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Blanching of papaya: effect on osmotic dehydration and characterization of the fruit invertase

Branqueamento de mamão: efeito na desidratação osmótica e caracterização da invertase da fruta

ABSTRACT:

This research evaluated the influence of blanching on osmotic dehydration in sucrose solutions of papaya of Formosa cultivar. The characterization of invertase present in the fruits was also done. Blanching possibly caused damages to the cellular structure resulting in higher water loss, sugar gain and, thus, effective diffusion coefficients than fresh papayas during osmotic dehydration. The invertase extracted from papaya pulp presented optimum temperature of 45 °C and optimum pH of 4.8. Considering the low production cost of papaya and the invertase characteristics, the fruit shows to be a potential source for the referred enzyme extraction.

Key words:
Carica papaya L.; diffusion coefficient; plant invertase; sugar composition

RESUMO:

O objetivo desse trabalho foi avaliar a influência do branqueamento na desidratação osmótica de mamão Formosa em soluções de sacarose. A caracterização da invertase presente nos frutos também foi realizada. O branqueamento possivelmente danificou a estrutura celular do vegetal resultando em maior perda de água, ganho de açúcar e, consequentemente, maior coeficiente de difusão do que os mamões frescos após a desidratação osmótica. A invertase extraída da polpa do mamão apresentou temperatura ótima de 45 °C e pH ótimo de 4.8. Considerando o baixo custo de produção do mamão e as características da invertase, essa fruta apresenta-se como potencial fonte de extração da enzima.

Palavras-chave:
Carica papaya L.; coeficiente de difusão; invertase vegetal; composição de açúcares.

INTRODUCTION:

Papaya is a typical fruit of tropical regions presenting high amounts of vitamin C and mineral salts. The fruit does not present high pro-vitamin A activity; however, because it has long periods of crop and low cost of production, it becomes an important source of carotenoids (RODRIGUEZ-AMAYA, 1996RODRIGUEZ-AMAYA, D. B. Assessment of the provitamin A contents of foods - the Brazilian experience. Journal of Food Composition and Analysis, v.3, p.196-229, 1996. Available from: <Available from: https://doi.org/10.1006/jfca.1996.0028 >. Accessed: Jun. 09, 2020. doi: 10.1006/jfca.1996.0028.
https://doi.org/10.1006/jfca.1996.0028...
).

In Brazil, losses of fruits and vegetables in harvest and post-harvest are great, achieving 30% of the crop (SANTOS et al., 2020SANTOS, F. S. dos et al. Post-harvest losses of fruits and vegetables in supply centers in Salvador, Brazil: Analysis of determinants, volumes and reduction strategies. Waste Management, v.101, p.161-170, 2020. Available from: <Available from: https://doi.org/10.1016/j.wasman.2019.10.007 >. Accessed: Jun. 25, 2020. doi: 10.1016/j.wasman.2019.10.007.
https://doi.org/10.1016/j.wasman.2019.10...
). Because of that, processing the fruit could represent an alternative to minimize these losses, adding value to the final product.

Osmotic dehydration (OD) is a process based on water removal from a product by its immersion in a hypertonic solution. During the process, solutes gain from the solution to the food and loss of some intracellular constituents with low molecular weight from the food to the solution is verified. Result of these transfers is a decrease on moisture content with a simultaneous increase on solids, besides changes on chemical composition of the dehydrated food (FERNANDES et al., 2006FERNANDES, F. A. N. et al. Optimization of osmotic dehydration of papaya followed by air-drying. Food Research International, v.39, p.492-498, 2006. Available from: <Available from: https://doi.org/10.1016/j.foodres.2005.10.004 >. Accessed: Jun. 09, 2020. doi: 10.1016/j.foodres.2005.10.004.
https://doi.org/10.1016/j.foodres.2005.1...
).

