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Mushroom Jam (Sweet Concentrated Mushroom Preserve)

Mushroom jam · mushroom-jam · sweet mushroom jam · oyster mushroom jam · oyster-mushroom jam · Pleurotus mushroom jam · mushroom pulp jam · mushroom-based jam · mushroom preserve · banana-mushroom blended jam · banana mushroom mixed jam · milky mushroom jam · Calocybe indica jam · mushroom fruit spread · sweetened mushroom spread

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An experimental sweet mushroom preserve developed in Indian food-processing research, made by cooking mushroom pulp with sugar, added pectin and citric acid until concentrated into a thick, spreadable jam.

A bowl of smooth, glossy chestnut-brown sweet mushroom jam with a fine pulped texture and a small spoon.

What it is

Mushroom jam is an experimental sweet preserve made by cooking edible mushroom pulp with sugar, added pectin and acid until it reaches a thick, spreadable consistency. Unlike savoury mushroom-and-onion spreads, this preparation belongs to the sweet jam-making tradition and is intended to resemble fruit jam in appearance, consistency and sweetness. It has been developed mainly by Indian agricultural researchers seeking new uses for cultivated oyster mushrooms. The finished product can be golden, amber or brown, depending on the mushroom, ingredients and cooking process.

The basic formulation begins with fresh mushrooms that are cleaned, blanched and ground into a pulp. Sugar provides sweetness and contributes to preservation through its effect on water availability. Pectin gives the gel structure familiar from fruit jam, and citric acid supplies the acidity pectin needs to set and adds flavour. Cooking evaporates water and concentrates the mixture. ICAR's Directorate of Mushroom Research in Solan describes a formulation containing equal weights of mushroom pulp and sugar, with pectin and citric acid each added at 1% of the pulp weight.

The main ingredient in the early ICAR work was oyster mushroom (Pleurotus species). Later work used Pleurotus ostreatus in a banana-mushroom blended jam. A separate Indian study used milky mushroom, Calocybe indica, and investigated pectin obtained from different sources.

Mushroom makes the jam different from fruit jam. Edible mushrooms contain cell-wall materials such as chitin and beta-glucans, whereas many fruits supply appreciable pectin. Mushroom pulp has no natural pectin-and-acid system like a jam fruit. So pectin and citric acid are added to get the structure.

Mushroom jam is non-fermented. No bacteria, yeasts, koji moulds or other starter organisms are deliberately cultivated during its production. The transformation depends on blanching, mechanical pulping, evaporation, sugar concentration, acidification and pectin gelation. Any microbial fermentation developing during storage would normally indicate unwanted deterioration rather than successful manufacture. The finished food should also be kept distinct from mushroom murabba, which preserves larger mushroom pieces in syrup, and mushroom candy, which includes further sugar impregnation and drying.

Standards for fruit jam generally assume a fruit-based ingredient system. A product composed principally of mushroom pulp may require separate regulatory assessment depending on where it is sold.

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History

Mushroom jam has a modern research history, not a traditional regional origin. The earliest paper on the sweet oyster-mushroom product is Development and evaluation of oyster mushroom value added products, by G. C. Wakchaure, Mahantesh Shirur, K. Manikandan and Lekh Raj Rana. It appears in volume 19, issue 1 of Mushroom Research, dated 2010. The paper describes mushroom jam alongside biscuits, pickle, soup, patties and pakoda. ICAR's online catalogue lists it under 2015.

The work arose from a specific agricultural problem. Fresh oyster mushrooms spoil fast, especially in tropical heat and when a seasonal surplus is hard to sell. Growers can lose value when large quantities become available at the same time. Indian research institutions therefore tried dried powders, biscuits, pickles, sweet preserves and other products that might increase the proportion of a harvest that could be sold. Mushroom jam was one experimental product in this programme, not an inherited household speciality.

ICAR News supplied clearer public documentation in July–September 2013. An article by G. C. Wakchaure and Kamlesh K. Meena, then affiliated with the National Institute of Abiotic Stress Management in Baramati, included a photograph explicitly labelled oyster mushroom jam. It reported that mushroom pickle and jam had stayed stable at ambient temperature for six to eight months, and recommended incorporating oyster-mushroom powder at 5–10% in certain products by desired flavour and nutritional properties. The brief article did not disclose complete pH, water-activity or thermal-validation results for the photographed jam.

