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Deciphering the file "test-acids nucleici.

xml"

$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids / 2.1.2.1.
DNA structure picture:

Name the structures shown in the illustration:

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:

Name the structures shown in the illustration:

1 (uracil)

2 (cytosine)

3 (adenine)

4 (ribose)

5 (N-glycosidic bond)

6 (phosphodiester bond)

(Deoxyribose)

(Hydrogen bond)

(Guanine)

(Thymine)

Call functions structures shown in the illustration:


1 (serves for binding amino acid)

4 (ribosome binding)

2 (fixed aminoacyl-tRNA synthetase)

(GTP-binding site)

(Binding protein initiation factors, and elongation)

3 (adapted amino acid codon of the mRNA)

(Binds to the nucleosome)

(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)

(Containing the nucleotide sequence of the ACC serving of protein synthesis


termination signal)

(Nitrogenous base contains phosphorylated)

3 (containing a complementary nucleotide triplet codon in mRNA)

(Containing the initiation codon)

(Introns and exons is made of)

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nitrogenous bases:

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:

That meet the following nucleotide positions?

(Secondary messenger signal is a hormonal)

(It is the DNA monomer)

(RNA is the monomer)

(It is a cofactor)

(Composed macroergic)
(Participating in the synthesis of glycogen)

That meet the following nucleotide positions?

(Participating in the synthesis of glycogen)

(A substrate for the synthesis of RNA)

(Secondary messenger signal is a hormonal)


(It is the RNA monomers)

(A substrate for DNA synthesis)

(Participating in the synthesis of phospholipids)

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nucleotides:

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:

Name the structures indicated in the 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 the minor nitrogen base

target composed "cap" site of mRNA

are part of cyclic GMP

it is guanine

it is GMP

$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.1.


nitrogenous bases:

selectI saidţSTATEMENTS RELATING TO CORRECT chemical structureA: (Many)

DNA is present in

FAD's are part

It is pyrimidine nitrogen base

it is nucleoside

are part cGMP

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nucleosides:

selectI saidţSTATEMENTS RELATING TO CORRECT chemical structure A: (Many)


it is nucleoside

It is part of the ATP

are part of the DNA

it is adenine

It contains a phosphodiester bond

$ 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 represents the primary structure of DNA

It contains deoxyribose
It contains uracil
containing peptide bonds

RNA secondary structure is of

Regarding the structure shown in the picture are correct statements: (Many)

contain phosphodiester bonds,

containing thymine, cytosine and adenine

is a polypeptide chain

containing ribose

RNA is the primary structure of

$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.5. Special
structures:

Select correct statements on the chemical structure: (Many)


Cyclic GMP is

second messenger signal is a hormonal

It was synthesized from ATP by the action of adenylate cyclase

It is part of FMN's

are part of the DNA

$ 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 represents the primary structure of RNA

It contains N-glycosidic
It contains thymine

containing peptide bonds

It is the secondary structure of the DNA

Regarding the structure shown in the picture are correct statements: (Many)

contain phosphodiester bonds,

containing uracil, cytosine and adenine

is a polypeptide chain

It contains deoxyribose

It is the primary structure of the DNA

$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.3.


nucleotides:

Select correct statements on the chemical structure: (Many)


It contains two links macroergic

It is a precursor in the synthesis of RNA

second messenger signal is a hormonal

it is nucleoside

It contains guanine

$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.1.


nitrogenous bases:

Select correct statements on the chemical structure: (Many)

It is present in the RNA

are part of the DNA

the nitrogen base is purine

It is the minor nitrogen base

UDP-glucose are part of

$ 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

It is part of the DNA

It contains a phosphodiester bond

cAMP is the precursor

NADP + contained in

selectI saidţSTATEMENTS RELATING TO CORRECT chemical structure A: (Single)

it is nucleotide

is CDP

a substrate for DNA synthesis

It is the precursor of cyclic GMP

It is a dezoxiribonucleozidă

$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.2.


nucleosides:
selectI saidţSTATEMENTS RELATING TO CORRECT chemical structure A: (Single)
It is a nucleotide

It is a component of ATP

are part of the DNA

it is adenosine

acquis are part of NAD +

selectI saidţSTATEMENTS RELATING TO CORRECT chemical structure A: (Many)

