Professional Documents
Culture Documents
xml"
$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids / 2.1.2.1.
DNA structure picture:
1 (thymine)
2 (cytosine)
3 (adenine)
4 (deoxyribose)
5 (phosphodiester bond)
6- (N-glycosidic bond)
(Ribose)
(Hydrogen bond)
(Guanine)
(Uracil)
$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids / 2.1.2.2.
RNA structure images:
1 (uracil)
2 (cytosine)
3 (adenine)
4 (ribose)
5 (N-glycosidic bond)
6 (phosphodiester bond)
(Deoxyribose)
(Hydrogen bond)
(Guanine)
(Thymine)
4 (ribosome binding)
(GTP-binding site)
(Binding to DNA)
What structural and functional features are characteristic of sectors shown in the illustration:
1 (containing the nucleotide sequence which binds to the amino acid CCA)
4 (containing pseudouridina)
2 (containing dihidrouridina)
AppointedCHEMICAL STRUCTURE:
(Adenine)
(Cytosine)
(Guanine)
(Guanosine)
(Cytidine)
(Adenylic acid)
AppointedCHEMICAL STRUCTURE:
(Thymine)
(Uracil)
(Cytosine)
(Cytidine)
(Uridylate)
(TMP)
$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.4. Mixed
structures:
(It is a cofactor)
(Composed macroergic)
(Participating in the synthesis of glycogen)
AppointedCHEMICAL STRUCTURE:
(Adenylic acid)
(Adenosine)
(DTMP)
(Deoxythymidine)
(Cytidylate)
(PMU)
AppointedCHEMICAL STRUCTURE:
(DCMP)
(DTMP)
(Deoxyguanylate acid)
(Deoxyguanosine)
(Uridylate acid)
(Uridine)
$ COURSE $ / 2.1. NUCLEIC ACID / 2.1.1. BA STRUCTURES nucleotide nucleoside / 2.1.1.2. nucleosides:
AppointedCHEMICAL STRUCTURE:
(Adenosine)
(Deoxythymidine)
(Deoxyguanosine)
(Adenine)
(TMP)
(Deoxyguanylate acid)
AppointedCHEMICAL STRUCTURE:
(Deoxycytidine)
(Guanosine)
(Uridine)
(PMU)
(Deoxycytosine)
(Guanylic acid)
AppointedCHEMICAL STRUCTURE:
(Cytidine)
(Deoxyadenosine)
(Uridine)
(Cytosine)
(DAMP)
(Uridylate)
$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids / 2.1.2.1.
DNA structure picture:
1 (nucleosomes)
2 (solenoid)
3 (loops)
4 (chromosome)
5 (histone protein)
(subunitsAnd of the ribosome)
(The ribosome)
(ARNT)
(Aa)
$ COURSE $ / 2.1. NUCLEIC ACID / 2.1.1. BA STRUCTURES nucleotide nucleoside / 2.1.1.4. JOINT
STRUCTURES:
AppointedCHEMICAL STRUCTURE:
(Cytosine)
(Cytidine)
(Adenosine)
(ACID adenylate)
(Deoxythymidylate)
(Deoxythymidine)
AppointedCHEMICAL STRUCTURE:
(7-methylguanine)
(Guanosine)
(Deoxyadenosine)
(Deoxyguanosine)
(Deoxycytidylate)
(Cytidine)
AppointedCHEMICAL STRUCTURE:
(Dihidrouridină)
(Uridylate acid)
(Guanine)
(Guanylate)
(DCMP)
(Dump)
AppointedCHEMICAL STRUCTURE:
(Ribotimidina)
(Thymine)
(DAMP)
(Deoxyadenosine)
(GMPciclic)
(AMPciclic)
$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.5. Special
structures:
SELECT statements accurate information on the chemical structure: (MANY)
it is guanine
it is GMP
DNA is present in
it is nucleoside
it is adenine
$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids / 2.1.2.1.
DNA structure picture:
Regarding the structure shown in the picture are correct statements: (Many)
It contains deoxyribose
It contains uracil
containing peptide bonds
Regarding the structure shown in the picture are correct statements: (Many)
is a polypeptide chain
containing ribose
$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.5. Special
structures:
It is part of FMN's
$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids / 2.1.2.2.
