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UNIVERSITI PUTRA MALAYSIA
THERMAL PROCESS REQUIREMENT AND STORAGE STABILITY OF CANNED GUAVA DRINK
ISHAK BIN SULAIMAN
FSMB 1993 3
THERMAL PROCESS �1Rl'.}U'lff AND S'roRAGE STABILITY OF CANNED GUAVA DRINK
BY
ISHAK BIN SULAIMAN
Thesis Sul:mi.tted in Fulfilment of the Requirements for the Degree of Master of Science in the Faculty
of Food Science and Biotechnology, Universiti PertanianMalaysia
February, 1993
I l ike to take the opportunity to acknowl edge my
i ndebtedness to the chai rman of my supervisory carmi ttee, Dr.
Asbi Ali and the ccmn:i. ttee members, Dr . Sal mah Yusof and Dr.
Jinap Sel amat for their guidance, supervision and suggestions
throughout the runni ng of the project and the preparation of the
thesis.
My sincere gratitude is also extended to the Mini stry of
Educati on, Malaysia for providi ng me the fi nancial support under
Training Scheme Fel lowship (Worl d Bank Loan VII) .
I would l ike tQ thank my col l eagues and fel l ow friends in
the Facul ty of Food Science and Biotechnology, Uni versi ti
Pertani an Mal aysia for their val uabl e assistance .
Final l y, I l ike to affectionately acknowl edge my wife,
Shamsiah, for her constant encouragement and support .
11
t
TABLE OF <XIfl'9fl'S
Page
ACKNCML�S • • • • • • • • • • • • • • • • • • • • • • • • • I • • • • • • • • • • • • • • • ii
LIST OF TABLES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . vi
LIST OF FIGURES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . viii
ABSTRACT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . , . . . . . . . . . . . . . . . x
ABSTRAK . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . xiii
I INTRODUCTION 1
I I LlTERA'1t1RE REVIEW 5
Guava . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Bioch�cal Characteristics of Guava 6
Guava Processing . . . . . . . . . . . . . . . .. . . . . . . . . . . . 11
Thermal Processing of Fruit Juices and Beverages 15
Enzyme Inactivation in Fruit Juices 23
Pectinesterase Inactivation as Basis of Themel Process Evaluation . . . . . . , . . . . . . . . . . . . . 31
storage Stability of Fruit Juices and Beverages 38
III THERMOSTABILITY OF PECTINESTERASE IN GJAVA DRINK 43
Introduction . . . . , . . . . . . . . . . . . . . . . . . .. . . . . . . . . . . . . . . 43
Materials and Methods . . . . . . . . . . . . . " " . . . . . . . . . . " . . . 45
Materials . . . . . . . . . . . . . . , . . . . , . . . . . . . . . . . . . . . . . 45
iii
IV
v
Preparation of Guava Drink . . , . . . . . . . . . . . .. . , . . . 45
Detennination of Therrral Inactivation Time of Pectinesterase ... . . . . . . . . . . . . . . . . . . . . . . . . . . 46
Quantitative Estimation of Pectinesterase Activity . . tI • • • • • • • • • • • • • • • • • • • • • • • • , • • • • • • • • • • 47
Calculation of Lethality of the 'come-up Time' . . 47
Determination of Decimal Reduction Time
Results and Discussion . . . . . . . . .. . . . . . . . . . . .. . . . . . . .
50
50
Thermal Inactivation Time of Pectinesterase 50
Decimal Reduction Time of Pectinesterase
Conclusion . . . . . . . . , . . . , . . . . . . . . . . . . . . . . . . . . , . . , , . .
THERMAL PROCESS REQUIREMENT OF CANNED GUAVA DRINK • •
Introduction .. . . . .. . . . . . . . . . . . .. . . . , . . . . . . . . . , . . . .
Materials and Methods
Materials . . . . . . . . . . . . . . , . . . . . . . . . . . . . . . . . . .. , . .
Heat Penetration Studies . . . . . , . . . . . . . . . .. . . . . .
calculations of Process Time
58
63
65
65
67
67
67
68
Microbiological Examdnation of Processed cans .. 69
Results and Discussion . . ... . .. . . , . . . ... . . . . . ... . . .
Thermal Process calculation • • • • , • • • • • • • • II • • • • •
Microbiological Safety of Process Evolved
Conclusion
STORAGE STABILITY OF CANNED GUAVA DRINK
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Materials and Methods .. . . . .. .. . . . . , . .. . . . . . . . . .. . . .. .. . .
iv
71
71
78
82
84
84
85
Processing and Sample Preparation
Analyses of Guava Drink SaJTI)le . . . . . . . . . . . . . . ..