It contains an N-glycosidic bond

it is nucleoside

it is guanosine

It is composed macroergic

is GMPciclic

selectI saidţSTATEMENTS RELATING TO CORRECT chemical structure A: (Many)


It is part of the DNA

It contains an N-glycosidic bond

it is timidilatul

It contains links macroergic

It is a minor nucleoside

$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.5. Special
structures:

Select correct statements on the chemical structure: (Many)

are part tRNA

It is the minor nitrogen base

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 composed of two antiparallel polynucleotide chains

it is solenoid

it is the nucleosome

It is localized in the cytosol

Regarding the structure shown in the picture are correct statements: (Many)

It is stabilized by hydrogen bonds between complementary nitrogenous bases


It is made up of two complementary polynucleotide chains

It represents the primary structure of nucleic acids

is tRNA

containing peptide bonds


$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.5. Special
structures:

selectI saidţSTATEMENTS RELATING TO CORRECT chemical structureA: (Many)

Cyclic GMP is

second messenger signal is a hormonal

GTP is synthesized by the action of guanylate cyclase

it is nucleoside

are part of the DNA

$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.3.


nucleotides:

selectI saidţSTATEMENTS RELATING TO CORRECT chemical structure A: (Many)

cGMP is the precursor

It is used as a substrate in the processes of replication and transcription

ATP is

it is nucleoside

It does not contain links macroergic


$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.1.
nitrogenous bases:

selectI saidţSTATEMENTS RELATING TO CORRECT chemical structureA: (Many)

It is part of the DNA

are part of cyclic GMP

It is the minor nitrogen base

it is guanosine

It is part of the FAD-by

$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids / 2.1.2.3.
structure and functions
DNA:

ON ARE CORRECT TO histone saidţSTATEMENTS: (Many)


They are basic protein

binds to DNA via ionic bonds

They are structural components of the ribosome

covalently binds to DNA

are protein rich and Glu Asp

Select the chemical bonds involved in stabilizing the DNA double helix: (Many)

hydrogen

hydrophobic

peptide
O-glycoside

disulfide

Select the chemical bonds present in the polynucleotide chain: (Many)

phosphodiester

N-glycoside

peptide

O-glycoside

disulfide

Select correct statements on nucleosomes: (Many)

OctaMic histone is wrapped with the double helix of DNA

between histone and DNA form ionic bonds

is the top level of organization of chromosome material

between DNA and histone phosphodiester bonds are established


tetramethyl histone is wrapped a strand of DNA with a length of 10 nucleotides

$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids / 2.1.2.1.
DNA structure picture:

Select correct statements about the structure shown: (Many)


represent hydrogen bonds between complementary nitrogenous bases

bonds are currently on the stabilization of the secondary structure of DNA

It represents a purine base pair

is the ionic bonds between DNA and histone

the connections shown can be present in the rRNA

Select correct statements about the structure shown: (Many)


the bond shown participates in the formation of the secondary structure of the tRNA

bonds are currently on the stabilization of the secondary structure of DNA

It is a pyrimidine nitrogen base pair

It represents three phosphodiester bonds between nucleotide

bonds are currently on the stabilization of the solenoid

$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.5. Special
structures:

selectI saidţSTATEMENTS RELATING TO CORRECT chemical structureA: (Many)

are part tRNA

it is pseudouridina

it is dihidrouridina

are part of the DNA


it is deoxyuridine

Select correct statements on the chemical structure: (Many)

It is part of the tRNA

it is ribotimidina

thymidylic acid

It is part of the DNA

It contains a phosphodiester bond

$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids / 2.1.2.3.
structure and functions
DNA:

Select correct statements concerning DNA (complementary laws) (Many)

The nucleotide composition of DNA from different species is different

All types of DNA, A = T and G = C

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

All types of DNA, A = G and T = C


$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids / 2.1.2.4.
structure and functions
RNA:
selectI saidţSTATEMENTS RELATING TO THE FAIR RNA: (Many)

RNA contains uracil, cytosine, adenine and guanine

the amount of RNA in the cell may vary

It is mainly double-stranded RNA

the composition according to the laws nucleotide complementarity to RNA

RNA in the nucleus and mitochondria containing only

$ 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

polynucleotide chains are complementary

polynucleotide chains are parallel

nitrogenous bases are complementary, covalently linking the

polynucleotide strands are the same as the nucleotide sequence

$ Course $ / 2.1. Nucleic acids / 2.1.2. The structure and function of nucleic acids / 2.1.2.4. structure
and functions
RNA:

ON TO mRNA ARE CORRECT saidţSTATEMENTS: (Single)

It serves a template for protein synthesis

participates in the activation of amino acids

It is an exact copy of the DNA coding strand

a polyadenylated sequence at the 5'conţine


It is part of ribosomes
ON TO rRNA ARE CORRECT saidţSTATEMENTS: (Single)

are structural components of ribosomes

are two-chain macromolecules

serve a template for protein synthesis

contained only in the core

It is a conformation "clover leaf"

selectI saidţSTATEMENTS RELATING TO THE FAIR ARNT: (Many)

Ribosomes, tRNA carrying the amino acids (protein synthesis headquarters)

TRNA have conformation "clover leaf"

the tRNA anticodon loop contains a codon triplet of nucleotides in the mRNA

same tRNA molecule can carry more amino acids

TRNA do not contain nitrogen bases minor

$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.1.


nitrogenous bases:

selectI saidţSTATEMENTS RELATING TO CORRECT chemical structureA: (Single)

It is present in all the RNA

UDP-glucose are part of

the nitrogen base is purine

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:

selectI saidţSTATEMENTS RELATING TO CORRECT chemical structureA: (Many)

participates in the synthesis of glycogen

It is the active form of glucose

It is part of the tRNA

It is CDP-glucose

is cyclic nucleotide

$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.3.


nucleotides:

selectI saidţSTATEMENTS RELATING TO CORRECT chemical structureA: (Many)

RNA is the monomer

acid uridylate

is cyclic nucleotide

It is composed macroergic
It contains a phosphodiester bond

$ Course $ / 2.1. Nucleic acids / 2.1.1. Nucleosides, nucleotides structure BA / 2.1.1.1.


nitrogenous bases:

selectI saidţSTATEMENTS RELATING TO CORRECT chemical structureA: (Many)

It is present in the RNA

UDP-glucose are part of

the nitrogen base is purine

It is the minor nitrogen base

are part cGMP


Deciphering the file "test-Glucide1.xml"

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.1. stereoisomeric monosaccharides en:

What is the number for aldohexose stereoisomers? (Single)

12

16

How many stereoisomers form aldotetrozele? (Single)

How many stereoisomers form cetotetrozele? (Single)

12

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.4. en carbohydrates properties:


The reduction to give the alcohol polyatomic monosaccharides, known as galactitol (dulcitol)?
(Single)

ribose

glucose

mannose

galactose

fructose

Metabolically active form of D-glucose is: (Single)

in the form of ether

in the form of glycoside

in the form of acetilglucoza

in the form of phosphoester

in the form of glucose sulphate

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:

The most common monosaccharide in free form in nature is: (Single)

fructose

ribose

glucose

xylose

arabinose

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.3. en heteropolysaccharides ties monomers:


The composition of the polysaccharide which fall β-D-glucosamine? (Single)
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:

The disaccharide that is obtained from hydrolysis of starch is (Single)

sucrose

cellobiose

maltose

lactose

hondrozina

Which type of glycoside bonds listed below contain glycogen macromolecule? (Single)

α (1-4) and β (1-4)

β (1-4) and α (1-6)

α (1-4) and α (1-6)

β (1-3) and α (1-4)

β (1-4) and α (1-3)

In the acid hydrolysis of sucrose to yield: (Single)

glucose and mannose


glucose and galactose

glucose and fructose

galactose and fructose

galactose and mannose

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.1. stereoisomeric monosaccharides en:

How many stereoisomers for cetohexoze: (Single)

12

16

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:

The lactose hydrolysis in acid medium is obtained: (Single)

glucose and mannose

glucose and galactose

glucose and fructose

galactose and fructose

galactose and mannose

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.3. en heteropolysaccharides ties monomers:

The substances listed below heparin composition includes: (Single)

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:

Cellulose glycosidic linkages in the macromolecule are of the type: (Single)

α (1-4) and β (1-6)

β (1-4)

α (1-4)

β (1-4) and α (1-6)

β (1-4) and α (1-3)

Glycoside bonds of macromolecule amylose are type: (Single)

α (1-6)

β (1-4)

α (1-4)

β (1-6)

α1-3)

