An Increase in Mechanical Extensibility during the Period of Light-stimulated Growth

The sporangiophore of Phycomyces responds to a temporary increase in light intensity with a transient increase in growth rate that begins 2 to 3 minutes after the initiation of the stimulus and continues until approximately the 12th minute. Tensile tests conducted on the stage IVb sporangiophore demonstrate that an increase in mechanical extensibility of the cell wall occurs 2 minutes after the initiation of a light stimulus and continues until approximately the 15th minute. This finding supports the theory that light-stimulated plant cell expansion and rate of expansion is a function of the mechanical extensibility of the cell wall.     

Phycomyces: a change in mechanical properties after a light stimulus

Tensile tests were conducted on the photoresponsive stage IVb sporangiophore of the fungus Phycomyces before and after a saturating light stimulus. The results demonstrate that an increase in the mechanical extensibility of the cell wall occurs after the light stimulus. This increase in mechanical extensibility occurs in the growing zone of the sporangiophore. The majority of this increase occurs in the region about 300 ųmeters beneath the sporangium.     

Phycomyces: An Increase in Mechanical Extensibility during the Avoidance Growth Response

The sporangiophore of Phycomyces shows a transient response to a double barrier, the avoidance growth response. Tensile tests conducted on the stage IV sporangiophore demonstrate that an increase in mechanical extensibility occurs about a minute after a double barrier stimulus. This change in mechanical extensibility is similar to the one that occurs after a light stimulus. We have concluded that the avoidance stimulus occurs somewhere on the same pathway between the photoreceptor mechanism and the final growth response.     

Evidence that Blastocladiella emersonii zoospore chitin synthetase is located at the plasma membrane

Blastocladiella emersonii zoospores are not encased by a cell wall and do not detectably synthesize or contain chitin; accompanying de novo cell wall formation during zoospore encystment, chitin rapidly accumulates and is incorporated into the cell wall. Essential for understanding this abrupt change in chitin synthesis is the location of zoospore chitin synthetase. The enzyme has previously been reported to the sequestered with distinctive cytoplasmic organelles (gamma particles) characteristic for the zoospore cell type. Using similar differential and equilibrium density centrifugation procedures to those reported previously, we have observed the vast majority of zoospore homogenate chitin synthetase activity in fractions distinct from the gamma particle-enriched fractions. Over 90% of the homogenate enzyme activity could be recovered in a sucrose buoyant density region (1.14–1.18 g/ml) containing membranous elements and well separated from the region enriched for gamma particles (1.30–1.34 g/ml). When zoospores were surface-labelled with [³H]concanavalin A prior to homogenization, the buoyant density regions of radioactivity and of chitin synthetase activity exhibited nearly complete coincidence. At least the bulk of zoospore chitin synthetase appears to be located at the plasma membrane, rather than in gamma particles.     

Photo-reactions in Phycomyces; growth and tropic responses to the stimulation of narrow test areas

Sporangiophores of Phycomyces in stage IV b have been stimulated by parallel light in test areas 0.2 mm. wide. The growth responses to large stimuli are very large, owing probably to light scattered within the specimen. For medium stimuli the sensitive zone coincides with the growth response zone obtained previously and excludes the region of maximum stretch. Sustained stimulations were used to elicit tropic responses. The bends formed travel away from the sporangium at a speed equal to the growth speed. Thus they remain very close to the stimulus when this is held at a constant level relative to ground but separate from it for stimuli programmed differently. The existence of a protoplasmic structure, the "inner wall," with the following properties is postulated: it is attached to the lower, non-growing part of the sporangiophore and grows by addition above the sensitive zone. It neither stretches nor twists in the sensitive zone. It is the seat of the light receptors and gives growth and tropic responses. The cell wall follows its bends by elastic stretch.     