A separate experiment published in October 2013 by researchers at Dr. MGR Educational and Research University in Chennai used Calocybe indica, the milky mushroom. The authors compared pectin sources, and jam made with natural guava pectin scored highest in sensory tests.

In Pakistan, researchers at the University of Agriculture, Peshawar, developed a banana-mushroom blended jam. Their paper was received in October 2015, accepted in June 2016 and published on 30 April 2017. The study used oyster mushrooms and bananas obtained from the Tarnab area. Six mushroom-and-banana combinations were compared with a banana-only control, and the products were evaluated during ninety days of storage. The preferred formulation combined 400 g banana, 600 g mushroom, 1 kg sugar and 2 g citric acid.

The jam was also shown at an ICAR mushroom-awareness event held at the Indian Agricultural Research Institute in New Delhi on 21 February 2018. The exhibition displayed mushroom jam among preserved, dried and cooked mushroom products contributed by multiple organisations and businesses.

ICAR-DMR's June 2020 manual, Technologies Developed by ICAR-DMR for Commercial Use, gives the most explicit institutional manufacturing formula. It describes grinding blanched mushrooms, adding sugar, pectin and citric acid, concentrating the mixture to 68°Brix and hot-filling glass containers.

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How it works: chemistry and preservation

Mushroom jam is formed through heat concentration and pectin gelation. Fresh mushrooms are mostly water, and some is released in blanching and pulping. Further heating evaporates moisture and concentrates the soluble substances. Sugar dissolves into the pulp and changes both sweetness and the availability of water. Added pectin forms a network that gives the finished product a soft, spreadable structure. These processes are physical and chemical, not microbial fermentation.

The fungal material behaves differently from fruit pulp. Mushroom cell walls contain chitin, beta-glucans and other polysaccharides that contribute to tissue structure and texture. They do not supply the same established pectin-rich cell-wall system found in many jam-making fruits. For this reason, ICAR's formulation adds commercial pectin at 1% of mushroom pulp weight. This matters because ordinary high-methoxyl pectin depends on sugar and acid, while low-methoxyl pectin gels through calcium.

Pectin consists principally of polymers containing galacturonic acid residues. Under suitable conditions, pectin chains associate to form a network that retains water and suspended solids. In conventional high-sugar jam, dissolved sugar reduces competition from water around the polymer chains, while acidity changes the electrical interactions between pectin molecules. Penn State Extension gives about pH 2.8 to 3.3 as the range where traditional fruit jam gels; that is general pectin chemistry, not a measured value for this jam.

Citric acid serves both a flavour and formulation role. It provides tartness that balances the sugar and can move the mixture towards conditions suitable for pectin gel formation. The ICAR manual specifies citric acid at 1% of mushroom pulp weight, but does not report the resulting equilibrium pH. Mushrooms buffer acid, so a fixed amount of citric acid will not give the same final pH in every batch. Acidity must be measured rather than inferred from the ingredient list.

The manual's concentration target is 68°Brix. Brix is a refractometric measure of soluble solids expressed against a sucrose calibration. In a complex food it is not the same as the percentage of sucrose, because acids and other soluble compounds add to the reading. 68°Brix on its own does not show a low enough water activity. Higher soluble-solids concentration can reduce water activity and improve the effectiveness of sugar as a preservative. However, Brix and water activity are different measurements.

Cooking also affects colour and flavour. Fresh mushrooms contain enzymes, including polyphenol oxidases, involved in postharvest browning. Blanching can reduce enzymatic activity, while subsequent concentration can darken the mixture through nonenzymatic reactions and changes in pigments. Amino compounds from the mushrooms may participate in heat-induced flavour reactions when appropriate conditions are present. The balance between sweetness and natural mushroom savouriness is therefore part of the sensory character of the finished product.

The central food-safety concern is the combination of a low-acid starting ingredient and an enclosed, moist finished product. Mushroom jam may become sufficiently acidic and concentrated under a validated process, but neither sugar addition nor hot filling alone guarantees that outcome. The relevant measurements include finished equilibrium pH, water activity, soluble solids, packaging integrity and the thermal treatment used.

