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Book of Abstracts (PDF) - International Mycological Association

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IMC7 Main Congress Theme V: CELL BIOLOGY AND PHYSIOLOGY Posters<br />

in complete darkness. We also revealed proteins spots that<br />

were newly expressed after light stimulation and localized<br />

in pileus. These suggests that many <strong>of</strong> proteins involved in<br />

fruit body induction in F. velutipes are expressed after<br />

temperature reduction, and involved in pileus induction are<br />

expressed after light stimulation.<br />

1170 - Ultrastructure and biochemistry <strong>of</strong> hyphae <strong>of</strong><br />

different zone <strong>of</strong> growth in a fruiting colony <strong>of</strong><br />

Pleurotus pulmonarius<br />

C. Sánchez 1* , G. Díaz-Godínez 1 & D. Moore 2<br />

1 Universidad Autónoma de Tlaxcala, Apartado Postal 129,<br />

Tlaxcala, Tlax. C.P. 90000, Mexico. - 2 The University <strong>of</strong><br />

Manchester, School <strong>of</strong> Biological Sciences, Manchester<br />

9PT, U.K. - E-mail: sanher6@hotmail.com<br />

In a fungus colony, hyphae from the peripheral zone (i.e.<br />

young hyphae) are responsible for colony expansion. On<br />

the other hand, hyphae from the central zone (i.e. mature<br />

hyphae) may differentiate into reproductive structures. It<br />

has previously been observed that when P. pulmonarius<br />

cultures were stained by using conventional histological<br />

stains the peripheral zone <strong>of</strong> the colony (PZC) and the<br />

fruiting structures were stained, but the central zone <strong>of</strong> the<br />

colony (CZC) was unstained. In this research, the<br />

ultrastructure and biochemistry <strong>of</strong> hyphae from the PZC<br />

and CZC <strong>of</strong> a fruiting colony <strong>of</strong> P. pulmonarius, developed<br />

on potato dextrose agar were studied. The wall thickness <strong>of</strong><br />

hyphae from the CZC was approx. twice that <strong>of</strong> hyphae<br />

from the PZC (0.15 and 0.07 µm, respectively). Hyphae<br />

from the PZC had about twice glycogen content and 50%<br />

higher protein content (501 and 18 mg/g dry biomass (dX),<br />

respectively) than those from the CZC (237 and 11 mg/g<br />

dX, respectively). The cell wall <strong>of</strong> hyphae from the CZC<br />

had about twice soluble and insoluble glucans content (7.7<br />

and 6.4 mg/g dX, respectively) that <strong>of</strong> hyphae from the<br />

PZC (3.8 and 3.4 mg/g dX, respectively). The histological<br />

differences between young and mature hyphae <strong>of</strong> a colony<br />

<strong>of</strong> P. pulmonarius, particularly in the cell wall and the<br />

amount <strong>of</strong> cytoplasmic material present in the hyphae,<br />

suggest that the wall is used as a temporary nutrient reserve<br />

during development <strong>of</strong> Pleurotus.<br />

1171 - Stability <strong>of</strong> some commercial mushrooms in<br />

Thailand after continuous subcultures <strong>of</strong> mycelia for<br />

production<br />

W. Sattayaphisut 1 , N. Boonkerd 1 , N. Teaumroong 1 & S.<br />

Rodtong 2*<br />

1 School <strong>of</strong> Biotechnology, Institute <strong>of</strong> Agricultural<br />

Technology, Suranaree University <strong>of</strong> Technology, Nakhon<br />

Ratchasima 30000, Thailand. - 2 School <strong>of</strong> Microbiology,<br />

Institute <strong>of</strong> Science, Suranaree University <strong>of</strong> Technology,<br />

Nakhon Ratchasima 30000, Thailand. - E-mail:<br />

sureelak@ccs.sut.ac.th<br />

The decrease in fruiting body yields commonly occurs in<br />

the mushroom production in Thailand when mycelia<br />

obtained from continuous subcultures are used. The<br />

stability <strong>of</strong> commercial mushrooms: Auricularia auricula,<br />

Agrocybe cylindracea, Lentinula edodes, Lentinus<br />

polychrous, L. squarrossulus, Pleurotus ostreatus,<br />

Pleurotus species under names P. cystidiosus and P. sajorcaju,<br />

and Tricholoma crassum, after continuous<br />

subcultures <strong>of</strong> mycelia for production twenty times was<br />

investigated. Mycelial growth rates and fruiting body<br />

yields were determined. The PCR-RFLP technique was<br />

also tried to be employed for the preliminary detection <strong>of</strong><br />

fungal genetic stability. After the twentieth subculture,<br />

growth rates and fruiting body yields <strong>of</strong> all mushrooms<br />

were found to be rather consistent except Auricularia<br />

auricula giving the decrease in both its growth and yield<br />

after the third subculture then reversing to be stable<br />

through the subsequent subcultures. For the detection <strong>of</strong><br />

genetic stability, all fungal species gave consistent DNA<br />

patterns (600-800bp PCR products from ITS4 and ITS5<br />

primers, and the unique RFLP pattern <strong>of</strong> each species when<br />

the DNA was digested with either AluI, TaqI, MboI, or<br />

HinfI) except A. auricula giving the different pattern <strong>of</strong><br />

HinfI digest after the third subculture which was<br />

corresponding to its growth and yield reduction. The<br />

genetic stability <strong>of</strong> mushrooms should be examined after<br />

continuous subcultures <strong>of</strong> mycelia prior to application in<br />

the large scale production.<br />

1172 - Long-term exposure <strong>of</strong> lichens to high<br />

atmospheric CO 2 under controlled conditions: effects<br />

on morphology and chemistry<br />

M. Saunders * & D. Armaleo<br />

Duke University, Department <strong>of</strong> Biology, Box 90338,<br />

Durham, NC 27708, U.S.A. - E-mail: saunders@duke.edu<br />

The lichens Usnea strigosa and Parmotrema hypotropum<br />

were collected at the FACE (Free Air CO2 Enrichment) site<br />

in operation near Duke University. FACE technology is<br />

able to monitor and maintain open-air sites with<br />

atmospheric CO2 levels kept either at ambient (^500 ppm)<br />

or enriched (^700 ppm) values. Flora is grown under<br />

natural conditions realistically simulating future<br />

concentrations <strong>of</strong> atmospheric CO 2. This setup, in<br />

operation for 15 years, is ideal for monitoring long-term<br />

effects <strong>of</strong> CO 2 enrichment throughout the lichens' lifespan,<br />

with a degree <strong>of</strong> control not possible in earlier studies. Both<br />

species <strong>of</strong> lichens were collected almost exclusively from<br />

the bark <strong>of</strong> Sweetgum (Liquidambar styraciflua) trees from<br />

both CO2-enriched and control sites. Each specimen was<br />

photographed, sectioned, and observed by standard and<br />

fluorescence microscopy. The secondary compounds were<br />

extracted to near completion (^95%) and quantified (in<br />

reference to thallus dry weight) by digital analysis <strong>of</strong> Thin<br />

Layer Chromatography data. Significant differences in<br />

micro-anatomy and chemistry were found between the<br />

lichens collected in the high CO2 and control sites.<br />

<strong>Book</strong> <strong>of</strong> <strong>Abstracts</strong> 355

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