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(1)

Effects of Continuous Application of CO

2

on

Fruit Quality Attributes and Shelf Life during Cold Storage in Cherry Tomato

Adanech Melaku Taye, Shimeles Tilahun, Do Su Park, Mu Hong Seo, and Cheon Soon Jeong*

Department of Horticulture, Kangwon National University, Chuncheon 24341, Korea

*Corresponding author: [email protected]

‘Unicon’ cherry tomato (

Solanum lycopersicum

) is one of the most highly perishable horticultural crops due to its high water content and respiration rate. This study was carried out to assess the effect of continuous application of CO2 (control [air], 3%, and 5%) on the quality and shelf life of cherry tomato fruits stored at 10°C and 85 ± 5% relative humidity (RH) at two maturity stages (pink and red). Continuous application of CO2 did not affect the soluble solids content (SSC) or titratable acidity (TA) of the fruit at either maturity stage during storage.

However, there was a significant difference among treatments in terms of flesh firmness, cell wall thickness, pectin content, vitamin C content, skin color, lycopene content, weight loss, ethylene production rate, respiration rate, and acetaldehyde and ethanol production. Fruits treated with 5% CO2 maintained their high quality with regards to vitamin C, skin color (

a

*), lycopene content, weight loss, physiological parameters (ethylene production rate, respiration rate, and volatile compounds), flesh firmness, cell wall thickness, and pectin content at both maturity stages compared with 3% CO2 treatment and the control. Continuous application of CO2 (5%) reduced the ethylene production rate and the production of volatile compounds during storage. Therefore, cherry tomato ‘Unicon’ fruit can be stored for two weeks without losing fruit quality at both maturity stages under continuous application of 5% CO2 as a postharvest treatment.

The work was supported by the Korea Institute of Planning and Evaluation for Technology in Food, Agriculture, Forestry, and Fisheries (IPET) through the Agri-Bioindustry Technology Development Program, funded by the Ministry of Agriculture, Food, and Rural Affairs (MAFRA) (314086-3) and by a 2015 Research Grant from Kangwon National University (No.

520150123).

HORTICULTURAL SCIENCE and TECHNOLOGY 35(3):300-313, 2017

URL: http://www.kjhst.org pISSN : 1226-8763 eISSN : 2465-8588

This is an Open-Access article distributed under the terms of the Creative Commons Attribution NonCommercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Copyrightⓒ2017 Korean Society for Horticultural Science.

OPEN ACCESS Received:

Revised:

Accepted:

September 1, 2016 March 20, 2017 March 24, 2017

Abstract

Additional key words: cell wall thickness, maturity stage, perishable, postharvest, volatile compounds

Introduction

Tomatoesareconsumedbroadlythroughouttheworld

,

andtheirconsumptionhasrecentlybeenshown tohavehealthbenefitsduetotheirhighphytonutrientcontents

(

LevyandSharoni

,

2004

;

Hsuetal

.,

2008

).

Postharvestrecommendationsindicatethattomatoes

,

includingcherrytomatoes

,

shouldbestoredat10

°

C orhighertoavoidchillinginjury

(

JimenezandCantwell

,

1996andRobertsetal

.,

2002

)

andthateven10

°

C maybeharmfultotomatoflavor

(

Mauletal

.,

2000

).

Oneofthemostcharacteristicphytonutrientsin tomatoislycopene

,

acarotenoidwithahighcapacityforreducingtheriskofchronicdiseasesthat represents

-

80

%

ofthetotalcarotenoidcontentsintomatofruit

(

Raoetal

.,

1998

).

Lycopeneaccountsfor

(2)

thereddeningoftomatoesduetothedifferentiationofchloroplastsintochromoplasts

(

Egeaetal

.,

2011

).

Hence

,

thiscarotenoid isfundamentalforthenutritionalqualityandcommercialvalueofthisfruit

(

Dumasetal

.,

2003

).

ThestorabilityofapplescanbeincreasedbytreatingfruitswithhighconcentrationsofCO2forashortperiodoftime

.

Burg andBurg

(

1967and1969

)

foundthatCO2functionsasacompetitiveinhibitorofethyleneaction

.

Beyer

(

1979

)

reportedthat suchanactionisrelatedtoethylenemetabolism

;

CO2canaffectthismetabolismbyinhibitingethyleneoxidation

.

Theactivity ofCO2indelayingtheagingrateisassociatedwithreducedrespiratorymovementandahindranceofthesuccinicoxidase complex

,

particularlysuccinicdehydrogenase

(

Ransonetal

.,

1960andShipwayandBramlage

,

1973

).

