Bio(degradation/remediation/catalysis) Flashcards

1
Q

Biodegredation

A

organisms do during metabolism, reduction of complex chemicals, can be complete or partial

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2
Q

Bioremediation

A

exploit biodegradation for clean-up purposes, remove unwanted chemicals or detoxify

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3
Q

Biocatalysis

A

exploit microbes for industrial use

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4
Q

Spill cleanup

A

hydrocarbon degrading microbes clean up sites- bioremediation

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5
Q

Complete Biodegradation

A

Mineralization- conversion of C,N,P,S and other elelments to inorganic products eg.CO2,NH4)

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6
Q

Partial Biodegradation

A

Biotransformation- transform compound to a more stable/less toxic/more useful compound

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7
Q

Principle of Microbial infallibility

A

no natural organic compound is totally resistant to biodegration in fav conditions

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8
Q

Xenobiotic

A

chemical that isnt normally found in a living organism or expected to be produced by it

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9
Q

factors influencing biodegradability/rate of biodegradation

A

pH, temp, organic matter content, availability of target compounds, only dissolved hydrocarbon units are available to degraders

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10
Q

Compound degradability depends on

A
element composition, structure: branching, repeating units, linkage, arrangement
of substituents (more Cl- increases persistence)
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11
Q

Hydrocarbon biodegradation

A

degraders are found everywhere, most are aerobic using oxygenases

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12
Q

Methane and Hydrocarbon biodegradation

A

degraded my specialized C1 microorganisms (methanotrophs)

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13
Q

Aliphatics and degradation

A
  • up to C9 can be toxic, biodegradable, volatile
  • C10-C24 or branching decrease biodegradability
  • unsaturated are more rapidly degraded than saturated
  • (most to least degraded ) alkanes, aromatics, alicyclics
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14
Q

Beta - Oxidation of fatty acids

A
2C units (acetyl CoA)
feeds into central metabolism (TCA Cycle) and reducing power (FADH, NADH), used to generate ATP or directly in biosynthesis
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15
Q

oxidation of aromatic hydrocarbons

A

-oxygenases (di- or mono-)
-initial steps lead to catechols, protocatechuate (aromatic rings with adjacent –OHs)
-subsequent ring cleavage between hydroxyl groups (ortho fission), beside the hydroxyl groups (meta fission)
eventual formation of compounds that enter central metabolic pathways (TCA cycle)
“funnelling” of many different aromatic compounds (including substituted aromatics) through a few key intermediates (e.g., catechols) to common pathways

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16
Q

anaerobic biodegradation of aromatic compounds

A

ring reduction followed by ring cleavage to form fatty acid
β-oxidation to acetyl-CoA & propionyl-CoA units
added oxygen is from H2O not O2
BTEX compounds may be slowly biodegraded by similar pathway in absence of oxygen

17
Q

cometabolism

A

transformation of a substanve while a second serves as a primary growth substrate

18
Q

Biocatalysis example

A

naphthalene dioxygenase catalyzes first step of aerobic naphthalene degradation
- has a broad substrate range, can be used for lots of catalysis

19
Q

Biodegradation of xenobiotics

A

loss can be from biotic and abiotic reasons: volatile rxns, leaching, spontaneous decomposition, biological reactions

20
Q

Reductive dechlorination

A

PCE or TCE, requires electrons + H+; Cl- is released

  • cis-DCE is usual DCE intermediate in biological reduction
  • this pathway occurs in anoxic, low redox environments
  • microorganisms most efficient at this conduct dehalorespiration (chloroalkene = terminal electron acceptor in anaerobic respiration)
21
Q

Biodegradation of 2,4,5-T by Burkholderia cepacia

A
  • O2 required (i.e., oxic environments)
  • note –Cl replacement by -OH
  • note substituted catechol formation; subsequent ring fission
  • note 2,4,5-T is used as a growth substrate; succinate, acetate feed into central metabolic pathways
22
Q

Plastics

A
  • polymers of polyethylene, polypropylene, PVC

- recalcitrant xenobiotic compounds

23
Q

Biodegradable plastics

A

starch linked polymers, plastics based on microbial storage polymers