Fruit Ripening Room Market Outlook

The global fruit ripening room market size was valued at approximately USD 1.2 billion in 2023 and is expected to reach around USD 2.4 billion by 2032, growing at a compound annual growth rate (CAGR) of 8.1% during the forecast period from 2024 to 2032. This remarkable growth is driven by the increasing demand for fresh fruits that maintain consistent quality and the need for efficient ripening processes to meet consumer expectations. The rise in urbanization, changing food consumption habits, and advancements in ripening technologies are significant factors contributing to market growth.

One of the primary growth factors for the fruit ripening room market includes the increasing consumer preference for fresh and ready-to-eat fruits. As urban populations grow and lifestyles become busier, there is heightened demand for fruits that are ready for consumption, driving the need for effective ripening technologies. Furthermore, with an expanding middle-class population, particularly in developing countries, disposable incomes are rising, enabling consumers to afford high-quality fruits, thereby boosting market demand. Additionally, the global trend towards healthy eating and the consumption of fruit as a natural source of vitamins and minerals have also been instrumental in propelling market growth.

Technological advancements in fruit ripening processes have significantly impacted market dynamics, offering more efficient, controlled, and environmentally friendly solutions. Innovations such as controlled atmosphere storage and ethylene control technologies are becoming increasingly popular as they ensure fruits ripen uniformly, thus reducing wastage and enhancing shelf life. Furthermore, the advent of digital monitoring systems and automation in ripening rooms allows for precise control over temperature, humidity, and ethylene levels, which are critical parameters in the fruit ripening process. These advancements not only improve the quality of the ripened fruit but also enhance operational efficiency, thereby driving market growth.

Government regulations and initiatives aimed at reducing food wastage and ensuring food safety have also played a crucial role in the growth of the fruit ripening room market. Many countries have implemented stringent regulations regarding the use of artificial ripening agents like calcium carbide, which can be harmful to health. This has led to a rise in the adoption of safer and more controlled ripening methods such as ethylene generators and ripening chambers. Additionally, subsidies and incentives provided by governments to promote the adoption of advanced ripening technologies are further catalyzing market growth.

From a regional perspective, the Asia Pacific region is expected to witness the highest growth in the fruit ripening room market during the forecast period. This is attributed to the region's large population base, increasing disposable incomes, and the rising demand for high-quality fruits. Additionally, countries like India and China are major producers and consumers of fruits, necessitating efficient ripening infrastructure to meet both domestic and export demands. North America and Europe are also significant markets due to the high consumption of fruits and the presence of advanced ripening technologies. Latin America and the Middle East & Africa are emerging markets with potential growth opportunities driven by increasing fruit production and exports.

Product Type Analysis

The fruit ripening room market can be segmented by product type into ethylene generators, ripening controllers, and ripening chambers. Ethylene generators play a crucial role in the ripening process by releasing ethylene gas, which is a natural plant hormone that accelerates fruit ripening. These generators are widely used due to their efficiency and ease of use. They ensure uniform ripening, which helps maintain the quality and taste of the fruit. The demand for ethylene generators is expected to grow significantly, driven by their ability to provide consistent ripening results and improve the overall shelf life of the fruit.

Ripening controllers are another essential product type in this market, offering advanced solutions for monitoring and controlling the ripening environment. These controllers are equipped with sensors and digital interfaces that allow for precise regulation of temperature, humidity, and ethylene levels. The adoption of ripening controllers is increasing due to their ability to enhance operational efficiency and reduce human error. They also enable the implementation of automated ripenin

Fruit Ripening System Market Analysis

The Fruit Ripening System Market is experiencing significant growth, accord...

The market size of the Fruit Ripening System Market is categorized based on Type (Ethylene, Ethephon, 1-MCP, Calcium Carbide, Ozone Generator) and Application (Banana, Mango, Tomato, Avocado, Apple) and geographical regions (North America, Europe, Asia-Pacific, South America, and Middle-East and Africa).

The provided report presents market size and predictions for the value of Fruit Ripening System Market, measured in USD million, across the mentioned segments.