Inadditiontoits respiration

-

blockingactivity

,

CO2athighlevelsdiminishesethyleneevolutioninfruits

,

suchasapple

,

pears

,

andtomato

(

Bramlage

,

etal

.,

1977

;

Buescher

,

1979

;

Looney

,

1975

;

MarcellinandChaves

,

1983andWangandMellenthin

,

1975

).

According toFarber

(

1991

),

theoptimumconditionsformodifiedatmospherepackaging

(

MAP

)

storageoffruitsandvegetablesare3

-

8

%

CO2 and2

-

5

%

O2

.

Duetothelowstorabilityofcherrytomatofruit

,

manystudieshavefocusedondesigningvariouspracticalapproachesfor extendingthestorageperiod

,

includingcontrolledatmosphere

(

CA

)

storage

.

Short

-

termexposureoftomatofruitto80

%

CO2 stimulatestheethylenebiosyntheticpathwayduetotheinhibitionoftheripeningprocess

(

Hirofumietal

.,

1998

).

Treatmentwith 60

%

CO2for24hrreducedethyleneproductionintomatofruit

,

butitsharplyincreasedimmediatelyaftertheCO2treatment

.

Surfaceblemishes

,

increasedsoftening

,

andunevenripeningwerealsoobservedinfruitsafterremovalfromelevatedCO2 levels

(

Kuboetal

.,

1990andMorris

,

1977

).

However

,

nostudieshaveinvestigatedtheeffectsofcontinuousapplicationof

CO2 atlowtemperatureonfruitqualityattributesandshelflifeincherrytomato

.

Maintainingfruitqualityandaddingcommercial valuewillbenefitbothproducersandconsumers

.

Tomatofruitisperishable

,

chillingsensitive

,

andeasilyaffectedbynumerous fungaldiseases

(

Hoeberichtsetal

.,

2002

).

Inaddition

,

tomatofruithasashortshelflifeduetoitshighwatercontent

,

andits climactericnatureleadstoethyleneproductionandahighrespirationrateafterharvest

.

Therefore

,

inthecurrentstudy

,

we examinedtheeffectsofcontinuousapplicationof

CO2onfruitqualityattributesandshelflifeincherrytomato

.

Materials and Methods

Plant Material and Treatments

Cherrytomato

(Solanum lycopersicum) ‘

Unicon

fruitswereharvestedatthepinkandredmaturitystagesfromacommercial farminKangwonProvince

,

RepublicofKoreaonOctober15

,

2015

.

ThefruitswereimmediatelytransportedtothePostharvest QualityManagementLaboratory

,

DepartmentofHorticulture

,

KangwonNationalUniversityinanair

-

ventilatedautomobile within30minofharvest

.

Uponarrival

,

defect

-

freefruitsofuniformcolorweresorted

,

washedwithcoldwater

,

andair

-

driedfor 6hrs

.

Thesortedfruitwerecarefullytransferredto0

.

75Lplasticcontainers

(

16fruitspercontainer

)

forCO2treatment

.

The treatmentswereconductedusingacontinuousapplicationofCO2

(

control

[

untreated

,

air

],

3

%,

and5

% )

withtwomaturitystages offruit

(

pinkandred

)

inacompletelyrandomizeddesign

(

CRD

).

CO2wastakenfromagascylinderusingasyringeand immediatelyinjectedintothecontainer

,

andtherequiredpercentageofCO2wasconfirmedusingahandheldPBIDansensor gasanalyzer

(

CheckMate9900

,

Ringsted

,

Denmark

).

Thetreatedfruitswerestoredat10

°

Cand85

±

5

%

RH

.

Evaluationswere madeoncherrytomatofruitstoredinanevaluationroom

,

anddatawerecollectedfromeachtreatmentat2

-

dayintervals

.

(3)

Weight Loss, Flesh Firmness, Surface Color, Titratable Acidity, Soluble Solids Content, Ethylene Production Rate, and Respiration Rate

Weightlosswasdeterminedbymeasuringthefreshweightoffruitandcomparingthevaluetotheinitialfreshweight

.

Fresh weightwasmeasuredeverytwodaysfor15d

,

andweightlosswascalculatedbysubtractingfreshweightsfromtheinitial weightofthefruit

.

FleshfirmnesswasmeasuredusingaRheometer

(

modelcompact

-

100II

,

Meschede

,

Germany

)

witha maximumforceof10kganda3mmdiameterroundstainlesssteelprobewithaflattip

.

Surfacecolor

(a*

value

)

wasmeasured onfruitsmarkedalongtheirequatorregions

,

withthreereadingstakenusingaChromameter

(

modelCR

-

400

,

MinoltaCo

.,

Tokyo

,

Japan

).

Cherrytomatojuicewasanalyzedforsolublesolidscontent

(

SSC

)

usingarefractometer

(

Model

-

AtagoInc

.,

Tokyo

,

Japan

);

theresultswereexpressedin

°

Brix

.