RNA structure images:
Regarding the structure shown in the picture are correct statements: (Many)
It contains N-glycosidic
It contains thymine
Regarding the structure shown in the picture are correct statements: (Many)
is a polypeptide chain
It contains deoxyribose
it is nucleoside
It contains guanine
$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids / 2.1.2.1.
DNA structure picture:
Select DNA components: (Many)
(CORRECT)
(INCORRECT)
(INCORRECT)
(CORRECT)
(CORRECT)
$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids / 2.1.2.2.
RNA structure images:
Select RNA components: (MANY)
(CORRECT)
(CORRECT)
(CORRECT)
(INCORRECT)
(INCORRECT)
$ COURSE $ / 2.1. NUCLEIC ACID / 2.1.1. BA STRUCTURES nucleotide nucleoside / 2.1.1.3. nucleotides:
selectI saidţSTATEMENTS RELATING TO CORRECT chemical structure A: (Many)
it is nucleotide
NADP + contained in
it is nucleotide
is CDP
It is a dezoxiribonucleozidă
It is a component of ATP
it is adenosine
it is nucleoside
it is guanosine
It is composed macroergic
is GMPciclic
it is timidilatul
It is a minor nucleoside
$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.5. Special
structures:
it is dihidrouridina
it is uracil
it is deoxyuridine
$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids /
2.1.2.1. DNA structure picture:
Regarding the structure shown in the picture are correct statements: (Many)
represents the DNA double helix
it is solenoid
it is the nucleosome
Regarding the structure shown in the picture are correct statements: (Many)
is tRNA
Cyclic GMP is
it is nucleoside
ATP is
it is nucleoside
it is guanosine
$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids / 2.1.2.3.
structure and functions
DNA:
Select the chemical bonds involved in stabilizing the DNA double helix: (Many)
hydrogen
hydrophobic
peptide
O-glycoside
disulfide
phosphodiester
N-glycoside
peptide
O-glycoside
disulfide
$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids / 2.1.2.1.
DNA structure picture:
$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.5. Special
structures:
it is pseudouridina
it is dihidrouridina
it is ribotimidina
thymidylic acid
$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids / 2.1.2.3.
structure and functions
DNA:
from the same species, DNA from different tissues have a different nucleotide composition
The nucleotide composition of DNA from the same species depends on the age, food
intake, environmental conditions
$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids / 2.1.2.3. structure
and functions
DNA:
Refer to the secondary structure of DNA (double helix) correct statements: (Many)
are the two polynucleotide chains double helix coiled around the common shaft
$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids / 2.1.2.4. structure
and functions
RNA:
the tRNA anticodon loop contains a codon triplet of nucleotides in the mRNA
It is a minor nucleoside
It is part of dezoxitimidilatului
$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.5. Special
structures:
It is CDP-glucose
is cyclic nucleotide
acid uridylate
is cyclic nucleotide
It is composed macroergic
It contains a phosphodiester bond
12
16
12
ribose
glucose
mannose
galactose
fructose
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
fructose
ribose
glucose
xylose
arabinose
Hyaluronic acid
dexstran
condroitinsulfuric acid
cellulose
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
sucrose
cellobiose
maltose
lactose
hondrozina
Which type of glycoside bonds listed below contain glycogen macromolecule? (Single)
12
16
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
D-galactosamine
D-Glucosamine
D-mannosamine
D-fructose
D-ribose
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
β (1-4)
α (1-4)
α (1-6)
β (1-4)
α (1-4)
β (1-6)
α1-3)
(Correct)
(incorrect)
(incorrect)
(Correct)
(Correct)
Hyaluronic acid
heparin