Fruit Ripening Process Dataset and Model

This dataset contains images of the classes below:

• freshripe
• freshunripe
• overripe
• ripe
• rotten
• unripe

Usage

This is an object detection model that can be used to possibly identify where in the Fruit Ripening Process fruit at stores are and when to take them off the shelves and put them in composting.

The Fruit Ripening Agents Market size was valued at USD 2.8 USD Billion in 2023 and is projected to reach USD 6.11 USD Billion by 2032, exhibiting a CAGR of 11.78 % during the forecast period. Ripening agents are chemical compounds employed to hasten the process of ripening fruits thereby making the fruits more tender and palatable, besides extending their shelf life. Such agents include ethylene which is a natural hormone that initiates fruit ripening, and calcium carbide which generates acetylene gas mimicking the effects of ethylene. Ethylene can be used in the form of gaseous ethylene or products that release ethylene such as ethylene releasing compounds. Gibberellins are the hormonal ripening agents that help in fruiting and maturation. Chemical agents such as sodium chloride help in increasing appropriate ripening conditions. Some of the characteristics of these agents are that they make the bananas ripen uniformly, they can reduce losses through spoilage, and increase the storage life. They are used in agriculture and the food industry for the maturation of fruits like bananas, tomatoes, and avocados up to identical quality and the degree of ripeness perfect for selling. Key drivers for this market are: Increasing Adoption of Precision Farming Techniques to Propel Agricultural Sprayer Demand. Potential restraints include: Prevalence of Less Organized Industry Across Developing Economies to Hinder Growth. Notable trends are: Subsidizing Agricultural Machinery to Propel Market to Next Height.

Fruit Ripening Room Market Analysis

The Fruit Ripening Room Market is experiencing significant growth, according...

Trihelix proteins are plant-specific transcription factors that play crucial roles in plant development and stress responses. However, the involvement of trihelix proteins in fruit ripening and transcriptional regulatory mechanisms remains largely unclear. In this study, we cloned a trihelix gene SlGT31, whose relative expression was significantly induced by the application of exogenous ethylene but repressed by 1-methylcyclopropene (1-MCP). Suppression of SlGT31 resulted in delayed fruit ripening, decreased accumulation of total carotenoids and ethylene content, and inhibition of relative expression of genes related to ethylene and fruit ripening. Conversely, the opposite results were observed in SlGT31-overexpression lines. Yeast one-hybrid and dual-luciferase assays suggested that SlGT31 could bind to the promoters of two key ethylene biosynthesis genes ACO1 and ACS4. These results indicate that SlGT31 may act as a positive modulator during fruit ripening.

Plant Materials and Growth Conditions

Tomato (Solanum lycopersicum Mill.var. Ailsa Craig) was used as the wild type (WT) in this study. WT and transgenic lines were grown in a glasshouse under controlled conditions with 16-h-light/8-h-dark cycles, 25°C-day/18°C-night temperatures, 80% relative humidity, and 250 μmol m⁻² sec⁻¹ luminous intensity. Flowers were tagged at the anthesis stage, immature green was defined as 20 DPA (days post-anthesis), and mature green was defined as 35 DPA. Breaker fruits were defined as fruits of 38 DPA with the color starting to generate a slight yellow color. Other fruits from the 4th and 7th days after breaker were also used. Fruits at different ripening stages were collected, frozen immediately in liquid nitrogen, and stored at -80°C until use.

Sequence analysis and subcellular localization

For SlGT31-GFP construction, the cDNA with the termination codon removed from SlGT31 was amplified with SlGT31-GFP-F/R primers (Supplementary Table.S1). The amplified products were digested with the restriction enzymes Pst I/Sal I and inserted into the pHB vector to form the SlGT31-GFP vector (Supplementary Fig.S2). The SlGT31-GFP fusion construct and the control vector GFP were transformed into Agrobacterium tumefaciens strain GV3101 separately, and then infiltrated into tobacco (Nicotiana benthamiana) leaves about 5 weeks old. Studies have shown that the transcription factor HY5 is localized in the nucleus (Burman et al., 2018), so the subcellular localization of SlGT31 was studied using HY5-RFP localization. Tobacco was cultured in darkness for 24 hours, then cultured under normal conditions for 2–3 days. The fluorescence images of localization samples were acquired on a confocal laser scanning microscope (Leica TCS SP8) after 72h of infiltration. Excitation wavelengths used were 488 nm for GFP and 563 nm for RFP, emission wavelengths used were 507 nm for GFP and 582 nm for RFP. All the primers used in this experiment were listed in Supplementary Table.S1.