Titratableacidity

(

TA

)

wasanalyzedusingaDL22FoodandBeverage Analyzer

(

MettlerToledoLtd

.,

Zurich

,

Switzerland

).

Dilutedjuice

(

1mLofjuice

:

19mLofwater

)

wastitratedwith0

.

1Nsodium hydroxideandtheresultswereexpressedasmg

·

100g-1ofcitricacid

.

TheethyleneproductionratewasmeasuredusingaGC

-

2010Shimadzu

(

ShimadzuCorporation

,

Tokyo

,

Japan

)

fittedwithaBP20waxcolumn

(

30m

×

0

.

25mm

×

0

.

25µm

)

andaflame ionizationdetector

(

FID

).

Thedetectorandinjectorwereoperatedat127

°

Candtheovenwassetat50

°

C

.

Thecarriergas

(

N

)

flow ratewas0

.

67mL

·

s-1

(

Parketal

.,

2000

).

TherespirationratewasmeasuredwithaPBIDan

-

sensor

(

CheckMate9900

,

Ringsted

,

Denmark

).

Vitamin C and Lycopene Content, Ethanol and Acetaldehyde Production

VitaminCwasanalyzedusinghighperformanceliquidchromatography

(

HPLC

) (

model

:

WatersAssociates

,

Milford

,

MA

,

USA

)

througha717plusautosamplerusingaZORBAXEclipseXDB

-

C18analyticalcolumn

(

4

.

6cm

×

250mm

×

5μm

,

Agilent Co

.,

Torrance

,

USA

),

aWaters600controllerpump

,

andaWaters486tunableabsorbancedetectorat265nm

.

Themobilephase was1

:

9and100

%

MeOH

:

0

.

1MKH2PO4

,

andtheflowratewas1

.

0mL

·

min-1

(

LiandChen

,

2001

).

Frozenfruittissue

(

1g

)

was mixedwith10mLof

5

%

metaphosphoricacidandhomogenizedusingaT25Ultra

-

Turrax

(

IKAKorea

.

Ltd

.,

Seoul

,

Republic ofKorea

)

untilcombined

.

Themixturewascentrifugedat20

,

000rpmfor10minutesat4

°

Candfilteredthrougha0

.

45μmfilter membrane

.

Thesample

(

1mL

)

wasanalyzedbyHPLCwiththreereplicates

(

Kimetal

.,

2011

).

Thelycopenecontentofthefruit wasanalyzedasdescribed

,

withslightmodifications

(

Fishetal

.,

2002

).

Frozenfruitwasgroundwithamortarandpestle

,

and1 ggroundsamplewashomogenizedwith1mLdistilledwaterusingaT25Ultra

-

Turraxstainlesssteelblender

(

IKAKorea

.

Ltd

.,

Seoul

,

RepublicofKorea

).

Tubescontaininghomogenizedsampleswerecoveredwithaluminumfoilandplacedoniceand combinedwith20mLofhexane

-

ethanol

-

acetone

(

2

:

1

:

1

),

followedbygentleshaking

.

Thesampleswerecentrifugedat 15

,

000rpmfor20min

,

followedbytheadditionof3mLdistilledwaterpervial

.

Thesampleswereagitatedfor2min

,

incubated atambienttemperatureforafewmin

,

andreadusingaspectrophotometer

(

ThermoFisherScientific

,

Madison

,

WI

,

USA

)

at503 nm

.

Hexanewasusedasablank

.

Ethanolandacetaldehydeweremeasuredusingthesameprocedureusedtomeasurethe ethyleneproductionrate

.

Cell wall Thickness and Water-soluble Pectin

Cellwallthicknesswasmeasuredunderascanningelectronmicroscope

(

SEM

,

Supra55VP

,

CarlZeiss

,

Germany

)

as describedbyIslametal

. (

2016

).

WatersolublepectinwasanalyzedbasedontheprotocolofBlumenkrantzandAsoe

-

Hansen

(

1973

).

(4)

Statistical Analysis

Significancetestswereconductedbyanalysisofvariance

(

ANOVA

)

usingSASVersion9software

(

SASInstitute

,

Cary

,

NC

,

USA

)

andExcel2010

(

MicrosoftCo

.,

WA

,

USA

).

Meancomparisonsweremadeusingleastsignificancedifference

(

LSD

)

at5

%

probability

.

Result and Discussion

Weightlossleadstoquantitativecroplosses

,

aswellasareductioninqualityduetoshrivelingandwilting

,

softeningoftissue

,

andalossofcrispness

(

Kader

,

1986

).

Wedetectedasignificant

( p <

0

.

05

)

differenceincherrytomatofruitqualityamong treatmentsatbothmaturitystages

(

Fig. 1AandB)

.