Glycoside bonds of amylopectin are macromolecule type: (Single)

β (1-4) and β (1-6)

α (1-4) and β (1-6)

β (1-3) and α (1-6)


α (1-4) and α (1-6)

β (1-4) and α (1-3)

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.4. en carbohydrates properties:

selectNon-reducing disaccharide I: (Single)

(Correct)

(incorrect)

(incorrect)

selectReducing disaccharide I: (Many)


(incorrect)

(Correct)

(Correct)

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.3. en heteropolysaccharides ties monomers:

Heteropolysaccharide composed of the β-D-galactosamine fall? (Single)

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:

Which has branched polysaccharides presented? (Single)

amylose

amylopectin

cellulose

hyaluronic acid

condroitinsulfuric acid

Which of the polysaccharides listed below is animal? (Single)

amylose

amylopectin

cellulose

dextrans

glycogen

Polysaccharide composed of the β-D-glucose enter? (Single)

amylose

amylopectin

glycogen

pulp

dextran

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.4. en carbohydrates properties:


From the monosaccharide yield ascorbic acid (vit.C)? (Single)
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:

Glycosidic bond in sucrose molecule is of the type: (Single)

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:

Which two polysaccharide fractions, constituting the starch granule? (Single)

amylose and amylopectin

amylose and polyglucosamine

amylose and poligalactozamina

amylose and N-acetylgalactosamine

amylopectin and N-acetylglucosamine

Disaccharide unit structure of amylose is: (Single)

maltose

cellobiose

lactose

sucrose

muramic acid

What glycosidic bond in the macromolecule of amylopectin meet? (Single)

α (1-4) and α (1-6)

β (1-4) and α (1-6)

β (1-4) and β (1-6)


α (1-3) and α (1-6)

α (1-4) and β (1-6)

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.1. stereoisomeric monosaccharides en:

Monosaccharides which are presented epimers? (Many)

D-glucose and D-galactose

D-ribose and D-galactose

D-mannose and D-galactose

D-ribose and D-glucose

D-mannose and D-glucose

Monosaccharides which are presented diastereomers? (Many)

D-glucose and D-galactose

D-ribose and D-galactose

D-mannose and D-galactose

D-ribose and D-glucose

D-mannose and D-glucose

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:

Sucrose hydrolysis products are obtained: (Many)

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

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.4. en carbohydrates properties:

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

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.1. stereoisomeric monosaccharides en:

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

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.3. en heteropolysaccharides ties monomers:

The composition of heparin enter acids: (Many)

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

Aminoglucidelor most important representatives are: (Many)

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
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.3. en heteropolysaccharides ties monomers:

Hyaluronic acid constituent components are: (Many)

β-D-galacturonic acid

β-D-glucuronic acid

β-D-gluconic acid

N-acetylmannosamine
N-acetylglucosamine

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.4. en carbohydrates properties:

Polyalcohols are obtained from the reduction of D-fructose are: (Many)

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:

Is obtained from acid hydrolysis of sucrose? (Many)

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:

The hydrolysis products of lactose are: (Many)

D-mannose

α-D-galactose

β-D-galactose

D-glucose

D-fructose

Polysaccharides which are listed below homopolysaccharides? (Many)

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

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.1. stereoisomeric monosaccharides en:

Which of the given monosaccharide epimer D-glucose? (Single)


D-ribose

D-xylose

D-galactose

D-arabinose

D-fructose

The number of stereoisomers for aldopentoze is: (Single)

12

16

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.4. en carbohydrates properties:


What substance and in what environment it is necessary to interact with a monosaccharide to
obtain a glycoside? (Single)

with an acid in a basic medium

with an acid in an acid medium

with an alcohol in acidic medium

with an alcohol in basic medium

with an acidic ether

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.1. stereoisomeric monosaccharides en:

How many stereoisomers cetopentozele? (Single)

1
2

6
Deciphering the file "test-Glucide2.xml"

$ Course $ / 2.2. /2.2.2 carbohydrates. Joint structure carbohydrate / 2.2.2.3. oligosaccharides


structures en:

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)

$ Course $ / 2.2. /2.2.2 carbohydrates. Joint structure carbohydrate / 2.2.2.2. monosaccharides


ring structures en:

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)

$ Course $ / 2.2. /2.2.2 carbohydrates. Joint structure carbohydrate / 2.2.2.1. monosaccharides


linear structures en:

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)

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.1. stereoisomeric monosaccharides en:

What is the number for aldohexose stereoisomers? (Single)

12

16

How many stereoisomers form aldotetrozele? (Single)

4
6

8
How many stereoisomers form cetotetrozele? (Single)

12

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.4. en carbohydrates properties:

The reduction to give the alcohol polyatomic monosaccharides, known as galactitol (dulcitol)?
(Single)

ribose

glucose

mannose

galactose

fructose

Metabolically active form of D-glucose is: (Single)

in the form of ether

in the form of glycoside

in the form of acetilglucoza

in the form of phosphoester

in the form of glucose sulphate


$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:
The most common monosaccharide in free form in nature is: (Single)

fructose

ribose

glucose

xylose

arabinose

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.3. en heteropolysaccharides ties


monomers:

The composition of the polysaccharide which fall β-D-glucosamine? (Single)

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:

The disaccharide that is obtained from hydrolysis of starch is (Single)

sucrose

cellobiose

maltose

lactose
hondrozina

Which type of glycoside bonds listed below contain glycogen macromolecule? (Single)

α (1-4) and β (1-4)

β (1-4) and α (1-6)

α (1-4) and α (1-6)

β (1-3) and α (1-4)

β (1-4) and α (1-3)

In the acid hydrolysis of sucrose to yield: (Single)

glucose and mannose

glucose and galactose

glucose and fructose

galactose and fructose

galactose and mannose

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.1. stereoisomeric monosaccharides en:

How many stereoisomers for cetohexoze: (Single)

12

16
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:

The lactose hydrolysis in acid medium is obtained: (Single)

glucose and mannose

glucose and galactose

glucose and fructose

galactose and fructose

galactose and mannose

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.3. en heteropolysaccharides ties


monomers:

The substances listed below heparin composition includes: (Single)

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:

Cellulose glycosidic linkages in the macromolecule are of the type: (Single)

α (1-4) and β (1-6)

β (1-4)

α (1-4)
β (1-4) and α (1-6)

β (1-4) and α (1-3)


Glycoside bonds of macromolecule amylose are type: (Single)

α (1-6)

β (1-4)

α (1-4)

β (1-6)

α1-3)

Glycoside bonds of amylopectin are macromolecule type: (Single)

β (1-4) and β (1-6)

α (1-4) and β (1-6)

β (1-3) and α (1-6)

α (1-4) and α (1-6)

β (1-4) and α (1-3)

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.4. en carbohydrates properties:

Select non-reducing disaccharide: (Single)

(Correct)
(INCORRECT)

(INCORRECT)

selectReducing disaccharide I: (MANY)

(INCORRECT)

(CORRECT)

(CORRECT)
$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.3. en heteropolysaccharides ties monomers:

Heteropolysaccharide composed of the β-D-galactosamine fall? (Single)

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:

Which has branched polysaccharides presented? (Single)

amylose

amylopectin

cellulose

hyaluronic acid

condroitinsulfuric acid

Which of the polysaccharides listed below is animal? (Single)

amylose

amylopectin

cellulose

dextrans

glycogen
Polysaccharide composed of the β-D-glucose enter? (Single)

amylose

amylopectin

glycogen

pulp

dextran

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.4. en carbohydrates properties:

From the monosaccharide yield ascorbic acid (vit.C)? (Single)

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:

Glycosidic bond in sucrose molecule is of the type: (Single)

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)

$ 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:

Which two polysaccharide fractions, constituting the starch granule? (Single)

amylose and amylopectin

amylose and polyglucosamine

amylose and poligalactozamina

amylose and N-acetylgalactosamine


amylopectin and N-acetylglucosamine

Disaccharide unit structure of amylose is: (Single)


maltose

cellobiose

lactose

sucrose

muramic acid

What glycosidic bond in the macromolecule of amylopectin meet? (Single)

α (1-4) and α (1-6)

β (1-4) and α (1-6)

β (1-4) and β (1-6)

α (1-3) and α (1-6)

α (1-4) and β (1-6)

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.1. stereoisomeric monosaccharides en:

Monosaccharides which are presented epimers? (Many)

D-glucose and D-galactose

D-ribose and D-galactose

D-mannose and D-galactose

D-ribose and D-glucose

D-mannose and D-glucose


Monosaccharides which are presented diastereomers? (Many)