Phycomyces: Mechanical Analysis of the Living Cell Wall

Stress relaxation measurements were conducted on stage IVb Phycomycessporangiophores in order to correlate the effect of imposedstress on cell wall growth. It was found that the cell wallshowed maximum growth when subjected to maximum stress. Growthunder stress decreased as the stress decreased. This techniquewas used to measure the response of the sporangiophore to alight stimulus; the response is measured directly from the stressrelaxation curve. Stress/strain measurements were also conducted on the stageIVb Phycomyces sporangiophores in order to further characterizethe mechanical properties of the growing zone. It was foundthat the stress/strain ratio was invariant to the strain ratewithin the ranges tested but the stress/strain ratio did increasewith larger loads, i.e., the stress/strain ratio shows non-linearbehaviour.     

Some properties of chitinase from Phycomyces blakesleeanus

The cytosol of the sporangiophore of $\text{Phycomyces}$$\text{blakesleeanus}$ has considerable chitinolytic activity. This activity is strongly dependent on the presence of a dialyzable activator. Maximal activity is achieved at pH 5.5; and ionic strength and Ca⁺⁺ or Mg⁺⁺ have little effect. Ungerminated spores do not contribute activity. The possibility is discussed that chitinase might be involved in the growth response system by transiently loosening the rigid framework of chitin at specific and defined points.     

Growth rate fluctuations in phycomyces sporangiophores

The growth rate of the Phycomyces sporangiophore fluctuates under constant environmental conditions. These fluctuations underlie the well-characterized sensory responses to environmental changes. We compared growth fluctuations in sporangiophores of unstimulated wild type and behavioral mutants by use of maximum entropy spectral analysis, a mathematical technique that estimates the frequency and amplitude of oscillations in a time series. The mutants studied are believed to be altered near the input (“night-blind”) or output (“stiff” and “hypertropic”) of the photosensory transduction chain. The maximum entropy spectrum of wild type shows a sharp drop-off in spectral density above 0.3 millihertz, several minor peaks between 0.3 and 10 millihertz, and a broad maximum near 10 millihertz. Similar spectra were obtained for a night-blind mutant and a hypertropic mutant. In contrast, the spectra of three stiff mutants, defective in genes madD, madE, or madG, had distinctive peaks near 1.6 mHz and harmonics of this frequency. A madF stiff mutant, which is less stiff than madD, madE, and madG mutants, had a spectrum intermediate between wild type and the three other stiff mutants. Our results indicate that alterations in one or more steps associated with growth regulation output cause the Phycomyces sporangiophore to express a rhythmic growth rate.     

The effect of auxin (indole-3-acetic acid) on the growth rate and tropism of the sporangiophore of <Emphasis Type="Italic">Phycomyces blakesleeanus</Emphasis> and identification of auxin-related genes

The roles of fungal auxins in the regulation of elongation growth, photo-, and gravitropism are completely unknown. We analyzed the effects of exogenous IAA (indole-3-acetic acid), various synthetic auxins including 1-NAA (1-naphthaleneacetic acid) and 2,4-D (2,4-dichlorophenoxyacetic acid), and the auxin transport inhibitor NPA (N-1-naphtylphtalamic acid) on the growth rate and bending of the unicellular sporangiophore of the zygomycete fungus, Phycomyces blakesleeanus. Sporangiophores that were submerged in an aqueous buffer responded to IAA with a sustained enhancement of the growth rate, while 1-NAA, 2,4-D, and NPA elicited an inhibition. In contrast, sporangiophores kept in air responded to IAA with a 20 to 40% decrease of the growth rate, while 1-NAA and NPA elicited an enhancement. The unilateral and local application of IAA in the growing zone of the sporangiophore elicited in 30 min a moderate negative tropic bending in wild type C2 and mutant C148madC, which was, however, partially masked by a concomitant avoidance response caused by the aqueous buffer. Auxin transport-related genes ubiquitous in plants were found in a BLAST search of the Phycomyces genome. They included members of the AUX1 (auxin influx carrier protein 1), PILS (PIN-LIKES, auxin transport facilitator protein), and ABCB (plant ATP-binding cassette transporter B) families while members of the PIN family were absent. Our observations imply that IAA represents an intrinsic element of the sensory transduction of Phycomyces and that its mode of action must very likely differ in several respects from that operating in plants.     