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How it is made and why each ingredient and step matters

The ICAR-DMR process starts with fresh edible mushrooms. They are washed, blanched and ground into a relatively uniform paste. Washing removes visible debris, while blanching softens the mushroom tissues and reduces vegetative microorganisms and some browning-enzyme activity. Mechanical grinding makes a continuous pulp suitable for concentration and gel formation. The June 2020 manual gives no mushroom species, blanching temperature, blanching time or particle size for its jam formula, and the pickle and candy recipes in the same book do not fill the gap.

Sugar is then added at a ratio of one part sugar to one part mushroom paste by weight. Pectin and citric acid are each specified at 1% of mushroom pulp weight. The manual instructs heating the mixture with continuous stirring to prevent it sticking to the pan. Evaporation concentrates the soluble solids, while the pectin and acid influence the setting properties. The stated endpoint is 68°Brix. No universal cooking time or numerical temperature is supplied for this particular formula.

For the endpoint to be meaningful in food production, soluble solids need to be measured appropriately. Penn State Extension recommends a refractometer, with representative samples cooled before measurement as the instrument instructions say. Measuring a thick, heterogeneous pulp requires particular care to obtain a representative sample. The ICAR manual gives the concentration target but does not describe the calibration, sampling or measurement procedure used during the original development work.

After concentration, the ICAR process hot-fills the prepared jam into sterilised glass containers, leaving approximately 0.8–1.0 cm headspace. The containers are then sealed. The manual recommends cool, dry storage, but does not give a separate validated sealed-container heat process with an exact product temperature, time, container size or cooling schedule. Hot filling a clean or sterilised jar does not by itself make a low-acid mixture safe to keep at room temperature.

A separate Pakistani experiment provides more numerical operating details for a different recipe. The authors blended banana and Pleurotus ostreatus in several proportions. Their preferred BM6 formulation used 400 g banana, 600 g mushroom, 1 kg sugar and 2 g citric acid. The mushrooms and bananas were washed and sliced, briefly treated in acidified water at 80°C for two minutes, pulped and concentrated by cooking. The paper reports a cooking temperature of 104°C and a target of 68–70°Brix. These temperatures and ingredient quantities belong to the fruit-blended experiment, not the Indian mushroom-only formula.

The Peshawar researchers packed their jams into glass containers autoclaved at 121°C for fifteen minutes, sealed them and stored them at about 31°C for ninety days. That is a laboratory test, not a home canning schedule.

Other mushroom preparations require separate methods. Mushroom murabba retains recognisable pieces in concentrated sugar syrup, while mushroom candy undergoes additional treatment and drying. A savoury mushroom jam may contain onion, oil, vinegar and much less sugar. Neither its method nor its storage behaviour is interchangeable with the sweet ICAR formulation. For publication, the actual sweet jam process should retain its own substrate, ingredient proportions and analytical endpoints.

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Regional and historical variations

Mushroom jam is best understood as a family of experimental food-processing formulations rather than a single traditional dish with a recognised regional recipe. The variations come from research institutions and differ in mushroom species and pectin source.

The ICAR work in Solan, Himachal Pradesh, made oyster-mushroom jam one of several products meant to raise the value of cultivated mushrooms. The 2013 ICAR News article describes processing of fresh and dried oyster mushrooms, including experimental jam, pickle and biscuits. It also mentions using oyster-mushroom powder at 5–10% in selected preparations to balance nutritional composition with sensory acceptability.

A distinct variation was studied in Chennai, Tamil Nadu, in 2013. Researchers used Calocybe indica, commonly called milky mushroom, and compared pectin sources. Their conclusion was that a formulation using natural pectin derived from guava gave the highest sensory score among the treatments evaluated. Guava contributes a fruit-derived gelling component, potentially alongside flavour and other constituents depending on its preparation.

The Peshawar banana-mushroom formulation represents another approach. Instead of relying almost entirely on mushroom pulp, it blends oyster mushroom with ripe banana. The 2017 study compared formulations with different banana-to-mushroom ratios and with or without added citric acid. BM6, containing 400 g banana and 600 g mushroom alongside sugar and citric acid, received favourable overall quality assessments. This recipe has a recognisable fruit component and a different flavour profile from a jam made principally from mushrooms.