D-glucose and D-galactose

D-ribose and D-galactose

D-mannose and D-galactose


D-ribose and D-glucose

D-mannose and D-glucose

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.2. monomers in the oligo and
homopolysaccharides links en:

Sucrose hydrolysis products are obtained: (Many)

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

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.4. en carbohydrates properties:


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

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.1. stereoisomeric monosaccharides en:

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

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.3. en heteropolysaccharides ties monomers:


The composition of heparin enter acids: (Many)

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

Aminoglucidelor most important representatives are: (Many)

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

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.3. en heteropolysaccharides ties monomers:

Hyaluronic acid constituent components are: (Many)

β-D-galacturonic acid

β-D-glucuronic acid

β-D-gluconic acid

N-acetylmannosamine

N-acetylglucosamine

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.4. en carbohydrates properties:

Polyalcohols are obtained from the reduction of D-fructose are: (Many)

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:

Is obtained from acid hydrolysis of sucrose? (Many)

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:
The hydrolysis products of lactose are: (Many)

D-mannose

α-D-galactose

β-D-galactose

D-glucose
D-fructose

Polysaccharides which are listed below homopolysaccharides? (Many)

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

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.1. stereoisomeric monosaccharides en:


Which of the given monosaccharide epimer D-glucose? (Single)

D-ribose

D-xylose

D-galactose

D-arabinose

D-fructose

The number of stereoisomers for aldopentoze is: (Single)

12

16

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.4. en carbohydrates properties:

What substance and in what environment it is necessary to interact with a monosaccharide to


obtain a glycoside? (Single)

with an acid in a basic medium

with an acid in an acid medium

with an alcohol in acidic medium

with an alcohol in basic medium

with an acidic ether

$ Course $ / 2.2. /2.2.3 carbohydrates. Paul / 2.2.3.1. stereoisomeric monosaccharides en:


How many stereoisomers cetopentozele? (Single)

6
$ Course $ / 2.2. /2.2.1 carbohydrates. Carbohydrate structure functions properties:

Choose carbohydrate present in the human body: (Single)

amylose

cellobiose

glycogen

cellulose

amylopectin

Choose carbohydrate present in the human body: (Single)

amylose

cellobiose

galactose

cellulose

amylopectin

Disaccharide on correct statements: (Single)

lactose in the milk of mammals is

lactose hydrolysis is received from two molecules of alpha-galactose

both hexoses in the furanose form are lactose


sucrose is the main carbohydrate in the blood

sucrose is composed of two glucose molecules of alpha-

Disaccharide on correct statements: (Single)

disaccharide maltose is mainly mammals milk


hydrolysis of lactose produces two molecules of alpha-galactose

maltose starch hydrolysis product is call the action of pancreatic amylase

sucrose is the main carbohydrate in the blood

sucrose is composed of two glucose molecules of alpha-

FRUCTOSE: (Single)

It is a aldopentoză

It is a ketosis

it contains lactose

Blood is mainly monosaccharides

It is the monomer cellulose

FRUCTOSE: (Single)

It is a aldopentoză

It is an isomer of glucose

are part of the lactose

Blood is mainly monosaccharides

It is the monomer cellulose

officeIA carbohydratesţOF THE IS: (Single)

structure

genetics

emulsifying

catalysis

transport
Carbohydrates function is: (Single)
energy

genetics

emulsifying

catalysis

transport

glycogen: (Single)

stored blood

It is stored in the adipose tissue

It is stored in the gut

Liver glycogen helps to maintain blood glucose levels

glycogen in the body can provide energy for 15 to 20 days

glycogen: (Single)

It is stored in the liver

It is stored in the adipose tissue

It is stored in the gut

amylose and amylopectin consists of

glycogen in the body can provide energy for 15 to 20 days

Glucose: (Single)

It has two anomers - α and β

It is a ketosis

It is a polysaccharide
It has no asymmetric carbon atoms
It is a aldopentoză

TO Cleavage of sucrose is ODBţBEHINDcomplicatedfollowing 2 monosaccharides: (Single)

α-maltose and glucose

α-glucose and β-galactose

α-β-fructose and glucose

α-α galactose and fructose

α-glucose and β-fructose

LACTOSE: (Single)