Phenotypic characterization of a trifluoperazine-resistant mutant ofMucor rouxii

A trifluoperazine-resistant (TFP¹) mutant (strain G5) ofMucor rouxii was isolated and some biochemical and physiological parameters were studied. It resisted up to 250 μM TFP compared to 100 μM observed for the wild-type strain. At this drug concentration the mutant strain G5 germinated, grew, exhibited yeast-mycelium transition, and chitin synthesisin vivo. The mutant strain presentedin vitro levels of calmodulin activity similar to those of the wild-type, but with less sensitivity to inhibition by TFP. Also, with regard to spore germination and cell growth, mutant G5 presented cross-resistance to calmidazolium, another potent anticalmodulin drug. Partially purified chitin synthetase preparations of mutant G5 exhibited a diminished enzymatic activity, compared to the wild-type. The results presented in this work suggest the participation of a Ca²⁺-calmodulin complex in growth and differentiative processes ofMucor and substantiate the role of this complex in chitin synthesis.     

Spiral growth in the radially-expanding piloboloid mutants ofPhycomyces blakesleeanus

The growth zone of the sporangiophore of a piloboloid mutant,pil, ofPhycomyces expands radially at an increased rate until the growth zone becomes nearly spherical, in sharp contrast to that of the wild-type sporangiophore which exhibits longitudinal elongation only and is conical. The rotation of thepil sporangiophore reverses its direction from clockwise (CW) to counterclockwise (CCW) during the period of increased radial expansion, and the CCW rotation continues as long as does the radial expansion. The direction of rotation and the time of reversal are correlated with the relative rates of cell-wall expansion in the longitudinal and transverse directions. The CCW rotation of the sporangiophore of this mutant can be explained by the behavior of the microfibrils, as previously proposed to explain the rotation of the wild-type sporangiophore.Abbreviations CW clockwise - CCW counterclockwise — both as viewed from above     

Tropic Responses of Phycomyces Sporangiophores to Gravitational and Centrifugal Stimuli

A low-speed centrifuge was used to study the tropic responses of Phycomyces sporangiophores in darkness to the stimulus of combined gravitational and centrifugal forces. If this stimulus is constant the response is a relatively slow tropic reaction, which persists for up to 12 hours. The response is accelerated by increasing the magnitude of the gravitational-centrifugal force. A wholly different tropic response, the transient response, is elicited by an abrupt change in the gravitational-centrifugal stimulus. The transient response has a duration of only about 6 min. but is characterized by a high bending speed (about 5°/min.). An analysis of the distribution of the transient response along the growing zone shows that the active phase of the response has a distribution similar to that of the light sensitivity for the light-growth and phototropic responses. Experiments in which sporangiophores are centrifuged in an inert dense fluid indicate that the sensory mechanism of the transient response is closely related to the physical deformation of the growing zone caused by the action of the gravitational-centrifugal force on the sporangiophore as a whole. However, the response to a steady gravitational-centrifugal force is most likely not connected with this deformation, but is probably triggered by the shifting of regions or particles of differing density relative to one another inside the cell.     

The Effect of Polarized Light on the Growth of a Transparent Cell : A theoretical analysis

It is shown that light lost by reflection before entering a clear and homogeneous sphere or infinite cylinder is precisely compensated by light retained within these bodies by internal reflection; compensation means that the total rate of light absorption by infinitely dilute photoreceptors as integrated through the whole of these bodies or even through any concentric or coaxial shell making them up is independent of surface reflection. In the Phycomyces sporangiophore this theorem precludes a reflection explanation of R, the polarization dependence of the light growth response. An alternative explanation based upon anisotropic absorption by the receptors is explored and found tenable. Formulae are derived for R in any transparent cylindrical cell as a function of the constants of anisotropic absorption by the photoreceptors taken as a group (C_H' and C_L'), of the radial position of the receptors, and of the refractive indices of the cell (n) and of the medium (N). It is inferred that the photoreceptors in the Phycomyces sporangiophore are most absorbent for light vibrating in the direction of a hoop around a barrel. Orientation of the receptors by linkage to the cell wall is then shown to be a plausible explanation of the inferred anisotropy. On the basis of anisotropic reception, it is predicted that R should be constant for any N > n, and it is shown how C_H', C,_L' and the radial position of the receptors may all be obtained from a careful determination of R as a function of N.     

