 1–136; https://doi.org/10.1007/s13225-019-00430-9.
- Hawksworth, D. L., The fungal dimension of biodiversity: magnitude, significance, and conservation. Mycol. Res., 1991, 95, 641– 655.
- Arnold, A. E., Maynard, Z., Gilbert, G. S., Coley, P. D. and Kursar, T. A., Are tropical fungal endophytes hyperdiverse? Ecol. Lett., 2000, 3, 267–274.
- Hyde, K. D., Ho, W. H., Taylor, J. E. and Hawksworth, D. L., Estimating the extent of fungal diversity in the tropics. In Nature and Human Society: The Quest for a Sustainable World (eds Raven, P. H. and Williams, T.), National Academy Press, Washington, DC, 2000, pp. 156–175.
- Hyde, K. D. (ed.), Where are the missing fungi? Mycol. Res., Cambridge University Press, 2001, pp. 1422–1518.
- Suryanarayanan, T. S. and Hawksworth, D. L., Fungi from littleexplored and extreme habitats. In Bio-diversity of Fungi: Their role in Human Life (eds. Deshmukh S. K. and Rai, M. K.), Oxford & IBH Publishing, New Delhi, 2005, pp. 33–48.
- Manoharachary, C., Sridhar, K., Singh, R., Adholeya, A., Suryanarayanan, T. S., Rawat, S. and Johri, B. N., Fungal biodiversity: distribution, conservation and prospecting of fungi from India. Curr. Sci., 2005, 89, 58–71.
- Suryanarayanan, T. S., Kumaresan, V. and Johnson, J. A., Foliar fungal endophytes from two species of the mangrove Rhizophora. Can. J. Microbiol., 1998, 44, 1003–1006.
- Suryanarayanan, T. S., Murali, T. S. and Venkatesan, G., Occurrence and distribution of fungal endophytes in tropical forests across a rainfall gradient. Can. J. Bot., 2002, 80, 818–826.
- Suryanarayanan, T. S., Murali, T. S., Thirunavukkarasu, N., Govinda Rajulu, M. B., Venkatesan, G. and Sukumar, R., Endophytic fungal communities in woody perennials of three tropical forest types of the Western Ghats, southern India. Biodiver. Conserv., 2011, 20, 913–928.
- Suryanarayanan, T. S., Govinda Rajulu, M. B. and Vidal, S., Biological control through fungal endophytes: Gaps in knowledge hindering success. Curr. Biotechnol., 2018, 7, 185–198.
- Devarajan, P. T. and Suryanarayanan, T. S., Evidence for the role of phytophagous insects in dispersal of non-grass fungal endophytes. Fungal Divers., 2006, 23, 111–119.
- Mohandoss, J. and Suryanarayanan, T. S., Effect of fungicide treatment on foliar fungal endophyte diversity in mango. Sydowia, 2009, 61, 11–24.
- Devarajan, P. T., Suryanarayanan, T. S. and Geetha, V., Endophytic fungi associated with the tropical seagrass Halophila ovalis (Hydrocharitaceae). Indian J. Mar. Sci., 2002, 31, 73–74.
- Venkatachalam, A., Thirunavukkarasu, N. and Suryanarayanan, T. S., Distribution and diversity of endophytes in seagrasses. Fungal Ecol., 2015, 13, 60–65.
- Suryanarayanan, T. S., Venkatachalam, A., Thirunavukkarasu, N., Ravishankar, J. P., Doble, M. and Geetha, V., Internal mycobiota of marine macroalgae from the Tamil Nadu coast: distribution, diversity and biotechnological potential. Bot. Mar., 2010, 53, 456–468.
- Suryanarayanan, T. S., Fungal endosymbionts of seaweeds. In Biology of Marine Fungi (ed. Raghukumar, C.), Progress in Molecular and Subcellular Biology 53, Springer-Verlag, Berlin, Heidelberg, 2012, pp. 53–69.
- Suryanarayanan, T. S., Gopalan, V., Sahal, D. and Sanyal, K., Establishing a national fungal genetic resource to enhance the bioeconomy. Curr. Sci., 2015, 109, 1033–1037.
- Suryanarayanan, T. S., Govindarajulu, M. B., Rajamani, T., Tripathi, M. and Joshi, Y., Endolichenic fungi in lichens of Champawat district, Uttarakhand, northern India. Mycol. Prog., 2017, 16, 205–211.