It is made up of two molecules of α-galactose

It contains the bond β (1 → 4) glycosidic

glycogen is the monomer

It is a non-reducing disaccharide

It can not be synthesized by human cells

LACTOSE: (Single)

It is made up of two molecules of α-glucose

contains the bond α (1 → 4) glycosidic

glycogen is the monomer

It is a reducing disaccharide

It can not be synthesized by human cells

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 made up of two molecules of β-glucose

It is a monomer cellulose

MALTOSE: (Single)

It is a homopolysaccharides

It is a reducing disaccharide

It contains the bond β (1 → 4) glycosidic

It is made up of two molecules of β-glucose

It is the monomer cellulose

monosaccharides ARE: (Single)

compounds polihidroxicarbonilici

polyol

esters

ethers

aldehydes

selectI saidţTHE RIGHTcomplicated ON monosaccharides: (Single)

can be hydrolyzed

They are compounds polihidroxicarbonilici

all monosaccharides form intramolecular hemiacetals

are classified into essential and non-essential


all monosaccharides can have two anomers - α and β
Select correct statements about homopolysaccharides: (Single)

maltose cellulose is the structural unit

Cellulose is a polysaccharide in plants

consisting of alpha-fructose starch

beta-glucose is glycogen

Cellulose is the main point of the α- 1,6-glycosidic

$ Course $ / 2.2. /2.2.2 carbohydrates. Joint structure carbohydrate / 2.2.2.3. oligosaccharides


structures en:

Select lactose monomers: (Many)

(Correct)

(incorrect)

(incorrect)
(CORRECT)

(INCORRECT)

selectI MONOMERS Sucrose: (MANY)

(CORRECT)

(INCORRECT)

(INCORRECT)
(incorrect)

(Correct)

$ Course $ / 2.2. /2.2.2 carbohydrates. Joint structure carbohydrate / 2.2.2.4.


homopolysaccharides structures en:

selectMonomers STARCH: (Single)

(Correct)

(incorrect)

(incorrect)
(incorrect)

(incorrect)

selectMonomers PULP: (Single)

(incorrect)

(Correct)

(incorrect)
(incorrect)

(incorrect)

Select monomer glycogen: (Single)

(Correct)

(incorrect)

(incorrect)
(incorrect)

(incorrect)

$ Course $ / 2.2. /2.2.2 carbohydrates. Joint structure carbohydrate / 2.2.2.3. oligosaccharides


structures en:

selectMonomers maltose: (Single)

(Correct)

(incorrect)

(incorrect)
(incorrect)

(incorrect)

$ Course $ / 2.2. /2.2.1 carbohydrates. Carbohydrate structure functions properties:

sucrose: (Single)

It is made up of two molecules of α-galactose

It is a reducing disaccharide

is obtained from starch hydrolysis

contains the bond α (1 → 4) glycosidic

It can be hydrolyzed alpha and beta-glucose-fructose

sucrose: (Single)

It is made up of two molecules of β-glucose

It is a reducing disaccharide

is obtained from hydrolysis of glycogen

It contains the bond α, 1 → β 2 glycoside

can be hydrolyzed to α-glucose and β-galactose


Deciphering the file "test-Vitamine.xml"

$ 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)

(NAD + (NADP +))

(FADH2 (FMNH2))

AppointedI coenzymes:

(Pyridoxamine phosphate)
(NADH (NADPH))

(Thiamin pyrophosphate)

(FAD (FMN))

(Pyridoxal phosphate)

(NAD + (NADP +))

(FADH2 (FMNH2))

Name of chemical compounds:

(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:

Select correct statements about the chemical structure: (MANY)

the two reduction reactions tetrahydrofolic acid was converted into


it is vitamin
pantothenic acid

it is coenzyme

NAD + target composed acquis

Select correct statements about the chemical structure: (Many)

are part of coenzyme A

are part fosfopantoteinei

FAD's are part

folic acid

it is coenzyme

$ Course $ / 2.3. Vitamins /2.3.1. vitamin coenzymes structure functions / 2.3.1.4. coenzymes
role en:

Select correct statements about the chemical structure: (Many)

It is coenzyme A

tetrahydrofolic acid

participates in the activation of fatty acids

participates in the transamination reactions of amino acids


$ COURSE $ / 2.3. VITAMINS /2.3.1.Coenzyme vitamins STRUCTURE FUNCTION / 2.3.1.5. Coenzyme SIDE EN :