The 2018 mushroom-awareness exhibition in India shows the wider food-development effort. Mushroom jam appeared alongside mushroom candy, murabba, pickle, biscuits, soup mixes, snacks and other preparations. The exhibition was designed to introduce growers and consumers to opportunities for mushroom processing.

Sweet mushroom jam must also be distinguished from unrelated modern savoury products using the same English name. Savoury mushroom jam can be made from fried mushrooms, onions, vinegar, miso, wine or oil and may contain relatively little sugar. Such products depend mainly on cooking and flavour concentration rather than conventional high-sugar pectin gelation. They may be suitable as refrigerated condiments, but their ingredients and preservation hazards are different.

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How it is eaten and used

The intended finished product is a sweet, thick mushroom spread resembling conventional jam. The ICAR manual describes a smooth mushroom paste concentrated with sugar and set using pectin. Its purpose was to create an acceptable processed food from a highly perishable agricultural ingredient.

As a culinary preparation, a sweet mushroom jam can potentially be spread on bread or toast or used as a filling in baked goods and other desserts. These are applications consistent with the intended spreadable texture. However, the ICAR publication does not document individual serving recipes or the performance of mushroom jam in baking.

The flavour is expected to differ from familiar fruit preserves. Mushrooms contain savoury amino compounds and other substances associated with umami, while the concentrated sugar and citric acid create a sweet-sour background. Oyster mushroom pulp may also contribute a noticeable earthy or fungal aroma. The extent to which this flavour remains acceptable depends on ingredient proportion and processing. Research formulations generally aim to make the mushroom component compatible with familiar sweet-preserve characteristics rather than reproduce a conventional fruit flavour exactly.

The 2017 Peshawar study tested taste. Ten judges evaluated colour, taste, texture and overall acceptability using a nine-point hedonic scale. The blend of 60% mushroom and 40% banana pulp with added citric acid did well among the experimental blends, judged by a small panel.

Quality fell in storage. Colour, taste, texture and overall scores all dropped over the ninety days. This matters when interpreting preservation claims: a product can remain physically concentrated while becoming less desirable to eat. Commercial acceptability therefore involves flavour, colour, texture and microbiological safety, not merely achieving a particular Brix reading.

Mushroom jam is sometimes promoted as a way to increase the nutritional value of sweet products. Mushrooms contain protein, fibre-type polysaccharides and some micronutrients, but the jam is also half sugar. Processing, concentration and the ratio of mushroom to other ingredients affect its composition.

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Reading results and problems

The intended result is a homogeneous, spreadable product without obvious separation between syrup and mushroom solids. It should be thick enough to resemble jam but not so stiff that it will not spread. The precise colour depends on the mushroom and processing method. A golden or brown colour is normal after concentration, but colour says nothing about quality or safety.

One measurable process endpoint is total soluble solids. ICAR specifies 68°Brix for its mushroom-pulp formula; the 2017 banana-mushroom study aimed for 68 to 70°Brix. Measure soluble solids with a calibrated refractometer. Sugar concentration, other soluble compounds and water availability need to be considered separately. A thick product may still have an unsafe combination of pH and water activity.

The Pakistan study tracked changes over ninety days. Across its treatments, soluble solids rose from about 67.94 to 69.78°Brix while pH fell from about 3.45 to 3.26. Titratable acidity and reducing sugars increased, while non-reducing sugars and sensory scores decreased.

Texture defects can arise from unsuitable proportions of pectin, sugar and acid. Too little effective pectin or insufficient concentration can produce a soft, poorly setting spread. Excessive acid or unsuitable gel conditions may cause water separation, known as syneresis. Prolonged heating can degrade pectin and weaken gel formation. A stiff or rubbery result may indicate excessive concentration or an inappropriate pectin system.

Excessive cooking may also cause scorching and undesirable flavour changes. Mushroom pulp contains suspended solids and can adhere to a hot cooking surface as water evaporates. Continuous stirring is explicitly required by the ICAR method. Browning may result from enzymatic changes before blanching or from heat-induced reactions during concentration. A darker finished colour is therefore not automatically proof of spoilage, but unexplained changes during storage require separate assessment.