condroitinsulfuric acid
muramina
pectic acid
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
amylose
amylopectin
cellulose
hyaluronic acid
condroitinsulfuric acid
amylose
amylopectin
cellulose
dextrans
glycogen
amylose
amylopectin
glycogen
pulp
dextran
galactose
ribose
glucose
xylose
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
α (1-4)
β (1-4)
α, β (1-2)
α, β (1-4)
α, β (1-6)
What type of glycosidic bonds link the side chains of the main chain of glycogen
macromolecule? (Single)
β (1-4)
α (1-4)
α (1-3)
β (1-6)
α (1-6)
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.3. en heteropolysaccharides ties
monomers:
What type of glycosidic bonds links between them disaccharide units of hyaluronic acid
macromolecule? (Single)
α (1-4)
β (1-3)
α (1-3)
β (1-4)
α (1-6)
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
maltose
cellobiose
lactose
sucrose
muramic acid
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
D-galactose
D-mannose
D-glucose
D-ribose
D-fructose
Let the name of substances that are obtained from the hydrolysis of lactose: (Many)
mannose
fructose
galactose
cellobiose
glucose
D-glucose in the presence of ATP interaction with the enzyme glucokinase in turn: (Single)
gluconic acid
glucuronic acid
glucose-1-phosphate
glucose-6-phosphate
glucose-5-phosphate
After configuration of chiral center which takes place ranking in series stereochemistry
aldohexozelor enantiomers D- and L? (Single)
C-1
C-2
C-3
C-4
C-5
After configuration of chiral center which takes place ranking in series stereochemistry
aldopentozelor enantiomers D- and L? (Single)
C-1
C-2
C-3
C-4
hyaluronic
D-gluconic
D-glucuronic
L-galactonic
L-iduronic
The macromolecule chondroitin sulfuric acid containing monomer units is: (Many)
β-D-galacturonic acid
β-D-glucuronic acid
N-acetyl-β-D-glucose
N-acetyl-β-D-glucosamine
N-acetyl-β-D-galactosamine
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.4. en carbohydrates properties:
Gangliosides containing sialic acids in the brain, the blood and other tissues. Since the substances
in the body to yield N-acetyl-neuraminic acid?(Many)
lactic acid
pyruvic acid
N-acetyl-D-glucosamine
N-acetyl-D-galactosamine
N-acetyl-D-mannosamine
D-ribozoamina
D-xilozoamina
D-Glucosamine
D-fructosamine
D-galactosamine
The epimers of D-glucose, which differ only in the configuration of the chiral center C-4 and C-2
are:
(Many)
fructose
ribose
mannose
cellobiose
galactose
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.3. en heteropolysaccharides ties monomers:
β-D-galacturonic acid
β-D-glucuronic acid
β-D-gluconic acid
N-acetylmannosamine
N-acetylglucosamine
D-galactitol
D-ribitol
D-xylitol
D-sorbitol
D-mannitol
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
α-D-fructose
β-D-glucose
β-D-fructose
α-D-glucose
not hydrolyze
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.4. en carbohydrates properties:
The correct name of the product the new interaction of α-D-glucose with methyl alcohol: (Single)
α-methylglucose
O-methyl-α-D-glucopyranose
α-metilglucopiranoză
O-methyl-α-D-glucopyranoside
2-methyl-α-D-glucopyranoside
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
D-mannose
α-D-galactose
β-D-galactose
D-glucose
D-fructose
Hyaluronic acid
heparin
cellulose
glycogen
starch
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.3. en heteropolysaccharides ties monomers:
The product names are obtained from acid hydrolysis of the acid was completely condroitinsulfuric are:
(Many)
β-D-glucuronic acid
Hyaluronic acid
sulfuric acid
β-D-glucosamine
β-D-galactosamine
D-xylose
D-galactose
D-arabinose
D-fructose
12
16
1
2
6
Deciphering the file "test-Glucide2.xml"
AppointedCHEMICAL STRUCTURE:
(maltose)
(lactose)
(Sucrose)
(glucose)
(fructose)
(Galactose)
(Mannose)
(Cellobiose)
$ Course $ / 2.2. /2.2.2 carbohydrates. Joint structure carbohydrate / 2.2.2.4.
