Lesson
14 of 25

🌿 Protein and Fat Synthesis

Protein and Fat Synthesis.

This lesson provides exam-focused context on key concepts in crop physiology and connects the section topics for quick revision.


Biosynthesis of protein

Protein is a complex organic nitrogenous substance found in all living tissues of

plants and animals. They are polymer of amino acids in linear order. Synthesis of protein

may take place from amino acids produced by direct amination of organic acids or by

degradation of protein. Former is known as primary protein synthesis while the latter is

called secondary protein synthesis . Protein synthesis occurs in pre – DNA synthesis phase

(G1 phase) of cell cycle.

Biosynthesis of protein takes place in prokaryotes as well as in eukaryotes. Kinds of

protein to be synthesized depend upon the gene (DNA segment). Gene is continuous

uninterrupted sequence of nucleotides which codes for a single polypeptide chain. Now it is

believed that the sequence of some eukaryotic genes is found to be interrupted by nucleotides

that are not represented with the amino acid sequence of protein. They are non-coding

(silent). Genes control all metabolic processes by synthesizing proteins (enzymes).

Structure of an eukaryotic gene showing Exon (coding part) and Intron (non-coding part).

Mechanism of protein synthesis: Protein synthesis takes place in following two stages:

I. Transcription

II. Translation

Transcription: Transcription occurs throughout inter phase and continues up to early

prophase of cell division. It is primary stage of protein synthesis. When DNA produces

DNA the process is called replication but when DNA produces RNA the process is called

transcription. In the former case DNA is duplicated while in the latter case protein is

synthesized. During transcription RNA is synthesized on DNA template. Here, information

or order contained in DNA is passed on the mRNA for synthesis of particular protein. The

information is in coded form and consists of three nitrogenous bases (triplet codons). The

part of DNA responsible for synthesis of mRNA is which leads to one polypeptide chain is

called cistron (functional gene). New strands of mRNA are synthesized on DNA template

making use of RNA nucleotides present in surroundings in 5’ 3’ director just like DNA

chains.

Single DNA strand serves as template for RNA polymerase and synthesizes RNA.

DNA strand which serves as template for transcription is called the sense strand. The

complementary strand is antisense strand. In SV – 40 viruses both strands of DNA are

transcribed and it is called symmetrical transcription, but when only one strand is transcribed

it is called asymmetrical transcription. Former type of transcription also occurs in Polymer

virus DNA and in the mitochondria genome.

Mechanism of transcription

Transcription involves following events:

I. Uncoiling of DNA molecule

II. Synthesis and action of enzyme RNA polymerase

III. Synthesis of hn RNA / mRAN.

Uncoiling of DNA molecule: As per “nucleosome model” of chromosome.

Chromosomes are ‘matarmala’ like beaded structure. Beads are separated by string and are

making up of DNA and histone protein. Histone proteins are of 5 kinds: H2A, H2B, H3, H4

and H5 or H1. First four constitute the bead core and H1 links two beads. The DNA

molecules are wrapped on histone protein cores and linker protein core in beaded and linker

regions respectively.

Structure and function of enzyme RNA polymerase: RNA polymerase is a

holoenzyme. Core particle consists of sub units α’β, β’ and ψ. Cofactor consists of sigma

factor. For functional RNA polymerase formation the two (core enzyme and sigma factor)

gene united. Sigma factor recognized correct start signal at DNA template and core enzyme

continues transcription. Sigma factor dissociates after initiation of transcription to adjure

with other core enzyme of RNA polymerase. In prokaryotes RNA polymerase is only one

type while in eukaryotes.

Production of mRNA / hnRNA: In prokaryotes where nucleus is not well organized

mRNA is the direct product of transcription, while in eukaryotes the direct product of

transcription is hnRNA (heteronucleic RNA) and mRNA is derived from hnRNA by cutting

and splicing. HnRNA has coding and non-coding sequences. Coding sequences are

interrupted by non-coding sequences. Non coding sequences are removed by splicing

(cutting) by endonuclease enzyme and coding sequences are ligased together to from mRNA.

The spliced non-coding sequences are degraded within nucleus. It never goes out of nucleus.

Thus, only fraction of hnRNA is translocated to cytoplasm from nucleus via nuclear pore.

In eukaryotes migration of mRNA from nucleus to cytoplasm via nuclear pore occurs

through poly a tail. According to another view, ribosome’s pull the mRNA from nucleus to

cytoplasm. Now mRNA gets established in cytoplasm.

Translation: Translation is a process in which order (message) given by DNA to mRNA for

synthesis of particular protein is implemented (conveyed). Genetic information concealed in

mRNA directs the synthesis of particular protein. These orders are in coded form. This

coded information (expressed through codons) is recognized by tRNA having anticodons.

Anticodons are opposite to codons (codons and anticodons are complementary to each other).

