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H00102--00A, Front mat Genesis

Page 38

by Charles Baum


  formed deep in the crust. Samples are widely available commercially, but the

  outcrops occur on the San Carlos Indian reservation, so access and collect-

  ing is restricted.

  p. 126

  100 parts per million carbon: Keppler et al. (2003) disagree

  with this claim for San Carlos olivine. Their experiments on olivine growth

  under carbon-saturated conditions produced crystals with no more than 0.5

  part per million carbon.

  p. 126

  “I ran a sample . . .”: [George R. Rossman to Anne M.

  Hofmeister, 20 December 2002] Many mineralogists and solid-state chem-

  272

  GENESIS

  ists discount Freund’s findings as experimental artifacts resulting from sur-

  face contamination. See, for example, Keppler et al. (2003) and M. Wilson

  (2003).

  p. 127

  no single dominant source: A few authors imply that it re-

  mains a mystery which of several sources of organic molecules—Miller-type

  surface synthesis, hydrothermal processes, impacts, or deep-space synthe-

  sis—was dominant. Orgel (1998a, p. 491), for example, states: “Three popu-

  lar hypotheses attempt to explain the origin of prebiotic molecules: synthesis

  in a reducing atmosphere, input in meteorites and synthesis on metal sul-

  fides in deep-sea vents. It is not possible to decide which is correct.” Simi-

  larly, Miller and his colleagues have at times discounted both hydrothermal

  zones and extraterrestrial sources as trivial (S. L. Miller and Bada 1988;

  Stanley Miller and Jeffrey Bada as quoted in Radetsky 1992, 1998). Other

  more ecumenical estimations of multiple organic sources include Chyba and

  Sagan (1992) and Lahav (1999).

  INTERLUDE—

  MYTHOS VERSUS LOGOS

  p. 129

  “People of the past . . .”: Armstrong (2000, p. xiii). She contin-

  ues, “Myth looked back to the origins of life, to the foundations of culture,

  and to the deepest levels of the human mind. Myth was not concerned with

  practical matters, but with meaning.” By contrast, “Logos was the rational, pragmatic, and scientific thought.” Armstrong argues, “People of Europe and

  America [have] achieved such astonishing success in science and technology

  that they began to think that logos was the only means to truth and began to discount mythos as false and superstitious.”

  p. 129

  “Whoa, . . .”: [Margaret H. Hazen to RMH, 30 May 2004]

  10

  THE MACROMOLECULES OF LIFE

  p. 133

  “To purify . . .”: Lehninger et al. (1993, p. 5).

  p. 133

  One of the transforming discoveries: Lehninger et al. (1993).

  The extraordinary Web site http://biocyc.org/ECOO157/new-image?object=

  Compounds tabulates all known small organic molecules from the microbe

  Escherichia coli.

  p. 134

  “I can no longer . . .”: Friedrich Wöhler to his teacher Jacob

  Berzelius, February 28, 1828. This discovery (Wöhler 1828) was made in the

  same year that Wöhler isolated and named the element beryllium.

  p. 134

  Four key types of molecules: For an overview of the character-

  NOTES

  273

  istics of sugars, amino acids, carbohydrates, and nucleic acids, see Lehninger

  et al. (1993).

  p. 135

  Sugars are the basic building blocks: Estimates of Earth’s total

  biomass place cellulose, the abundant glucose polymer that forms leaves,

  stems, trunks, and other plant support structures, at the top of the list

  (Lehninger et al. 1993, pp. 298 et seq).

  p. 135

  For every useful molecule: Of the several proposed prebiotic

  mechanisms for biomolecular synthesis, Miller’s original spark experiments

  produce perhaps the highest percentage of useful molecules. Fully 6 percent

  of the carbon atoms introduced as CH in some of his experiments were

  4

  incorporated into amino acids, for example (S. L. Miller and Urey 1959a).

