Inoculum 56(4) - Mycological Society of America
Inoculum 56(4) - Mycological Society of America
Inoculum 56(4) - Mycological Society of America
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MSA ABSTRACTS<br />
Okada, Gen 1 *, Takematsu, Akiko 1 , Ogawa, Hiroyuki 2 , Wakabayashi, Keiko 2 ,<br />
Goto, Keiichi 2 , Attili de Angelis, Derlene 3 and Canhos, Vanderlei P. 3 1 Microbe<br />
Division / Japan Collection <strong>of</strong> Microorganisms, RIKEN BioResource Center, 2-1<br />
Hirosawa, Wako, Saitama 351-0198, Japan, 2 Laboratory <strong>of</strong> Beverage Development,<br />
Food Research Laboratories, Mitsui Norin Co., Ltd., 223-1 Miyahara, Fujieda,<br />
Shizuoka 426-0133, Japan, 3 Andre Tosello Foundation, Rua Latino Coelho,<br />
1301, Campinas 1889, SP, Brazil. okada@jcm.riken.jp. Undescribed anamorphic<br />
basidiomycete producing white synnemata and dikaryotic blastoconidia.<br />
White synnematous hyphomycete with basidiomycetous affinities was collected<br />
and isolated from dead inflorescence <strong>of</strong> palm (Phoenix rupicola) in Sao<br />
Paulo, Brazil on October 1993 (Specimens GO 1675 & 1676; cultures JCM<br />
12448 & 12449). Synnemata were white and indeterminate with parallel stipe and<br />
loose fertile zone. Hyphae were hyaline, septate, and lacking clamp connections.<br />
Conidia were produced blastically in dry chain, hyaline, non-septate, subglobose,<br />
and dikaryotic. Conidiogenesis superficially looks like those <strong>of</strong> the anamorphs <strong>of</strong><br />
Botryobasidium: (e.g., Haplotrichum, Parahaplotrichum), though the hyphae and<br />
conidia were completely hyaline and thin-walled. Based on 18S and 28S (D1/D2)<br />
rDNA sequence data, however, the fungus probably belongs to the Sebacinales<br />
phylogenetically far from Botryobasidium. Although its phylogenetic position has<br />
not yet decided clearly, we think that a new genus should be established for this<br />
undescribed anamorphic basidiomycete. poster<br />
Okane, Izumi* and Nakagiri, Akira. Biological Resource Center (NBRC), Department<br />
<strong>of</strong> Biotechnology, National Institute <strong>of</strong> Technology and Evaluation, 2-<br />
5-8, Kazusakamatari, Kisarazu, Chiba 292-0818, Japan. okane-izumi@nite.go.jp.<br />
Studies on xylariaceous fungi from plant leaves and other substrates.<br />
Xylariaceous fungi are known mainly as decomposers <strong>of</strong> angiosperms, and<br />
a few species have been reported to be plant pathogens. Some species have been<br />
found to live within living plant tissues, and considered as important endophytes.<br />
In this study, we surveyed diversity <strong>of</strong> the xylariaceous fungi from symptomless<br />
leaves <strong>of</strong> various vascular plants. Some strains were obtained from the fruit bodies<br />
on the pieces <strong>of</strong> wood, soil, and the nests <strong>of</strong> termites to investigate the wide<br />
range <strong>of</strong> xylariaceous fungi. We carried out taxonomical studies on isolates from<br />
leaves and other substrates by investigating morphology and molecular phylogeny.<br />
As a result, a sequence analysis based on the ITS regions <strong>of</strong> rDNA showed<br />
that the isolates from leaves were separated into two groups, namely Nemania and<br />
Xylaria clades, and two isolates from a nest <strong>of</strong> termite were included in the former<br />
clade. A cluster in the Nemania clade consisted <strong>of</strong> many isolates from various<br />
plants (evergreen-woody plants, orchids and pteridophytes) and two strains <strong>of</strong><br />
Nemania bipapillata, whose data were derived from DNA database. All isolates<br />
from leaves in the cluster were similar in their colony appearances on media.<br />
These results suggested that most <strong>of</strong> the xylariaceous fungi inhabiting various vascular<br />
plants belong to the genus Nemania and Xylaria. It was confirmed that some<br />
species behave as not only saprophytes, but also endophytes. Fresh plants and termite-living<br />
environment must be important materials to investigate on biodiversity<br />
<strong>of</strong> xylariaceous fungi. poster<br />
Okazaki, Koei* and Niwa, Osami. Kazusa DNA Research Institute, 2-6-7<br />
Kazusa-Kamatari, Kisarazu, Chiba 292-0818, Japan. kokazaki@kazusa.or.jp.<br />
Molecular mechanisms for the conjugate division: analysis using the fission<br />
yeast dikaryon.<br />
Many basidiomycetes use clamp connection to maintain the two different<br />
nuclei during mitotic division. However, the dikaryons <strong>of</strong> some basidiomycetes<br />
