- Research article
- Open Access
The dynamic behavior of bacterial macrofibers growing with one end prevented from rotating: variation in shaft rotation along the fiber's length, and supercoil movement on a solid surface toward the constrained end
© Mendelson et al; licensee BioMed Central Ltd. 2003
- Received: 28 April 2003
- Accepted: 16 August 2003
- Published: 16 August 2003
Bacterial macrofibers twist as they grow, writhe, supercoil and wind up into plectonemic structures (helical forms the individual filaments of which cannot be taken apart without unwinding) that eventually carry loops at both of their ends. Terminal loops rotate about the axis of a fiber's shaft in contrary directions at increasing rate as the shaft elongates. Theory suggests that rotation rates should vary linearly along the length of a fiber ranging from maxima at the loop ends to zero at an intermediate point. Blocking rotation at one end of a fiber should lead to a single gradient: zero at the blocked end to maximum at the free end. We tested this conclusion by measuring directly the rotation at various distances along fiber length from the blocked end. The movement of supercoils over a solid surface was also measured in tethered macrofibers.
Macrofibers that hung down from a floating wire inserted through a terminal loop grew vertically and produced small plectonemic structures by supercoiling along their length. Using these as markers for shaft rotation we observed a uniform gradient of initial rotation rates with slopes of 25.6°/min. mm. and 36.2°/min. mm. in two different fibers. Measurements of the distal tip rotation in a third fiber as a function of length showed increases proportional to increases in length with constant of proportionality 79.2 rad/mm. Another fiber tethered to the floor grew horizontally with a length-doubling time of 74 min, made contact periodically with the floor and supercoiled repeatedly. The supercoils moved over the floor toward the tether at approximately 0.06 mm/min, 4 times faster than the fiber growth rate. Over a period of 800 minutes the fiber grew to 23 mm in length and was entirely retracted back to the tether by a process involving 29 supercoils.
The rate at which growing bacterial macrofibers rotated about the axis of the fiber shaft measured at various locations along fibers in structures prevented from rotating at one end reveal that the rate varied linearly from zero at the blocked end to maximum at the distal end. The increasing number of twisting cells in growing fibers caused the distal end to continuously rotate faster. When the free end was intermittently prevented from rotating a torque developed which was relieved by supercoiling. On a solid surface the supercoils moved toward the end permanently blocked from rotating as a result of supercoil rolling over the surface and the formation of new supercoils that reduced fiber length between the initial supercoil and the wire tether. All of the motions are ramifications of cell growth with twist and the highly ordered multicellular state of macrofibers.
- Rotation Rate
- Fiber Length
- Viscous Drag
- Fiber Elongation
- Fiber Growth
Filaments of Bacillus subtilis, consisting of chains of cells linked in tandem, twist as they grow, writhe, supercoil, and by repetition self-assemble into highly ordered fibers of mm in length called macrofibers [1, 2]. The direction of twisting can be either left or right handed, and the degree of twist can be varied giving rise to fibers that range from very tightly twisted to those so loose that they barely retain their integrity as fibers. Helix hand and the degree of twist are both governed by genes and environmental factors such as temperature, or the presence of certain ions or compounds in the growth medium . In any given culture all the fibers grow with the same handedness and degree of twist [4, 5]. All fibers carry loops at both ends of the fiber shaft that rotate during growth in contrary directions about the axis of the shaft [6, 8]. If the loops are removed the ends of the shaft also rotate in contrary directions. We have shown previously that the sum of the angles turned through at the ends of such fibers is a linear function of their length  which strongly suggests that fibers grow with constant twist, and that the rate at which a fiber shaft rotates must decrease from a maximum at the ends to zero at some point along the length of a fiber.
The presumed gradient of rotation rate along the shaft of a macrofiber has never been observed directly although pivoting motions observed as fibers grow on solid surfaces clearly show a gradient of velocity of rotation in the horizontal plane which is the result of rolling over the surface that correspondes to the rate of rotation in the fiber [7, 8]. Simple theory predicts that if rotation is prevented at only one end of a fiber the other should rotate at twice the rate it normally would, and that the rotation rate should vary linearly along the shaft from zero at the blocked end to maximum at the other.
In all previous work on macrofibers it has been evident that anything that impedes fiber rotation during growth simultaneously at two locations along a fiber's length results in supercoiling in the region between the impediments [4, 10]. In particular impediment to rotation at the free end of fibers blocked at their other end has previously been shown to induce supercoiling . In fiber populations blocking rotation at one end of a fiber caused by fiber/fiber interactions followed later by blocking the other end has been shown to result in supercoiling and the dragging of the two ends together. The work described here deals with the characterization of the rotation rate gradient in fibers experimentally blocked at one end, as well as the ramifications of later preventing rotation at the free end of such fibers.