Thehighestweightlosswasfoundinthecontrol

,

followedby3

%

CO2 treatment

,

whiletheleastweightlosswasobservedinfruitsafter5daysof5

%

CO2treatmentatthepinkmaturitystage

.

However

,

therewasnodifferencebetween3

%

CO2and5

%

CO2treatmentsuntilday13

,

afterwhichweightlossincreased significantlyinfruitstreatedwith3

%

CO2

.

Thecontrolfruitsatbothmaturitystagesshowedmoreweightlossthanthetreated fruitsduetohigherrespirationratesandethyleneproduction

(

Fig. 3CandD, 4AandB), whichinturnresultedinwaterlossor shrinkageofthefruitsurface

.

Theseresultsindicatethatthecontinuousapplicationof5

%

CO2reducesweightlossintomato fruitduetoreducedethyleneproductionandrespirationduringcoldstorage

.

Therewassignificantdifference

( p <

0

.

05

)

infleshfirmnessamongtreatmentsatbothmaturitystages

(

Fig. 1CandD). Fruits treatedwith5

%

CO2weremuchfirmerthanthosetreatedwith3

%

CO2andthecontrolatbothmaturitystagesduringtheentire storageperiod

(

Fig. 1CandD). Attheredmaturitystage

,

untreatedfruitwerethesoftest

,

followedbyfruitsunder3

%

CO2 treatmentandthoseunder5

%

CO2treatment

.

Atthepinkmaturitystage

,

however

,

therewasnosignificantdifferencebetween fruitstreatedwith3

%

CO2anduntreatedfruitsthroughoutthestorageperiod

.

Atbothmaturitystages

,

fruitstreatedwith5

%

CO2maintainedfirmnessthroughoutthestorageperiod

.

Similarly

,

PorrittandMeheriuk

(

1977

)

reportedthattreatmentwith20

-

30

%

CO2at

0

°

Cfortwoweeksreducedthesofteningof

Newton

applefruitwithoutinducingCO2injury

.

Inthecurrentstudy

,

5

%

CO2

-

treatedfruitswerefirmerthanthosetreatedwith3

%

CO2andthecontrol

.

Atthepinkmaturitystage

,

fleshfirmnesswas reducedfrom9

.

80Nto5

.

48Nand7

.

85Nincontroland5

%

CO2

-

treatedfruits

,

respectively

.

ThehigherthelevelofCO2 treatment

,

thefirmerthefleshandthehigherthecellwallthickness

.

Treatmentwith10to20

%

CO2for10

-

14daysreducedthe degradationoffleshfirmnessin

GoldenDelicious

applefruit

(

Lauetal

.,

1977

).

Asthestorageperiodincreases

,

thethicknessof thefruitcellwalldecreases

,

alongwithcellwallbreakage

(

KashmireandKader

,

1978

).

Continuousapplicationof

CO2treatmentsignificantly

( p <

0

.

05

)

affectedthesurfacecolorchangeoftomatofruitduringcold storage

(

Fig. 2AandB)

.

Fruitcolorpeakedearlierinuntreatedfruitsthanintreatedfruits

.

After11days

,

thecolorvaluesof controlfruitsandfruitstreatedwith3

%

CO2weresignificantlylowerthanthoseof5

%

CO2

-

treatedfruits

.

ContinuousCO2 applicationdelayedthecolorchangeatthepinkmaturitystage

.

Thisresultissupportedbythefindingof

Sozzietal

. (

1999

)

that redcolordevelopedslowlyintomatofruitatthebreakerstageasaresultof

CO2treatment

.

Aharonietal

. (

1989

)

andMitcham

(

1997

)

alsoreportedthathighCO2concentrationssignificantlyreducedchlorophylldegradationingreenvegetablescompared withtheuntreatedcontrol

.

Similarly

,

thefruitsmaintainedtheirredcolorattheendofstorage

.

Colordevelopmentincherry tomatoesatthepinkstagebeganonday3and5under3

%

and5

%

CO2treatment

,

respectively

.

Bycontrast

,

colordevelopment inuntreatedfruitbeganonday5andreacheditspeakonday7

.

However

,

under3

%

CO2treatment

,

colordevelopmentbegan

(5)

earlierthaninuntreatedfruitandincreasedslowlyuntilitreachedaclimactericpeakonday11

.

Similarly

,

attheredmaturity stage

,

fruitunder5

%

CO2treatmentmaintainedbettercolorthanfruitundercontroland3

%

CO2treatmentthroughoutthe storageperiod

(

Fig. 2B)

.

Therewasnosignificantdifference

( p <

0

.