  For this reason alone, Miller and his supporters often argue that electric

  discharge in a reducing atmosphere is the most likely origin scenario.

  p. 136

  life is even choosier: See, for example, Bonner (1995). The

  problem of chiral selection is discussed in more detail in Chapter 13.

  p. 136

  molecular phylogeny: See, for example, Pace (1997), Pennisi

  (1998), and Sogin et al. (1999).

  p. 137

  The Canterbury Tales: Barbrook et al. (1998). Similar tech-

  niques of textual comparison have long been employed for shorter manu-

  scripts, but this study used the same computer algorithms as applied to

  genomic data.

  p. 138

  Carl Woese: The original proposal for three domains of life,

  including the Archaea, appears in Woese and Fox (1977). See also Woese

  (1978, 1987, 2000, 2002). A biographical sketch of Carl Woese, including an

  overview of his work, is provided by Morell (1997).

  p. 139

  thrive at elevated temperature: Perspectives on the proposi-

  tion that the last common ancestor was an extremophile are provided, for

  example, by Gogarten-Boekels et al. (1995), Forterre (1996), and Reysenbach

  et al. (1999).

  Bruce Runnegar writes, “There is a last common ancestor and it was a

  highly derived organism. It tells us very little about Earth’s earliest cells in

  the same way that living birds do not reveal the attributes of dinosaurs.” [B.

  Runnegar to RMH, 4 March 2005]

  p. 141

  swap sections of DNA: Gogarten et al. (1999), Doolittle (2000),

  and Woese (2002).

  p. 141

  “last common ancestor”: See, for example, Woese (1998) and

  Ellington (1999). An important conclusion of recent studies is that, because

  of gene transfer, there is no single last common cellular ancestor. Woese

  (1998, p. 6854) writes: “The universal ancestor is not a discrete entity. It is,

  rather, a diverse community of cells that survives as a biological unit. The

  universal ancestor has a physical history but not a genealogical one.”

  p. 141

  all cells employ RNA: Woese (2002).

  274

  GENESIS

  p. 141

  simple metabolic strategy: Woese (1998, p. 6855) states that

  the biochemical repertoire of the universal ancestor included “a complete

  tricarboxylic acid cycle, polysaccharide metabolism, both sulfur oxidation

  and reduction, and nitrogen fixation.” Pace (1997, p. 734) comments that

  “the earliest life was based on inorganic nutrition.”

  p. 142

  primordial “oil slick”: Lasaga et al. (1971). See also Morowitz

  (1992).

  11

  ISOLATION

  p. 143

  “The self-assembly process . . .”: Deamer (2003, p. 21).

  p. 143

  Lipid molecules: For an accessible overview of lipid molecules

  and their spontaneous organization into bilayers, see Tanford (1978) and

  Segré et al. (2001).

  p. 144

  Alec Bangham: See, for example, Bangham et al. (1965). Some

  researchers initially called these structures “banghasomes.” [Harold Morowitz

  to RMH, 10 August 2004]

  p. 144


  Luisi and co-workers: Luisi (1989, 2004), Luisi and Varela

  (1989), Luisi et al. (1994), Bachmann et al. (1992), and Szostak et al. (2001).

  See also Segré et al. (2001).

  p. 145

  counted as classics: Pasteur (1848), Miller (1953), and

  Bernstein et al. (1999b).

  p. 146

  Deamer returned: Deamer and Pashley (1989). For additional

  information, see Zimmer (1993) and Deamer and Fleischaker (1994).

  p. 146

  Murchison meteorite: For a description of the Murchison me-

  teorite and related research, see Grady (2000, pp. 350-352).

  p. 147

  Their straightforward procedure: The eclectic mix of organic

  molecules in Murchison included some species, like amino acids, that were

  soluble in water; some, like lipids, that were soluble in chloroform or other

  organic solvents; and a complex tarry residue, called by the generic name

  “kerogen,” which is difficult to analyze. Recent studies by Cody et al. (2001a)

  suggest that this residue consists of a complexly linked mass of rings, chains,

  and other smaller groups of atoms. It is not evident that such insoluble mat-

  ter could have played much of a role in prebiotic chemistry.