A bacterial macrofiber was suspended in growth medium from a textile fiber which was floated on the surface. The textile fiber remained fixed in orientation on the fluid surface as the bacterial fiber grew vertically toward the floor of the chamber. Macrofiber growth was observed using a CCD video camera fitted with a telephoto lens aimed horizontally at the chamber. The optics chosen permitted visualization of the full depth (approximately 10 mm) of the growth fluid. It also allowed resolution of macrofiber details adequate to quantify the rates of fiber growth and rotation of the shaft and distal tip of the elongating structure. Time-lapse video images were produced and used to analyze these parameters for three macrofibers designated 8, 9, and 82.
Additional File 4: Time-lapse dual-view video film sequence of a tethered macrofiber growing horizontally above the floor of the growth chamber. The upper image is the view from above and is not pertinent to this analysis. The lower image shows the view from the side including a mirror image reflection of the fiber from the glass floor. The fiber grew from the large mass attached to the wire at the left toward the right of the field of view. Writhing motions, supercoiling, and supercoil movement toward the left can be seen in the lower images. The entire sequence spans 136 minutes in real time. The initial frame of this sequence corresponds to 336 min on Fig. 9. For purposes of orientation two triangles and a connecting horizontal line drawn on panel B of figure 9 indicate where the starting and ending time frames are of additional file 4 in the context of the entire growth and retraction process. (MOV 30 MB)
The experiments described here illustrate that in growing bacterial macrofibers that are tethered at one end, rotation rate gradients develop, that the rate at which the free end of a tethered fiber rotates increases as a function of fiber elongation, and that a second block to fiber rotation at a distance from the tether induces plectoneme supercoils that migrate on solid surfaces toward the tether. All of these observations can be understood in terms of the behavior of a deformable filament that twists as it elongates, and when twisting is impeded develops torque that is relieved by changing shape. Earlier work has suggested that all of the cells in a macrofiber grow, even those at its center . Individual cells, and therefore macrofibers, grown without constraint expand , toward both poles of their approximately cylindrical structure. The methods we used to block macrofiber rotation at one end also imposed a constraint on growth expansion. The cell mass produced by growth of cells in a tethered fiber must be taken up by expansion solely toward the free end of the fiber. A similar situation arises in natural macrofiber populations when mature fibers form ball-like structures that harbor younger fibers growing outward from their surface . These young fibers can neither rotate at the end attached to the ball structure as they grow, nor expand into the ball structure. Their behavior is the same as that found in the tethered fibers described here.
A single cell positioned within a macrofiber at its tethered end, unlike a free cell, can rotate as it grows only at its distal pole. The twist generated by its growth can influence only the downstream neighboring cell to which the initial cell is attached by a septum. Growth of the downstream cell is subject to the same constraints but it is also influenced by the twist generated by its upstream neighbor. This polarity continues throughout the entire fiber and is the key mechanical reason for rotation gradient behavior and the fact that the downstream tip of the fiber rotates faster and faster as more cells are produced by growth all along the length of the macrofiber. We modeled mathematically the dynamic behavior of a macrofiber tethered at one end making the following simplifying assumptions: i. the macrofibers have uniform diameter throughout their length, ii. there is uniform twist throughout the fiber structure, and iii. the fibers grow at an exponential rate. The model predicts that the rotation rate at any point in a tethered fiber is proportional to the rate of growth of the segment between the tether and that point and depends solely on the fiber's twist. The argument is essentially the same for unconstrained macrofibers ; thus:
where Ωx is the rotation rate at length x from the tether and N is twist in turns/unit length. When the fiber growth rate is exponential (ν) as the measurements in Figs. 1 and 6 indicate it is, the relationship becomes
Ωx = 2πNνx (2)
where x = xoeντ and ν = (ln2)/Td, Td is the doubling time.
Integrating (2) with respect to time gives the angle turned through θ
θx = 2πNxo(eντ -1) = 2πN(x - xo) (3)
which is the form the data takes in Fig. 3 for markers along the length of the shaft and in Fig. 7 for measurements of rotation at the distal tip. Using this relationship we are able to solve for N in fiber 9 given ν = 0.0083 min-1. The inferred twist is 12.1 turns/mm. The same calculation using measurements from fiber 82 (that from which distal tip rotation rate was measured) results in an inferred twist of 12.6 turns/mm. That for fiber 8 however results in a twist of only 8.7 turns/mm. All three fibers were grown under the same conditions so that a common twist value should be expected. The most likely reason for fiber 8 twist being different is that, although the plectoneme markers on fiber 9 moved away from the surface tether at a speed corresponding to the whole fiber growth rate, those on fiber 8 did so at speeds that on average were only 0.70 times the corresponding fiber growth rate. It is clear that elongation of plectonemes reduces the rate of elongation of the macrofiber shaft, but there is no simple theory relating this to rotation rate, so the fact that 8.7/12.1 = 0.71 is probably coincidence.