An advantageous of this minimal process is the possibility of modifying food formulation by incorporating different solutes in the porous structure of fruits and vegetables. Desirable effects in maintenance of tissue firmness were verified adding calcium to osmotic solutions (HEREDIA et al., 2007HEREDIA, A. et al. Drying of cherry tomato by a combination of different dehydration techniques. Comparison of kinetics and other related properties. Journal of Food Engineering, v.80, n.1, p.111-118, 2007. Available from: <Available from: https://doi.org/10.1016/j.jfoodeng.2006.04.056 >. Accessed: Jun. 09, 2020. doi: 10.1016/j.jfoodeng.2006.04.056.
https://doi.org/10.1016/j.jfoodeng.2006....
; RODRIGUES et al. 2003RODRIGUES, A. C. C. et al. Rheological properties and colour evaluation of papaya during osmotic dehydration processing. Journal of Food Engineering , v.59, p.129-135, 2003. Available from: <Available from: https://doi.org/10.1016/S0260-8774(02)00442-9 >. Accessed: Jun. 09, 2020. doi: 10.1016/S0260-8774(02)00442-9.
https://doi.org/10.1016/S0260-8774(02)00...
), since calcium ions can bind to the pectin present in the cellular wall and middle lamella reinforcing their structural integrity (PEREIRA et al., 2009PEREIRA, L. M. et al. Microscopic features, mechanical and thermal properties of osmotically dehydrated guavas. LWT - Food Science and Technology, v.42, p.378-384, 2009. Available from: <Available from: https://doi.org/10.1016/j.lwt.2008.06.002 >. Accessed: Jun. 09, 2020. doi: 10.1016/j.lwt.2008.06.002.
https://doi.org/10.1016/j.lwt.2008.06.00...
; ALZAMORA et al., 1997ALZAMORA, S. M. et al. In: Food Engineering 2000. Structural changes in the minimal processing of fruits: some effects of blanching and sugar impregnation. New York: Chapman and Hall, 1997, p.117-139.).

Blanching is widely used for minimally processed food preparation aiming enzymatic inactivation, microorganisms destruction or injury to reduce initial microbial load of the food or awareness of the survivor microorganisms to posterior procedures (ALZAMORA et al., 1997ALZAMORA, S. M. et al. In: Food Engineering 2000. Structural changes in the minimal processing of fruits: some effects of blanching and sugar impregnation. New York: Chapman and Hall, 1997, p.117-139.). The great inconvenient of thermal treatment is the structural damage to the food resulting in its softening (SILVA et al., 2011SILVA, K. S. et al. Osmotic dehydration process for low temperature blanched pumpkin (Cucurbita moschata). Journal of Food Engineering , v.82, p.509-517, 2011. Available from: <Available from: https://doi.org/10.1016/j.jfoodeng.2011.01.025 >. Accessed: Jun. 09, 2020. doi: 10.1016/j.jfoodeng.2011.01.025.
https://doi.org/10.1016/j.jfoodeng.2011....
; KOWALSKA et al., 2008KOWALSKA, A. et al. The effect of blanching and freezing on osmotic dehydration of pumpkin. Journal of Food Engineering , v.86, p.30-38, 2008. Available from: <Available from: https://doi.org/10.1016/j.jfoodeng.2007.09.006 >. Accessed: Jun. 09, 2020. doi: 10.1016/j.jfoodeng.2007.09.006.
https://doi.org/10.1016/j.jfoodeng.2007....
; PAREDES ESCOBAR et al., 2007PAREDES ESCOBAR, M. et al. Effect of long-term storage and blanching pre-treatment on the osmotic dehydration kinetics of carrots (Daucus carota L. cv. Nerac). Journal of Food Engineering , v.81, p.313-317, 2007. Available from: <Available from: https://doi.org/10.1016/j.jfoodeng.2006.11.005 >. Accessed: Jun. 09, 2020. doi: 10.1016/j.jfoodeng.2006.11.005.
https://doi.org/10.1016/j.jfoodeng.2006....
; ALZAMORA et al., 1997). When applied prior to drying or another treatment, researchers verified higher dehydration rates and/or reduced time of process (KOWALSKA et al., 2008; PAREDES ESCOBAR et al., 2007).