05

)

intitratableacidityamongtreatmentsatbothmaturitystages

,

althoughthe acidityvaluesofthefruitsdecreasedwithincreasingstorage

(

Fig. 2CandD)

.

Riquelmeetal

. (

1994

)

reportedthatstoring strawberriesunderlowO2andhighCO2concentrationsdidnotaffecttitratableacidity

.

Similarly

,

Biale

(

1960

)

reportedthat treatmentwith60

%

CO2hadnoeffectontitratableacidityin

Valencia

orangefruit

,

whereasstorageunderhighCO2levels increasedtheorganicacidcontentsinlemon

.

Atthepinkmaturitystage

,

wedetectedadecreaseinaciditylevelsfromday3to day7inthecontrolgroup

,

whichsubsequentlybecamesimilartothoseoftheothertreatments

.

Therewasreductioninacidity Fig. 1. Effect of continuous application of CO2 on weight loss and flesh firmness in ‘Unicon’ cherry tomato fruit at two maturity

stages stored at 10°C for up to 15 days. A and C=pink and B and D=red maturity stages. Vertical bars represent mean +/- SE (n=5) when larger than the symbols.

Weight loss (%)Weight loss (%)

0 0.5 1 1.5 2 2.5 3 3.5

0 2 4 6 8 10 12

0 1 3 5 7 9 11 13 15 0 1 3 5 7 9 11 13 15

A

C

B

D

Storage time (days) Storage time (days)

Control 3% CO2

5% CO2

(6)

levelfrom0

.

89mg

·

100g-1to0

.

59mg

·

100g-1inuntreatedfruit

,

from0

.

89mg

·

100g-1to0

.

57mg

·

100g-1infruitstreatedwith3

%

CO2

,

andfrom0

.

89mg

·

100g-1to0

.

65mg

·

100g-1infruitstreatedwith5

%

CO2

.

Thisresultisinagreementwiththefindingsof CouveyandOlsen

(

1977

).

Nosignificantdifference

( p <

0

.

05

)

wasobservedbetweentreatmentswithregardtosolublesolidscontent

(

SSC

)

atboth maturitystages(Fig. 3AandB)

.

RyallandPentez

(

1982

)

reportedthatSSCwasnotaffectedbyCO2levelorlong

-

termapplication ofCO2

.

However

,

SSClevelsshowedadecreasingtrendonthelastdayatbothmaturitystages

,

whichmightbeassociatedwith utilizationof

SSCduringrespiration

.

AnalysisofvarianceoftheeffectsofcontinuousapplicationofCO2onethyleneproductionrevealedasignificantdifference

( p <

0

.

05

)

amongtreatmentsatbothmaturitystages (Fig. 3CandD)

.

Theethyleneproductionratewaslowerinfruitstreatedwith 5

%

CO2fromthebeginningoftheexperiment

,

followedby3

%

CO2treatment

,

comparedtountreatedfruitsatbothmaturity Fig. 2. Effect of continuous application of CO2 on surface color (a* value) and titratable acidity in ‘Unicon’ cherry tomato fruit at

two maturity stages stored at 10°C for up to 15 days. A and C=pink and B and D=red maturity stages. Vertical bars represent mean +/- SE (n = 9 for surface color and n = 5 for titratable acidity) when larger than the symbols.

Surface color (Hunter a*)Titiratable acidity (mg · 100g-1 )

-5 0 5 10 15 20

0 0.2 0.4 0.6 0.8 1 1.2

0 1 3 5 7 9 11 13 15 0 1 3 5 7 9 11 13 15

A

C

B

D

Storage time (days) Storage time (days)

Control 3% CO2

5% CO2

(7)

stages

.

TheseobservationsaresimilartothoseofBurgandBurg

(

1967

),

whodetectedinhibitedethyleneproductionunderCO2 treatmentduetoitscompetitiveaction

,

whichinturnhelpsregulateethylenebiosynthesisduringstorage

.

Eventhoughall treatedfruitsatbothmaturitystagesexhibitedpeakethyleneproductiononthesameday

,

5

%

CO2

-

treatedfruitsproducedthe lowestethylenelevels

,

whichdeclineddrastically

.

Indeed

,

areducedO2uptakerateduringhighCO2treatment

,

accompaniedby inhibitedethyleneproduction

,

wasfoundtoextendtheshelflifeoftomatofruit

(

Kuboetal

.,

1985

).

Atthepinkmaturitystage

,

bothcontroland3

%

CO2

-

treatedfruithadahighethyleneproductionrateuntilday5

,

followedbyaslightdecrease

.

Asimilar trendwasobservedattheredmaturitystageaswell

.

Therespirationratewaslowerunder5

%

CO2treatmentcomparedwith3

%

CO2andthecontrolthroughouttheentirestorageperiod

,

regardlessoffruitmaturity

(

Fig. 4AandB)

.