Select reaction, the chemical structure of coenzyme participates as shown: (Single)

(Correct)

(incorrect)

(incorrect)

(incorrect)
Select reaction, the chemical structure shown participates as cofactor: (Single)

(Correct)

(incorrect)

(incorrect)
(INCORRECT)

Select reactions, the chemical compound acting as a cofactor attendees: (MANY)

(CORRECT)

(CORRECT)
(incorrect)

(incorrect)

$ Course $ / 2.3. Vitamins /2.3.1. vitamin coenzymes structure functions / 2.3.1.4. coenzymes role
en:

selectI saidţSTATEMENTS FAIR ON CHEMICAL STRUCTUREA: (Many)

participate in the decarboxylation reactions of the amino acids

participate in transamination reactions of amino acids

participate in reactions of oxidative decarboxylation of alpha-keto acids

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:

selectI saidţSTATEMENTS FAIR ON CHEMICAL STRUCTUREA: (Single)

transfer part of the fragments in the reactions of the carbon atom

participate in transamination reactions of amino acids

participate in reactions of oxidative decarboxylation of alpha-keto acids

it is tiaminpirofosfatul

pantothenic acid

selectI saidţSTATEMENTS RELATING TO CORRECT chemical structureA: (Many)

It is thiamin pyrophosphate

It is Pyridoxamine phosphate

participate in reactions of oxidative decarboxylation of alpha-keto acids

participates in the transamination reactions of amino acids


$ Course $ / 2.3. Vitamins /2.3.1. vitamin coenzymes structure functions / 2.3.1.3. vitamins role
en:

selectI saidţSTATEMENTS RELATING TO CORRECT chemical structure A: (Many)

FAD's are part

it is vitamin

it is piridoxol

it is cofactor

NAD + target composed acquis

Select correct statements about the chemical structure: (Many)

participating in the carboxylation of pyruvate to acetyl-CoA, propionyl-CoA

is the prosthetic group of carboxilazelor

it is piridoxol

participate in the decarboxylation of amino acids

NAD + target composed acquis


$ Course $ / 2.3. Vitamins /2.3.1. vitamin coenzymes structure functions / 2.3.1.5. en coenzyme
reactions:
Select the reaction, the compound shown in the capacity of chemical prosthetic group: (Single)

(incorrect)

(incorrect)

(incorrect)
(Correct)

$ Course $ / 2.3. Vitamins /2.3.1. vitamin coenzymes structure functions / 2.3.1.3. vitamins
role en:

Select correct statements on the chemical structure: (Many)

acquis are part of NAD +

it is vitamin

FAD's are part

nicotinic acid

it is cofactor

$ Course $ / 2.3. Vitamins /2.3.1. vitamin coenzymes structure functions / 2.3.1.1. General
vitamins en:

Select the possible causes of hypovitaminosis: (Many)

Structural analogues of vitamin action (antivitaminele)

absorption disorders in the gastrointestinal tract vitamins

the lack of carbohydrates in the diet

excess protein in the diet

obesity

Select the possible causes of hypovitaminosis: (Many)


deficiency of vitamins in the diet

eridare defects of the enzymes involved in the processing of vitamins

the lack of carbohydrates in the diet

excess protein in the diet


obesity

$ Course $ / 2.3. Vitamins /2.3.1. vitamin coenzymes structure functions / 2.3.1.3. vitamins
role en:

selectVITAMIN coenzymes I В12: (Many)

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:

selectI FUNCţILE VITAMINS: (Many)

are part of coenzymes

antioxidant

energy

immunological

contractile

selectI FUNCţILE VITAMINS: (Many)


are part of coenzymes

hormone

role of intercellular interaction

immunological
contractile

Select the vitamins: (Single)

are part of coenzymes

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

transamination of amino acids

amino acid decarboxylation

decarboxylation of alpha-keto acids

activating fatty acids

Select chemical process involving vitamin С: (Single)

hydroxylation of proline and lysine residues in collagen composition

amino acid decarboxylation


activating fatty acids

carboxylation of pyruvate to acetyl-CoA, propionyl-CoA


transamination of amino acids
Select chemical process involving the structure shown: (Single)

hydroxylation of proline and lysine residues in collagen composition

decarboxylation of alpha-keto acids

transferring fragments of a carbon atom

isomerization reaction

transamination of amino acids

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