Invertase (β-fructofuranosidase) is the enzyme that catalysis enzymatic hydrolysis of sucrose in equal proportions of glucose and fructose (GUIMARÃES et al., 2007GUIMARÃES, L. H. S. et al. Production and characterization of a thermostable extracellular β-d-fructofuranosidase produced by Aspergillus ochraceus with agroindustrial residues as carbon sources. Enzyme and Microbial Technology, v.42, p.52-57, 2007. Available from: <Available from: https://doi.org/10.1016/j.enzmictec.2007.07.021 >. Accessed: Jun. 09, 2020. doi: 10.1016/j.enzmictec.2007.07.021.
https://doi.org/10.1016/j.enzmictec.2007...
). Traditionally this enzyme is obtained by the lysis of fungi cells such as Saccharomyces cerevisiae, Saccharomyces carlsbergenses and Aspergillus ochraceus (GUIMARÃES et al., 2007; ROMERO-GÓMEZ et al., 2000ROMERO-GÓMEZ, S. J. et al. Invertase production by Aspergillus niger in submerged and solid-state fermentation. Biotechology Letters, v.22, n.15, p.1255-1258, 2000. Available from: <Available from: https://doi.org/10.1023/A:1005659217932 >. Accessed: Jun. 09, 2020. doi: 10.1023/A:1005659217932.
https://doi.org/10.1023/A:1005659217932...
). CHAN & KWOK (1975CHAN JR., H. T.; KWOK, S. C. M. Importance of enzyme inactivation prior to extraction of sugars from papaya. Journal of Food Science, v.40, p.770-771, 1975. Available from: <Available from: https://doi.org/10.1111/j.1365-2621.1975.tb00552.x >. Accessed: Jun. 09, 2020. doi: 10.1111/j.1365-2621.1975.tb00552.x.
https://doi.org/10.1111/j.1365-2621.1975...
) verified that invertase activity in papayas of Solo cultivar was 0.821 U mg-1 of protein and that if the enzyme was not inactivated, half of the original sucrose in the fruits would be lost in 2.66 min.

As enzyme activity can affect the mass transfer during OD, the objectives of this research were to evaluate the effect of blanching on OD kinetics of papaya of Formosa cultivar, characterizing the invertase present in papaya, regarding its stability, optimum operating pH and temperature and their kinetics parameters.

MATERIALS AND METHODS:

Samples preparation

Papaya of Formosa cultivar from São Paulo State (Brazil) were purchased at São José do Rio Preto Supplying Center (CEAGESP - São José do Rio Preto, São Paulo, Brazil). Ripe fruits with orange peels weighting around 1.6 kg were used in the experiments.

Papayas were longitudinally cut in four pieces, peels and seeds were removed, and each portion was sectioned in cylinders of 3.6 cm of internal diameter with a manual cutter. These pieces were cut in slices with 1.0 cm of thickness. Samples were kept and mixed in a plastic bag from where the slices to be used in the experiments were randomly removed. These samples were used immediately after cutting procedure, which took about 1 h.

For the enzymatic assays, two ripe fruits with orange peels weighting about 0.950 g were used. fruits were cut longitudinally in four pieces and two opposites sections of each one were taken to be used in the experiments. They were crushed and 100 g of pulp were used to extract the enzyme.

Soluble solids content and total solids of the pulp fruits were measured at each experiment.

Blanching and osmotic dehydration

Papaya slices were put in a stainless basket and dipped in boiling water (98.3 °C at São José do Rio Preto - SP - Brazil) for 2 min. After this time, the samples were cooled in tap water for 1 min.

Osmotic solutions were prepared with commercial sucrose (refined sugar) purchased in a local market, food grade calcium lactate pentahydrate in powder form from PURAC Synthesis - Brazil (1% w/w concentration), food grade L (+)-lactic acid in 85% solution from PURAC Synthesis - Brazil (concentration of 0.1 M) and distilled water.

The OD experiments of fresh and blanched fruits were conducted in 40%, 50% and 60% w/w sucrose aqueous solutions with 1% w/w of calcium lactate and 0.1 M of lactic acid. Processing times were 30, 60, 120, 240 and 360 min.

OD experiments were conducted into a stainless steel vat with an external jacket for water circulation at 27 °C. Osmotic solutions were continuously stirred using a 1.6 kW mechanical stirrer (Marconi, model MA-261 - Brazil) with a 10 cm diameter propeller and rotation of 1000 rpm. The ratio between sample and solution mass were at least 1:10.