homopolysaccharides structures en:
AppointedCHEMICAL STRUCTURE:
(Amylose)
(Amylopectin)
(cellulose)
(Cellobiose)
(maltose)
(lactose)
(Sucrose)
(Mannose)
AppointedCHEMICAL STRUCTURE:
(Amylose)
(Glycogen)
(cellulose)
(Cellobiose)
(maltose)
(lactose)
(Sucrose)
(Mannose)
AppointedCHEMICAL STRUCTURE:
(Α-D-fructofuranoza)
(Α-D-ribofuranose)
(Β-D-galactopyranose)
(Β-D-fructofuranoza)
(Α-D-glucofuranose)
(Β-D-ribofuranose)
AppointedCHEMICAL STRUCTURE:
(Α-D-glucopyranose)
(Α-D-galactopyranose)
(Β-D-fructofuranoza)
(Α-D-glucofuranose)
(Β-D-ribofuranose)
(Β-D-fructopyranose)
AppointedCHEMICAL STRUCTURE:
(Α-D-galactopyranose)
(Β-D-galactopyranose)
(Β-D-fructofuranoza)
(Β-D-ribofuranose)
(Β-D-fructopyranose)
(Β-D-glucopyranose)
AppointedCHEMICAL STRUCTURE:
(Α-D-ribofuranose)
(Α-D-glucopyranose)
(Β-D-galactopyranose)
(Β-D-fructofuranoza)
(Α-D-glucofuranose)
(Β-D-dezoxiribofuranoza)
AppointedCHEMICAL STRUCTURE:
(D-glucose)
(D-galactose)
(D-ribose)
(D-fructose)
(L-glucose)
(L-ribose)
AppointedCHEMICAL STRUCTURE:
(D-glucose)
(D-galactose)
(D-ribulose)
(D-fructose)
(L-ribose)
(L-galactose)
AppointedCHEMICAL STRUCTURE:
(D-glucose)
(D-galactose)
(D-ribulose)
(D-fructose)
(L-ribose)
(L-fructose)
12
16
4
6
8
How many stereoisomers form cetotetrozele? (Single)
12
The reduction to give the alcohol polyatomic monosaccharides, known as galactitol (dulcitol)?
(Single)
ribose
glucose
mannose
galactose
fructose
fructose
ribose
glucose
xylose
arabinose
starch
Hyaluronic acid
dexstran
condroitinsulfuric acid
cellulose
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
sucrose
cellobiose
maltose
lactose
hondrozina
Which type of glycoside bonds listed below contain glycogen macromolecule? (Single)
12
16
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
D-galactosamine
D-Glucosamine
D-mannosamine
D-fructose
D-ribose
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
β (1-4)
α (1-4)
β (1-4) and α (1-6)
α (1-6)
β (1-4)
α (1-4)
β (1-6)
α1-3)
(Correct)
(INCORRECT)
(INCORRECT)
(INCORRECT)
(CORRECT)
(CORRECT)
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.3. en heteropolysaccharides ties monomers:
Hyaluronic acid
heparin
condroitinsulfuric acid
muramina
pectic acid
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
amylose
amylopectin
cellulose
hyaluronic acid
condroitinsulfuric acid
amylose
amylopectin
cellulose
dextrans
glycogen
Polysaccharide composed of the β-D-glucose enter? (Single)
amylose
amylopectin
glycogen
pulp
dextran
mannose
galactose
ribose
glucose
xylose
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
α (1-4)
β (1-4)
α, β (1-2)
α, β (1-4)
α, β (1-6)
The type of glycosidic bonds that link the side chains of the main chain of the macromolecule
glycogen? (Single)
β (1-4)
α (1-4)
α (1-3)
β (1-6)
α (1-6)
What type of glycosidic bonds links between them disaccharide units of hyaluronic acid
macromolecule? (Single)
α (1-4)
β (1-3)
α (1-3)
β (1-4)
α (1-6)
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
cellobiose
lactose
sucrose
muramic acid
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
D-galactose
D-mannose
D-glucose
D-ribose
D-fructose
Let the name of substances that are obtained from the hydrolysis of lactose: (Many)
mannose
fructose
galactose
cellobiose
glucose
gluconic acid
glucuronic acid
glucose-1-phosphate
glucose-6-phosphate
glucose-5-phosphate