Ascorbic Acid Measurement .................... .
Browning Measurement ......................... .
Total Soluble Solids and pH Measurements . . . • . . . .
Titratable Acidity Measurement ............... .
Cloud stability Measurement .................. .
Viscosity Measurement
Orgarl.ol eptic study . . . . . . . . . . . . . . . . . . . . . . . . . . . .
statistical Treatment
Results and Discussion
Ascorbic Acid Degradation . . . • • . . . . . . • • • . . . . . . .
The Development of Browning
Cloud stability ...................... " . . . . .. . . .
Changes in Viscosity
Changes in Acidity and pH . • . . . • . . . . . . • • • • . . . • .
Changes in Total Soluble Solid content ....... .
Sensory Evaluation . I I • • • • • • I I I I • • • • • • • • • • • • • I I
COncl'llSion ., . . . . . I • • • • • • • • • • • • • • • • • • • • • , • • • • • • • • • •
VI SUMMARY AND �ATIONS ...................... .
BIBLlOORAPtIY .............. , . . . . . . . , .. . . . . , . . . . . . . . . . .... .
APPmDlCES • • • • • • • • • • • • • • . • • • • • • • • • • . • • • • • • • . , . . • • • • . . • . . .
BIOGRAPHICAL SKETCH . .. . . . . . . . . . . . . . . .. . . . . . . . . . . . � . . . . . . .
v
85
86
86
87
87
87
88
89
89
89
90
90
97
101
105
108
112
112
118
119
125
139
152
LIST OF TABLES
Table Page
1 Nutrient and Proximate Composition of Guava Fruit 7
2 Classification of Canned Foods on Basis of Processing Requirements . . ...................... . . .. 18
3 Range of Processing Temperatures Used for Fruit Products . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
4 Flash Pasteurisation Conditions for Fruit Juices 24
5 Batch Process Requirements for Canned Fruit Juices 26
6 Thermal Inactivation Data of Pectinesterase in Various Types of Fruits . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
7 F, D and Z-Values of Pectinesterase in Guava Drink 57
8 Process Time Calculated by Fo�la Method to Achieve 1.5 D Process for Guava Drink canned in 300 x 305 Carls . . , . ,' • • • . , . • • • . , • • • • • • t, ' • • • • • • • • • , I , , 76
9 The Process Times for Different F Values 10 Means of Sensory Panel Score for COlour, Flavour,
80
Taste, Cloudiness and Overall Acceptability . . . . ... . 114
11 ANOVA Table for Vitamin C in canned Guava Drink D'uI"ing storage .. ... . . . . .. . ..... .. .... . . , ........ ,.. 142
12 ANOVA Table for Browning in Canned Guava .Drink During storage ........ " . . . . . . .. .. . . ....... . . . . . . , . . , 1 43
13 ANOVA Table for Cloud Loss in canned Guava Drink During storage ... " . . . . . . . . II • • • • • • • • • • • • • • • • I • • • • • • • 144
14 ANOVA Table for Viscosity in Canned Guava Drink During storage ... . ... .... . . . ..... III • • • • • • • • • • • • • • , • • 145
15 ANOVA Table for Total Acidity in Canned Guava Drink D'uI"ing storage . . • . . . . . . . . • . . . • . . . . . . . . . . . . . . . 146
vi
16 "PJ.-{OVA Table for pH of Canned Guava Drink During storage . " " .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 147
17 "PJ.-{OVA Table for Total Soluble Solid in Canned Guava Drink During Storage . . . . . . . . . . . . . . . . . . . . . . . . . 148
18 Analysis of Variance of Sensory Scores for Canned Guava Drinlt .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. , 149
vii
LIST OF FIClJRES
Figure Page
1 Pectinesterase Inactivation at 900C for Various Heating Times and Soluble Solid Concentrations (100 - 3SOsrix) .......... , ........... , . . . . . . . . . . . .. . 34
2 A Typical Heat Penetration Curve and Lethality CUrve of Came-up Time .............................. 49
3 Percent Residual Activity of Pectinesterase as a Function of Heating Temperature and Time . . . . • . . . . . . 52
4 Uncorrected Thermal Inactivation Time CUrve of Pectinesterase . . . . . . . . . . . . . . . . . . . . . . .. . . . . . . . . . . . . . , 54
5 Thermal Inactivation Time and Thermal Resistance CUrves of Pectinesterase in Guava Drink ............ 55
6 Thermal Inactivation Rates CUrves of Pectinesterase . 60
7 Heat Penetration Curves of Canned Guava Drink
8 Heating CUrves of canned Guava Drink
9 Cooling CUrves' of canned Guava Drink
10 Process Time as a Function of Heat Treatment
72
73
74
Level and Fill-in Temperature ...................... 79
11 Percent Retention of Ascorbic Acid in canned Guava Drink as a Function of Storage Temperature and Heat Treattnent Level ........ , . . . . . . . .. . . . . . . . 11 • • • • • 91
:2 Log Percent Retention of Ascorbic Acid in Canned Guava Drink as a Function of storage Temperature and Heat Treatment Level ........................... 95
13
14
Browning in Canned Guava Drink as Affected by storage Temperature and Heat Treatment Level
Cloud Loss in canned Guava Drink as Affected by Storage Temperature- and Heat Treatment Level