Equilibrium experiments were conducted with fresh and blanched cylindrical slices of 4 mm thickness, immersed in the solutions, in flasks kept in a BOD incubator at 27 °C, on a platform with orbital agitation of 117.5 rpm, until the equilibrium was reached (about 48 h). The rate between sample and solution mass was 1:10.

After osmotic treatments, samples were removed from the solutions, washed with distilled water for 10 s and dried on absorbing paper.

Total solids, reducing and total sugar contents were determined before and after process.

Calculations

Water and sucrose contents during OD were considered for diffusivities determination. However, for the fresh samples, as sucrose was not detected because it was enzymatically hydrolyzed to reducing sugars by invertase, the variation of the reducing sugars content during OD was used to calculate sucrose diffusion. For the blanched fruits, sucrose content was used.

The effective diffusion coefficients of water and sugar (sucrose/reducing sugar, D k ) in papaya slices was calculated by Fick´s second law applied to an infinite slab (Equation 1). The analytical solutions in terms of the mean water or sugar contents in the slice at time t of OD, w̅kt , is (CRANK, 1975CRANK, J. The Mathematics of Diffusion. Oxford, UK: Clarendon Press., 1975, 414p.):

wk=w̅kt-wkeqwk0-wkeqinf.slab=8π2e-π24Dλtz2+19e-9π24Dλtz2+125e-254π2z2+ (1)

in which k represents the species: w is the water, sc is sucrose and rs is reducing sugar; superscript eq indicates equilibrium; superscript 0 indicates initial (at t = 0); w k represents mass fraction of the specie; w̅ is the average content of the specie at time t; D k is the effective diffusion coefficient of the specie, in m2 s-1; z is the half initial thickness of the samples.

Extraction of invertase from papaya and enzymatic assays

The activity of invertase was assessed in the papaya fruits because sucrose was not detected in non-blanched samples during OD process or in crushed fresh fruit after a few minutes. Thus, independent assays were carried out to characterize the invertase enzyme in papaya.

Based on the methodology used by Chan & Kwok (1975), 100 g of papaya pulp were homogenized and submitted to an extraction process using ketone at 4 °C. It was obtained 4.35 g of dried extract (DE). Enzymatic extract was obtained shaking a solution of 0.5 g of DE in 100 mL of acetate buffer pH 5.0 (0.01 M) during 20 min. After this time the suspension was centrifuged at 800 rpm for 15 min at 13 °C and then filtered in glass wool.

Enzymatic assays were conducted with 150 µL of acetate/phosphate buffer 0.2 M, 100 µL of substrate (sucrose 1 M), enzyme and distilled water completing a final volume of 500 µL. The reducing sugars were determined using Somogy-Nelson method. To determine optimum pH the range of 3.0-8.0 was analyzed. To find optimum operating temperature the range of 30-65 °C was studied. Michaelis and Menten’s kinetic parameters, K m and V m , were estimated from Lineweaver-Bulk plots in the range of 0.03-0.4 μM of sucrose concentration.

Analytical methodologies

Total solid contents of fresh, blanched, and osmotically dehydrated fruits were determined in triplicate in a vacuum oven at 60 °C, 10 kPa, until constant weight. Total and reducing sugars of fresh, blanched, and osmotically dehydrated samples were determined in replicate by redox titration (WILLIAM, 1970WILLIAM, H. Official Methods of Analysis, 11th ed. Arlington: Association of Official Analytical Chemists, AOAC, 1970.).

Statistical analysis and fitting

Results were statistically analyzed by an Analysis of Variance (ANOVA) and Tukey test in a 5% significance level, using Excel 2007 (Microsoft - USA). Effective diffusion coefficients were calculated according to equation 1 using experimental data by minimizing the squares of the deviations between predicted and observed values, with the aid of a statistic software. The fitting efficiency was evaluated by the correlation coefficient R 2 and the mean relative error root square (RRMS); the latter according to Equation 2.

RRMS%=1001Nn=1Mxcalc-xexpxexp12 (2)

where x calc represents water or sugar contents calculated according to Equation 1; x exp is the observed value; N represents the number of observations.