TheAspergillus nidulans geneschsA andchsD encode chitin synthases which have redundant functions in conidia formation

We previously isolated three chitin synthase genes (chsA, chsB, andchsC) fromAspergillus nidulans. In the present work, we describe the isolation and characterization of another chitin synthase gene, namedchsD, fromA. nidulans. Its deduced amino acid sequence shows 56.7% and 55.9% amino acid identity, respectively, with Cal1 ofSaccharomyces cerevisiae and Chs3 ofCandida albicans. Disruption ofchsD caused no defect in cell growth or morphology during the asexual cycle and caused no decrease in chitin content in hyphae. However, double disruption ofchsA andchsD caused a remarkable decrease in the efficiency of conidia formation, while double disruption ofchsC andchsD caused no defect. Thus it appears thatchsA andchsD serve redundant functions in conidia formation.     

Cell wall extension behavior of Phycomyces sporangiophores during the pressure response.

The cylindrical, single-celled sporangiophore of Phycomyces blakesleeanus grows (enlarges) predominantly in the longitudinal direction during two stages of development; stage I and stage IVb. Cell enlargement (cell wall extension) occurs in a distinct region termed the "growing zone." It was previously reported that a large step-up or pulse-up in turgor pressure, greater than approximately 0.02 MPa, will elicit a transient decrease in longitudinal growth rate of the stage I and stage IVb sporangiophore. This transient decrease in longitudinal growth rate is termed the "pressure response." Both the magnitude and duration of the pressure response depend on the magnitude of the turgor pressure step-up or pulse-up. Qualitatively, the pressure response is similar to the stretch response, which is produced with the application of a longitudinal force (load) on the sporangiophore. In this investigation, the growth (extension) behavior of the cell wall in the growing zone is studied during the pressure response. It is found that both the extension rate of the cell wall in the growing zone and the length of the growing zone decrease during the pressure response, and that together they account for the observed decrease in longitudinal growth rate.     

Negative phototropism in the piloboloid mutants of Phycomyces blakesleeanus Bgff.

The sporangiophore (spph) of a piloboloid mutant, genotype pil, of Phycomyces ceases elongation and expands radially in the growth zone shortly after reaching the developmental stage IV b. The pil spph is always negatively phototropic to unilateral visible light when its diameter exceeds 210 m. Photoinduction of spph initiation, light-growth response, threshold of light energy fluence rate for the negative phototropism, avoidance and gravitropism in the pil mutant are all normal. In liquid paraffin, the pil spph shows negative phototropism as does the wild-type spph. Genetic analyses indicate that the negative phototropism of the pil mutant is governed by the phenotypic characteristics of pil but not by specific gene(s) responsible for negative phototropism. These facts imply that the reverse phototropism of the pil mutant results from a loss of the convergent lens effect of the cell because of the increase in cell diameter.Abbreviations spph(s) sporangiophore(s) - wt(s) wild type(s)     

Presence of GTP-Binding Proteins in the Plasma Membrane of the Phycomyces Sporangiophore