  p. 148

  breakthrough moment: The discovery paper by Deamer and

  Pashley (1989) was entitled “Amphiphilic components of the Murchison car-

  bonaceous chondrite: Surface properties and membrane formation.” In this

  article they state, “If amphiphilic substances derived from meteoric infall

  and chemical evolution were available on the prebiotic earth following con-

  densation of oceans, it follows that surface films would have been present at

  air-water interfaces. . . . This material would thereby be concentrated for

  NOTES

  275

  self-assembly into boundary structures with barrier properties relevant to

  function as early membranes.”(p. 37) This paper was especially noteworthy

  because it followed by a year the publication of a theoretical paper by

  Morowitz et al. (1988) that proposed such an origin scenario.

  p. 148

  NASA Ames team: Dworkin et al. (2001).

  p. 149

  a colorful photograph: The Washington Post (Kathy Sawyer,

  “IN SPACE; CLUES TO THE SEEDS OF LIFE,” January 30, 2001, p. A1).

  p. 149

  astrobiology meetings: The First Astrobiology Science Con-

  ference was held April 3–5, 2000, at the NASA Ames Research Center, Moffett

  Field, California. Deamer’s lecture was entitled “Self-assembled Vesicles of

  Monocarboxylic Acids and Alcohols: A Model Membrane System for Early

  Cellular Life” (Apel et al. 2000).

  p. 151

  we had made bilayer membranes: These results were reported

  at the 221st Annual Meeting of the American Chemical Society, held in San

  Diego, California, April 1-5, 2001.

  p. 151

  Recent work: Knauth (1998) provides estimates of higher sa-

  linity in the Archean ocean. Salt inhibition of amphiphile self-organization

  is reported in Monnard et al. (2002).

  p. 152

  atmospheric aerosols: Dobson et al. (2000). See also Ellison et

  al. (1999), Tuck (2002), and Donaldson et al. (2004). These studies, which

  present theoretical analyses of aerosol dynamics and atmospheric residence

  times, build on earlier speculative comments regarding the possible roles of

  aerosols by Woese (1978) and Lerman (1986, 1994a, 1994b, 1996). Regard-

  ing Lerman’s contributions, James Ferris writes: “Unfortunately a head in-

  jury in an automobile accident had a major effect on his life and he was

  unable to get a full paper written on this proposal. He discussed this pro-

  posal at meetings and it was well known in the origins of life community.”

  [James Ferris to RMH, 22 August 2004].

  12

  MINERALS TO THE RESCUE

  p. 155

  “But I happen to know . . .” : Updike (1986, pp. 328-329).

  p. 155

  The first living entity: Portions of this chapter were adapted

  from Hazen (2001).

  p. 156

  Mineralogist Joseph V. Smith: J. V. Smith (1998), Parsons et al.

  (1998), and J. V. Smith et al. (1999). Other authors, including Cairns-Smith

  et al. (1992), have also proposed that porous minerals might have provided a

  measure of protection for proto-life.

  p. 157

  a primitive slick: The oil-slick hypothesis was championed by

  Morowitz (1992) in his influential book The Beginnings of Cellular Life: Me-

  tabolism Recapitulates Biogenesis. See also Lasaga et al. (1971), who estimated

  276

  GENESIS

  that a primordial oil slick on the Archean ocean could have achieved a thick-

  ness of 1 to 10 meters.

  p. 157

  British biophysicist John Desmond Bernal: Bernal (1949,

  1951). The Swiss-born geochemist Victor Goldschmidt also suggested that

  minerals played a role in life’s origin, but his thoughts, presented as a lecture

  in 1945 and published posthumously (Goldschmidt 1952), had little impact

  on the origins community (Lahav 1999, p. 250).

  p. 157

  In a 1978 study: Lahav et al. (1978). See also Lahav and Chang

  (1976) and Lahav (1994).

  p. 157

  NASA-sponsored teams: Among the chemists who have stud-

  ied roles of clays and other fine-grained minerals in prebiotic processes, two

  NASA Specialized Center of Research and Training (NSCORT) groups at

  Scripps Institution of Oceanography (La Jolla, California) and Rensselaer

  Polytechnic Institute (Troy, New York) have made notable contributions.

