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MOLECULAR MACHINES:

Experimental Support for the Design Inference

Michael J.=20 Behe

A Series of Eyes

How do we see? In the 19th century the anatomy of the eye was known = in great=20 detail and the sophisticated mechanisms it employs to deliver an = accurate=20 picture of the outside world astounded everyone who was familiar with = them.=20 Scientists of the 19th century correctly observed that if a person were = so=20 unfortunate as to be missing one of the eye's many integrated features, = such as=20 the lens, or iris, or ocular muscles, the inevitable result would be a = severe=20 loss of vision or outright blindness. Thus it was concluded that the eye = could=20 only function if it were nearly intact.

As Charles Darwin was considering possible objections to his theory = of=20 evolution by natural selection in The Origin of Species he = discussed the=20 problem of the eye in a section of the book appropriately entitled = "Organs of=20 Extreme Perfection and Complication." He realized that if in one = generation an=20 organ of the complexity of the eye suddenly appeared, the event would be = tantamount to a miracle. Somehow, for Darwinian evolution to be = believable, the=20 difficulty that the public had in envisioning the gradual formation of = complex=20 organs had to be removed.

Darwin succeeded brilliantly, not by actually describing a real = pathway that=20 evolution might have used in constructing the eye, but rather by = pointing to a=20 variety of animals that were known to have eyes of various = constructions,=20 ranging from a simple light sensitive spot to the complex vertebrate = camera eye,=20 and suggesting that the evolution of the human eye might have involved = similar=20 organs as intermediates.

But the question remains, how do we see? Although Darwin was able to = persuade much of the world that a modern eye could be produced gradually = from a=20 much simpler structure, he did not even attempt to explain how the = simple light=20 sensitive spot that was his starting point actually worked. When = discussing the=20 eye Darwin dismissed the question of its ultimate mechanism (1):

How a nerve comes to be sensitive to light hardly concerns us more = than how=20 life itself originated.

He had an excellent reason for declining to answer the question: = 19th=20 century science had not progressed to the point where the matter could = even be=20 approached. The question of how the eye works--that is, what happens = when a=20 photon of light first impinges on the retina--simply could not be = answered at=20 that time. As a matter of fact, no question about the underlying = mechanism of=20 life could be answered at that time. How do animal muscles cause = movement? How=20 does photosynthesis work? How is energy extracted from food? How does = the body=20 fight infection? Nobody knew.

Calvinism

Now, it appears to be a characteristic of the human mind that when = it is=20 unconstrained by knowledge of the mechanisms of a process, then it seems = easy to=20 imagine simple steps leading from non-function to function. A happy = example of=20 this is seen in the popular comic strip Calvin and Hobbes. Little boy = Calvin is=20 always having adventures in the company of his tiger Hobbes by jumping = in a box=20 and traveling back in time, or grabbing a toy ray gun and = "transmogrifying"=20 himself into various animal shapes, or again using a box as a duplicator = and=20 making copies of himself to deal with worldly powers such as his mom and = his=20 teachers. A small child such as Calvin finds it easy to imagine that a = box just=20 might be able to fly like an airplane (or something), because Calvin = does not=20 know how airplanes work.

A good example from the biological world of complex changes = appearing to be=20 simple is the belief in spontaneous generation. One of the chief = proponents of=20 the theory of spontaneous generation during the middle of the 19th = century was=20 Ernst Haeckel, a great admirer of Darwin and an eager popularizer of = Darwin's=20 theory. From the limited view of cells that 19th century microscopes = provided,=20 Haeckel believed that a cell was a "simple little lump of albuminous = combination=20 of carbon," (2) not much different from a piece of microscopic Jello. = Thus it=20 seemed to Haeckel that such simple life could easily be produced from = inanimate=20 material. In 1859, the year of the publication of The Origin of = Species,=20 an exploratory vessel, H.M.S. Cyclops, dredged up some curious looking = mud from=20 the sea bottom. Eventually Haeckel came to observe the mud and thought = that it=20 closely resembled some cells he had seen under a microscope. Excitedly = he=20 brought this to the attention of Thomas Henry Huxley, Darwin's great = friend and=20 defender. Huxley, too, became convinced that it was Urschleim = (that is,=20 protoplasm), the progenitor of life itself, and Huxley named the mud=20 Bathybius Haeckelii after the eminent proponent of = abiogenesis.

