Hominids started using primitive stone tools millions of years ago. The earliest stone tools were little more than a fractured rock, but approximately 75, years ago,  pressure flaking provided a way to make much finer work. Control of fire by early humans The discovery and utilization of firea simple energy source with many profound uses, was a turning point in the technological evolution of humankind. As the Paleolithic era progressed, dwellings became more sophisticated and more elaborate; as early as ka, humans were constructing temporary wood huts.
For a typical small molecule e. Bacteria that do induce currents for their benefit e. Another postulated function of primitive motility, swimming for the sake of running into more molecules, also does not work: Thus, if diffusion of molecules into the cell is the only matter of concern, a bacterium will do just as well by sitting still as it will by stirring or swimming.
The reason bacteria swim is not to increase diffusion but to find locations with a higher local concentration of nutrient molecules Purcell, ; Berg, ; Vogel, However, a typical value for a is 0. Thus, fundamental physical considerations make the hypothesized stirring filament an unlikely intermediate.
Similarly, Rizzotti implies that the F0-c subunit Crabb theory critique essay example homologous with the flagellar motor proteins MotAB, but sequence homology has instead been discovered homology between MotAB and a phylogenetically widespread family of proteins that couple protonmotive force to diverse membrane transport processes.
The homologies could be explained by invoking additional independent cooption events, but this would require a rather more complex scenario than that presented by Rizzotti. Therefore several of the ideas proposed here have been previously raised in informal debates about flagellar evolution.
Millerand Musgrave review this aspect of the debate in detail, and Musgrave proposes a model that is similar in outline to that presented here, although his account is more general.
Phylogenetic context and assumed starting organism The paradigm for prokaryote phylogeny, if there is one, is the universal rRNA tree. This shows a number of widely separated bacterial lineages, with archaea and eukaryotes separated from them all by a very long branch. This tree is unrooted, and many possible rootings have been proposed in the literature.
As these are the most remote and difficult phylogenetic events it is possible to study, and as there is by definition no outgroup to life in general, the debate can be expected to continue for some time. For current purposes the most important point is that flagella are widespread across the bacterial phylogenetic tree, with losses in various taxa and no clearly primitive nonflagellate taxa.
It is therefore assumed that flagella evolved near the base of the bacterial tree. Rizzotti and others e. However, the very general consideration that most of the bacterial phyla are gram negative, including the many different taxa that come out as basal on different analyses, weighs against this hypothesis.
Therefore, we shall side with Cavalier-Smith, who argues that the last common ancestor was gram-negative. He has put forward the most detailed model for the origin of bacteria and the double membrane Cavalier-Smith, a, a. The model thus begins with a generic double-membraned, gram-negative bacterium.
The present model will begin with a reasonably complex bacterium, already possessing the general secretory pathway and type II secretion system, as well as signal transduction, a peptidoglycan cell wall, and F1F0-ATP synthetase.
Cavalier-Smith a hypothesizes that chlorobacteria may be the most basal offshoot of the tree and be primitively nonflagellate. An export system plus a mechanism to cross the outer membrane forms a secretion system. Bacteria make use of a number of distinct secretion systems, reviewed as a group elsewhere Hueck, ; Thanassi and Hultgren, a; van Wely et al.
Six major well-characterized secretion systems Figure 4aFigure 5 are reviewed by Thanassi and Hultgren a. It is likely that systems will be added to the list in time. Systems with components homologous to flagellar components. For components with well-documented homology to flagellar components, the name according to the unified nomenclature for type III secretion systems proposed by Hueck is given Sct: Secretion and Cellular Translocation first, followed by the currently accepted name for the Hrp protein.
The name of the flagellar homolog is shown in brackets.
Further possible homologies are discussed in the text. Various secretion systems of prokaryotes. Based on several sources Jarrell et al. Another nucleotide may be substituted for ATP in some cases.
See Table 4 for description of the functions of the systems.Abstract: The bacterial flagellum is a complex molecular system with multiple components required for functional motility. Such systems are sometimes proposed as puzzles for evolutionary theory on the assumption that selection would have no function to act on until all components are in place.
possible worlds and other essays by j. b. s. haldane sir william dunn reader in biochemistry. in the university of cambridge. Medical Dark Ages Quotes. By Wade Frazier.
Revised in July Introduction. Section 1. Section 2. Section 3. Section 4. Section 5. Section 6.
Section 7. Preface. The opportunity to write this manuscript came chiefly as the result of two extended speaking engagements. The bulk of the material was written to complement the Spring Lectureship which I presented at Western (Conservative Baptist) Seminary in Portland, Oregon.
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