RESULTS AND DISCUSSION:

As can be seen in tables 1, 2 and 3, OD experiments showed that blanching resulted in decrease of total solids (9.33 ± 0.01 kg/100 kg) of papaya samples comparing to the respective fresh fruits (approximately 11.0 kg/100 kg), due to losses of soluble solids during thermal treatment. This lost was reflected in the reducing sugars content which was higher in fresh (approximately 7.5 kg/100 kg) than in blanched fruits (4.14 ± 0.05 kg/ 100 kg).

Table 1
Mean ± SD of total solids (w ts ), sucrose (w sc ) and reducing sugars (w rs ) contents in unblanched and blanched papaya slices during OD in 40% w/w sucrose solution with 1% w/w of calcium lactate and 0.1 M of lactic acid.
Table 2
Mean ± SD of total solids (w ts ), sucrose (w sc ) and reducing sugars (w rs ) contents in unblanched and blanched papaya slices during OD in 50% w/w sucrose solution with 1% w/w of calcium lactate and 0.1 M of lactic acid.
Table 3
Mean ± SD of total solids (w ts ), sucrose (w sc ) and reducing sugars (w rs ) contents in unblanched and blanched papaya slices during OD in 60% w/w sucrose solution with 1% w/w of calcium lactate and 0.1 M of lactic acid.

The total solids content of fresh fruits is presented in tables 1, 2 and 3 when the time of OD is equal zero (0). The absence of sucrose is explained by the enzymatic activity of invertase. The total solids content of blanched fresh fruits is also shown at the initial instant in the same Tables.

As noticed by KOWALSKA et al. (2008KOWALSKA, A. et al. The effect of blanching and freezing on osmotic dehydration of pumpkin. Journal of Food Engineering , v.86, p.30-38, 2008. Available from: <Available from: https://doi.org/10.1016/j.jfoodeng.2007.09.006 >. Accessed: Jun. 09, 2020. doi: 10.1016/j.jfoodeng.2007.09.006.
https://doi.org/10.1016/j.jfoodeng.2007....
) and SILVA et al. (2011SILVA, K. S. et al. Osmotic dehydration process for low temperature blanched pumpkin (Cucurbita moschata). Journal of Food Engineering , v.82, p.509-517, 2011. Available from: <Available from: https://doi.org/10.1016/j.jfoodeng.2011.01.025 >. Accessed: Jun. 09, 2020. doi: 10.1016/j.jfoodeng.2011.01.025.
https://doi.org/10.1016/j.jfoodeng.2011....
) for pumpkins, thermal treatment possibly damaged the cellular tissue of papayas, since, for the same process time, higher solute gain was observed for the blanched fruits in relation to the fresh samples independently of solution concentration. Sugar gain of fresh samples (reducing sugar) increased when increasing dewatering time and low dependence with solution concentration was observed, as can be seen in tables 1, 2 and 3. Sucrose gain of blanched fruits presented low dependence with solution concentration for short OD times and increasing solution concentration increased sucrose gain of these samples for dewatering times up to 120 min (Tables 1, 2 and 3).

Tables 1, 2 and 3 shows that for the fresh papayas, after equal process time, the higher the osmotic concentration, the higher the total solid and reducing sugar contents measured in the dehydrated samples in sucrose solutions at 40% and 50%. However, minor changes were observed for fresh papayas dehydrated in solutions at 50% and 60%. For the blanched fruits, the higher the osmotic concentration, the higher were the total solid in the dehydrated samples after the same time of OD. Considering sucrose content, few differences between blanched samples dehydrated in 50% and 60% solutions were observed.

Sucrose was not detected in the fresh fruits as a result of the fast sugar inversion that occurred during samples manipulation. In fact, as can be seen in tables 1, 2 and 3, during OD of fresh samples, independently of process time, sucrose was not detected. Conversely, reducing sugars average contents of osmo-treated fresh slices increased with process time in relation to the initial value corroborating the hypothesis of the fast inversion of these sugars.