The mud failed to grow. In later years, with the development of new=20 biochemical techniques and improved microscopes, the complexity of the = cell was=20 revealed. The "simple lumps" were shown to contain thousands of = different types=20 of organic molecules, proteins, and nucleic acids, many discrete = subcellular=20 structures, specialized compartments for specialized processes, and an = extremely=20 complicated architecture. Looking back from the perspective of our time, = the=20 episode of Bathybius Haeckelii seems silly or downright embarrassing, = but it=20 shouldn't. Haeckel and Huxley were behaving naturally, like Calvin: = since they=20 were unaware of the complexity of cells, they found it easy to believe = that=20 cells could originate from simple mud.

Throughout history there have been many other examples, similar to = that of=20 Haeckel, Huxley and the cell, where a key piece of a particular = scientific=20 puzzle was beyond the understanding of the age. In science there is even = a=20 whimsical term for a machine or structure or process that does = something, but=20 the actual mechanism by which it accomplishes its task is unknown: it is = called=20 a 'black box.' In Darwin's time all of biology was a black box: not only = the=20 cell, or the eye, or digestion, or immunity, but every biological = structure and=20 function because, ultimately, no one could explain how biological = processes=20 occurred.

Ernst Mayr, the prominent biologist, historian, and guiding force = behind the=20 neo-Darwinian synthesis, has pointed out that (3):

Any scientific revolution has to accept all sorts of black boxes, = for if=20 one had to wait until all black boxes are opened, one would never have = any=20 conceptual advances.

That is true. But in earlier days when black boxes were finally = opened=20 science, and sometimes the whole world, appeared to change. Biology has=20 progressed tremendously due to the model that Darwin put forth. But the = black=20 boxes Darwin accepted are now being opened, and our view of the world is = again=20 being shaken.

Proteins

In order to understand the molecular basis of life it is necessary = to=20 understand how things called "proteins" work. Although most people think = of=20 protein" as something you eat, one of the major food groups, when they = reside in=20 the body of an uneaten animal or plant proteins serve a different = purpose.=20 Proteins are the machinery of living tissue that builds the structures = and=20 carries out the chemical reactions necessary for life. For example, the = first of=20 many steps necessary for the conversion of sugar to biologically-usable = forms of=20 energy is carried out by a protein called hexokinase. Skin is made in = large=20 measure of a protein called collagen. When light impinges on your retina = it=20 interacts first with a protein called rhodopsin. As can be seen even by = this=20 limited number of examples proteins carry out amazingly diverse = functions.=20 However, in general a given protein can perform only one or a few = functions:=20 rhodopsin cannot form skin and collagen cannot interact usefully with = light.=20 Therefore a typical cell contains thousands and thousands of different = types of=20 proteins to perform the many tasks necessary for life, much like a = carpenter's=20 workshop might contain many different kinds of tools for various = carpentry=20 work.

What do these versatile tools look like? The basic structure of = proteins is=20 quite simple: they are formed by hooking together in a chain discrete = subunits=20 called amino acids. Although the protein chain can consist of anywhere = from=20 about 50 to about 1,000 amino acid links, each position can only contain = one of=20 twenty different amino acids. In this way they are much like words: = words can=20 come in various lengths but they are made up from a discrete set of 26 = letters.=20 Now, a protein in a cell does not float around like a floppy chain; = rather, it=20 folds up into a very precise structure which can be quite different for=20 different types of proteins. When all is said and done two different = amino=20 sequences--two different proteins--can be folded to structures as = specific as=20 and different from each other as a three-eighths inch wrench and a = jigsaw. And=20 like the household tools, if the shape of the proteins is significantly = warped=20 then they fail to do their jobs.

