Spinning Tales About the Bacterial Flagellum
However, there are strong reasons to doubt these hypotheses.
First, leading biologists argue that phylogenetic data implies the T3SS could not have been a precursor to the flagellum.34 As New Scientist reported:
One fact in favour of the flagellum-first view is that bacteria would have needed propulsion before they needed T3SSs, which are used to attack cells that evolved later than bacteria. Also, flagella are found in a more diverse range of bacterial species than T3SSs. "The most parsimonious explanation is that the T3SS arose later," says biochemist Howard Ochman at the University of Arizona in Tucson.35Second, the T3SS is composed of only about Â¼ of the proteins in the flagellum, and does not help one account for how the fundamental function of the flagellum--its propulsion system--evolved. The unresolved challenge that the irreducible complexity of the flagellum continues to pose for Darwinian evolution is starkly summarized by William Dembski: "At best the TSS represents one possible step in the indirect Darwinian evolution of the bacterial flagellum. But that still wouldn't constitute a solution to the evolution of the bacterial flagellum. What's needed is a complete evolutionary path and not merely a possible oasis along the way. To claim otherwise is like saying we can travel by foot from Los Angeles to Tokyo because we've discovered the Hawaiian Islands. Evolutionary biology needs to do better than that."36
Dembski's critique is apt because it recognizes that Miller wrongly characterizes irreducible complexity as focusing on the non-functionality of sub-parts. In contrast, Behe properly tests irreducible complexity by assessing the plausibility of the entire functional system to assemble in a step-wise fashion, even if sub-parts can have functions outside of the final system. The "leap" required by going from one functional sub-part to the entire functional system is indicative of the degree of irreducible complexity in a system. Contrary to Miller's assertions, Behe never argued that irreducible complexity mandates that sub-parts can have no function outside of the final system.
Miller misconstrued the proper way of testing irreducible complexity, and his argument amounts to this: if my laptop's power cord could also be used to power my toaster, then my laptop is no longer irreducibly complex. Because a laptop requires a number of parts necessary for function, this is preposterous. So is Dr. Miller's straw method of testing irreducible complexity, as illustrated in the following 2 diagrams:
Figure A: Consider an irreducibly complex functional arch, divided up into many pieces, including s and t:
Figure B: Take away the keystone of the arch, t, and the arch falls down. But piece s may be left standing:
Does the fact that part of the arch, s, remains standing imply that the rest of the arch is not irreducibly complex? Of course not. In the same way, the fact that a fraction of the flagellum helps form a T3SS does not imply that the flagellum itself is not irreducibly complex. To refute irreducible complexity, Dr. Miller would have to show how a fully functional flagellum could form in a step-by-step fashion. He hasn't shown anything close to that.
In contrast, pro-ID microbiologist Scott Minnich has properly tested for irreducible complexity through genetic knock-out experiments he performed in his own laboratory at the University of Idaho. He presented this evidence during the Dover trial, which showed that the bacterial flagellum is irreducibly complex with respect to its complement of thirty-five genes. As Minnich testified: "One mutation, one part knock out, it can't swim. Put that single gene back in we restore motility. Same thing over here. We put, knock out one part, put a good copy of the gene back in, and they can swim. By definition the system is irreducibly complex. We've done that with all 35 components of the flagellum, and we get the same effect."37
Moreover, Scott Minnich explained that even if Miller's speculative scenario turned out to be true, it would not be sufficient to prove a Darwinian explanation for the origin of the flagellum because there is still a huge leap in complexity from a T3SS to a flagellum. Unfortunately, Judge Jones ignored Scott Minnich's research and testimony supporting irreducible complexity of the flagellum, and instead ruled that Miller refuted the irreducible complexity of the flagellum. Ironically, a review article in Nature Reviews Microbiology the following year admitted that "the flagellar research community has scarcely begun to consider how these systems have evolved."38 Did Miller actually demonstrate the flagellum could have evolved by Darwinian evolution?
|G. Truth or Dare: Why does Dr. Miller promote an improper way of testing for irreducible complexity and misconstrue Behe's theories as prohibiting the use of sub-parts in other systems? Has Dr. Miller actually provided anything close to a complete evolutionary pathway for the origin of the flagellum? Has anyone done this? How does Miller's evidence refute Scott Minnich's genetic knockout experiments which show the flagellum is irreducibly complex with respect to its complement of about 35 genes?|
[Editor's Note: Ken Miller speaks regularly on intelligent design (ID), and for years has repeatedly promoted the same misrepresentations of ID when speaking on the topic. This is Part 5 of a series of 7 posts that comprise a lecture guide for those listening to lectures by Dr. Miller against ID. When this series is complete, the entire lecture guide will be released as a single document.]
[33.] Kitzmiller v. Dover ruling, p. 76
[34.] See Milton H. Saier, Jr., "Evolution of Bacterial Type III Protein Secretion Systems," Trends in Microbiology 113:12 (2004).
[35.] Dan Jones, "Uncovering the evolution of the bacterial flagellum," New Scientist (Feb 16, 2008).
[37.] Day 20 PM Testimony, pp. 107-108.
[38.] Pallen & Matzke, "From The Origin of Species to the Origin of Bacterial Flagella," Nat. Revs. Microbiology, Vol. 4:788 (2006).