- Tan, R. X. and Zou, W. X., Endophytes: a rich source of functional metabolites. Nat. Prod. Rep., 2001, 18, 448–459.
- Schulz, B., Boyle, C., Draeger, S., Römmert, A. K. and Krohn, K., Endophytic fungi: a source of novel biologically active secondary metabolites. Mycol. Res., 2002, 106, 996–1004.
- Nisa, H., Kamili, A. N., Nawchoo, I. A., Shafi, S., Shameem, N. and Bandh, S. A., Fungal endophytes as prolific source of phytochemicals and other bioactive natural products: a review. Microb. Pathog., 2015, 82, 50–59.
- Kusari, S., Verma, V. C., Lamshöft, M. and Spiteller, M., An endophytic fungus from Azadirachta indica A. Juss. that produces azadirachtin. World J. Microbiol. Biotechnol., 2012, 28, 1287–1294.
- Vasanthakumari, M. M. et al., Restoration of camptothecine production in attenuated endophytic fungus on re-inoculation into host plant and treatment with DNA methyltransferase inhibitor. World J. Microbiol. Biotechnol., 2015, 31, 1629–1639.
- Suryanarayanan, T. S., Thirunavukkarasu, N., Govindarajulu, M. B., Sasse, F., Jansen, R. and Murali, T. S., Fungal endophytes and bioprospecting. Fungal Biol. Rev., 2009, 23, 9–19.
- Kumaresan, V. and Suryanarayanan, T. S., Endophyte assemblages in young, mature and senescent leaves of Rhizophora apiculata: evidence for the role of endophytes in mangrove litter degradation. Fungal Divers., 2002, 9, 81–91.
- Maria, G. L., Sridhar, K. R. and Raviraja, N. S., Antimicrobial and enzyme activity of mangrove endophytic fungi of southwest coast of India. J. Agric. Technol., 2005, 1, 67–80.
- Paranetharan, M. S., Thirunavukkarasu, N., Rajamani, T., Murali, T. S. and Suryanarayanan, T. S., Salt-tolerant chitin and chitosan modifying enzymes from Talaromyces stipitatus, a mangrove endophyte. Mycosphere, 2018, 9, 215–226.
- Sengupta, A., Zabala, A., Tan, S. Y., Broadstock, A., Suryanarayanan, T. S. and Gopalan, V., Characterization of an ionic liquidtolerant β -xylosidase from a marine-derived fungal endophyte. Biochem. Cell Biol., 2017, 95, 585–591.
- Nagarajan, A., Thirunavukkarasu, N., Suryanarayanan, T. S. and Gummadi S. N., Screening and isolation of novel glutaminase free l-asparaginase from fungal endophytes. Res. J. Microbiol., 2014, 9, 163–176.
- Østergaard, L. H. and Olsen, H. S., Industrial applications of fungal enzymes. In The Mycota (ed. Hofrichter, X. M.), Springer, Berlin, 2010, pp. 269–290.
- Ellis, J. J., Preserving fungus strains in sterile water. Mycologia, 1979, 71, 1072–1075.
- Suryanarayanan, T. S. and Kumaresan, V., A simple method for storing and transporting fungal cultures. Mycologist, 1998, 12, 173.
- Suryanarayanan, T. S. and Uma Shaanker, R. (Guest eds), Fungal Endophytes – Biology and Bioprospecting. Preface, Curr. Sci., 2015, 109, 37–38.
- Suryanarayanan, T. S., Endophyte research: going beyond isolation and metabolite documentation. Fungal Ecol., 2013, 6, 561–568.
- Thirunavukkarasu, N., Suryanarayanan, T. S., Girivasan, K. P., Venkatachalam, A., Geetha, V., Ravishankar, J. P. and Doble, M., Fungal symbionts of marine sponges from Rameswaram, southern India: species composition and bioactive metabolites. Fungal Divers., 2012, 55, 37–46.
- Govinda Rajulu, M. B., Lai, L. B., Murali, T. S., Gopalan, V. and Suryanarayanan, T. S., Several fungi from fire-prone forests of southern India can utilize furaldehydes. Mycol. Prog., 2014, 13, 1049–1056.
- Thirunavukkarasu, N., Suryanarayanan, T. S., Murali, T. S., Ravishankar, J. P. and Gummadi, S. N., L-asparaginase from marine derived fungal endophytes of seaweeds. Mycosphere, 2011, 2, 147–155.