The Eyesight of Man

In general, biological processes on the molecular level are = performed by=20 networks of proteins, each member of which carries out a particular task = in a=20 chain.

Let us return to the question, how do we see? Although to Darwin the = primary=20 event of vision was a black box, through the efforts of many biochemists = an=20 answer to the question of sight is at hand. (4) When light strikes the = retina a=20 photon is absorbed by an organic molecule called 11-cis-retinal, = causing=20 it to rearrange within picoseconds to trans-retinal. The change = in shape=20 of retinal forces a corresponding change in shape of the protein, = rhodopsin, to=20 which it is tightly bound. As a consequence of the protein's = metamorphosis, the=20 behavior of the protein changes in a very specific way. The altered = protein can=20 now interact with another protein called transducin. Before associating = with=20 rhodopsin, transducin is tightly bound to a small organic molecule = called GDP,=20 but when it binds to rhodopsin the GDP dissociates itself from = transducin and a=20 molecule called GTP, which is closely related to, but critically = different from,=20 GDP, binds to transducin.

The exchange of GTP for GDP in the transducinrhodopsin complex = alters its=20 behavior. GTP-transducinrhodopsin binds to a protein called = phosphodiesterase,=20 located in the inner membrane of the cell. When bound by rhodopsin and = its=20 entourage, the phosphodiesterase acquires the ability to chemically = cleave a=20 molecule called cGMP. Initially there are a lot of cGMP molecules in the = cell,=20 but the action of the phosphodiesterase lowers the concentration of = cGMP.=20 Activating the phosphodiesterase can be likened to pulling the plug in a = bathtub, lowering the level of water.

A second membrane protein which binds cGMP, called an ion channel, = can be=20 thought of as a special gateway regulating the number of sodium ions in = the=20 cell. The ion channel normally allows sodium ions to flow into the cell, = while a=20 separate protein actively pumps them out again. The dual action of the = ion=20 channel and pump proteins keeps the level of sodium ions in the cell = within a=20 narrow range. When the concentration of cGMP is reduced from its normal = value=20 through cleavage by the phosphodiesterase, many channels close, = resulting in a=20 reduced cellular concentration of positively charged sodium ions. This = causes an=20 imbalance of charges across the cell membrane which, finally, causes a = current=20 to be transmitted down the optic nerve to the brain: the result, when=20 interpreted by the brain, is vision.

If the biochemistry of vision were limited to the reactions listed = above,=20 the cell would quickly deplete its supply of 11-cis-retinal and = cGMP=20 while also becoming depleted of sodium ions. Thus a system is required = to limit=20 the signal that is generated and restore the cell to its original state; = there=20 are several mechanisms which do this. Normally, in the dark, the ion = channel, in=20 addition to sodium ions, also allows calcium ions to enter the cell; = calcium is=20 pumped back out by a different protein in order to maintain a constant=20 intracellular calcium concentration. However, when cGMP levels fall, = shutting=20 down the ion channel and decreasing the sodium ion concentration, = calcium ion=20 concentration is also decreased. The phosphodiesterase enzyme, which = destroys=20 cGMP, is greatly slowed down at lower calcium concentration. = Additionally, a=20 protein called guanylate cyclase begins to resynthesize cGMP when = calcium levels=20 start to fall. Meanwhile, while all of this is going on, metarhodopsin = II is=20 chemically modified by an enzyme called rhodopsin kinase, which places a = phosphate group on its substrate. The modified rhodopsin is then bound = by a=20 protein dubbed arrestin, which prevents the rhodopsin from further = activating=20 transducin. Thus the cell contains mechanisms to limit the amplified = signal=20 started by a single photon.

Trans-retinal eventually falls off of the rhodopsin molecule = and must=20 be reconverted to 11-cis-retinal and again bound by opsin to = regenerate=20 rhodopsin for another visual cycle. To accomplish this = trans-retinal is=20 first chemically modified by an enzyme to transretinol, a form = containing two=20 more hydrogen atoms. A second enzyme then isomerizes the molecule to=20 11-cis-retinol. Finally, a third enzyme removes the = previouslyadded=20 hydrogen atoms to form 11-cis-retinal, and the cycle is complete.