After configuration of chiral center which takes place ranking in series stereochemistry
aldohexozelor enantiomers D- and L? (Single)
C-1
C-2
C-3
C-4
C-5
After configuration of chiral center which takes place ranking in series stereochemistry
aldopentozelor enantiomers D- and L? (Single)
C-1
C-2
C-3
C-4
hyaluronic
D-gluconic
D-glucuronic
L-galactonic
L-iduronic
The macromolecule chondroitin sulfuric acid containing monomer units is: (Many)
β-D-galacturonic acid
β-D-glucuronic acid
N-acetyl-β-D-glucose
N-acetyl-β-D-glucosamine
N-acetyl-β-D-galactosamine
Gangliosides containing sialic acids in the brain, the blood and other tissues. Since the substances
in the body to yield N-acetyl-neuraminic acid?(Many)
lactic acid
pyruvic acid
N-acetyl-D-glucosamine
N-acetyl-D-galactosamine
N-acetyl-D-mannosamine
D-ribozoamina
D-xilozoamina
D-Glucosamine
D-fructosamine
D-galactosamine
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.1. stereoisomeric monosaccharides en:
The epimers of D-glucose, which differ only in the configuration of the chiral center C-4 and C-2 are:
(Many)
fructose
ribose
mannose
cellobiose
galactose
β-D-galacturonic acid
β-D-glucuronic acid
β-D-gluconic acid
N-acetylmannosamine
N-acetylglucosamine
D-galactitol
D-ribitol
D-xylitol
D-sorbitol
D-mannitol
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
α-D-fructose
β-D-glucose
β-D-fructose
α-D-glucose
not hydrolyze
The correct name of the product the new interaction of α-D-glucose with methyl alcohol: (Single)
α-methylglucose
O-methyl-α-D-glucopyranose
α-metilglucopiranoză
O-methyl-α-D-glucopyranoside
2-methyl-α-D-glucopyranoside
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
The hydrolysis products of lactose are: (Many)
D-mannose
α-D-galactose
β-D-galactose
D-glucose
D-fructose
Hyaluronic acid
heparin
cellulose
glycogen
starch
The product names are obtained from acid hydrolysis of the acid was completely condroitinsulfuric are:
(Many)
β-D-glucuronic acid
Hyaluronic acid
sulfuric acid
β-D-glucosamine
β-D-galactosamine
D-ribose
D-xylose
D-galactose
D-arabinose
D-fructose
12
16
6
$ Course $ / 2.2. /2.2.1 carbohydrates. Carbohydrate structure functions properties:
amylose
cellobiose
glycogen
cellulose
amylopectin
amylose
cellobiose
galactose
cellulose
amylopectin
FRUCTOSE: (Single)
It is a aldopentoză
It is a ketosis
it contains lactose
FRUCTOSE: (Single)
It is a aldopentoză
It is an isomer of glucose
structure
genetics
emulsifying
catalysis
transport
Carbohydrates function is: (Single)
energy
genetics
emulsifying
catalysis
transport
glycogen: (Single)
stored blood
glycogen: (Single)
Glucose: (Single)
It is a ketosis
It is a polysaccharide
It has no asymmetric carbon atoms
It is a aldopentoză
LACTOSE: (Single)
It is a non-reducing disaccharide
LACTOSE: (Single)
It is a reducing disaccharide
MALTOSE: (Single)
It is a polysaccharide
It is a non-reducing monosaccharide
glycogen is the hydrolysis product of the action of pancreatic amylase
It is a monomer cellulose
MALTOSE: (Single)
It is a homopolysaccharides
It is a reducing disaccharide
compounds polihidroxicarbonilici
polyol
esters
ethers
aldehydes
can be hydrolyzed
beta-glucose is glycogen
(Correct)
(incorrect)
(incorrect)
(CORRECT)
(INCORRECT)
(CORRECT)
(INCORRECT)
(INCORRECT)
(incorrect)
(Correct)
(Correct)
(incorrect)
(incorrect)
(incorrect)
(incorrect)
(incorrect)
(Correct)