- Kaushik, N. K., Murali, T. S., Sahal, D. and Suryanarayanan, T. S., A search for antiplasmodial metabolites among fungal endophytes of terrestrial and marine plants of southern India. Acta Parasitol., 2014, 59, 745–757.
- Thirunavukkarasu, N., Jahnes, B., Broadstock, A., Govinda Rajulu, M. B., Murali, T. S., Gopalan, V. and Suryanarayanan, T. S., Screening marine-derived endophytic fungi for xylan-degrading enzymes. Curr. Sci., 2015, 109, 112–120.
- Suryanarayanan, T. S., Govinda Rajulu, M. B., Thirumalai, E., Reddy, M. S. and Money, N. P., Agni’s fungi: heat-resistant spores from the Western Ghats, southern India. Fungal Biol., 2011, 115, 833–838.
- Thirunavukkarasu, N., Suryanarayanan, T. S., Rajamani, T. and Paranetharan, M. S., A rapid and simple method for screening fungi for extracellular protease. Mycosphere, 2017, 8, 131–136.
- Geetha, V., Venkatachalam, A., Suryanarayanan, T. S. and Doble, M., Isolation and characterization of new antioxidant and antibacterial compounds from algicolous marine fungus Curvularia tuberculata. International Conference on Bioscience, Biochemistry and Bioinformatics (IPCBEE), IACSIT Press, Singapore, 2011, vol. 5, pp. 302–304.
- Govinda Rajulu, M. B., Thirunavukkarasu, N., Babu, A. G., Aggarwal, A., Suryanarayanan, T. S. and Reddy, M. S., Endophytic Xylariaceae from the forests of Western Ghats, southern India: distribution and biological activities. Mycology, 2013, 4, 29–37.
- Govinda Rajulu, M. B., Thirunavukkarasu, N., Suryanarayanan, T. S., Ravishankar, J. P., El Gueddari, N. E. and Moerschbacher, B. M., Chitinolytic enzymes from endophytic fungi. Fungal Divers., 2011, 47, 43–53.
- Suryanarayanan, T. S., Ravishankar, J. P., Venkatesan, G. and Murali, T. S., Characterization of melanin pigment of a cosmopolitan fungal endophyte. Mycol. Res., 2004, 108, 974–978.
- Scientific Research: A Collaborative Endeavour is Unrivalled
Abstract Views :417 |
PDF Views:145
Authors
Affiliations
1 Vivekananda Institute of Tropical Mycology, Ramakrishna Mission Vidyapith, Mylapore, Chennai 600 004, IN
1 Vivekananda Institute of Tropical Mycology, Ramakrishna Mission Vidyapith, Mylapore, Chennai 600 004, IN
Source
Current Science, Vol 119, No 11 (2020), Pagination: 1739-1741Abstract
During the last few decades, advances in biology have motivated inventions in the form of bioinspired solutions. Such advances have resulted from the use of inter-disciplinary approaches to complex problems. Because of the specialized nature of tackling research problems, these scientific and technological developments have required collaborations with schools of different specialities. We emphasize the importance of such collaborations using as an example of our success with a small research programme in a teaching college, and to stress that the sum is greater than the parts in these joint global endeavours.- The fungal endobiome of seaweeds of the Andaman Islands, India
Abstract Views :325 |
PDF Views:151
Authors
Affiliations
1 Vivekananda Institute of Tropical Mycology, Ramakrishna Mission Vidyapith, Chennai 600 004, India, IN
2 Department of Biotechnology, Manipal School of Life Sciences, Manipal Academy of Higher Education, Manipal 576 104, India, IN
3 Jawaharlal Nehru Rajkeeya Mahavidyalaya College, Port Blair, Andaman and Nicobar Islands 744 101, India, IN
1 Vivekananda Institute of Tropical Mycology, Ramakrishna Mission Vidyapith, Chennai 600 004, India, IN
2 Department of Biotechnology, Manipal School of Life Sciences, Manipal Academy of Higher Education, Manipal 576 104, India, IN
3 Jawaharlal Nehru Rajkeeya Mahavidyalaya College, Port Blair, Andaman and Nicobar Islands 744 101, India, IN
Source
Current Science, Vol 123, No 12 (2022), Pagination: 1508-1514Abstract
Seventeen seaweed species (two green algae, nine brown algae and six red algae) of the Andaman Islands, India, were studied for their culturable fungal endophyte assemblage. A total of 796 endophytic isolates (67 species of fungi belonging to 22 genera and 10 sterile forms) were recovered from the 17 seaweeds. All the fungi were marine-derived forms and many belonged to Eurotiomycetes and Sordariomycetes of the Ascomycota group. More species of Aspergillus, Fusarium, Penicillium and Trichoderma were present as endophytes. While most endophytic species recovered were present in low frequency, some fungi like Aspergillus niger, Aspergillus sp. 1, Nodulisporium sp., Pestalotiopsis sp., Trichoderma yunnanense and Xylaria sp. 1 exhibited more than 40% frequency of colonization. Apart from yielding the maximum number of endophytic isolates, different Trichoderma species showed the highest colonization frequency in 11 of the 17 seaweeds. The results of this study indicate that fungi belonging to Eurotiomycetes which occur in low frequency as endophytes in terrestrial plants represent a significant percentage in the seaweeds and that the environment might have a more critical role than host specificity in determining the endophyte community of seaweed mycobiomeKeywords
Algal endophytes, eurotiomycetes, marine algae, Sordariomycetes, Trichoderma.References
- Dayton, P. K., Ecology of kelp communities. Annu. Rev. Ecol. Syst., 1985, 16, 215–245.