To Explain Life

Although many details of the biochemistry of vision have not been = cited=20 here, the overview just seven is meant to demonstrate that, ultimately, = this=20 is what it means to 'explain' vision. This is the level of = explanation that=20 Biological science eventually must aim for. In order to say that some = function=20 is understood, every relevant step in the process must be elucidated. = The=20 relevant steps in biological processes occur ultimately at the molecular = level,=20 so a satisfactory explanation of a biological phenomenon such as sight, = or=20 digestion, or immunity, must include a molecular explanation. It is no = longer=20 sufficient, now that the black box of vision has been opened, for an=20 'evolutionary explanation' of that power to invoke only the anatomical=20 structures of whole eyes, as Darwin did in the 19th century and as most=20 popularizers of evolution continue to do today. Anatomy is, quite = simply,=20 irrelevant. So is the fossil record. It does not matter whether or not = the=20 fossil record is consistent with evolutionary theory, any more than it = mattered=20 in physics that Newton's theory was consistent with everyday experience. = The=20 fossil record has nothing to tell us about, say, whether or how the = interactions=20 of 11-cis-retinal with rhodopsin, transducin, and = phosphodiesterase could=20 have developed stepby-step. Neither do the patterns of biogeography = matter, or=20 of population genetics, or the explanations that evolutionary theory has = given=20 for rudimentary organs or species abundance.

"How a nerve comes to be sensitive to light hardly concerns us more = than how=20 life itself originated," said Darwin in the 19th century. But both = phenomena=20 have attracted the interest of modern biochemistry. The story of the = slow=20 paralysis of research on life's origin is quite interesting, but space = precludes=20 its retelling here. Suffice it to say that at present the field of = originoflife=20 studies has dissolved into a cacophony of conflicting models, each = unconvincing,=20 seriously incomplete, and incompatible with competing models. In private = even=20 most evolutionary biologists will admit that science has no explanation = for the=20 beginning of life. (5)

The purpose of this paper is to show that the same problems which = beset=20 origin-of-life research also bedevil efforts to show how virtually any = complex=20 biochemical system came about. Biochemistry has revealed a molecular = world which=20 stoutly resists explanation by the same theory that has long been = applied at the=20 level of the whole organism. Neither of Darwin's black boxes--the origin = of life=20 or the origin of vision or other complex biochemical systems--has been = accounted=20 for by his theory.

Irreducible Complexity

In The Origin of Species Darwin stated (6):

If it could be demonstrated that any complex organ existed which = could not=20 possibly have been formed by numerous, successive, slight = modifications, my=20 theory would absolutely break down.

A system which meets Darwin's criterion is one which exhibits = irreducible=20 complexity. By irreducible complexity I mean a single system which = is=20 composed of several interacting parts that contribute to the basic = function, and=20 where the removal of any one of the parts causes the system to = effectively cease=20 functioning. An irreducibly complex system cannot be produced gradually = by=20 slight, successive modifications of a precursor system, since any = precursor to=20 an irreducibly complex system is by definition nonfunctional. Since = natural=20 selection requires a function to select, an irreducibly complex = biological=20 system, if there is such a thing, would have to arise as an integrated = unit for=20 natural selection to have anything to act on. It is almost universally = conceded=20 that such a sudden event would be irreconcilable with the gradualism = Darwin=20 envisioned. At this point, however, 'irreducibly complex' is just a = term, whose=20 power resides mostly in its definition. We must now ask if any real = thing is in=20 fact irreducibly complex, and, if so, then are any irreducibly complex = things=20 also biological systems.

Consider the humble mousetrap (Figure 1). The mousetraps that my = family uses=20 in our home to deal with unwelcome rodents consist of a number of parts. = There=20 are: (1) a flat wooden platform to act as a base; (2) a metal hammer, = which does=20 the actual job of crushing the little mouse; (3) a wire spring with = extended=20 ends to press against the platform and the hammer when the trap is = charged; (4)=20 a sensitive catch which releases when slight pressure is applied; and = (5) a=20 metal bar which holds the hammer back when the trap is charged and = connects to=20 the catch. There are also assorted staples and screws to hold the system = together.