such as Ustilago maydis and ascogenous hyphae <strong>of</strong> the filamentous ascomycetes<br />
do not form the clamp connection. This suggests that basic mechanisms for the<br />
conjugate division underlie before the clamp connection have evolved. We found<br />
that the fission yeast Schizosaccharomyces pombe could propagate as a dikaryon<br />
in a manner to guarantee maintaining heterokaryon. Using this model organism<br />
and video microscopy, we are now analyzing the mechanism for nuclear pairing,<br />
communication between the two mitotic spindles, coupling <strong>of</strong> the two mitotic<br />
spindles to the single cytokinetic ring, and other mechanisms for dikaryon. We<br />
identified the minus-end directed kinesin as a motor protein responsible for nuclear<br />
pairing. Without this kinesin, the binucleated cell underwent mitosis and<br />
septation at two distant places, which produced a central binucleated cell and two<br />
monokaryons at the ends. The septation initiation network (SIN) proteins are<br />
known to localize asymmentrically at the spindle poles. Distribution <strong>of</strong> Cdc7, a<br />
member <strong>of</strong> SIN, suggested that the two spindles are arranged in a head-to-head<br />
orientation. poster<br />
Okuda, Toru 1 * and Bennett, Joan W. 2 1 Tamagawa University Research Institute, 6-<br />
1-1 Tamagawa-Gakuen, Machida, Tokyo 194-0041, Japan, 2 Department <strong>of</strong> Cell<br />
and Molecular Biology, Tulane University, New Orleans, LA 70118, USA. torula@lab.tamagawa.ac.jp.<br />
Exhibition <strong>of</strong> Dr. Jokichi Takamine sponsored by<br />
Sankyo Co., Ltd. (APPENDIX to Special Symposium on Industrial Mycology).<br />
Filamentous fungi in the genus Aspergillus are involved in our daily life.<br />
Koji mold, A. oryzae is used for producing miso, soy sauce and sake by growing<br />
the fungus on steamed rice. Currently, Aspergillus is applied to the production <strong>of</strong><br />
various enzymes and organic acids. Enzymes are particularly essential for industrial<br />
production <strong>of</strong> cereal food, detergents, forest products, textiles, feed, and beverages.<br />
Dr. Jokichi Takamine for the first time applied the enzymatic activity <strong>of</strong><br />
46 <strong>Inoculum</strong> <strong>56</strong>(4), August 2005<br />
A. oryzae to modern industry. A hundred years ago, he recognized the diastatic<br />
activity <strong>of</strong> A. oryzae, patented the first microbial enzyme in USA, and launched<br />
Taka-diastase. The substance is still sold today as a digestive aid. He then hired<br />
Dr. Uenaka and together they isolated adrenalin (epinephrine), the first modern<br />
wonder drug. Dr. Takamine became increasingly wealthy, developed strong trade<br />
positions in several Japanese industries, and founded three companies including<br />
Sankyo Co. in Tokyo. As a private diplomat between US and Japan, he helped defray<br />
the cost <strong>of</strong> the now famous cherry trees planted in Washington, D. C. On this<br />
commemorative occasion <strong>of</strong> MSA/MSJ Joint Meeting, it is worthwhile to exhibit<br />
a number <strong>of</strong> historical photographs and materials related to Dr. Takamine,<br />
which are reproduced by the courtesy <strong>of</strong> The Great People <strong>of</strong> Kanazawa Memorial<br />
Museum in Kanazawa and Sankyo Co., Ltd., Japan. symposium presentation<br />
Ono, Yoshitaka. College <strong>of</strong> Education, Ibaraki University, Mito, Ibaraki 310-<br />
8512, Japan. herb-iba@mx.ibaraki.ac.jp. Life cycle and host specificity in<br />
Ochropsora and Aplopsora species.<br />
Species in rust genera Aplopsora and Ochropsora are presumed to have a<br />
macrocyclic heteroecious life cycle; however, only O. ariae and O. kraunhiae<br />
have been proven to be heteroecious. None <strong>of</strong> Aplopsora species is known its full<br />
life cycle. Species in the two genera produce a sessile, one-celled, thin-walled<br />
probasidium (teliospore), producing a metabasidium without dormancy; and the<br />
two genera differ only in the mode <strong>of</strong> metabasidium production (germination <strong>of</strong><br />
teliospores). However, the difference in the mode <strong>of</strong> metabasidium production is<br />
a matter <strong>of</strong> degree <strong>of</strong> apical elongation <strong>of</strong> the probasidium during maturation.<br />
Thus, the taxonomic separation <strong>of</strong> the two genera has been questioned. In addition,<br />
three species in a poorly circumscribed genus Cerotelium have been suggested<br />