Therespirationrate reacheditspeakonday1inalltreatments

.

Eventhoughtherespirationratedecreasedafterday1underalltreatments

,

therateof reductionwashigherundercontroland3

%

CO2treatmentsthanunder5

%

CO2treatmentthroughouttheexperimentalperiod

.

Fig. 3. Effect of continuous application of CO2 on soluble solids content (SSC) and ethylene production rate in ‘Unicon’ cherry tomato fruit at two maturity stages stored at 10°C for up to 15 days. A and C=pink and B and D=red maturity stages. Vertical bars represent mean +/- SE (n=5 for SSC and n=3 for ethylene production rate) when larger than the symbols.

Ethylene production (μL · kg-1· hr-1) 0 1 2 3 4 5 6 0 1 2 3 4 5 6

0 1 3 5 7 9 11 13 15 0 1 3 5 7 9 11 13 15

Storage time (days) Storage time (days)

Control 3% CO2

5% CO2

Soluble Solids content (°Brix)

A

C

B

D

(8)

ThisresultisinagreementwiththefindingsofKader

(

1986

),

whodetectedreducedrespirationratesduetoelevatedCO2 concentrations

,

whichisresponsibleforchangesintheactivitiesofvariousenzymesthathastenfruitripeningandsenescence

.

Therewasasignificantdifference

( p <

0

.

05

)

invitaminCcontentamongtreatmentsatbothmaturitystages

(

Fig. 5AandB)

.

Continuousapplicationof

5

%

CO2delayedthedecreaseinvitaminCcontentfor7daysatthepinkmaturitystage

.

Thevitamin Ccontentsoffruitsunder3

%

CO2andcontroltreatmentwerehigherthanthoseof5

%

CO2

-

treatedfruitsonday1atthepink maturitystage

.

Subsequently

,

vitaminClevelsdecreasedinboth3

%

CO2

-

treatedandcontrolfruitsattheendofstorageatboth maturitystages

.

Thisresultindicatesthatasfruitripeningadvances

,

organicacidcontentsdecline

.

Similarly

,

Islametal

. (

1996

)

detectedincreasedascorbicacidcontentsintomatofruitwithincreasingmaturity

,

withhighconcentrationsofvitaminCfound atthepinkmaturitystage

,

followedbyaslightdecreasewhenthefruitsreachedtheredmaturitystage

.

AsshowninFig. 5B

,

vitaminCcontentsweremaintainedunder5

%

CO2treatmentcomparedwiththecontroland3

%

CO2treatmentthroughoutthe storageperiod

.

Attheendofstorage

,

thehighestvitaminCcontent

(

31

.

78mg

·

100g-1and30

.

06mg

·

100g-1atbothmaturity stages

,

respectively

)

wasfoundinfruittreatedwith5

%

CO2

.

Atbothmaturitystages

,

vitaminClevelsremainedstableinfruit treatedwith5

%

CO2comparedto3

%

CO2andthecontrolthroughoutthestorageperiod

.

Theseresultsindicatethattherateof vitaminClosswaslowerinthe5

%

CO2

-

treatedgroupthaninthe3

%

CO2

-

treatedandcontrolgroupsatbothmaturitystages throughouttheentirestorageperiod

(

Fig. 5AandB)

.

VitaminCisgenerallyconsideredtobeagoodindicatorofnutritional qualityduringtheprocessingandstorageoffruits

;

ifvitaminClevelsarewellmaintained

,

theotherfruitqualityparametersare alsowellmaintained

(

Uddinetal

.,

2002

).

Therewassignificantdifference

( p <

0

.

05

)

inlycopenebiosynthesisand

/

orcontentamongtreatmentsatbothmaturitystages (Fig. 5CandD)

.

Atthepinkmaturitystage

,

thelycopenecontentsatharvestweresimilarforalltreatmentsbutincreasedover timeuntilreachingapeakonday7

(

24

.

96mg

·

kg-1

)

andday11

(

23

.

68mg

·

kg-1

)

aftercontroland3

%

CO2treatment

,

respectively

.

Similarly

,

in5

%

CO2

-

treatedfruitatthepinkmaturitystage

,

lycopenecontentsincreasedfrom6

.

65mg

·

kg-1onday1to20

.

65 mg

·

kg-1onday15

(

Fig. 5C)

.

Attheredmaturitystage

,

nosignificantchangeinlycopenecontentwasobservedunderany Fig. 4. Effect of continuous application of CO2 on respiration rate in ‘Unicon’ cherry tomato fruit at two maturity stages stored at

10°C for up to 15 days. A=pink and B=red maturity stages. Vertical bars represent mean +/- SE (n=3) when larger than the symbols.