Construction of RNAi and overexpression vectors and plant transformation

For overexpressing SlGT31, the open reading frame sequence of SlGT31 was introduced into the pBI121 expression vector under cauliflower mosaic virus (CaMV) 35S promoters. In order to down-regulate the relative expression of the SlGT31 gene, an RNAi vector was constructed (Supplementary Fig.S3). A 382 bp specific DNA fragment of SlGT31 was amplified, which had been tailed with Kpn I/Cla I restriction sites at the 5^’ end and Xba I /Xho I restriction sites at the 3^’ end. Then, the amplified products were digested with Cla I/Xba I and Kpn I/Xho I and linked into the pHANNIBAL plasmid at the Cla I/Xba I restriction site in the sense orientation and at the Kpn I/Xho I restriction site in the antisense orientation. Finally, the double-stranded RNA expression unit was purified and inserted into the plant binary vector pBIN19 with Sac I and Xba I restriction sites. The two vectors were sequenced, checked, and transformed into Agrobacterium tumefaciens LBA4404 strain (An, 1987), and then transformed into Solanum Lycopersicum cv. Ailsa Craig as described in the previous study (Chen et al., 2004). We obtained SlGT31-OE (overexpression) and SlGT31-RNAi (RNA interference) transgenic plants.

Total RNA extraction and quantitative reverse-transcription PCR analysis

Total RNA was extracted from samples using Trizol reagent (Invitrogen, Shanghai, China). Quantitative reverse-transcription PCR (qRT-PCR) was performed by using a CFX96™ Real-Time System (Bio-Rad, USA). The RNA extraction method and PCR reaction system were based on previous reports (Zhang et al., 2018). The tomato SlCAC gene was used as an internal control for expression analysis (Nicot et al., 2005; Exposito-Rodriguez et al., 2008), the relative expression levels of the genes were analyzed using the 2^−ΔΔCT method (Livak et al., 2001), and all experiments were repeated three biological replicates.

Ethylene content determination and ethylene triple response experiment

The fruits at different ripening stages were picked and placed in jars for 3 hours to eliminate the effect of wound-induced ethylene caused by fruit picking (Zhu et al., 2014). The ethylene content was determined after being sealed for 24 hours (Chung et al., 2010). The seeds of wild type and transgenic lines were sown on MS medium supplemented with 0 and 5.0 µM ACC (1-aminocyclopropane-1-carboxylicacid) and then cultured in the dark at 25°C. Hypocotyl and root elongation were measured at 6 days after sowing, and at least 30 seedlings were measured for each line. The relative expression levels of ACS4 in treated wild-type and transgenic seedlings were determined by qRT-PCR. All experiments were repeated three biological replicates.

Pigment extraction

A 0.5 g sample of each line was cut from the pericarp in a 5-mm-wide strip around the equator of B+4 (4 days after breaker fruits) and B+7 (7 days after breaker fruits) fruits. Then, 5 mL of 60:40 (v/v) hexane: acetone was added, and total carotenoids of wild-type, SlGT31-RNAi fruits, and SlGT31-OE fruits were extracted. The extract was centrifuged at 4,000g for 5 min, and the absorbance of the supernatant was measured at 450 nm. Carotenoid content was calculated with the following equation: total carotenoid (mg mL⁻¹) = 4×(OD₄₅₀ nm) × 5 mL/0.5 g (Fray et al., 1993; Forth et al., 2006). All experiments were repeated three biological replicates.

The lycopene extraction was performed according to the previous method (Fish et al., 2002). A 0.5 g sample of each line was cut from the same area of pericarp around the equator of fruits at the breaker, B+4, and B+7 stages. Firstly, the samples were triturated in the liquid nitrogen, then 20 mL 0.05% (w/v) BHT in acetone: 95% ethanol: hexane (1:1:2, v/v) was added to the 50 mL centrifuge tube with samples. After shaking for 15 min at 180 rpm, the ice-deionized water (3 mL) was added into each tube, the tubes were shaken for 5 min and kept at room temperature for 5 min to allow for phase separation. The supernatant (hexane layer) was used to measure the absorbance at 503 nm. Carotenoid content was calculated with the following equation: lycopene (mg/kg) = (OD₅₀₃nm×31.2)/g tissue. All experiments were repeated in three biological replicates.

