Localized, Cold-Induced Inhibition of Translocation in Mycelia and Strands of Serpula lacrimans

Thompson, W., Brownlee, C, Jennings, D. H. and Mortimer, A.M. 1987. Localized, cold-induce inhibition of translocationin mycelia and strands of Serpula lacrimans. —J. exp.Bot. 38: 889–899 The effect has been investigated of localized low temperatureon translocation of ³²P across myceliui of Serpula lacrimansusing two gas-flow detectors capable of recording radioactivitycontinuously. When the temperature of a band of mycelium wasreduced to 0 ? C, radioactivity ceased to accumulai and in factdeclined under the detector (number 2) separated from the sourceof radioactivity by tr cold-treated mycelium. In the myceliumbeneath the other detector (number 1), closest to the sourceradioactivity, the rate of accumulation of radioactivity increased.When the temperature was raised t 20 ?C, radioactivity beganto accumulate in the mycelium under detector 2 and, apart froma sma fluctuation, continued to accumulate at a uniform rate.In the mycelium under detector 1, the accumulation of radioactivitystopped for a short time but then recommenced at a rate similarto thi found at 0 ?C. In other experiments the distributionof radioactivity (¹⁴C) throughout the myceliui was measuredat the end in homogenized samples. In these experiments a bandof mycelium we subjected to 0 ?C or to 20 ?C for the whole experimentalperiod, or only after the mycelium had bee translocating radioactivityalready for 16 h. These experiments showed that the changesin the rate of accumulation of ³²P in living mycelium underthe two gas flow detectors used for in situ measurements werenot due to a reversal of the flow of translocation. The resultsare consistent with an hypothesis that a turgor-driven massflow of solution is the mechanism for translocation in thisfungus and are considered in relation to the results of similarexperiments on phloem translocation in higher plants. Key words: Serpula lacrimans, mycelium, translocation, low-temperature, phloem transport     

Internal Structure and Hydraulic Conductivity of Basidiomycete Translocating Organs

Eamus, D., Thompson, W., Cairney, J. W. G. and Jennings, D.H. 1985. Internal structure and hydraulic conductivity of basidiomycetetranslocating organs.–J. exp. Bot. 36: 1110–1116. The presence in rhizomorphs of Armillaria mellea and cords ofPhallus impudicus of wide diameter hyphae (5–20 {diaeresis}m),which run for considerable distances along these linear organs,has been demonstrated. The longitudinal hydraulic conductivityof these organs has been determined experimentally and similarvalues were obtained when the hydraulic conductivity was calculatedtheoretically on the basis that the vessel hyphae were the solechannel for water movement along these organs. The experimentaldata have been discussed in relation to other data for long-distancetranslocation in basidiomycete linear organs. It is concludedthat the vessel hyphae are the main channels for turgor-driventranslocation. Key words: -Basidiomycete fungi, translocation, hydraulic conductivity     

A population‐based temporal logic gate for timing and recording chemical events

Engineered bacterial sensors have potential applications in human health monitoring, environmental chemical detection, and materials biosynthesis. While such bacterial devices have long been engineered to differentiate between combinations of inputs, their potential to process signal timing and duration has been overlooked. In this work, we present a two‐input temporal logic gate that can sense and record the order of the inputs, the timing between inputs, and the duration of input pulses. Our temporal logic gate design relies on unidirectional DNA recombination mediated by bacteriophage integrases to detect and encode sequences of input events. For an E. coli strain engineered to contain our temporal logic gate, we compare predictions of Markov model simulations with laboratory measurements of final population distributions for both step and pulse inputs. Although single cells were engineered to have digital outputs, stochastic noise created heterogeneous single‐cell responses that translated into analog population responses. Furthermore, when single‐cell genetic states were aggregated into population‐level distributions, these distributions contained unique information not encoded in individual cells. Thus, final differentiated sub‐populations could be used to deduce order, timing, and duration of transient chemical events.