Regarding OD of blanched papayas, it was verified the increase on sucrose content with time due to solids incorporation. Reducing sugars content of blanched samples remained practically constant during the first hour of OD. For longer dehydration times, slight decrease of reducing sugars was noticed, which were probably transferred to the dehydrating solution (Tables 1, 2 and 3).

Comparing OD of fresh and blanched samples, it could be concluded that papaya of Formosa cultivar presented high activity of invertase enzyme which is responsible for sucrose hydrolysis in glucose and fructose. This fact explained the failure to measure the sucrose contents of osmo-dehydrated fresh fruits and the increases in their reducing sugar contents over dehydration. Blanching inactivated the enzyme, so sucrose contents of blanched fruits increased during OD. The invertase present in papaya of Formosa cultivar was characterized.

The effective diffusion coefficients of fresh and blanched papayas submitted to OD in 40%, 50% and 60% w/w sucrose aqueous solutions with calcium lactate (1% w/w) and lactic acid (0.1 M) are presented in table 4. For the fresh fruits, it was calculated the effective diffusion coefficients of water and reducing sugars and, for the blanched slices, the coefficients of water and sucrose.

Table 4
Effective diffusion coefficients of water (D w x 1010, in m2 s-1) and sugar (D s x 1010, in m2 s-1) during OD of fresh and blanched papayas of Formosa cultivar, calculated according to equation 1.

As for pure sucrose solutions, for each treatment time, the diffusion coefficients decreased when the concentration of the osmotic solution increased, except for the water diffusivities of blanched samples osmo-treated at 50% and 60% solutions. It was expected that the last samples presented lower diffusivities, but, probably due to great tissue damages, enhancing diffusion processes, they resulted higher than the slices dehydrated in the solution at 50%.

Diffusion coefficients of blanched fruits were higher than the fresh ones. These results are in agreement with the hypothesis that thermal treatment caused cellular tissue damages leading to loss of selective permeability of the plasmalemma and thus facilitating diffusive process.

The effective diffusion coefficients calculated for papaya of Formosa cultivar were lower than the ones calculated for pumpkins by SILVA et al. (2011SILVA, K. S. et al. Osmotic dehydration process for low temperature blanched pumpkin (Cucurbita moschata). Journal of Food Engineering , v.82, p.509-517, 2011. Available from: <Available from: https://doi.org/10.1016/j.jfoodeng.2011.01.025 >. Accessed: Jun. 09, 2020. doi: 10.1016/j.jfoodeng.2011.01.025.
https://doi.org/10.1016/j.jfoodeng.2011....
) and for carrots by PAREDES ESCOBAR et al. (2007PAREDES ESCOBAR, M. et al. Effect of long-term storage and blanching pre-treatment on the osmotic dehydration kinetics of carrots (Daucus carota L. cv. Nerac). Journal of Food Engineering , v.81, p.313-317, 2007. Available from: <Available from: https://doi.org/10.1016/j.jfoodeng.2006.11.005 >. Accessed: Jun. 09, 2020. doi: 10.1016/j.jfoodeng.2006.11.005.
https://doi.org/10.1016/j.jfoodeng.2006....
), but within the range reported for pumpkins by KOWALSKA et al. (2008KOWALSKA, A. et al. The effect of blanching and freezing on osmotic dehydration of pumpkin. Journal of Food Engineering , v.86, p.30-38, 2008. Available from: <Available from: https://doi.org/10.1016/j.jfoodeng.2007.09.006 >. Accessed: Jun. 09, 2020. doi: 10.1016/j.jfoodeng.2007.09.006.
https://doi.org/10.1016/j.jfoodeng.2007....
).