Figure 1. A household mousetrap. The working parts of the trap = are=20 labeled. If any of the parts are missing the trap does not = function.

If any one of the components of the mousetrap (the base, hammer, = spring,=20 catch, or holding bar) is removed, then the trap does not function. In = other=20 words, the simple little mousetrap has no ability to trap a mouse until = several=20 separate parts are all assembled.

Because the mousetrap is necessarily composed of several parts, it = is=20 irreducibly complex. Thus, irreducibly complex systems exist.

Molecular Machines

Now, are any biochemical systems irreducibly complex? Yes, it turns = out that=20 many are.

Earlier we discussed proteins. In many biological structures = proteins are=20 simply components of larger molecular machines. Like the picture tube, = wires,=20 metal bolts and screws that comprise a television set, many proteins are = part of=20 structures that only function when virtually all of the components have = been=20 assembled. A good example of this is a cilium. (7) Cilia are hairlike = organelles=20 on the surfaces of many animal and lower plant cells that serve to move = fluid=20 over the cell's surface or to "row" single cells through a fluid. In = humans, for=20 example, epithelial cells lining the respiratory tract each have about = 200 cilia=20 that beat in synchrony to sweep mucus towards the throat for = elimination. A=20 cilium consists of a membrane-coated bundle of fibers called an axoneme. = An=20 axoneme contains a ring of 9 double microtubules surrounding two central = single=20 microtubules. Each outer doublet consists of a ring of 13 filaments = (subfiber A)=20 fused to an assembly of 10 filaments (subfiber B). The filaments of the=20 microtubules are composed of two proteins called alpha and beta tubulin. = The 11=20 microtubules forming an axoneme are held together by three types of = connectors:=20 subfibers A are joined to the central microtubules by radial spokes; = adjacent=20 outer doublets are joined by linkers that consist of a highly elastic = protein=20 called nexin; and the central microtubules are joined by a connecting = bridge.=20 Finally, every subfiber A bears two arms, an inner arm and an outer arm, = both=20 containing the protein dynein.

But how does a cilium work? Experiments have indicated that ciliary = motion=20 results from the chemically-powered "walking" of the dynein arms on one=20 microtubule up the neighboring subfiber B of a second microtubule so = that the=20 two microtubules slide past each other (Figure 2). However, the protein=20 cross-links between microtubules in an intact cilium prevent neighboring = microtubules from sliding past each other by more than a short distance. = These=20 cross-links, therefore, convert the dynein-induced sliding motion to a = bending=20 motion of the entire axoneme.

Figure 2. Schematic drawing of part of a cilium. The power = stroke of=20 the motor protein, dynein, attached to one microtubule, against subfiber = B of a=20 neighboring microtubule causes the fibers to slide past each other. The = flexible=20 linker protein, nexin, converts the sliding motion to a bending = motion.

Now, let us sit back, review the workings of the cilium, and = consider what=20 it implies. Cilia are composed of at least a half dozen proteins: = alpha-tubulin,=20 beta-tubulin, dynein, nexin, spoke protein, and a central bridge = protein. These=20 combine to perform one task, ciliary motion, and all of these proteins = must be=20 present for the cilium to function. If the tubulins are absent, then = there are=20 no filaments to slide; if the dynein is missing, then the cilium remains = rigid=20 and motionless; if nexin or the other connecting proteins are missing, = then the=20 axoneme falls apart when the filaments slide.

What we see in the cilium, then, is not just profound complexity, = but also=20 irreducible complexity on the molecular scale. Recall that by = "irreducible=20 complexity" we mean an apparatus that requires several distinct = components for=20 the whole to work. My mousetrap must have a base, hammer, spring, = catch,=20 and holding bar, all working together, in order to function. Similarly, = the=20 cilium, as it is constituted, must have the sliding filaments, = connecting=20 proteins, and motor proteins for function to occur. In the absence of = any one of=20 those components, the apparatus is useless.