Fruit Storage Assay

Fruits of WT and transgenic lines were harvested at the B+4 stage. All fruits were disinfected with 10% bleach for 10 minutes, followed by rinsing with sterilized water and air-drying (Zhang et al., 2018). The fruits of WT and transgenic lines

The market size of the Fruit Ripening Room Market is categorized based on Type (Less than 10 Tons In Capacity, More than 10 Tons In Capacity) and Application (Fruit Factory, Fruit Grower) and geographical regions (North America, Europe, Asia-Pacific, South America, and Middle-East and Africa).

The provided report presents market size and predictions for the value of Fruit Ripening Room Market, measured in USD million, across the mentioned segments.

Get the sample copy of Fruit Ripening Gas Market Report 2024 (Global Edition) which includes data such as Market Size, Share, Growth, CAGR, Forecast, Revenue, list of Fruit Ripening Gas Companies (Saudi Basic Industries Corporation , Dow , Exxon Mobil , Shell , Sinopec , Chevron Phillips , Chevron Phillips , LyondellBasell Industries , National Petrochemical Company , INEOS Group AG), Market Segmented by Type (M Grade , L Grade , Others), by Application (Food Packaging , Automotive Industry , Others)

'Mango and Banana Dataset (Ripe Unripe)' is the RGB image dataset. This dataset of 5000 photos of bananas and mangoes focuses on identifying ripe and unripe fruits. Each photograph has metadata that identifies whether or not the banana in the image is considered ripe. The data set was gathered in indoor as well as outdoor lighting conditions, to identify ripe and unripe Bananas and Mangoes. Each image in this dataset has a YOLO.txt label attached to it. This data can be used to train all YOLO Object Detection models. The dataset has been divided into two sections: Train and Test each of which contains 80% and 20% of the total data. Train folder contains 4000 images with labels and Test folder contains 1000 images with labels. The purpose of collecting this dataset was to create 'Ripe Unripe Fruit Detection System' using YOLOv8 Object detection model. Dimensions of image : 640 x 480

The tomato (Solanum lycopersicum) MADS box FRUITFULL homologs FUL1 and FUL2 act as key ripening regulators and interact with the master regulator MADS box protein RIPENING INHIBITOR (RIN). Here, we report the large-scale identification of direct targets of FUL1 and FUL2 by transcriptome analysis of FUL1/FUL2 suppressed fruits and chromatin immunoprecipitation coupled with microarray analysis (ChIP-chip) targeting tomato gene promoters. The ChIP-chip and transcriptome analysis identified FUL1/FUL2 target genes that contain at least one genomic region bound by FUL1 or FUL2 (regions that occur mainly in their promoters) and exhibit FUL1/FUL2-dependent expression during ripening. These analyses identified 860 direct FUL1 targets and 878 direct FUL2 targets; this set of genes includes both direct targets of RIN and nontargets of RIN. Functional classification of the FUL1/FUL2 targets revealed that these FUL homologs function in many biological processes via the regulation of ripening-related gene expression, both in cooperation with and independent of RIN. Our in vitro assay showed that the FUL homologs, RIN, and tomato AGAMOUS-LIKE1 form DNA binding complexes, suggesting that tetramer complexes of these MADS box proteins are mainly responsible for the regulation of ripening.

This dataset is about books and is filtered where the book subjects is Fruit-Ripening. It has 9 columns such as book, author, ISBN, BNB id, and language. The data is ordered by publication date (descending).

Pepper fruits at four different developmental stages were collected: early fruit [EF; 1 cm long; 7 days after pollination (dap)], mature green fruit (MG; 6-7 cm length; 20 dap), breaking or turning red fruit (BR; fruit are partially red; 35 dap), and red ripe fruit (RR; fully red; 40 dap). Tomato fruits at corresponding developmental stages were also collected: EF (less than 1cm; 7 dap), MG (40 dap), BR (50 dap), and RR (55 dap). For the monitoring of fruit-specific and fruit ripening-related genes, we did array hybridization by using the leaves as a common reference and each corresponding fruit developmental stage sample.