To characterize the invertase present in papaya, independent experiments were carried out. The fruit pulp used in these analyses had 14.78 ± 0.005 of total solids content and 14.1% of soluble solids content. The optimum temperature of the enzyme was 45 °C and the optimum pH was 4.8. These values were close to the ones found for strawberries and Japanese pear (VIBERG & SJÖHOLM, 1998VIBERG, U.; SJOHOLM, I. Sucrose inversion during osmotic pre-treatment of strawberries. LWT - Food Science and Technology , v.31, p.546-551, 1998. Available from: <Available from: https://doi.org/10.1006/fstl.1998.0412 >. Accessed: Jun. 09, 2020. doi: 10.1006/fstl.1998.0412.
https://doi.org/10.1006/fstl.1998.0412...
; HASHIZUME et al., 2003HASHIZUME, H. et al. Purification and characterization of two soluble acid invertase isozymes from Japanese pear fruit. Phytochemistry, v.63, p.125-129, 2003. Available from: <Available from: https://doi.org/10.1016/S0031-9422(03)00107-9 >. Accessed: Jun. 09, 2020. doi: 10.1016/S0031-9422(03)00107-9.
https://doi.org/10.1016/S0031-9422(03)00...
). The fungal enzymes usually used in inverted sugar production present optimum pH around 4.5 and optimum temperature ranging from 55-60 °C (GUIMARÃES et al., 2007GUIMARÃES, L. H. S. et al. Production and characterization of a thermostable extracellular β-d-fructofuranosidase produced by Aspergillus ochraceus with agroindustrial residues as carbon sources. Enzyme and Microbial Technology, v.42, p.52-57, 2007. Available from: <Available from: https://doi.org/10.1016/j.enzmictec.2007.07.021 >. Accessed: Jun. 09, 2020. doi: 10.1016/j.enzmictec.2007.07.021.
https://doi.org/10.1016/j.enzmictec.2007...
; ROMERO-GÓMEZ et al., 2000ROMERO-GÓMEZ, S. J. et al. Invertase production by Aspergillus niger in submerged and solid-state fermentation. Biotechology Letters, v.22, n.15, p.1255-1258, 2000. Available from: <Available from: https://doi.org/10.1023/A:1005659217932 >. Accessed: Jun. 09, 2020. doi: 10.1023/A:1005659217932.
https://doi.org/10.1023/A:1005659217932...
).

Increasing pH values up to 6.5, enzymatic activity decreased 75%; pH values below 3.5 decreased invertase activity to 35% of its original value. Invertase contained in papayas of Formosa cultivar presented activity up to 30% when kept at 35 or 40 °C for until 4 h. At 55 °C its activity decreased 75% after 15 min. Enzymes presenting high optimum temperature and thermal stability are interesting for biotechnology application in many industries (GUIMARÃES et al., 2007GUIMARÃES, L. H. S. et al. Production and characterization of a thermostable extracellular β-d-fructofuranosidase produced by Aspergillus ochraceus with agroindustrial residues as carbon sources. Enzyme and Microbial Technology, v.42, p.52-57, 2007. Available from: <Available from: https://doi.org/10.1016/j.enzmictec.2007.07.021 >. Accessed: Jun. 09, 2020. doi: 10.1016/j.enzmictec.2007.07.021.
https://doi.org/10.1016/j.enzmictec.2007...
).

The kinetic parameters of papaya invertase was obtained according to Lineweaver-Burk model and were: K m = 66.31 mM and V m = 0.896 μM·min-1. The value of Michaellis-Menten constant (K m ) of the invertase extracted from papaya of Formosa cultivar was higher than the reported for bananas (2.7 mM), mango (5.0 to 0.9 mM) and Japanese pear (3.33 to 4.58 mM). The fungal invertases present K m ranging from 2 to 7 mM (GUIMARÃES et al., 2007GUIMARÃES, L. H. S. et al. Production and characterization of a thermostable extracellular β-d-fructofuranosidase produced by Aspergillus ochraceus with agroindustrial residues as carbon sources. Enzyme and Microbial Technology, v.42, p.52-57, 2007. Available from: <Available from: https://doi.org/10.1016/j.enzmictec.2007.07.021 >. Accessed: Jun. 09, 2020. doi: 10.1016/j.enzmictec.2007.07.021.
https://doi.org/10.1016/j.enzmictec.2007...
; HASHIZUME et al., 2003HASHIZUME, H. et al. Purification and characterization of two soluble acid invertase isozymes from Japanese pear fruit. Phytochemistry, v.63, p.125-129, 2003. Available from: <Available from: https://doi.org/10.1016/S0031-9422(03)00107-9 >. Accessed: Jun. 09, 2020. doi: 10.1016/S0031-9422(03)00107-9.
https://doi.org/10.1016/S0031-9422(03)00...
; ROMERO-GÓMEZ et al., 2000ROMERO-GÓMEZ, S. J. et al. Invertase production by Aspergillus niger in submerged and solid-state fermentation. Biotechology Letters, v.22, n.15, p.1255-1258, 2000. Available from: <Available from: https://doi.org/10.1023/A:1005659217932 >. Accessed: Jun. 09, 2020. doi: 10.1023/A:1005659217932.
https://doi.org/10.1023/A:1005659217932...
).

