Cavalier-Smith's model no longer separates prokaryotes and eukaryotes is the statement which differs from kingdom classification.
Explanation:
Cavalier-Smith in 1998 had reduced the kingdom numbers. The were brought down from 8 to 6. These are:
Animalia
Protozoa
fungi
plantae
chromista
bacteria
He divided eukaryotes into 6 kingdoms. The kingdoms are refined for better classification.
While Carolus Linnaeus divided the organisms into two kingdoms
Animalia and plantae.
The five kingdom classification:
Monera (prpkaryotes)
Protista ( unicellular eukaryotes)
fungi (multicellular decomposers)
plantae (multicellular producers)
Animalia (multicellular consumers)
It has drawbacks like in kingdom monera both autotrophs and heterotrophs are included. Phylogeny is not explained in lower organisms of monera and protista. Virus is also in classification. Cavalier-Smith introduced a new kingdom called chromista which are single- celled or multicellular eukaryotic organisms as diatoms, algae, oomycetes and protozoans which perform photosynthesis.
The second one or the third one, im not completely sure thi
Nowadays, different countries are constantly emerging and
expanding their liabilities which may include the field of medicine. The
disease that is being discussed by the instructor that is considered nearly
eradicated is probably the measles. This disease is caused by Paramyxovirus which
is a major respiratory pathogen among infants and young children. Measles is
also known as “rubeola virus”, an acute, highly respiratory symptoms and a
maculopapular rash that affects the mouth, head, body and extremities. It
begins with the appearance of Koplik spots which may end up to some
complications like symptomatic encephalitis and subacute sclerosing
panencephalitis(SSPE). In order to prevent this type of disease MMR(Measles, Mumps
& Rubella) Vaccine is needed. According to some of the reports, it is still
common to some of the countries, but WHO campaigns to eradicate the disease worldwide
by the year 2020.
Answer:
I'm going to go with a mixture sorry If this is wrong
Explanation:
The answer is D. For producing recombinant, first you need to cut the insert part and vector part to get the same end by using restriction enzyme. Then using DNA ligase to bind these two parts to get a new plasmids.