to belong to Aplopsora because <strong>of</strong> the similarity in probasidium morphology<br />
and a mode <strong>of</strong> metabasidium production. These necessitate the revision <strong>of</strong><br />
classification <strong>of</strong> Aplopsora, Ochropsora and their allies with species distinction<br />
by their life cycle and host specificity, i.e., circumscribing species by the reproductive<br />
isolation. Artificial inoculation experiments over ten years have revealed<br />
macrocyclic, heteroecious nature <strong>of</strong> the life cycle in two Aplopsora, one Ochropsora<br />
and one Cerotelium species in addition to two Ochropsora and one<br />
Cerotelium species, whose full life cycle was previously known. Thus, one<br />
Ochropsora and two Cerotelium species produces spermogonia/aecia on species<br />
<strong>of</strong> Corydalis/Dicentra (Fumariaceae), while spermogonia/ aecia <strong>of</strong> two Aplopsora<br />
and two Ochropsora species are produced on Anemone (Ranunculaceae). Each<br />
<strong>of</strong> the species has unique spermogonial/aecial host species. These results indicate<br />
that seven reproductively isolated species constitute a single genus with two subgroups<br />
that have differentiated in the spermogonial/aecial host preference during<br />
the course <strong>of</strong> evolution. symposium presentation<br />
Orihara, Takamichi 1 *, Sawada, Fumiko 2 , Ikeda, Shiho 3 , Yamato, Masahide 3 and<br />
Iwase, Koji 3 . 1 Dept. For. Sci., Fac. Agr., Kyoto Pref. Univ., 1-5 Shimogamohangi<br />
cho, Sakyo-ku, Kyoto 606-8522, Japan, 2 2-11-12 Tsujido-taiheidai, Fujisawa<br />
251-0044, Japan. 3 Biol. Environ. Inst., KANSO Technos Co., Ltd., 8-4 Ujimatafuri,<br />
Uji 611-0021, Japan. h_-berg-_f@io.ocn.ne.jp. Taxonomical<br />
reconsideration <strong>of</strong> Octaviania columellifera (Japanese name, jagaimo-take)<br />
and its phylogenetic relationship to Boletaceae.<br />
The semi-secotioid truffle-like fungus, Octaviania columellifera (Japanese<br />
name, jagaimo-take, literally means potato fungus) is an endemic species in<br />
Japan. It was originally described by Dr. Yoshio Kobayashi in 1936, but, since<br />
then, has not been authentically described. On the other hand, it has been suspected<br />
that the species which was described under the name <strong>of</strong> Octaviania asterosperma<br />
(Japanese name, Kurama-no-jagaimo-take, literally means potato fungus<br />
in Kurama) since 1972 in Japan corresponds to O. columellifera. It was clarified<br />
in this study that these two species are identical, by examining ITS regions <strong>of</strong> the<br />
nuclear rDNA as well as other chemical, morphological and ecological features.<br />
It was also revealed that the species is phylogenetically close to some groups in<br />
Boletaceae. Moreover, O. columellifera was placed in different lineage from other<br />
O. spp. in Boletales. In case <strong>of</strong> chemical reactions, the change <strong>of</strong> the length <strong>of</strong> the<br />
spore ornamentation in various reagents, which was previously described in Octavianina<br />
cyanescens (Trappe & Castellano, 2000), was also recognized, although<br />
this finding might be inconsistent to the results <strong>of</strong> molecular analysis. poster<br />
Osono, Takashi. Laboratory <strong>of</strong> Forest Ecology, Graduate School <strong>of</strong> Agriculture,<br />
Kyoto University Kyoto 606-8502, Japan. fujijun@kais.kyoto-u.ac.jp. Role <strong>of</strong><br />
phyllosphere fungi <strong>of</strong> forest trees in the development <strong>of</strong> decomposer communities<br />
and decomposition processes <strong>of</strong> leaf litter.<br />
The phyllosphere is the living leaf as a whole and includes the surface (phylloplane)<br />
and internal tissue. Phyllosphere fungi include epiphytes and endophytes<br />
that colonize the phylloplane and internal tissue, respectively, <strong>of</strong> living leaves.<br />
Phyllosphere fungi have been reported from a variety <strong>of</strong> plants including forest<br />
tree species. They have been studied intensively in terms <strong>of</strong> their ecological relationships<br />
with plants and other microorganisms on living leaves. In contrast, the<br />
ecology <strong>of</strong> phyllosphere fungi on leaf litter has received little attention even<br />
though they occur on various litters at initial stages <strong>of</strong> decomposition. At the leaf<br />
death, phyllosphere fungi can persist and have the advantage <strong>of</strong> gaining access to<br />
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