0 1 3 5 7 9 11 13 15 0 1 3 5 7 9 11 13 15

A B

Storage time (days) Storage time (days)

Control 3% CO2

5% CO2

Respiration rate (mg · kg-1 · hr-1 ) 0 0.2 0.4 0.6 0.8 1 1.2 1.4

(9)

treatmentuntilday11ofstorage

.

Thelycopenecontentstronglydecreasedfrom28

.

31mg

·

kg-1onday11to8

.

65mg

·

kg-1onday 15andfrom28

.

31mg

·

kg-1onday11to9

.

72mg

·

kg-1onday15incontroland3

%

CO2

-

treatedfruit

,

respectively

,

whereasthe lycopenecontentunder5

%

CO2treatmentdecreasedonlyslightlyduringthisperiod

,

from30

.

11mg

·

kg-1onday11to20

.

88 mg

·

kg-1onday15

.

Untreatedfruitshowedanimmediatedeclineatbothpinkandredstages

.

Therefore

,

treatmentwithhigh levelsof

CO2

(

5

%)

delayedtheformationoflycopeneand

/

ormaintainedthelycopenecontentattheendofthestorageperiod

.

Similarly

,

Sozzietal

. (

1999

)

reportedadelayintotalcarotenoidandlycopenebiosynthesisunderelevatedCO2levels

.

Volatilecompounds

,

suchasacetaldehydeandethanol

,

wereaffectedbythecontinuousapplicationofCO2atbothmaturity stages

.

Wedetectedverylowlevelsofethanolformationincherrytomatofruitduringcoldstorageunderalltreatments regardlessoffruitmaturity

(

Fig. 6AandB)

.

Afterday9

,

ethanollevelsinfruitsinthecontrolgroupwerelowerthanthoseof fruitstreatedwith3

%

and5

%

CO2atthepinkmaturitystage

.

Acetaldehydeformationwasaffectedbythecontinuousapplication Fig. 5. Effect of continuous application of CO2 on vitamin C and lycopene contents in ‘Unicon’ cherry tomato fruit at two maturity stages stored at 10°C for up to 15 days. A=pink and B=red maturity stages. Vertical bars represent mean +/- SE (n=3) when larger than the symbols.

Lycopene content (mg · kg-1) 0 10 20 30 40 50 60

0 1 3 5 7 9 11 13 15 0 1 3 5 7 9 11 13 15

A

C

B

D

Storage time (days) Storage time (days)

Control 3% CO2

5% CO2

Vitamin C (mg · 100g-1 )

0 5 10 15 20 30 40

25 35

(10)

ofCO2(Fig. 6CandD)

.

Therateofacetaldehydeformationwaslowuntilday1foralltreatmentsatbothmaturitystages

,

after whichthelevelsofthiscompoundinthecontroland3

%

CO2treatmentgroupsincreaseduptoday5andthendecreasedslowly atthepinkmaturitystage

.

Bycontrast

,

attheredmaturitystage

,

acetaldehydelevelsincontroland3

%

CO2

-

treatedfruits decreasedafterday3

.

Irrespectiveoffruitmaturity

,

acetaldehydeformationdecreasedafterafewdaysunderalltreatments

.

Theseresultsindicatethatfruitripeningleadstotheincreasedproductionofvolatiles

,

suchasethanolandacetaldehyde

,

infruits storedforlongperiodsoftimewithoutanti

-

agingpostharvesttreatment

.

Indeed

,

JanesandFrenkel

(

1978

)

andNanosetal

. (

1992

)

found thatfruitssuchaspearandstrawberryproduceethanolandacetaldehydewhentheyareallowedtoripen

.

Therewassignificantdifference

( p <

0

.

05

)

incellwallthicknessamongtreatmentsatbothmaturitystages

(

Fig. 9A, B, C, D, E, andF). Cellwallthicknessdecreasedwithincreasingstorageatbothmaturitystages

,

exceptforfruitstreatedwithCO2

.

Atboth maturitystages

,

wedetectedrapiddegradationofcellwallthickness

(

outer

,

middle

,

andinner

)

inthecontrol

,

followedby3

%

CO2treatment

,

throughoutthestorageperiod

.

Fruitstreatedwith5

%

CO2appearedmorecompactthantheotherfruitsatboth maturitystages

(

Fig. 7and8)

.

Theseresultsareinagreementwiththefindingthat5

%

CO2treatmentaffectstheactivitiesof enzymes

,

suchaspolygalacturonase

(

PG

)

andpectinmethylesterase

(

PME

),

whichareresponsibleforfruitsofteningduring storage

(

GoulaoandOliveira

,

2008

).