The central safety concern is that mushrooms are low-acid foods before formulation. In an inadequately acidified, sealed container, conditions may allow Clostridium botulinum to grow and produce botulinum neurotoxin. The US FDA defines acidified foods using a finished equilibrium pH of 4.6 or below together with other applicable criteria, while safe shelf-stable preservation requires a suitable validated process. A jar being hot-filled or sealed does not independently prove that the necessary controls have been achieved.

ICAR's published storage statements require careful interpretation. Its 2013 bulletin reports ambient stability of oyster-mushroom jam for six to eight months, whereas the 2020 manual describes one-year preservation as a development objective.

The National Center for Home Food Preservation warns that low-acid additions can make otherwise tested jam recipes unsafe by changing the acidity of the finished product. Mushrooms present exactly this kind of formulation problem. A separately tested process is required for unrestricted shelf-stable home preservation.

Mould or unexpected fermentation during storage is unacceptable. The National Center for Home Food Preservation advises discarding an entire mouldy jam rather than scraping off the visible growth, because contamination and potentially harmful metabolites may extend beyond the surface.

Publishing it as a general shelf-stable home-canning recipe would require verification of the mushroom species and pulp composition, pectin type, acidification, equilibrium pH, water activity, processing temperature and duration, container size, packaging integrity and shelf life.

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History

Wakchaure, Shirur, Manikandan and Rana described oyster mushroom jam among experimental value-added products in Mushroom Research, volume 19, issue 1 (2010). ICAR News reported oyster mushroom jam in July to September 2013 with a claimed ambient stability of six to eight months. A 2013 Chennai study made jam from Calocybe indica with different pectins, and a 2017 University of Agriculture, Peshawar study tested banana-oyster mushroom jams. ICAR's 2020 processing manual gives a general formula of equal weights of sugar and pulp, 1% pectin, 1% citric acid and a 68°Brix endpoint. This is modern experimental development, not an older regional tradition.

Ingredients

Scaling: scale by the weight of the mushroom paste: sugar 1:1, pectin and citric acid 1% each of pulp weight.

Fresh edible mushroomsFresh, sound mushrooms, washed, blanched and ground to a uniform paste before weighing
1 part by weight
Reference ingredient: the weight of the paste after blanching and grinding. No batch weight or species is given for the 2020 formula; earlier ICAR work used oyster mushrooms (Pleurotus).
SugarAdded to the mushroom paste before concentrating
1 part by weight
1:1 by weight with the paste, not with the raw mushrooms.
PectinAdded to the paste and sugar before concentrating
1 % of mushroom pulp weight
Grade and degree of esterification are not given; different pectins are not interchangeable.
Citric acidAdded with the pectin before concentrating
1 % of mushroom pulp weight
Anhydrous or monohydrate is not stated, and no finished pH is published.
WaterClean water for washing and blanching the mushrooms
Amount not stated
No volume is given, and water is not a separate jam ingredient.

Method

Risks and precautions · High risk
Clostridium botulinum in inadequately acidified mushroom preserves

Fresh mushrooms are low-acid foods. If the concentrated mushroom product retains conditions permitting growth inside an oxygen-limited sealed container, Clostridium botulinum may produce dangerous neurotoxin. Ordinary blanching and hot filling are not independently validated controls for this recipe.

Hazard source
Unverified finished equilibrium pH

The formula specifies citric acid at 1% of mushroom pulp weight but does not report a measured finished equilibrium pH. Ingredient acidity alone cannot establish safe acidification in a low-acid mushroom matrix.

Hazard source
Unverified water activity

The 68°Brix target measures soluble solids, not water activity. Mushroom solids, sugars, acids and other compounds influence the relationship between water content and microbial water availability. Final water activity has not been reported.

Hazard source
Inadequate thermal processing

The ICAR formula describes hot filling into sterilised glass containers but supplies no validated packaged-product heat treatment with container dimensions, product temperature, holding time and cooling conditions. Hot filling alone does not establish safe shelf-stable processing.

Hazard source
Low-acid ingredient substitution in jam

Mushroom pulp has a different acid and pectin composition from conventional jam-making fruit. A tested fruit-jam processing schedule may become unsafe if low-acid mushroom pulp is substituted without independent validation.