Spontaneous mutations associated with the tomato transcription factors COLORLESS NON-RIPENING (SPL-CNR), NON-RIPENING (NAC-NOR), and RIPENING-INHIBITOR (MADS-RIN) result in fruit that do not undergo the normal hallmarks of ripening but are phenotypically distinguishable. Here, we expanded knowledge of the physiological, molecular, and genetic impacts of the ripening mutations on fruit development beyond ripening. We demonstrated through phenotypic and transcriptome analyses that Cnr fruit exhibit a broad range of developmental defects before the onset of fruit ripening, but fruit still undergo some ripening changes similar to wild type. Thus, Cnr should be considered as a fruit developmental mutant and not just a ripening mutant. Additionally, we showed that some ripening processes occur during senescence in the nor and rin mutant fruit, indicating that while some ripening processes are inhibited in these mutants, others are merely delayed. Through gene expression analysis and direct measurement of hormones, we found that Cnr, nor, and rin have alterations in the metabolism and signaling of plant hormones. Cnr mutants produce more than basal levels of ethylene, while nor and rin accumulate high concentrations of abscisic acid. To determine genetic interactions between the mutations, we created for the first time homozygous double mutants. Phenotypic analyses of the double ripening mutants revealed that Cnr has a strong influence on fruit traits and that combining nor and rin leads to an intermediate ripening mutant phenotype. However, we found that the genetic interactions between the mutations are more complex than anticipated, as the Cnr/nor double mutant fruit has a Cnr phenotype but displayed inhibition of ripening-related gene expression just like nor fruit. Our reevaluation of the Cnr, nor, and rin mutants provides new insights into the utilization of the mutants for studying fruit development and their implications in breeding for tomato fruit quality.

• An annotated benchmark image dataset for training and validation of strawberry ripeness detection systems based on Machine learning (ML) and, Deep Learning (DL).
• 247 Raw RGB digital images (.jpg) of strawberry fruits were taken in an orchard of the Central Laboratory for Agricultural Climate (CLAC), Agricultural Research Center, Cairo - Egypt. -The images have been captured from the fruit top view considering different view angles using Sony Xperia Z2 LTE-A D6503 smartphone 20.7 MP camera with a CMOS sensor system and resolution of 3840 x 2160 pixels (Mpix). The dataset images, which contain both fully-visible strawberry fruits and partially-visible strawberry fruits concealed by leaves or by other fruits, were manually annotated, using Roboflow Annotate annotation tool. The data formats of files in Strawberry-DS dataset are RGB digital images (.jpg) and their corresponding YOLO format (.txt) annotation files.

Fruits 360 dataset: A dataset of images containing fruits and vegetables Version: 2020.05.18.0 Content The following fruits and are included: Apples (different varieties: Crimson Snow, Golden, Golden-Red, Granny Smith, Pink Lady, Red, Red Delicious), Apricot, Avocado, Avocado ripe, Banana (Yellow, Red, Lady Finger), Beetroot Red, Blueberry, Cactus fruit, Cantaloupe (2 varieties), Carambula, Cauliflower, Cherry (different varieties, Rainier), Cherry Wax (Yellow, Red, Black), Chestnut, Clementine, Cocos, Corn (with husk), Cucumber (ripened), Dates, Eggplant, Fig, Ginger Root, Granadilla, Grape (Blue, Pink, White (different varieties)), Grapefruit (Pink, White), Guava, Hazelnut, Huckleberry, Kiwi, Kaki, Kohlrabi, Kumsquats, Lemon (normal, Meyer), Lime, Lychee, Mandarine, Mango (Green, Red), Mangostan, Maracuja, Melon Piel de Sapo, Mulberry, Nectarine (Regular, Flat), Nut (Forest, Pecan), Onion (Red, White), Orange, Papaya, Passion fruit, Peach (different varieties), Pepino, Pear (different varieties, Abate, Forelle, Kaiser, Monster, Red, Stone, Williams), Pepper (Red, Green, Orange, Yellow), Physalis (normal, with Husk), Pineapple (normal, Mini), Pitahaya Red, Plum (different varieties), Pomegranate, Pomelo Sweetie, Potato (Red, Sweet, White), Quince, Rambutan, Raspberry, Redcurrant, Salak, Strawberry (normal, Wedge), Tamarillo, Tangelo, Tomato (different varieties, Maroon, Cherry Red, Yellow, not ripened, Heart), Walnut, Watermelon.