Ashktorab, H., and Cohen, R. J. 1994. Presence of GTP-binding proteins in the plasma membrane of the Phycomyces sporangiophore. Experimental Mycology 18, 139-149. When a plasma membrane-enriched fraction isolated from the sporangiophore of the Zygomycete Phycomyces blakesleeanus was subject to immunoblotting, two polypeptide bands reacted with an antibody directed to a conserved sequence of the ∝ subunit of G-proteins; their apparent molecular masses were 40 and 51 kDa. Upon treating the plasma membrane preparation with cholera toxin, bands at 40 and 51 kDa appeared to be ADP-ribosylated but no band appeared with pertussis toxin incubation. Apparent dissociation constants for the binding of GTPγS were determined for plasma membrane from Phycomyces sporangiophore grown in the light (K_D = 39 ± 16 nM) (±SD) and in the dark (K_D = 11 ± 6 nM). GTP served as a strong competitor for binding as did GDP, although somewhat less well, while ATP competed considerably more weakly. Northern analysis of sporangiophore mRNA displayed two bands hybridizing to the Gα2 probes coding for a G_α subunit from Dictyostelium discoideum. Furthermore, Western blotting of plasma membrane revealed several bands containing polypeptides with presumptive covalently attached immunoreactive flavins. (The prevailing evidence from the action spectra of Phycomyces is that the photoreceptor is a flavoprotein residing in the plasma membrane.) Immunoblotting also detected a H⁺ ATPase similar to the plasma membrane enzyme of yeast, corroborating our isolation of plasma membrane and suggesting another possible player in the signal responses of Phycomyces . This is apparently the first evidence for a G-protein in this class of eukaryotes. G-proteins may serve a role in the flavoprotein-mediated phototransduction system of P. blakesleeanus.     

The avoidance behavior of Phycomyces blakesleeanus: Is mediation by natural convection significant?

The sporangiophore of Phycomyces avoids nearby objects by detecting perturbations in the concentration of an emitted volatile effector. Gravity plays no significant role in modifying the distribution of gas. Thus avoidance cannot be mediated by natural convection.     

Chitin synthesis and localization in cell division cycle mutants of Saccharomyces cerevisiae.

Growth of Saccharomyces cerevisiae cell cycle mutants cdc3, cdc4, cdc7, cdc24, and cdc28 at a nonpermissive temperature (37 degrees C) resulted in increased accumulation of chitin relative to other cell wall components, as compared with that observed at a permissive temperature (25 degrees C). Wild-type cells showed the same chitin/carbohydrate ratio at both temperatures, whereas mutants cdc13 and cdc21 yielded only a small increase in the ratio at 37 degrees C. These results confirm and extend those reported by B. F. Sloat and J. R. Pringle (Science 200:1171-1173, 1978) for mutant cdc24. The distribution of chitin in the cell wall was studied by electron microscopy, by specific staining with wheat germ agglutinin-colloidal gold complexes. At the permissive temperature, chitin was restricted to the septal region in all strains, whereas at 37 degrees C a generalized distribution of chitin in the cell wall was observed in all mutants. These results do not support a unique interdependence between the product of the cdc24 gene and localization of chitin deposition; they suggest that unbalanced conditions created in the cell by arresting the cycle at different stages result in generalized activation of the chitin synthetase zymogen. Thus, blockage of an event in the cell cycle may lead to consequences that are not functionally related to that event under normal conditions.     

Complementation betweenPhycomyces mutants of mating type (+) with abnormal phototropism

Summary Twelve mutants ofPhycomyces blakesleeanus with defects in sporangiophore phototropism (genotypemad) were obtained from a wild type of the (+) mating type by mutagenesis with nitrosoguanidine. These mutants were tested for genetic complementation against standard (+)mad mutants derived from sexual crosses between the isogenic (+) strain and established (-)mad mutants (Ootaki et al., 1974; Eslava et al., 1976). Heterokaryons for complementation tests were obtained by grafting stage I sporangiophores. The (+) mutants were also investigated for their sensory responses such as photoinduction of sporangiophores and avoidance. The mutants were grouped into two classes, based on the phenotypic classification scheme of Bergman et al. (1973). There were eleven class 1.2 mutants and one class 2 mutant. Complementation tests revealed that all eleven class 1.2 mutants carry the genemadC and the class 2 mutant carriesmadD. There was no evidence that any were double mutants. These results are consistent with the phenotypic classification and with the complementation results of themad mutants of the (-) mating type.