viii
99
102
15 Viscosity in canned Guava Drink as Affected by storage Temperature and Heat Treatment Level . . . . . . .
16 Total Titratable Acidity in canned Guava Drink as Affected by storage Temperature and Heat Treatment
106
Level . . , . . , . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 109
17 PH of canned Guava Drink as Affected by storage Temperature and Heat Treatment Level . • . . . . . . . • . . . . . 111
18 Total Sol uble Solid in canned Guava Drink as Affected by Storage Temperature and Heat Treatment Level 113
ix
Abstract of the Thesis Subndtted to the senate of the Universiti Pertanian Malaysia in Fulfilment of the
Requirements for the Degree of Master of Science
'J.'H!»W, PROCESS �IREJotm'l' AND STCJWlE STABILITY OF CANNED GJAVA mINK
By
ISfAK BIN SULAIMAN
February , 1993
Chairman Asbi bin Ali, Ph.D.
Faculty Food Science and Biotechnology
A thermal process for canned guava drink was evolved on the
basis of inactivation of pectinesterase (PE) , the most heat
resistant enzyme naturally present in guava. The
thermostability of PE in guava drink was deterrrdned according
to the thermal inactivation time tube method. The kinetics of
themal inactivation of PE in guava drink showed it obeyed
first-order reactions. '!'he therrral inactivation time curve of
the enzyme was analogous to the themal death time curve of
bacteria. As the heat resistance of spoilage rrUcroorganisms is
lower than PE in acidic conditions, the enzyme was used in the
thermal process evaluation of canned guava drink.
x
The F and D values of PE in the guava drink (pH 3.7) at
100.4oC were 1.0 minute and 0.67 minute, respecti vel y . The F
value was equivalent to 1.5 D. This data was used as the
basis for the calculation of process time by the formula method.
The heat penetration study was carried out in 300 x 305 cans.
The �rocess requirements under different initial temperatures
were determined. It was found that when the filling temperature
was 750C, to achieve F i�O.4 = 1 . 0 , no processing was required if
1.5 D process was considered as the minimum lethal i ty . For 2 D
process, the filling temperature required was 80oC.
The microbial and storage stability s�udy of the canned
drink showed that the process rendered the product
microbiologically safe and organoleptically acceptable. The 1.5
D was the minimum safe process for the canned guava drink .
However, a 2 D process is recommended for commercial processing,
when variation of PE concentration in guava is taken into
consideration.
Significant changes during storage of canned guava drink
processed with 2 D and 3 D indicated the effect of heat
treatment levels on the quality of the product. storage
temperature had appreciable effect on the ascorbic acid content,
colour, cloudiness, acidity, pH, viscosity and total soluble
solid. Sensory quality scores were most affected by storage
xi
temperatures rather than the heat processing levels . Thus, a 2
D process and storage at refrigerated terrperatures (SoC) is
recarmended for canned guava drink as it was the most stabl e
during storage .
xii
Abstrak Tesis Yang Dikemukakan Kepada Senat Universiti Pertanian Malaysia Sebagai Memenuhi Syarat
Keperluan untuk Ijazah Master Sains
� PDtPROSESM 'lDHA OM RES'l'ABILAN PEl'fYIMPMAN MI� JltMBJ BA'l'U l:\ALMl TIN
Oleh
IsmK BIN SULAIMAN
Februari, 1993
Pengerusi: Asbi bin Ali, Ph.D.