Dataset properties Total number of images: 90483.

Training set size: 67692 images (one fruit or vegetable per image).

Test set size: 22688 images (one fruit or vegetable per image).

Number of classes: 131 (fruits and vegetables).

Image size: 100x100 pixels.

Filename format: image_index_100.jpg (e.g. 32_100.jpg) or r_image_index_100.jpg (e.g. r_32_100.jpg) or r2_image_index_100.jpg or r3_image_index_100.jpg. "r" stands for rotated fruit. "r2" means that the fruit was rotated around the 3rd axis. "100" comes from image size (100x100 pixels).

Different varieties of the same fruit (apple for instance) are stored as belonging to different classes.

How we made it Fruits and vegetables were planted in the shaft of a low-speed motor (3 rpm) and a short movie of 20 seconds was recorded.

A Logitech C920 camera was used for filming the fruits. This is one of the best webcams available.

Behind the fruits, we placed a white sheet of paper as background.

However, due to the variations in the lighting conditions, the background was not uniform and we wrote a dedicated algorithm that extracts the fruit from the background. This algorithm is of flood fill type: we start from each edge of the image and we mark all pixels there, then we mark all pixels found in the neighborhood of the already marked pixels for which the distance between colors is less than a prescribed value. We repeat the previous step until no more pixels can be marked.

All marked pixels are considered as being background (which is then filled with white) and the rest of the pixels are considered as belonging to the object.

The maximum value for the distance between 2 neighbor pixels is a parameter of the algorithm and is set (by trial and error) for each movie.

Pictures from the test-multiple_fruits folder were taken with a Nexus 5X phone.

Research papers Horea Muresan, Mihai Oltean, Fruit recognition from images using deep learning, Acta Univ. Sapientiae, Informatica Vol. 10, Issue 1, pp. 26-42, 2018.

The paper introduces the dataset and implementation of a Neural Network trained to recognize the fruits in the dataset.

Alternate download This dataset is also available for download from GitHub: Fruits-360 dataset

History Fruits were filmed at the dates given below (YYYY.MM.DD):

2017.02.25 - Apple (golden).

2017.02.28 - Apple (red-yellow, red, golden2), Kiwi, Pear, Grapefruit, Lemon, Orange, Strawberry, Banana.

2017.03.05 - Apple (golden3, Braeburn, Granny Smith, red2).

2017.03.07 - Apple (red3).

2017.05.10 - Plum, Peach, Peach flat, Apricot, Nectarine, Pomegranate.

2017.05.27 - Avocado, Papaya, Grape, Cherrie.

2017.12.25 - Carambula, Cactus fruit, Granadilla, Kaki, Kumsquats, Passion fruit, Avocado ripe, Quince.

2017.12.28 - Clementine, Cocos, Mango, Lime, Lychee.

2017.12.31 - Apple Red Delicious, Pear Monster, Grape White.

2018.01.14 - Ananas, Grapefruit Pink, Mandarine, Pineapple, Tangelo.

2018.01.19 - Huckleberry, Raspberry.

2018.01.26 - Dates, Maracuja, Plum 2, Salak, Tamarillo.

2018.02.05 - Guava, Grape White 2, Lemon Meyer

2018.02.07 - Banana Red, Pepino, Pitahaya Red.

2018.02.08 - Pear Abate, Pear Williams.

2018.05.22 - Lemon rotated, Pomegranate rotated.

2018.05.24 - Cherry Rainier, Cherry 2, Strawberry Wedge.

2018.05.26 - Cantaloupe (2 varieties).

2018.05.31 - Melon Piel de Sapo.

2018.06.05 - Pineapple Mini, Physalis, Physalis with Husk, Rambutan.

2018.06.08 - Mulberry, Redcurrant.

2018.06.16 - Hazelnut, Walnut, Tomato, Cherry Red.