(incorrect)
(incorrect)
(incorrect)
(Correct)
(incorrect)
(incorrect)
(incorrect)
(incorrect)
(Correct)
(incorrect)
(incorrect)
(incorrect)
(incorrect)
sucrose: (Single)
It is a reducing disaccharide
sucrose: (Single)
It is a reducing disaccharide
$ Course $ / 2.3. Vitamins /2.3.1. vitamin coenzymes structure functions / 2.3.1.2. coenzyme
vitamins structures en:
AppointedI coenzymes:
(Pyridoxal phosphate)
(NADH (NADPH))
(Thiamin pyrophosphate)
(FAD (FMN))
(Pyridoxamine phosphate)
(FADH2 (FMNH2))
AppointedI coenzymes:
(Pyridoxamine phosphate)
(NADH (NADPH))
(Thiamin pyrophosphate)
(FAD (FMN))
(Pyridoxal phosphate)
(FADH2 (FMNH2))
(Piridoxol)
(Pyridoxal)
(Pyridoxamine)
(Thiamine)
(Niacin)
(Biotin)
AppointedCHEMICAL STRUCTURE:
(folic acid)
(Coenzyme А)
(Fosfopantoteină)
(Tetrahydrofolic acid)
(Tiaminpirofosfat)
(Vitamin Н)
(Pantothenic acid)
(Piridoxalfosfat)
AppointedCHEMICAL STRUCTURE:
(folic acid)
(Coenzyme А)
(Fosfopantoteină)
(Tetrahydrofolic acid)
(Tiaminpirofosfat)
(Biotin)
(Pantothenic acid)
(Piridoxalfosfat)
AppointedI VITAMINS:
(Nicotinamide)
(Pyridoxal)
(Thiamine)
(Nicotinic acid)
(Piridoxol)
Call vitamins:
(Nicotinic acid)
(Pyridoxamine)
(Riboflavin)
(Nicotinamide)
(Thiamine)
(Piridoxol)
$ Course $ / 2.3. Vitamins /2.3.1. vitamin coenzymes structure functions / 2.3.1.3. vitamins
role en:
it is coenzyme
folic acid
it is coenzyme
$ Course $ / 2.3. Vitamins /2.3.1. vitamin coenzymes structure functions / 2.3.1.4. coenzymes
role en:
It is coenzyme A
tetrahydrofolic acid
(Correct)
(incorrect)
(incorrect)
(incorrect)
Select reaction, the chemical structure shown participates as cofactor: (Single)
(Correct)
(incorrect)
(incorrect)
(INCORRECT)
(CORRECT)
(CORRECT)
(incorrect)
(incorrect)
$ Course $ / 2.3. Vitamins /2.3.1. vitamin coenzymes structure functions / 2.3.1.4. coenzymes role
en:
it is tiaminpirofosfatul
it is pyridoxine
$ Course $ / 2.3. Vitamins /2.3.1. vitamin coenzymes structure functions / 2.3.1.5. en coenzyme
reactions:
Select reactions, the chemical compound of coenzyme participates as shown: (MANY)
(CORRECT)
(CORRECT)
(INCORRECT)
(INCORRECT)
$ Course $ / 2.3. Vitamins /2.3.1. vitamin coenzymes structure functions / 2.3.1.4. coenzymes role
en:
it is tiaminpirofosfatul
pantothenic acid
It is thiamin pyrophosphate
It is Pyridoxamine phosphate
it is vitamin
it is piridoxol
it is cofactor
it is piridoxol
(incorrect)
(incorrect)
(incorrect)
(Correct)
$ Course $ / 2.3. Vitamins /2.3.1. vitamin coenzymes structure functions / 2.3.1.3. vitamins
role en:
it is vitamin
nicotinic acid
it is cofactor
$ Course $ / 2.3. Vitamins /2.3.1. vitamin coenzymes structure functions / 2.3.1.1. General
vitamins en:
obesity
$ Course $ / 2.3. Vitamins /2.3.1. vitamin coenzymes structure functions / 2.3.1.3. vitamins
role en:
metilcobalamina
dezoxiadenozilcobalamina
piridoxalfosfat
piridoxaminfosfat
coenzyme А
fosfopantoteina
$ Course $ / 2.3. Vitamins /2.3.1. vitamin coenzymes structure functions / 2.3.1.1. General
vitamins en:
antioxidant
energy
immunological
contractile
hormone
immunological
contractile
structure
energy
genetics
transport
$ Course $ / 2.3. Vitamins /2.3.1. vitamin coenzymes structure functions / 2.3.1.4. coenzymes role
en:
Select chemical reactions in participating coenzymes derived from vitamin В12: (Many)
isomerization reaction
methylation reactions
isomerization reaction