Fakul ti Sains Makanan dan Bioteknologi
Suatu ketetapan pemprosesan terma untuk rrQnuman jambu batu
dalam tin telah dibuat berdasarkan penyahaktifan enzim
pektinesterase (PE). FE merupakan enzim semulajadi yang
terdapat dalam jambu batu. Kestabilan terma PE di dalam minuman
jambu batu telah ditentukan mengikut kaedah tiub masa
penyahaktifan terma. Kinetik bagi penyahaktifan terma FE
menunjukkan ianya mematuhi tindakbalas tertib-pertama.
Keluk masa penyahaktifan terma (TIT) bagi enzim tersebut
menyerupai keluk masa kenusnahan terma (TOT) bakteria. Dalam
keadaan berasid, kerintangan haba bagi mikroorganisma perosak
1 ebih rendah daripada FE. Dengan demikian, enzim tersebut
xiii
digunakan sebagai asas penilaian perrprosesan terma pengetinan
minunan jambu batu.
Nilai-nilai F dan D bagi PE di dalam �numan jambu batu ( pH
3 . 7) pada 100. 4°C adal ah masing-masing 1.0 min dan O. 67 min.
Nilai F adalah setara dengan 1. 5 D. Data ini digunakan sebagai
asas pengiraan mas a perrprosesan dengan menggunakan kaedah
formula . Ujian penusukan haba telah dijalankan dalam tin
berukuran 300 x 305. Keperl uan perrprosesan bagi suhu awal yang
berl ainan telah ditentukan. Didapati jika pemprosesan dilakukan
berdasarkan kemusnahan �nimum 1.5 D , tiada perrprosesan
diperlukan bila suhu pengisian 7SoC . Bagi pElTQ?rosesan 2 Df suhu
pengisian yang diperlukan adalah SOoC .
Kajian kestabilan mikrob dan penyimpanan minuman jambu batu
menunjukkan pemprosesan tersebut selamat daripada segi
mikrobiologi dan baik daripada segi organoleptik . Pemprosesan
1.5 D adalah tahap minimum yang selamat bagi pengetinan minuman
jambu batu. Walau bagairranapun , pefIi>rosesan 2 D disyorkan untuk
pemprosesan komersial apabila variasi kepekatan PE di dalam
jambu batu diambil kira.
Perubahan bererti serrasa penyimpanan minuman jambu batu
yang diproses pada 2 D dan 3 D menunjukkan kesan paras perl akuan
haba terhadap kuali ti produk . Suhu penyimpanan memberi kesan
xiv
�ang ketara ke atas kandungan asid askorbik, warna, kekel adakan,
keasidan, pH, kelikatan dan jumlah pepejal l arut. Suhu
penyilll?anan rnemberi kesan yang 1 ebih ketara pada skor atdbut
deria berbanding dengan paras pemprosesan haba . Ol eh itu,
PEI'I'Prosesan 2 D dan penyinpanan dingin (SoC) disyorkan bagi
min\lTBIl jambu batu yang ditin . Keadaan ini menghasilkan minuman
yang paling stabil semasa penyinpanan.
xv
0IAPl'ER I
INTROIXJCTION
Guava (Psidium guajava L.) is one of the fruits that has
been cultivated on a commercial scale. There are approximately
1,322 hectares of guava farms in Peninsular Malaysia. Its total
production for the year 1990 was about 25,200 metric tonnes.
About 70% of this was of the Vietnamese variety, and 26% of the
Taiwan variety. The seedless, Glohmsahlee and Kampuchea
varieties constitute around 1% to 2%, respectively (FAMA, 1988;
F;MA, 1989; Malaysia 1989).
Salmah (1985) found that the Vietnamese variety contained
the highest amount of vitarrdn C compared to several other local
guava varieties. Aside fram its high ascorbic acid content, the
flavour of guava is its most distinguishing characteristic.
Guava of the Vietnamese variety was found to be suitable for
processing (Salmah and Suhaila, 1987).
Guava can be processed into various products such as puree,
juice, nectar, jellies, jams, cheese, ketchup, juice powder and
canned product. Guava drink is one of the tropical fruit
beverages that has a good demand in the world market.
1
2
Thermal processing is an important step in guava processing ,
Fruit products such as puree and juices should be processed at
such temperatures and for such time periods as would render them
sterile without impairing their flavour and the nutritional
values. Therefore, it is important to find the optimum time and
temperature relationship required for the pasteurisation of
fruit juices.