The components of cilia are single molecules. This means that there = are no=20 more black boxes to invoke; the complexity of the cilium is final, = fundamental.=20 And just as scientists, when they began to learn the complexities of the = cell,=20 realized how silly it was to think that life arose spontaneously in a = single=20 step or a few steps from ocean mud, so too we now realize that the = complex=20 cilium can not be reached in a single step or a few steps. But since the = complexity of the cilium is irreducible, then it can not have functional = precursors. Since the irreducibly complex cilium can not have functional = precursors it can not be produced by natural selection, which requires a = continuum of function to work. Natural selection is powerless when there = is no=20 function to select. We can go further and say that, if the cilium can = not be=20 produced by natural selection, then the cilium was designed.

The Study of "Molecular Evolution"

Other examples of irreducible complexity abound, including aspects = of=20 protein transport, blood clotting, closed circular DNA, electron = transport, the=20 bacterial flagellum, telomeres, photosynthesis, transcription = regulation, and=20 much more. Examples of irreducible complexity can be found on virtually = every=20 page of a biochemistry textbook. But if these things cannot be explained = by=20 Darvvinian evolution, how has the scientific community regarded these = phenomena=20 of the past forty years? A good place to look for an answer to that = question is=20 in the Journal of Molecular Evolution. JME is a journal = that was=20 begun specifically to deal with the topic of how evolution occurs on the = molecular level. It has high scientific standards, and is edited by = prominent=20 figures in the field. In a recent issue of JME there were = published=20 eleven articles; of these, all eleven were concerned simply with the = analysis of=20 protein or DNA sequences. None of the papers discussed detailed models = for=20 intermediates in the development of complex biomolecular structures. In = the past=20 ten years JME has published 886 papers. Of these, 95 discussed = the=20 chemical synthesis of molecules thought to be necessary for the origin = of life,=20 44 proposed mathematical models to improve sequence analysis, 20 = concerned the=20 evolutionary implications of current structures, and 719 were analyses = of=20 protein or polynucleotide sequences. There were zero papers discussing = detailed=20 models for intermediates in the development of complex biomolecular = structures.=20 This is not a peculiarity of JME. No papers are to be found that = discuss=20 detailed models for intermediates in the development of complex = biomolecular=20 structures in the Proceedings of the National Academy of Science, = Nature,=20 Science, the Journal of Molecular Biology or, to my = knowledge, any=20 journal whatsoever.

Sequence comparisons overwhelmingly dominate the literature of = molecular=20 evolution. But sequence comparisons simply can't account for the = development of=20 complex biochemical systems any more than Darwin's comparison of simple = and=20 complex eyes told him how vision worked. Thus in this area science is = mute. This=20 means that when we infer that complex biochemical systems were designed, = we are=20 contradicting no experimental result, we are in conflict with no = theoretical=20 study. No experiments needs to be questioned, but the interpretation of = all=20 experiments must now be reexamined, just as the results of experiments = that were=20 consistent with a Newtonian view of the universe had to be reinterpreted = when=20 the waveparticle duality of matter was discerned.

Conclusion

It is often said that science must avoid any conclusions which smack = of the=20 supernatural. But this seems to me to be both bad logic and bad science. = Science=20 is not a game in which arbitrary rules are used to decide what = explanations are=20 to be permitted. Rather, it is an effort to make true statements about = physical=20 reality. It was only about sixty years ago that the expansion of the = universe=20 was first observed. This fact immediately suggested a singular = event--that at=20 some time in the distant past the universe began expanding from an = extremely=20 small size. To many people this inference was loaded with overtones of a = supernatural event--the creation, the beginning of the universe. The = prominent=20 physicist A.S. Eddington probably spoke for many physicists in voicing = his=20 disgust with such a notion (8):

Philosophically, the notion of an abrupt beginning to the present = order of=20 Nature is repugnant to me, as I think it must be to most; and even = those who=20 would welcome a proof of the intervention of a Creator will probably = consider=20 that a single winding-up at some remote epoch is not really the kind = of=20 relation between God and his world that brings satisfaction to the = mind.=20