Mechanism of translation: It involves following events:

I. Activation and selection of amino acids

II. Transfer of amino acids to tRNA molecules

III. Formation of protein synthesizing apparatus and chain initiation

IV. Chain elongation

V. Chain termination


FAT SYNTHESIS

Fat synthesis can be studied under the following heads:



Fat synthesis of Glycerol

There may be different methods of the formation of glycerol in plants, but one of the

very common methods is from dihydroxy acetone phosphate which is an intermediate of

glycolysis. Dihydroxyacetone phosphate is first reduced to α–glycerophosphate by the

enzyme glycerol – 3 – phosphate dehydrogenase. Co-enzyme NADH2 is oxidized in this

reaction. α–glycerophosphate is then hydrolysed by glycerol phosphatase to liberate

phosphoric acid and forming glycerol.



Synthesis of Fatty acids

Long chain saturated fatty acids* are synthesized in plants from active two carbon

units, the acetyl – CoA (CH3CO.CoA). Although the reactions of β – oxidation of fatty acids

are reversible, the fatty acids are not formed simply by the reverse reactions of β – oxidation.

Synthesis of fatty acids from CH3CO.CoA takes place step by step. In each step the fatty

acid chain is increased by two carbon atoms. Each step involves two reactions –

(i) In the first reaction which takes place in the presence of acetyl – CoA carboxylase, acetyl

  • CoA combines with CO2 to form malonyl – CoA (malonic acid is 3 – C compound). ATP

provides energy while Mn [++] and biotin are required as co-factors.

(ii) Malonyl CoA reacts with another molecule of CH3CO.CoA in the presence of fatty acid

synthetase and Coenzyme NADPH2 to form Coenzyme – A derivative butric acid (butyric

acid contains 4 – atoms). One mol. Of CO2, H2O and CoA are released while NADPH2

oxidised in the reaction.

Butyryl CoA, in the next step will combine with malonyl CoA to form CoA derivative of

fatty acid containing 6-C atoms. This process is repeated till Coenzymes-A derivative of

long chain fatty acid (which may contain up to 16-18C atoms) is produced.

(As a matter of fact the enzyme fatty acid synthetase is not simple but a complex of many

enzymes (multienzyme complex) and an acyl carrier protein called as ACP**. And actually

the reaction (ii) described above only summarises a number of reactions involved in the

synthesis of fatty acid from acetyl – CoA which can be grouped under 3 categories

Initiation reaction: In this reaction acetyl CoA transfers its acetyl group to one of the – SH

groups of multienzyme complex i.e. fatty acid synthatase.

Unsaturated fatty acids are synthesized by denaturation of saturated fatty acid. ACP is similar

to CoA in having phosphopantetheine as the functional unit in their structures. In CoA, it is

esterified to Adenosine 3, 5 – bisphosphate but in ACP, it is esterified to serine of a protein

chain consisting of 81 amino acids.


Chain elongation reactions

Six different reactions involved here are (i) malonyl transfer, (ii) condensation, (iii)

reduction, (iv) dehydration, (v) reduction and (vi) acyl transfer. Chain elongation starts with

the transfer of malonyl group from malonyl – CoA to second – SH group of the multienzyme

complex. Then, there is a condensation of the latter so that a 4 – C unit is produced. This

unit by next three reactions i.e. reduction, dehydration and reduction is converted into

saturated 4 – C unit (i.e. butyryl – CoA). In acyl transfer reaction the fatty acid residue is

transferred back to the – SH group to which the acetyl group was transferred in initiation

reaction. The cycle is repeated again and again with malonyl transfer, condensation etc. till

the fatty acid residue consists of up to 16 - 18 C atoms. Each such turn elongates fatty acid

chain by 2 – C atoms. Details of chain elongation reactions are given below


Termination reaction

When the fatty acid residue has attained a desired length the chain elongation stops at

reaction (v) and the cycle is not repeated. The acyl group instead of being transferred to the

  • SH of the enzyme is transferred to – SH group of Co-enzyme A (CoASH) molecule. Thus,

CoA derivate of the fatty acid is produced which can then be utilized in fat synthesis. The

enzyme becomes free.

It is believed that during this process of fatty acid synthesis, the acyl group of fatty acid

bound to the – SH group of ACP. The latter then passes it from one enzyme of the complex

to the other.


(3) Condensation of fatty acids and Glycerol

The fats or triglycerides are synthesized not from glycerol and free fatty acids but from

α – glycerophosphate and CoA derivatives of fatty acid, i.e. fatty acyl CoA residues. First,

there is acylation of α – glycerophosphate by two fatty acyl – CoA molecule to from

phosphatidic acid. Now dephosphorylation occurs in the presence of phosphatase and a

deglyceride is formed. The acylation of the free – OH groups of diglyceride completes the

biosynthesis of triglyceride or fat.


Summary Cheat Sheet

  • Review each concept section above in sequence to connect definitions, processes, and applied crop-physiology outcomes.
  • Focus on high-yield terms, pathways, and condition-dependent responses for exam-ready recall.
  • Use the listed examples, comparisons, and cycles as rapid-revision anchors before practice questions.

References

1 source

Lesson Doubts

Ask questions, get expert answers