- Schiel, D. R. and Foster, M. S., The population biology of large brown seaweeds: ecological consequences of multiphase life histories in dynamic coast. Annu. Rev. Ecol. Evol. Syst., 2006, 37, 343–372.
- Watt, C. A. and Scrosati, R. A., Experimental and mensurative data on the abundance of primary producers and consumers from intertidal habitats in Canada: Ecological Archives E095‐123. Ecology, 2014, 95, 1429.
- Vallet, M. et al., Chemically-mediated interactions between macro-algae, their fungal endophytes, and protistan pathogens. Front. Micro-biol., 2018, 9, 3161.
- Soleymani, M. and Rosentrater, K. A., Techno-economic analysis of biofuel production from macroalgae (seaweed). Bioengineering, 2017, 4, 92.
- Egan, S., Harder, T., Burke, C., Steinberg, P., Kjelleberg, S. and Tho-mas, T., The seaweed holobiont: understanding seaweed–bacteria interactions. FEMS Microbiol. Rev., 2013, 37, 462–476.
- Singh, R. P. and Reddy, C. R. K., Unravelling the functions of the macroalgal microbiome. Front. Microbiol., 2016, 6, 1488.
- Kohlmeyer, J. and Volkmann-Kohlmeyer, B., Marine ascomycetes from algae and animal hosts. Bot. Mar., 2003, 34, 1–35.
- Solis, M. J. L., Draeger, S. and dela Cruz, T. E. E., Marine-derived fungi from Kappaphycus alvarezii and K. striatum as potential causative agents of ice–ice disease in farmed seaweeds. Bot. Mar., 2010, 53, 587–594.
- Zuccaro, A., Schoch, C. L., Spatafora, J. W., Kohlmeyer, J., Draeger, S. and Mitchell, J. I., Detection and identification of fungi intimately associated with the brown seaweed Fucus serratus. Appl. Environ. Microbiol., 2008, 74, 931–941.
- Suryanarayanan, T. S., Venkatachalam, A., Thirunavukkarasu, N., Ravishankar, J. P., Doble, M. and Geetha, V., Internal mycobiota of marine macroalgae from the Tamil Nadu coast: distribution, diversity and biotechnological potential. Bot. Mar., 2010, 53, 456– 468.
- Schulz, B., Guske, S., Dammann, U. and Boyle, C., Endophyte–host interactions. II. Defining symbiosis of the endophyte–host interaction. Symbiosis, 1998, 25, 213–227.
- White, T. J., Bruns, T., Lee, S. J. and Taylor, J., Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics.In PCR Protocols: A Guide to Methods and Applications (eds Innis, M. A. et al.), Wiley, New York, USA, 1990, pp. 315–322.
- Thompson, J. D., Higgins, D. G. and Gibson, T. J., CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res., 1994, 22, 4673–4680.
- Tamura, K., Stecher, G., Peterson, D., Filipski, A. and Kumar, S., MEGA6: molecular evolutionary genetics analysis, version 6.0. Mol. Biol. Evol., 2013, 30, 2725–2729.
- Kimura, M., A simple method for estimating evolutionary rate of base substitutions through comparative studies of nucleotide sequences. J. Mol. Evol., 1980, 16, 111–120.
- Hata, K. and Futai, K., Endophytic fungi associated with healthy pine needles and needles infested by the pine needle gall midge Thecodiplo-sis japonensis. Can. J. Bot., 1995, 73, 384–390.