Nonetheless, the Big Bang hypothesis was embraced by physics and = over the=20 years has proven to be a very fruitful paradigm. The point here is that = physics=20 followed the data where it seemed to lead, even though some thought the = model=20 gave aid and comfort to religion. In the present day, as biochemistry = multiplies=20 examples of fantastically complex molecular systems, systems which = discourage=20 even an attempt to explain how they may have arisen, we should take a = lesson=20 from physics. The conclusion of design flows naturally from the data; we = should=20 not shrink from it; we should embrace it and build on it.

In concluding, it is important to realize that we are not inferring = design=20 from what we do not know, but from what we do know. We are not inferring = design=20 to account for a black box, but to account for an open box. A man from a = primitive culture who sees an automobile might guess that it was powered = by the=20 wind or by an antelope hidden under the car, but when he opens up the = hood and=20 sees the engine he immediately realizes that it was designed. In the = same way=20 biochemistry has opened up the cell to examine what makes it run and we = see that=20 it, too, was designed.

It was a shock to people of the nineteenth century when they = discovered,=20 from observations science had made, that many features of the biological = world=20 could be ascribed to the elegant principle of natural selection. It is a = shock=20 to us in the twentieth century to discover, from observations science = has made,=20 that the fundamental mechanisms of life cannot be ascribed to natural = selection,=20 and therefore were designed. But we must deal with our shock as best we = can and=20 go on. The theory of undirected evolution is already dead, but the work = of=20 science continues.

This paper was originally presented in the Summer of 1994 at the meeting = ofthe=20 C.S. Lewis Society, Cambridge University.

REFERENCES:

(1) Darwin, Charles (1872) Origin of Species 6th ed (1988), = p.151, New=20 York University Press, New York.

(2) Farley, John (1979) The=20 Spontaneous Generation Controversy from Descartes to Oparin, 2nd ed, = p.73,=20 The Johns Hopkins University Press, Baltimore.

(3) Mayr, Ernst = (1991)=20 One Long Argument, p. 146, Harvard University Press,=20 Cambridge.

(4) Devlin, Thomas M. (1992) Textbook of = Biochemistry,=20 pp.938954, WileyLiss, New York.

(5) University of Washington = rhetorician=20 John Angus Campbell has observed that "huge edifices of ideas such as = positivism=20 never really die. Thinking people gradually abandon them and even = ridicule them=20 among themselves, but keep the persuasively useful parts to scare away = the=20 uninformed." "The Comic Frame and the Rhetoric of Science: Epistemology = and=20 Ethics in Darwin's Origin," Rhetoric Society Quarterly 24, = pp.2750=20 (1994). This certainly applies to the way the scientific community = handles=20 questions on the origin of life.

(6) Darwin, p.154.

(7) = Voet, D.=20 & Voet, J.G. (1990) Biochemistry, pp.11321139, John Wiley = & Sons,=20 New York.

(8) Cited in Jaki, Stanley L. (1980) Cosmos and = Creator,=20 pp.56, Gateway Editions, Chicago.

Mike Behe received a Bachelor of Science degree in Chemistry from Drexel = University in 1974 and the Ph.D. in Biochemistry from the University of=20 Pennsylvania in 1978.

After doing postdoctoral work at the = National=20 institutes of Health he became assistant professor of Chemistry at the = City=20 University of New York/Queens College.

In 1985 he moved to Lehigh = University in Bethlehem, PA, where he is currently Associate Professor = in the=20 Department of Biological Sciences.

Mike is married to the former = Celeste=20 LaTassa. They are members of St. Theresa Parish in Hellertown, PA, where = they=20 are raising their six children: Grace, age 10; Benedict, 9; Clare, 7; = Leo, 5;=20 Rose, 3; and Vincent, 1.

Look for Dr. Behe's new book published by the Free Press, Darwin's = Black Box:=20 The Biochemical Challenge to Evolution.

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