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#Question id: 11902


A chemiosmotic model  has been proposed  to explain Polar transport , following steps are involve in the transport of auxin polarly;

a) IAA enters the cell either passively in the undissociated form (IAAH) or by secondary active cotransport in the anionic form (IAA–)

b) The cell wall is maintained at an acidic pH by the activity of the plasma membrane H+- ATPase

c) In the cytosol, which has acidic pH, the IAAH form predominates

d) The anions exit the cell via auxin anion efflux carriers that are concentrated at the basal ends of each cell in the longitudinal pathway

Which of the following is the correct statements about the polarly transporting of auxin?

#Unit 6. System Physiology – Plant
  1. A and B
  2. A, C and  D
  3. A, B and D
  4. B and D
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TLS Online TPP Program

#Question id: 3538

#Unit 8. Inheritance Biology

Monohybrid cross allowed between heterozygous Rr (Round) and RR (Round), all progeny having Round seeded plant were allowed to self-fertilize to produce numerous progeny that are 

TLS Online TPP Program

#Question id: 3542

#Unit 8. Inheritance Biology

All genes are not linked. The probability of a progeny being AaBBccDd from a corss between AABbccDd and aaBBccDD parents will be

TLS Online TPP Program

#Question id: 3545

#Unit 8. Inheritance Biology

Consider the accompanying pedigree of a rare autosomal recessive disease, PKU. Male with PKU marry with normal female whose father is PKU. What is probability of child affected with PKU?

TLS Online TPP Program

#Question id: 4900

#Unit 8. Inheritance Biology

The chlorophyll-deficient types occur in a particular plant species due to a mutation in the DNA of the chloroplast itself, Female cytoplasm chlorophyll-deficient organisms crossed with male normal chlorophyll will produce progeny

TLS Online TPP Program

#Question id: 17809

#Unit 8. Inheritance Biology

In humans, albinism (unpigmented skin, hair, and eyes) is due to an enzymatic deficiency, and it is an autosomal recessive trait. Suppose that in a small country of one million people (“Generation 1”), there are 500 aa albinos and 9000 Aa heterozygous carriers. What is the probability that a child will be albino if: Both parents are members of Generation 2, and one parent is albino and the other is non-albino.

TLS Online TPP Program

#Question id: 17808

#Unit 8. Inheritance Biology

In humans, albinism (unpigmented skin, hair, and eyes) is due to an enzymatic deficiency, and it is an autosomal recessive trait. Suppose that in a small country of one million people (“Generation 1”), there are 500 aa albinos and 9000 Aa heterozygous carriers. What is the probability that a child will be albino if: One parent is a non-albino member of Generation 2, and the other parent is a non-albino member of Generation 1.