Science is a investigation process
Answer:
This question lacks options, options are:
a) indirect
b) mosaic
c) determinative
d) regulative
e) direct.
The correct answer is d.
Explanation:
The egg (ovum) like the embryo during the first embryonic divisions, do not possess any sign of polarity. This development mechanism can be called regulative development(in contrast to the mosaic model) since the fate of the cells that originate is not fixed and can be modified during development. In regulative embryos, part of the embryo can be removed and the remaining cells can compensate for the loss and give a complete individual as the final product.The strongest evidence that continues to support this regulatory model is based on the plasticity or potential that mammalian cells possess before implantation. It is known that the blastomeres produced by the first divisions can be replaced with each other or even can be eliminated without apparently altering the embryonic development and therefore they are equivalent (without polarity).
Answer:
<u>Biofilms are</u> defined as complex communities of microorganisms that grow embedded in a self-produced polymeric organic matrix and adhered to a living or inert surface, and that can present a single microbial species or a range of different species
Explanation:
The bacteria that form the biofilm are in what is called sessile form, exhibiting a phenotype different from those of the same cells in unicellular or free form (planktonic form) with respect to the growth rate and gene transcription (Donlan, 2002 ).
<u>
The formation</u> of biofilms is an adaptive strategy of microorganisms, since growth in biofilm offers four important advantages: (I) protects microorganisms from the action of adverse agents, (II) increases the availability of nutrients for their growth, (III) facilitates the use of water, reducing the possibility of dehydration and (IV) enables the transfer of genetic material (DNA). All of these circumstances can increase your survival capabilities. As a consequence, <u>the usual methods of disinfection or the use of antibiotics are often ineffective against biofilm bacteria</u>.
In addition to the risk of contamination, the development of biofilms can interfere with different processes and cause damage to the equipment. In drinking water systems the formation of biofilms can obstruct the pipes reducing their speed and transport capacity causing an increase in energy consumption. The formation of biofilm in heat exchangers and cooling towers can reduce heat transfer and as a consequence its efficiency in the process. The formation of persistent biofilms on metal surfaces can cause corrosion due to acid production by bacteria.
An example of a missense mutation in a protein-encoding gene would most likely be a neutral mutation is option B: replacement of a polar amino acid with another polar amino acid at the protein's surface.
A frequent and well-known example of a missense mutation is the blood condition sickle-cell anemia. Missense mutations exist in the DNA at a single location in sickle-cell anemia patients. A different amino acid is required in this missense mutation, which also alters the overall structure of the protein. Similarly, replacement of a polar amino acid by another polar Ami no acid at the protein's surface is a missense mutation causing change in a single site.
A neutral mutation is one whose fixation is unrelated to natural selection. Therefore, the independence of a mutation's fixation from natural selection can be used to define the selective neutrality of a mutation.
To know more about mutations, refer to the following link:
brainly.com/question/20407521
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Complete question is:
Which example of a missense mutation in a protein-encoding gene would most likely be a neutral mutation?
a) Replacement of a polar amino acid with a nonpolar amino acid at the protein's outer surface
b) Replacement of a polar amino acid with another polar amino acid at the protein's surface
c) Replacement of a polar amino acid with another polar amino acid in the protein's interior
d) Replacement of a polar amino acid with a nonpolar amino acid in the protein's interior