- Magurran, A. E., Measuring Biological Diversity, Blackwell Science Limited, UK, 2004.
- Schoch, C. L., Sung, G.-H., Volkmann-Kohlmeyer, B., Kohlmeyer, J. and Spatafora, J. W., Marine fungal lineages in the Hypocreomy-cetidae. Mycol. Res., 2007, 111, 154–162.
- Sakayaroj, J., Preedanon, S., Supaphon, O., Jones, E. B. G. and Phongpaichit, S., Phylogenetic diversity of endophyte assemblages associated with the tropical seagrass Enhalus acoroides in Thailand. Fungal Divers., 2010, 42, 27–45.
- de Felício, R. et al., Antibacterial, antifungal and cytotoxic activities exhibited by endophytic fungi from the Brazilian marine red alga Bostrychia tenella (Ceramiales). Rev. Bras. Farmacogn., 2015, 25, 641–650.
- Flewelling, A. J., Johnson, J. A. and Gray, C. A., Isolation and bioassay screening of fungal endophytes from North Atlantic marine macro-algae. Bot. Mar., 2013, 56, 287–297.
- Loque, C. P., Medeiros, A. O., Pellizzari, F. M., Oliveira, E. C., Rosa, C. A. and Rosa, L. H., Fungal community associated with marine macroalgae from Antarctica. Polar Biol., 2010, 33, 641–648.
- Furbino, L. E. et al., Diversity patterns, ecology and biological activi-ties of fungal communities associated with the endemic macroalgae across the Antarctic Peninsula. Microb. Ecol., 2014, 67, 775–787.
- Thirunavukkarasu, N., Suryanarayanan, T. S., Girivasan, K. P., Venkatachalam, A., Geetha, V., Ravishankar, J. P. and Doble, M., Fungal symbionts of marine sponges from Rameswaram, southern India: species composition and bioactive metabolites. Fungal Divers., 2012, 55, 37–46.
- Devarajan, P. T., Suryanarayanan, T. S. and Geetha, V., Endophytic fungi associated with the tropical seagrass Halophila ovalis (Hy-drocharitaceae). Indian J. Mar. Sci., 2002, 31, 73–74.
- Venkatachalam, A., Thirunavukkarasu, N. and Suryanarayanan, T.S., Distribution and diversity of endophytes in seagrasses. Fungal Ecol., 2015, 13, 60–65.
- Yarden, O., Ainsworth, T. D., Roff, G., Leggat, W., Fine, M. and Hoegh-Guldberg, O., Increased prevalence of ubiquitous ascomy-cetes in an acropoid coral (Acropora formosa) exhibiting symptoms of brown band syndrome and skeletal eroding band disease. Appl. Environ. Microbiol., 2007, 73, 2755–2757.
- Kubanek, J., Jensen, P. R., Keifer, P. A., Sullards, M. C., Collins, D. O. and Fenical, W., Seaweed resistance to microbial attack: a targeted chemical defense against marine fungi. Proc. Natl. Acad. Sci. USA, 2003, 100, 6916–6921
- Raghukumar, C. and Ravindran, J., Fungi and their role in corals and coral reef ecosystems. In Biology of Marine Fungi. Progress in Molecular and Subcellular Biology 53 (ed. Raghukumar, C.),Springer-Verlag, Berlin, Germany, 2012, pp. 89–113.
- Zimmerman, N. B. and Vitousek, P. M., Fungal endophyte communi-ties reflect environmental structuring across a Hawaiian landscape. Proc. Natl. Acad. Sci. USA, 2012, 109, 13022–13027.
- Redman, R. S., Kim, Y. O., Woodward, C. J. D. A., Greer, C., Espino, L., Doty, S. L. and Rodriguez, R. J., Increased fitness of rice plants to abiotic stress via habitat adapted symbiosis: a strategy for miti-gating impacts of climate change. PLoS ONE, 2011, 6, e14823.
- Suryanarayanan, T. S., Repository of fungal endophytes at VINST-ROM, Chennai: waiting to be harnessed. Curr. Sci., 2019, 117, 1469–1474.
- Venkatachalam, A., Govinda Rajulu, M. B., Thirunavukkarasu, N. and Suryanarayanan, T. S., Endophytic fungi of marine algae and seagrasses: a novel source of chitin modifying enzymes. Myco-sphere, 2015, 6, 345–355