Structure and Significance of Amylose Molecule
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Questions and Answers

What causes iodine to turn from brown to blue-black when mixed with starch?

  • Iodine breaks down the helical structure of starch
  • Iodine forms a new chemical compound with starch
  • Iodine molecules fit into the helical structure of starch (correct)
  • Iodine neutralizes the acidity of starch
  • What is the primary function of cellulose in plant cell walls?

  • Facilitating cellular communication
  • Energy storage
  • Providing strength, rigidity, and support (correct)
  • Regulating metabolic processes
  • Which enzyme breaks the α(1->4) glycosidic bonds in glycogen during hydrolysis?

  • Debranching enzymes
  • Glycogen phosphorylase (correct)
  • Glycogenin
  • Amylase
  • How do cellulose chains establish strong cross-linking between each other?

    <p>Through hydrogen bonding</p> Signup and view all the answers

    What is the role of glycogenin in glycogen structure?

    <p>Acting as a core protein surrounded by glucose branches</p> Signup and view all the answers

    How do microfibrils contribute to plant cell walls?

    <p>By forming rigid structures through hydrogen bonding</p> Signup and view all the answers

    What type of bonds break upon hydrolysis of starch by amylase?

    <p>α(1-&gt;4) glycosidic bonds</p> Signup and view all the answers

    What is the main respiratory substrate obtained from starch breakdown?

    <p>Glucose</p> Signup and view all the answers

    What characteristic of amylose makes it ideal for storage?

    <p>Six glucose per turn in a helical shape</p> Signup and view all the answers

    Why is amylopectin considered highly branched?

    <p>Due to branch points maintained by α(1-&gt;6) glycosidic bonds</p> Signup and view all the answers

    What happens when debranching enzymes break α(1->6) glycosidic bonds in amylopectin?

    <p>Amylopectin converts into a linear structure</p> Signup and view all the answers

    Why does starch not affect the osmotic concentration in cells?

    <p>-OH groups in starch are unavailable due to intra-chain hydrogen bonding</p> Signup and view all the answers

    Study Notes

    Structure and Property of Starch

    • Composed of thousands of glucose linked by α(1→4) glycosidic bonds, storing large amounts of energy
    • α(1→4) glycosidic bonds can be broken by amylase, hydrolysing starch into glucose for respiration
    • Amylose chains are helical in shape, with six glucose per turn, maintained by intra-chain hydrogen bonding between hydroxyl groups of glucoses
    • Amylopectin are highly branched due to branch points maintained by α(1→6) glycosidic bonds, compact and ideal for storage
    • Debranching enzymes break α(1→6) glycosidic bonds, converting the branched structure of amylopectin into a more linear structure, increasing the accessibility of the remaining linear chains to amylase
    • -OH groups are occupied in intra-chain hydrogen bonding, making starch insoluble and osmotically inactive, thus does not affect osmotic concentration in cells

    Starch Test

    • In the presence of starch, iodine forms a complex with starch molecules, resulting in a color change from brown to blue-black
    • Iodine molecules fit into the helical structure of starch, changing the refractive index and causing the color change

    Glycogen

    • Branched chain polymer of α glucose, similar to amylopectin but larger and more highly branched
    • Easily hydrolysed to α glucose by debranching enzymes and glycogen phosphorylase
    • Functions as energy storage in animals, with a core protein of glycogenin surrounded by branches of glucose

    Cellulose

    • Comprises up to 50% of plant cell walls, providing strength, rigidity, and structural support to plant cells
    • Protects plant cells and cytoplasm from damage and mechanical injuries
    • Despite its strength, the cellulose cell wall is fully permeable to water and solutes, allowing for the functioning of plant cells
    • Structure consists of unbranched polysaccharide of β glucose linked by β(1→4) glycosidic bonds, with each chain consisting of 1000 or more β glucose residues
    • Formation of β(1→4) glycosidic bonds requires the 180º rotation of alternating glucose residues, resulting in straight chains of cellulose
    • Hydroxyl groups (-OH) project outwards, allowing for the formation of hydrogen bonds between adjacent chains, establishing a rigid cross-linking between the chains
    • Many unbranched linear chains run parallel to each other, forming microfibrils, macrofibrils, and fibers, contributing to the tensile strength of plant cell walls

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    Description

    Learn about the structure and significance of amylose, a polysaccharide composed of glucose molecules linked by α(1->4) glycosidic bonds. Discover how amylose stores energy, can be broken down by amylase into glucose for respiration, and its helical shape maintained by hydrogen bonding for compact storage.

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