Fig. 6. Effect of continuous application of CO2 on ethanol and acetaldehyde production in ‘Unicon’ cherry tomato fruit at two maturity stages stored at 10°C for up to 15 days. A and C=pink and B and D=red maturity stages. Vertical bars represent mean +/- SE (n=3) when larger than the symbols.

Acetaldehyde (μL · kg · hr-1 )Ethanol (μL · kg · hr-1 )

0 1 3 5 7 9 11 13 15 0 1 3 5 7 9 11 13 15

A

C

B

D

Storage time (days) Storage time (days)

Control 3% CO2

5% CO2

0 1 1.5 2 1.5 2.5 3 4 3.5 4.5 0 0.04 0.02 0.08

0.06 0.1 0.12 0.16 0.14

(11)

Fig. 7. Effect of continuous application of CO2 on cell wall thickness in ‘Unicon’ cherry tomato fruit at the pink maturity stage.

0 day 7th day 15th day

Cell wall

20 μm 20 μm

20 μm

20 μm

20 μm

Fig. 8. Effect of continuous application of CO2 on cell wall thickness in ‘Unicon’ cherry tomato fruit at the red maturity stage.

Control 5% CO2

0 day 7th day 15th day

20 μm 20 μm

20 μm

20 μm

20 μm

Control 5% CO2

(12)

ThecontinuousapplicationofCO2significantly

(p <

0

.

05

)

affectedwater

-

solublepectincontentsatbothmaturitystages(Fig. 10A andB). Water

-

solublepectinlevelsincreasedmorerapidlyincontrolfruitthaninCO2

-

treatedfruitatbothmaturitystages

.

At thepinkmaturitystage

,

water

-

solublepectinlevelsincreasedfrom40mg

·

kg-1to70mg

·

kg-1andfrom40mg

·

kg-1to60mg

·

kg-1 incontroland3

%

CO2

-

treatedfruits

,

respectively

.

However

,

5

%

CO2treatmentreducedtherateofsolubilizationofpectinat bothmaturitystagescomparedwiththecontroland3

%

CO2treatments

.

TreatingfruitswithhighCO2levelsdelayedtheonset oftheclimactericriseandprolongedtomatofruitripening

,

resultingindelayedfruitsoftening

.

Thisresultisinagreementwith thefindingofWillsetal

. (

1981

)

thatelevatedCO2levelsreducethebreakdownofpecticsubstancesresponsibleformaintaining afirmtextureinfruitforalongperiodoftime

.

Basedontheoverallresults

,

weconcludedthat

Unicon

cherrytomatofruitcanbestoredfor15daysat10

°

Cundercontinuous applicationof

5

%

CO2

,

comparedto3

%

CO2andcontrolfruits

.

Toobtainthebestsurfacecolorquality

,

alongwithanacceptable textureandothertomatoqualityparameters

,

werecommendthecontinuousapplicationof

5

%

CO2asapostharvesttreatment duringstorage

..

Fig. 9. Effect of continuous application of CO2 on cell wall thickness in the outer (A, D), middle (B, E), and inner (C, F) cortex in

‘Unicon’ cherry tomato fruit at the pink (A, B, C) and red (D, E, F) maturity stages stored at 10°C for up to 15 days. Vertical bars represent mean +/- SE (n=3) when larger than the symbols.

Cell wall thickness (um)Cell wall thickness (um)

0 2 4 6 8 10 14 12 16 0 2 4 6 8 10 14 12 16 0 2 4 6 8 10 14 12 16 Storage duration (days) Storage duration (days) Storage duration (days)

Outer Middle Inner

Control 5% CO2

0 10

5 20

15 25 30 35

0 10

5 20

15 25

A

D

C

F B

E

(13)

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Fig. 10. Effect of continuous application of CO2 on water soluble pectin in ‘Unicon’ cherry tomato fruit at two maturity stages stored at 10°C for up to 15 days. A=pink and B=red maturity stages. Vertical bars represent mean +/- SE (n=3) when larger than the symbols.

Water soluble pectin (mg · kg-1)

0 7 15 0 7 15

A B

Storage time (days) Storage time (days)

Control 3% CO2

5% CO2

0 20 10 40 30 50 60 80

70

(14)

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수치

Fig. 6. Effect of continuous application of CO 2  on ethanol and acetaldehyde production in ‘Unicon’ cherry tomato fruit at two  maturity stages stored at 10°C for up to 15 days
Fig. 7. Effect of continuous application of CO 2  on cell wall thickness in ‘Unicon’ cherry tomato fruit at the pink maturity stage
Fig. 9. Effect of continuous application of CO 2  on cell wall thickness in the outer (A, D), middle (B, E), and inner (C, F) cortex in
Fig. 10. Effect of continuous application of CO 2  on water soluble pectin in ‘Unicon’ cherry tomato fruit at two maturity stages  stored at 10°C for up to 15 days

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