Hazard source
Mould and yeast spoilage

Inadequate concentration, contamination, unsuitable packaging or moisture conditions may permit spoilage. A finished product that looks gelled or tastes sweet is not necessarily microbiologically stable.

Hazard source
Scorching during concentration

Mushroom paste contains suspended solids that can adhere to hot surfaces as water evaporates. The ICAR method explicitly requires continuous stirring to prevent burning.

Hazard source
Pectin-setting failure and syneresis

Gel formation depends on the type of pectin, sugar concentration, acidity and processing. The ICAR formula does not specify pectin grade or final pH. A weak gel or water separation may result from unsuitable conditions, although texture defects alone do not establish microbial spoilage.

Hazard source
Poisonous or misidentified mushrooms

Preservation and sugar concentration cannot be relied upon to neutralise toxins from poisonous mushroom species. Use reliably identified edible cultivated mushrooms rather than unverified wild mushrooms.

Hazard source
Unvalidated shelf life

Different Indian research publications report or propose six to eight months or up to one year of preservation, but the publicly available formula does not supply the complete validation parameters necessary to transfer those periods to home-prepared products.

Hazard source

Use reliably identified, sound, edible mushrooms.

Control source

Maintain the original ICAR ingredient proportions when describing its experimental formulation.

Control source

Concentrate the product to the documented analytical endpoint.

Control source

Prevent scorching during cooking.

Control source

Document the original container-filling specification without treating it as validated home canning.

Control source

Measure finished equilibrium pH as part of professional process validation.

Control source

Measure finished water activity rather than treating Brix as a substitute.

Control source

Use appropriate pectin and acid measurements to establish consistent gel formation.

Control source

Require a validated process before claiming shelf-stable home preservation.

Control source

Establish shelf life through product-specific laboratory assessment.

Control source

Avoid using visual appearance or taste to establish safety.

Control source

Experimental ICAR product, not a validated home-canning recipe.

The reference weight is the prepared mushroom paste, not the raw mushrooms.

The mushroom species, blanching and cooking times, fill temperature and yield are not published.

No pectin grade is given, and no finished pH was published.

68°Brix is a soluble-solids target, not a measurement of water activity or a guarantee of shelf stability.

No boiling-water or pressure-canning process is published; do not borrow times from fruit jam, mushroom pickle, murabba or banana-mushroom jam.

Hot filling sterilised jars does not by itself make sealed mushroom jam safe.

The claimed six to eight month stability needs its original validation before use as a storage rule.

Do not store at room temperature or assume a refrigerated shelf life.

Mushroom murabba, candy and savoury mushroom jam are different products.

Discard any jar that is mouldy, fermenting or leaking; do not taste it to check.

  1. Select fresh, sound, edible mushrooms for processing. Earlier ICAR work used oyster mushrooms; use a correctly identified species.
  2. Wash the mushrooms thoroughly to remove dirt, growing-medium particles and other debris.
  3. Blanch the mushrooms. No blanching time or temperature is published for this jam, so do not borrow those from other recipes.
  4. Grind the blanched mushrooms to a uniform paste.
  5. Weigh the paste; this weight sets the other amounts.
  6. Add sugar equal to the weight of the paste (1:1), pectin at 1% of the pulp weight and citric acid at 1% of the pulp weight, and combine in a cooking vessel.
  7. Heat the mixture, stirring continuously so the thick pulp does not stick and scorch.
  8. Keep concentrating until the mixture reaches 68°Brix total soluble solids. Measure it with a refractometer; thickness, a cold-plate test or sweetness cannot tell you.
  9. The ICAR manual reports hot-filling into sterilised glass containers with 0.8 to 1.0 cm of headspace. This is a description of the source, not a validated home-preservation step.
  10. Do not seal this preparation for storage. The published formula supplies no validated packaging process, heat treatment or shelf-life directions, so it must not be treated as a home-stored preserve.
  11. This record does not establish a safe home-use or storage method. Do not prepare it for storage or serve it on the assumption that concentration or hot filling makes it safe.

Places

Solan

Documented preparation · Locality evidence

India

Historical attestation · Country evidence

Chennai

Documented preparation · Locality evidence

New Delhi

Documented preparation · Locality evidence

Solan

Modern adaptation · Locality evidence

Peshawar and Tarnab

Documented preparation · Locality evidence

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