If we examine the film sequences shown in additional files 1, 2, and 3 all of which depict tethered macrofiber growth using the hanging wire protocol, we see that the first assumption of the model, uniform diameter throughout length, is true initially but not at later times after supercoil plectonemes arose. For technical reasons twist could not be measured directly in these fibers therefore we cannot assess the validity of the second assumption of our model. Figs 1 and 6 show that the third assumption of the model, uniform growth rate, is correct. Given these limitations we can nevertheless compare the rotation rate gradients with those predicted by our model of ideal behavior. Using the plectoneme markers shown in Figs. 2 and 5, the rates of rotation along the shaft (Figs. 3 and 4) and at the distal downstream tip (Fig. 7) were determined. In the two fibers measured the variation along the shaft of each fiber was linear (Fig. 4): in fiber 8 the gradient of rate of change as a function of distance from the tether was approximately 25.6°/min. mm, in fiber 9 it was 36.2°/min. mm.
Both fibers grew at an exponential rate. According to our simple model the rotation rate should have also increased at an exponential rate with time; but they did not. This was probably due to rotational viscous drag acting upon the macrofiber because the fiber surface moved relative to the fluid. The drag would have resulted in a torque about the longitudinal axis of the fiber. The effect of such a torque, Q is, in the simple theory given above, to reduce the effective twist 2πN in equation (1) by an amount Q/C where C is the torsional stiffness at the point under consideration. Because of their distance from the axis of rotation, the viscous drag on plectonemes is the major cause of macrofiber torque. This then depends on rotational speed, which does increase with time, so the effective twist decreases with time resulting in a non-exponential change in rotation rates. This does not affect the variation with position; the rates used in Fig. 4 were all initial rates. Better scaling proportionality was found however for the case of distal downstream tip rotation as a function of fiber length as shown in Fig. 7. During a 65 min. interval the rotation rate of the distal tip progressively increased from an initial rate of 286°/min. to 335, then to 382, and finally to 430°/min. The transitions between these rates were rather abrupt suggesting that there may be some thresholds that have to be overcome in order for the tip to increase its rate of rotation. The geometry of the tip markers may play some role in this. Their orientation with respect to the fiber shaft changed throughout the growth period examined. During the initial 8 minutes of Fig. 7, for example, two arms protruded perpendicular to the fiber shaft at the tip. These became aligned with the axis of the shaft between 8 and 10 minutes and remained in this orientation for the period corresponding to the second linear portion of the curve suggesting that changes in the viscous drag may be a contributing factor. For the purposes of modeling tip behavior however we have ignored this complication. Our mathematical model predicts a relationship between rotation rate and fiber length of:
θ l / π = 25.2(l-8.66) (4)
(where l is length in mm). Corresponding points based upon equation (4) have been superimposed upon the data of Fig. 7. The fit appears to be good suggesting proportionality between the growth rate of an entire fiber and the rate at which it's tip rotates. Because any torque due to viscous drag depends on the length of a macrofiber and the plectonemes beyond the section concerned, it should be zero at the tip. This explains why the rotation rate at the tip of a fiber (fiber 82 for example), unlike that at intermediate points, increases, on average, exponentially.
These findings establish that blocked rotation at one end during growth of macrofibers leads to the development of rotation rate gradients in which the further away from the point of impediment one gets, the faster the structure rotates as it elongates. Earlier we have shown using a similar floating wire protocol that preventing rotation at both ends during growth leads to supercoiling . In natural macrofiber populations blocked rotation usually results from contacts fibers make with the floor of the growth chamber . We describe here an inadvertent discovery in which a fiber prevented from rotating at one end by tethering to a wire later became prevented from rotating at various positions along its length as a result of touching the floor. Fig. 8 and additional file 4 show that plectoneme supercoils arose following the second impediment to rotation. Fig. 9 illustrates that the newly formed plectonemes migrated over the floor toward the initial tether eventually causing the entire length of the fiber (23 mm) to retract. The formation of new supercoils in the region between the tether and the plectoneme was responsible for retraction. Film sequence 4 clearly shows that the bulky plectoneme protruding from the fiber shaft prevented free shaft rotation and induced the secondary supercoils that shortened the length of fiber shaft between the plectoneme and the tether. A similar phenomenon has been observed in natural macrofiber populations when macrofibers bridging between two larger ball form structures were caused to supercoil, reduce their length and drag the two structures together .
