CHAPTER 1 Flashcards

THE MICROBIAL WORLD

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1
Q

Collection of cells that have been grown in or on a nutrient medium

A

CULTURE

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2
Q

liquid or solid nutrient mixture that contain all of the nutrients required for a microorganisms to grow

A

MEDIUM

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3
Q

the increase in cell number as a result of cell division

A

GROWTH

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4
Q

single microbial cell placed on a solid nutrient medium can grow and divide into millions or even billions of cells

A

COLONY

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5
Q

it is a type of cell that contain an assortment of membrane-enclosed cytoplasmic structure called organelles

A

EUKARYOTIC CELL

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6
Q

it is a type of cell that can be found within two different groups of organisms we know Bacteria and Archaea

A

PROKARYOTIC CELL

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7
Q

it has a few internal structures, they lack a nucleus, and they typically lack organelles

A

PROKARYOTIC CELL

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8
Q

full set of a genes in a cell

A

GENOME

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9
Q

segment of DNA that encodes a protein or a RNA molecule

A

GENE

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10
Q

living blueprint of an organisms

A

GENOME

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11
Q

proteins that have catalytic activity, carry out reactions that supply energy and perform biosynthesis within the cell

A

ENZYME

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12
Q

it is the process by which the information encoded in DNA sequences is copied into a RNA molecule

A

TRANSCRIPTION

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13
Q

it is a process whereby the information in an RNA molecule is used by a ribosome to synthesize a protein

A

TRANSLATION

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14
Q

it is a self-repulsion which allows the cell to relocate in response to environmental conditions

A

MOTILITY

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15
Q

many prokaryotic cells can exchange genes with neighboring cells, regardless of their species, in the process of

A

HORIZONTAL GENE TRANSFER

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16
Q

results when genes in a population of cells change in sequence and frequency over time, leading to descent with modification

A

EVOLUTION

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17
Q

transforming molecules to produce energy and building blocks

A

CATABOLISM

18
Q

synthesizing macromolecules

A

ANABOLISM

19
Q

first person to see bacteria

A

Antoni van Leeuwenhoek (1632-1723)

20
Q

capacity of microscope to enlarge an image

A

MAGNIFICATION

21
Q

ability to distinguish two adjacent object as distinct and separate. it also the one that govern our ability to see the very small

A

RESOLUTION

22
Q

Purpose of oil immersion

A

increase the light-gathering ability of a lens, that is increases the amount of light that is collected and viewed by the lens

23
Q

basic dyes

A

methylene blue, crystal blue and safranin

24
Q

stains that render the different kinds of cells different colors

A

differential stains

25
Q

Type of microscope that based on the principle that cells differ in refractive index (the ability of a material to alter the speed of light) from their surrounding liquid. Light passing through a cell thus differs in phase from light from passing through the surrounding. This subtle difference is amplified by a device in the objective lens of the phase-contrast microscope called the phase ring resulting in a dark image on a light background.

A

Phase-contrast Microscope

26
Q

-light does no pass through the specimen
-light is directed from the sides of the specimen and only light that is scattered when it hits the specimen reached the lens. Thus, the specimen appears light on dark background

A

Dark-field Microscope

27
Q

used to visualize cells in their natural habitats, such as soil, water, food, or a clinical specimen

A

DAPI(4’,6-diamidino-2-phenyliondole)

28
Q

a collection of practices that allow for the preparation and maintenance of sterile (without the presence of the living microorganisms) nutrient media and solutions

A

ASEPTIC TECHNIQUE

29
Q

those that contain cells from only a single type of microorganisms

A

PURE CULTURE

30
Q

person that construct a swan-necked flask, called Pasteur flask

A

Louis Pasteur

31
Q

-credited with the introduction of aseptic technique for surgeries

A

Joseph Lister (1827-1912)

32
Q

Koch Postulates

A
  1. The suspected pathogen must be present in all cases of the disease and absent from healthy animals’
  2. The suspected pathogen must be grown in pure culture.
  3. Cells from a pure culture of the suspected pathogen must cause disease in a healthy animal.
  4. The suspected pathogen must be reisolated and shown to be the same as the original.
33
Q

first to define chemolithotrophy, which is any metabolic process in which energy for growth is produced using only inorganic chemical compounds

A

Sergie Winogradsky (1856-1953)

34
Q

He reasoned that some molecule that contained genetic information must havebeen transferred from strain R to strain S in this process, andthis experiment showed that genetic transfer could be studied in bacteria

A

Frederick Griffith (1879-1941)

35
Q

this “transforming principle” was DNA. They treated the dead remains of cells of strain S with chemicals and enzymes that destroyed protein and left behind only DNA. They then repeated Griffith’s experiment with the pure DNA of strain S and showed that this DNA was sufficient to cause transformation, causing strain R cells to become S-type cells and virulent.They also demonstrated that transformation failed if the DNA from strain S was degraded

A

Avery–MacLeod–McCarty (1944),

36
Q

The structure of DNA was ultimately solved by James D. Watson (1928–) and Francis Crick (1916–2004) using X-ray diffraction images of DNA taken by their colleague Rosalind Franklin (1920–1958)

A

They revealed that DNA is composed of a double helix that contains four nitrogenous bases: guanine, cytosine, adenine, and thymine, which form the genetic code. Later research would reveal how the genetic code is read from DNA and translated into protein,

37
Q

proposed that molecular sequences could be used to reconstruct evolutionary relationships.

A

Emile Zuckerkandl
(1922–2013) and Linus Pauling (1901–1994)

38
Q

He realized in the 1970s that the sequence of ribosomal RNA (rRNA) molecules and the genes that encode them could be used to infer evolutionary relationships between organisms. He recognized that genes encoding rRNAs were excellent candidates for phylogenetic analysis because they were (1) present in all cells, (2) functionally constant, (3) highly conserved (slowly changing) in their nucleic acid sequences, and (4) of adequate length to provide a deep view of evolutionary relationships.

A

Carl Woese (1928–2012)

39
Q

he found that the rRNA sequences from methanogens were distinct from those of both Bacteria and Eukarya, the only two domains recognized at that time. He named this new group of prokaryotic cells the Archaea (originally Archaebacteria) and recognized them as the third domain of life alongside the Bacteria and the Eukarya

A

Carl Woese (1928–2012)

40
Q

He realized that Woese’s approach could be applied to rRNA molecules isolated directly from the environment as a way to probe the diversity of natural microbial communities without first cultivating their component organisms. These cultivation-independent methods of rRNA gene analysis pioneered by Pace greatly improved our picture of microbial diversity

A

Norman Pace (1942)

41
Q

He was the first to propose metagenomics, a technique in which fragments of microbial genomes (or even entire genomes) can be recovered from a sample of environmental DNA. Metagenomics, the study of genomic information recovered directly from the environment, is currently providing us
with profound insights on the evolution and diversity of life and new information on the metabolic potential of the microbial world.

A

Jo Handelsman (1959)