2018.06.17 - Cherry Wax (Yellow, Red, Black).

2018.08.19 - Apple Red Yellow 2, Grape Blue, Grape White 3-4, Peach 2, Plum 3, Tomato Maroon, Tomato 1-4 .

2018.12.20 - Nut Pecan, Pear Kaiser, Tomato Yellow.

2018.12.21 - Banana Lady Finger, Chesnut, Mangostan.

2018.12.22 - Pomelo Sweetie.

2019.04.21 - Apple Crimson Snow, Apple Pink Lady, Blueberry, Kohlrabi, Mango Red, Pear Red, Pepper (Red, Yellow, Green).

2019.06.18 - Beetroot Red, Corn, Ginger Root, Nectarine Flat, Nut Forest, Onion Red, Onion Red Peeled, Onion White, Potato Red, Potato Red Washed, Potato Sweet, Potato White.

2019.07.07 - Cauliflower, Eggplant, Pear Forelle, Pepper Orange, Tomato Heart.

2019.09.22 - Corn Husk, Cucumber Ripe, Fig, Pear 2, Pear Stone, Tomato not Ripened, Watermelon.

License MIT License

Copyright (c) 2017-2021 Mihai Oltean

Permission is hereby granted, free of charge, to any person obtaining a copy of this software and associated documentation files (the "Software"), to deal in the Software without restriction, including without limitation the rights to use, copy, modify, merge, publish, distribute, sublicense, and/or sell copies of the Software, and to permit persons to whom the Software is furnished to do so, subject to the following conditions:

The above copyright notice and this permission notice shall be included in all copies or substantial portions of the Software.

THE SOFTWARE IS PROVIDED "AS IS", WITHOUT WARRANTY OF ANY KIND, EXPRESS OR IMPLIED, INCLUDING BUT NOT LIMITED TO THE WARRANTIES OF MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE AND NONINFRINGEMENT. IN NO EVENT SHALL THE AUTHORS OR COPYRIGHT HOLDERS BE LIABLE FOR ANY CLAIM, DAMAGES OR OTHER LIABILITY, WHETHER IN AN ACTION OF CONTRACT, TORT OR OTHERWISE, ARISING FROM, OUT OF OR IN CONNECTION WITH THE SOFTWARE OR THE USE OR OTHER DEALINGS IN THE SOFTWARE.

La taille du marché du marché des salles de maturation des fruits est classée en fonction du type (moins de 10 tonnes de capacité, plus de 10 tonnes de capacité) et de l'application (usine de fruits, usine de fruits). Producteur) et régions géographiques (Amérique du Nord, Europe, Asie-Pacifique, Amérique du Sud, Moyen-Orient et Afrique).

Le rapport fourni présente la taille du marché et les prévisions concernant la valeur du marché des salles de maturation des fruits, mesurée en millions de dollars, à travers le segments mentionnés.

Fruit ripening is the summation of changes rendering fleshy fruit tissues attractive and palatable to seed dispersing organisms. For example, sugar content is influenced by plastid numbers and photosynthetic activity in unripe fruit and later by starch and sugar catabolism during ripening. Tomato fruit are sinks of photosynthate, yet unripe green fruit contribute significantly to the sugars that ultimately accumulate in the ripe fruit. Plastid numbers and chlorophyll content are influenced by numerous environmental and genetic factors and are positively correlated with photosynthesis and photosynthate accumulation. GOLDEN2-LIKE (GLK) transcription factors regulate plastid and chlorophyll levels. Tomato (Solanum lycopersicum), like most plants, contains two GLKs (i.e., GLK1 and GLK2/UNIFORM). Mutant and transgene analysis demonstrated that these genes encode functionally similar peptides, though differential expression renders GLK1 more important in leaves, while GLK2 is predominant in fruit. A latitudinal gradient of GLK2 expression influences the typical uneven coloration of green and ripe wild-type fruit. Transcriptome profiling revealed a broader fruit gene expression gradient throughout development. The gradient influenced general ripening activities beyond plastid development and was consistent with the easily observed yet poorly studied ripening gradient present in tomato and many fleshy fruits.

Dataset

This dataset was created by ML-50 Mudia Rahmah

Contents