Different fruit juices require different amount of heating.
The severity of the heat treatment and the resul ting extension
of shelf life are determined IOOstly by the pH of the product.
Since fruit juices are considered as acid food, severe heat
treatment is not necessary. It is sufficient to process them at
1000C or below (Woodroof, 1986).
Guava contains enzymes such as ascorbic acid oxidase,
polyphenoloxidase, peroxidase and pectinesterase.
Pectinesterase is the most heat stable enzyme in guava pulps
(Garces, 1963; Nath and Ranganna, 1983). In guava pulp (Garces,
1963), the inactivation time of peroxidase was found to be
minimum (7.5 minutes at 650C) and that of pectinesterase l'1as
found to be rraximum (5 minutes at 98oC). The presence of
pectinesterase will hydrolyse the pectin molecules resulting in
sedimentation of the colloidal particles in puree and juices.
3
The enzymes as well as the organisms present in the juice
have to be inactivated in order to avoid undesirable changes
during storage. The�l inactivation is extensively used as it
simultaneously destroys ndcroorganisms (Whitaker, 1972) .
TEfIl'eratures of 700 to 75°C are sufficient to destroy nomal
ndcrobial population. However, to inactivate pectinesterase,
heating at temperatures of 900 to 1000C is required (Desrosier,
1977) .
Since pectinesterase is the most heat stable enzyme, it has
to be considered in guava juice processing. Lund (1975b)
suggested considering enzymes instead of microorganisms in
thermal process evaluation of acid foods. In thermal process
calculation based on enzyme inactivation, the most heat
resistant enzyme is selected as the basis of the process, just
as the lOCIst heat-resistant pathogenic or spoilage organism is
used for microbial inactivation.
The�l processing of guava pulp has been evaluated based on
destruction of pectinesterase and microorganisms. It was found
that the thermal resistance of pectinesterase was higher than
that of microorganisms (Nath and Ranganna, 1983).
According to Chan (1983), pasteurisation of guava nectar is
best done in a plate heat exchanger and a few seconds at a
temperature of 73.90C or more are usually sufficient. However,
4
Luh (1980a) recommended that flash pasteurisation of guava drink
(nectar) should be done at 82. 2° - 87 . 80C for 60 seconds.
The objecti ve of the study was to establ i sh the thetl'T'al
process requirement for processing of canned guava drink. Since
pectinesterase is the most heat stabl e, the therroostabil ity of
the enzyme was dete�ned and used as the basis for the thetl'T'al
process eval uation . storage stabi lity of the canned guava drink
processed at different heat treatment levels and stored at
different temperatures was also evaluated .
<lIAPl'm II
LITmATORE RlWIBf
Guava
Traditionally, production of fruits in Malaysia has been
aimed mainly to meet the demands of the fresh market. However I
wi th the country's interest in general fruit processing and
development of the food products, the trend has been to upgrade
fruit growing frem the present subsistence level to a more
profit oriented plantation scale. Guava is one of the fruit
items that has been cultivated on a ccmnercial scale (FAMA,
1989). The potential of the guava industry in Malaysia is
excellent (Chan and Tee, 1976).
The guava (Psidi urn guajava L.) varieties found in Malaysia
are au 3, GU 4, GU 5, GU 6, GU 7, GU 8 (Kampuchea), GO 9
(Gl ohmsahlee or Hamsad), GU 10 (Kloontau), Maha 1, Pahang 4,
Serdang Bharu, Lebai Mel aka, Beaumont, Laknow, Indian guava,
Allahabad sateda, Taiwan rormd, Tai wan long, Vietnamese, Hong
Kong Pink, Mal acca seedless, Bentong seedless, Thai seedless and
Indonesian seedless (Chan and Tee, 1976; FAMA, 1989; Malaysia,
1989). However, only a few varieties are grown on large scale.
Based on the guava production in 1987, about 70% was of the
5
6
vietnamese variety, followed by Taiwan variety, 26%. The
seedless, Hamsad and Kampuchea varieties constitute around 1%
to 2%, respectively (FAMA, 1988) .
Biochemdcal Characteristics of Guava
Nutritionally guava is an excellent source of ascorbic acid.