  p. 157

  James Ferris: Reports by Ferris and colleagues on mineral-in-

  duced polymerization of RNA, principally by the common clay montmoril-

  lonite and the phosphate hydroxyapatite, include Ferris (1993, 1999), Holm

  et al. (1993), Ferris and Ertem (1992, 1993), Ferris et al. (1996), and Ertem

  and Ferris (1996, 1997). Images of organic molecules on ideally smooth min-

  eral surfaces have been published, for example, by Sowerby et al. (1996) and

  Uchihashi et al. (1999).

  p. 157

  “activated” RNA: Ferris writes: “My experiments work only if

  activated nucleotides are reacted. The thermodynamics is against self-con-

  densation of nucleotides to form the phosphodiester bond in aqueous solu-

  tion. That’s why nature uses ATP in place of AMP to form RNA. By the way,

  ATP and ADP do not work in the clay catalyzed reaction so we use the imi-

  dazole activating group that was introduced first by other workers and popu-

  larized by Lohrmann and Orgel.” [James Ferris to RMH, 22 August 2004]

  p. 158

  Leslie Orgel: Experiments on polypeptide formation are de-

  scribed in Ferris et al. (1996), Hill et al. (1998), and Liu and Orgel (1998).

  p. 158

  “polymerization on the rocks”: Orgel (1998b). See also

  Acevedo and Orgel (1986).

  p. 158

  One possible answer: Chen et al. (2004). Subsequent work by

  Szostak’s group reveals that a wide variety of powdered minerals promotes

  similar vesicle formation.

  p. 159

  Gustaf Arrhenius: Arrhenius and co-workers’ studies of

  d
ouble-layer hydroxides appear in Arrhenius et al. (1993), Gedulin and

  Arrhenius (1994), and Pitsch et al. (1995).

  p. 160

  Joseph Smith: Smith’s mineralogical proposal on “Biochemical

  evolution” appeared in J. V. Smith (1998), Parsons et al. (1998), and J. V.

  Smith et al. (1999).

  p. 160

  A. G. (Graham) Cairns-Smith: The clay-life hypothesis first

  NOTES

  277

  appeared in “The structure of the primitive gene and the prospect of gener-

  ating life” (manuscript dated October 1964). The first publication was

  Cairns-Smith (1968); see also Cairns-Smith (1977). Important book-length

  elaborations include Genetic Takeover and the Mineral Origins of Life (Cairns-Smith 1982) and Clay Minerals and the Origin of Life (Cairns-Smith and

  Hartman 1986). Popular accounts of these ideas include Seven Clues to the

  Origin of Life (Cairns-Smith 1985a) and a Scientific American article, “Clays and the origin of life” (Cairns-Smith 1985b).

  p. 160

  “I believe . . . ”: Cairns-Smith (1985b, p. 900).

  p. 160

  “Evolution did not . . . ”: Cairns-Smith (1985a, p. 107).

  p. 161

  “The answer”: Cairns-Smith (1985b, pp. 91-92).

  p. 161

  “I’m an organic chemist . . .”: A. G. Cairns-Smith seminar, “Clay

  Minerals and the Origin of Life,” Carnegie Institution, June 16, 2003.

  p. 162

  clay minerals commonly display: Varieties of clay defects are

  illustrated in Cairns-Smith (1988, 2001).

  p. 162

  “In two-dimensional . . . ”: Cairns-Smith (1985b, p. 96).

  p. 163

  particularly stable sequences: Cairns-Smith writes: “The word

  stable sounds like thermodynamically most stable whereas in fact any infor-

  mational structure has to be at least a little bit unstable. Like any genetic

  information it would owe its prevalence to indirect effects that favour its

  own survival and/or propagation—e.g., suppose that a particular defect ar-

  rangement catalyses (a little bit) the production of di- or tri-carboxylic ac-

  ids, which in turn assist clay synthesis by transporting aluminum.” [A.

  Graham Cairns-Smith to RMH, 31 August 2004]

  p. 164

  In 1988: Cairns-Smith (1988).

  p. 164

  “The first step . . .”: Cairns-Smith (1988, p. 244).

  p. 164

  “Can the material . . .”: [A. Graham Cairns-Smith to RMH, 18

  December 2003]

  13

  LEFT AND RIGHT

  p. 167

  “Assemblage on corresponding . . .”: Goldschmidt (1952,

 

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