Food Biochemistry and Food Processing (2 edition)

(Steven Felgate) #1

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
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