BLBS102-c27 BLBS102-Simpson March 21, 2012 13:25 Trim: 276mm X 219mm Printer Name: Yet to Come
27 Biochemistry of Fruits 539
Glucose-1-phosphate
ADP-glucose
pyrophosphorylase
UDP-glucose
pyrophosphorylase
ADP-glucose
Starch synthase
Amylopectin
Branching
enzyme
α-1-4-Glucan
primer
α-Glucosidase
α-Glucosidase Glucose
Glucose
Glucose-1-phosphate
Metabolic pool
Photosynthesis
Carbohydrate metabolism in fruits
Maltose
Maltose
(Amylose)
Hexokinase
Dextrins
α-Glucosidase
β-Amylase
H 2 O
α-Amylase
β-Amylase
AT P
AT P
ADP
UDP-glucose
Fructose-6-
phosphate
Sucrose
phosphate
synthase
Sucrose-6-phosphate
Phosphatase Pi
Sucrose
Starch
UDP-glucose
UDP-glucose
pyrophosphorylase
Starch
phosphorylase
Invertase Sucrose
synthase
Fructose
Glucose
+ fructose
PPi
PPi
PPi
UTP
UTP
UDP
Figure 27.2.Carbohydrate metabolism in fruits. UDP, Uridine diphosphate; UTP, Uridine triphosphate.
enzymes which cleaves theα-1,6-linkages in amylopectin and
releases linear units of the glucan chain.
In general, starch is confined to the plastid compartments of
fruit cells, where it exists as granules made up of both amylose
and amylopectin molecules. The enzymes that catabolise starch
are also found in this compartment and their activities increase
during ripening. The glucose-1-phosphate generated by starch
degradation (Fig. 27.2) is mobilised into the cytoplasm where
it can enter into various metabolic pools such as that of gly-
colysis (respiration), pentose phosphate pathway (PPP) or for
turnover reactions that replenish lost or damaged cellular struc-
tures (cell wall components). It is important to visualise that
the cell always tries to extend its life under regular develop-
mental conditions (the exceptions being programmed cell death
which occurs during hypersensitive response to kill invading
pathogens, thus killing both the pathogen and the cell/tissue;
formation of xylem vessels, secondary xylem tissues, etc.), and
the turnover reactions are a part of maintaining the homeostasis.
The cell ultimately succumbs to the catabolic reactions during
senescence. The compartmentalisation and storage of chemical
energy in the form of metabolisable macromolecules are all the
inherent properties of life, which is defined as a struggle against
increasing entropy.
The biosynthesis and catabolism of sucrose is an important
part of carbohydrate metabolism. Sucrose is the major form of
transport sugar and is translocated through the phloem tissues
to other parts of the plant. It is conceivable that carbon dioxide
fixed during photosynthesis in leaf tissues may be transported
to the fruits as sucrose during fruit development. Sucrose is
biosynthesised from glucose-1-phosphate by three major steps
(Fig. 27.2). The first reaction involves the conversion of glucose-
1-phosphate to UDP-glucose by UDP-glucose pyrophospho-
rylase in the presence of UTP (Uridine triphosphate). UDP-
glucose is also an important substrate for the biosynthesis of