TY - JOUR
T1 - The role of source-sink relationships in translocation during sclerotial formation by Morchella esculenta
AU - Amir, Rachel
AU - Levanon, Dan
AU - Hadar, Yitzhak
AU - Chet, Ilan
PY - 1994
Y1 - 1994
N2 - Sclerotia formed by Morchella esculenta were developed on square split plates. A trough separated two different media, effecting total separation between the sclerotia developing on one side, and the mycelium on the other. The translocation of two sugars, [14C]-d-glucose, or its analog, [14C]-3-O-methyl glucose, placed in the trough, was quantitatively measured during six stages of growth and sclerotial development. During this period, the direction of translocation changed three times: during extension of the colony, translocation was toward the hyphal tips of the mycelium; when the mycelium reached the edge of the plate, reverse translocation was observed, as a result of sclerotial formation; at maturation, the direction of translocation reversed again. In control experiments, the use of lanolin on the trough to prevent the wick effect, or ethylene oxide vapour to kill the fungus, showed that translocation to sclerotia was not the result of capillary action. The velocity of translocation was much greater than the utilization of nutrients in the developing sclerotia, probably due to sink strength. Most of the radioactivity was lost into the agar medium (up to 80% of the total radioactivity), rather than accumulating in the fungus. It is suggested that this loss originated from excess nutrients which were not converted to insoluble reserve materials. The labelled compounds that were lost to the medium were later reabsorbed by the mycelium, during the mature stage of sclerotial formation
AB - Sclerotia formed by Morchella esculenta were developed on square split plates. A trough separated two different media, effecting total separation between the sclerotia developing on one side, and the mycelium on the other. The translocation of two sugars, [14C]-d-glucose, or its analog, [14C]-3-O-methyl glucose, placed in the trough, was quantitatively measured during six stages of growth and sclerotial development. During this period, the direction of translocation changed three times: during extension of the colony, translocation was toward the hyphal tips of the mycelium; when the mycelium reached the edge of the plate, reverse translocation was observed, as a result of sclerotial formation; at maturation, the direction of translocation reversed again. In control experiments, the use of lanolin on the trough to prevent the wick effect, or ethylene oxide vapour to kill the fungus, showed that translocation to sclerotia was not the result of capillary action. The velocity of translocation was much greater than the utilization of nutrients in the developing sclerotia, probably due to sink strength. Most of the radioactivity was lost into the agar medium (up to 80% of the total radioactivity), rather than accumulating in the fungus. It is suggested that this loss originated from excess nutrients which were not converted to insoluble reserve materials. The labelled compounds that were lost to the medium were later reabsorbed by the mycelium, during the mature stage of sclerotial formation
UR - http://www.scopus.com/inward/record.url?scp=0028252126&partnerID=8YFLogxK
U2 - 10.1016/S0953-7562(09)81071-X
DO - 10.1016/S0953-7562(09)81071-X
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AN - SCOPUS:0028252126
SN - 0953-7562
VL - 98
SP - 1409
EP - 1414
JO - Mycological Research
JF - Mycological Research
IS - 12
ER -