Wilson ( 1980) reported that the average vitarrdn C content was as
high as 336.8 ITg/ 100 9 fruit. By far, the guava is more
nutritious than most of the irrq;>orted fruits (such as apple,
grape, pear, mandarin orange, avocado) in tet'TTG of vitamin C
content (Chan and Tee, 1976) . Ascorbic acid is not distributed
uniformly in the fruit tissues. The skin and outer flesh of
guava fruit contain most of the ascorbic acid (Agnihotri et al.,
1962; El-Zorkani, 1998; Salmah, 1985; Braverman, 1963) .
High vitarrdn C content is an important factor in selecting
fruit types for processing. Salmah ( 1985) found that the
Vietnamese variety contained the highest amount of vitamin C
(180 rng/100 9 fruit) compared to several other local guava
varieties. Ripening the fruits to a yellow-green stage would
further increase the vitamin C content (Salmah et ai., 1988).
The total sugar val ues in guava range from 4.3% to 9.0%
(Wilson, 1980). Glucose is the predarrnnant sugar, followed by
Table 1
Nutrient and Proximate Composition of Guava Fruit ---------------------------------------- ----------------------------------------------------------
Composition
Proximate Composition
Energy Moisture Protein Fat Carbohydrate Fibre Ash
Mineral s
Calcium Phosphorus Iron Sodium Potassi':lffi
Vitamins
Ascorbic acid Carotene RE B1 B2 Retinol Niacin
* Average
46 . 0 kcal 81 .2 9
1 . 1 g 0 . 2 9
10 . 0 9 6 . 8 9 0 . 7 9
33 . 0 rrg 15 .0 rrg
1 . 2rrg 23 .0 rrg 29 . 0 rrg
152 . 0 rrg 60 .0 J.lg 10 . 0 .llg
0 . 1 rrg 50 . 0 .llg
o .llg 1. 1rrg
================================================ *per 100 g edible portion
Adapted from Siang et al. (1988)
7
8
fructose and sucrose ( Salmah, 1989) . The total soluble solids
of the mature and ripened Vietnamese variety range fran 6% to 7%
( Salmah et al., 1988) . The predaninant organic acids in a
white-variety guava was citric acid . Mal ic and glycolic acids
present in much l esser amounts (Fang, 1965) . The acidity of
guavas range fran 0 . 33% to 0 .99% and the pH fran 3 .0 to 5 .4 .
The JOOre acid fruits are better for processing than sweeter
fruits (Wi lson, 1980; Luh, 1980a; Salmah, 1989) .
The acidity plays an important part in the fl avour
acceptance of the fruit and its processed products . Because of
the l ow acid, high sugar and total soluble sol ids contents, the
sugar-acid ratio and brix-acid ratio of guava are general ly high
but quite variabl e (Wilson , 1980) . For the Vietnamese variety,
the highest val ue of the brix-acid ratio was 16 . 3 , obtained
after ripening the fruits to a yel l ow-green stage ( Salmah et
al. , 1988) .
Guava is a potential source of pectin ( Pruthi et al., 1960;
Verma and Srivastava, 1966; Shastri and Shastri, 1975; Wilson,
1980). Values for total pectin range fran 0 . 5% to 1 . 8% . The
methoxyl content of purified guava pectin is rel atively l ow
( about 55%) , but pectin with characteristics sirrdlar to those of
commercial pectins has been prepared. The yield of pectin
t t
9
(about 11\ on dry weight basis) is larger than yields fran
citrus or pasion fruit peel (Muroki and Saint-Hilaire, 1977).
Good gel can be obtained at 65\ sol ubI e sol ids at pH 2 .1 to 2 .4
(Luh, 1980a).
The function of pectin in fruit juices is to hold the
colloidal material together and maintain them dispersed in
solution, thus contributing to the haze (commonly referred to as
, cloud') or body of the juice. Other product characteristics
affected by pectin include viscosity, colour stability and
flavour.
The enzyme, pectinesterase is also present in guava
(Rieckehoff and Rios, 1956; Garces, 1963; Shastri and Shastri ,
1975). They found most of the activity of the enzyme
associated with the peel and considerably less activity
associated with the flesh. The enzyme activity was fairly high
at immature stage, dec�eased considerably at mature stage, again
increased as the fruits became ripe. The acti vi ty was maxinrum
at overipe stage (Pal and Selvaraj, 1979). With the presence of
pectinesterase, pectin molecules can easily be hydrolysed
resul ting in sedimentation of the colloidal particles (cloud
loss) in frui t puree and juices. In guava processing,
pectinesterase has to be iHactivated.