Although bacterial macrofibers respond to forces as would any comparable deformable material their mechanical behavior is unique because all forces at play are derived from individual cell growth within the multicellular fibers and because impediments to the rotation that accompanies cell elongation set into play motions that when resisted can result in work being done. Macrofibers are therefore true self-organizing micromachines. The magnitude of forces they can generate is currently being measured using special force gauges and instrumentation that will be described in another publication.
The ends of freely growing macrofibers rotate in contrary directions as fibers elongate. If one end of a growing fiber is prevented from rotating the dynamic behavior of the fiber is disrupted and a new set of rules govern the motions that accompany growth. Tethered fibers develop rotation rate gradients along their length; the rate ranges from zero at the tether to a maximum at the other (free) end. The magnitude of maximum rate is governed by the twist state of the fiber and the fiber length. In a fiber whose twist was inferred to be approximately 12.6 turns/mm we observed a maximum tip rotation rate of 430°/min at a fiber length of approximately 10.7 mm. In similar fibers the rotation rate gradient along the fiber shaft was found to be constant at rates in two cases of 25.6°/min. mm. and 36.2°/min. mm. Tethered fibers allowed to make contact with a solid surface that blocked rotation at various distances from the tether developed plectoneme supercoils that migrated over the solid surface toward the tether eventually causing the entire length of the fiber (23 mm) to collapse back to the tether. Similar behavior has been observed in natural populations when fibers become tethered at one end as a result of their attachment to other structures.
Media and growth conditions
The complex medium, TB, consisted of 10 g Bacto Tryptose (Difco), 3 g Bacto Beef Extract (Difco) and 5 g of NaCl per L deionized water. Overnight cultures were grown at 20°C from toothpick transfer of fragmented mature fibers into fresh TB containing 50 mM MgSO4 . For hanging wire experiments the most uniform young and short macrofibers that carried a loop at one end large enough so that a wire could be inserted into it were selected from the populations and transferred into fresh medium of the same composition housed in a plastic chamber. The chamber was fabricated from an 85 × 22 × 45 mm (length, width, height) disposable tissue culture bottle by removing 20 mm of its height. Polyester textile microfilaments, 23 μm in diameter and 1 to 2 mm in length, were used to block terminal loop rotation. They were inserted by hand into a terminal loop and floated on the surface of the growth medium. The macrofibers hung down into the solution. The growth chamber was positioned on a glass plate, illuminated with diffuse fluorescent light from behind, and incubated at 24°C. The experiment involving horizontal growth of a tethered macrofiber near the floor of a growth chamber utilized a glass chamber, 56 × 25 × 13 mm (length, width, height). A 76 μm diameter stainless steel wire (Cal Fine wire) was inserted into the loop at one end of the fiber using a precision motorized micromanipulator (MP-285, Sutter Instrument Co., CA) and lowered to touch the floor of the glass chamber. Initially the opposite end of the fiber was tethered to a 10 μm diameter stainless steel wire designed to act as a force transducer. The transducer was raised above the glass surface to allow its movement in response to supercoiling but the fiber slid off the end of the wire before measurements could be taken. The fiber collapsed down in a supercoil onto the larger wire tether at its other end. The observations described in this paper began after the fiber grew out from cell mass clumped on the large wire tether. The tether remained in place throughout the the experiment.
Video film production and analysis
In the hanging wire experiments images of growth and motions were obtained using a Cohu charge-coupled device camera fitted with a Fujinon TV zoom lens (1/12 175/75 mm) to which Tiffen closeup lenses were added. The video images were written on VHS tape with a JVC time lapse tape deck prior to transfer to a PC via a Matrox frame grabber and Matrox Inspector software (Matrox Graphics, Montreal). Image analysis was done using the Image Pro Plus program (Media Cybernetics). Dual-view images of the macrofiber that grew horizontally above the floor of the growth chamber were captured using two Hitachi (Hitachi Denshi, Ltd.) charge-coupled device cameras fitted to Navitar optical tubes. Both images were sent to a Phase Eight screen splitter (Vicon Industries). The synchronized output was then routed to a GYYR time-lapse tape deck (Odetics). Both images were recorded simultaneously on the same film and a date and time stamp was printed on each frame. All figures were assembled using the Adobe Photoshop program (Adobe Systems). Graphs were constructed using Microsoft Excel (Microsoft Corporation). Curve fitting was done using the Psi Plot program (Poly Software International).
This work was supported by a grant from the National Center for Research Resources, NIH to NHM. D.R. and P.S. were supported by the University of Arizona Undergraduate Biology Research Program. We thank Elissa Reptowitz for help in organizing the video film libraries and providing indices for rapid location of particular sequences, and Michael Wagenheim for processing video film images for internet use.
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