Briefly, Michaellis-Menten constant indicated an apparent affinity of the enzyme by the substrate: higher its value, lower affinity. Therefore, it was verified that the invertase of papaya presented lower affinity to sucrose than the enzymes extracted from fungi and another fruits (GUIMARÃES et al., 2007GUIMARÃES, L. H. S. et al. Production and characterization of a thermostable extracellular β-d-fructofuranosidase produced by Aspergillus ochraceus with agroindustrial residues as carbon sources. Enzyme and Microbial Technology, v.42, p.52-57, 2007. Available from: <Available from: https://doi.org/10.1016/j.enzmictec.2007.07.021 >. Accessed: Jun. 09, 2020. doi: 10.1016/j.enzmictec.2007.07.021.
https://doi.org/10.1016/j.enzmictec.2007...
; HASHIZUME et al., 2003HASHIZUME, H. et al. Purification and characterization of two soluble acid invertase isozymes from Japanese pear fruit. Phytochemistry, v.63, p.125-129, 2003. Available from: <Available from: https://doi.org/10.1016/S0031-9422(03)00107-9 >. Accessed: Jun. 09, 2020. doi: 10.1016/S0031-9422(03)00107-9.
https://doi.org/10.1016/S0031-9422(03)00...
; ROMERO-GÓMEZ et al., 2000ROMERO-GÓMEZ, S. J. et al. Invertase production by Aspergillus niger in submerged and solid-state fermentation. Biotechology Letters, v.22, n.15, p.1255-1258, 2000. Available from: <Available from: https://doi.org/10.1023/A:1005659217932 >. Accessed: Jun. 09, 2020. doi: 10.1023/A:1005659217932.
https://doi.org/10.1023/A:1005659217932...
).

The velocity of hydrolysis (V m ) is proportional to the concentration of the sucrose-invertase compound, and to the fraction of the invertase which is combined with sucrose. Therefore, when the sucrose concentration is such that the velocity is at its maximum, then this proportion is equal 1 (NELSON & LARSON, 1927NELSON, J. M.; LARSON, H. W. Kinetics of invertase action. The Journal of Biological Chemistry, v.73, n.11, p.223-236, 1927. Available from: <Available from: https://www.jbc.org/content/73/1/223.short >. Accessed: Jun. 09, 2020. doi: 10.1016/S0021-9258(18)84308-3.
https://www.jbc.org/content/73/1/223.sho...
). Papaya of Formosa cultivar presented high invertase concentration since the V m value was almost 1.

Considering the low production cost of the fruit and its great harvest and post-harvest losses and the enzyme characteristics, papaya of Formosa cultivar is presented as a potential source to invertase extraction.

CONCLUSION:

Blanching of papaya damaged the cellular tissue since during OD process these samples presented higher water loss and sugar gain than the fresh fruits, in agreement with the diffusion coefficients which were higher for the blanched fruits than the fresh ones.

Invertase was detected in papaya of Formosa cultivar. Regarding the low cost of fruit production and the invertase characteristics, papaya of Formosa cultivar is presented as a potential source for invertase extraction.

ACKNOWLEDGEMENTS

Authors are grateful to Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) for the scholarship, to Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) for the financial support (Proc 07/07586-0 and Proc 09/00519-0) and to PURAC Synthesis - Brazil.

REFERENCES

  • CR-2020-0725.R1

Publication Dates

  • Publication in this collection
    11 June 2021
  • Date of issue
    2021

History

  • Received
    04 Aug 2020
  • Accepted
    22 Jan 2021
  • Reviewed
    19 Mar 2021
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