Method of cultivating mushrooms

Abstract

Method of cultivating mushrooms in a culture medium containing aluminum or a particular aluminum compound.

Description

This invention relates to a method of cultivating mushrooms in an improved culture medium.

Mushrooms have hitherto been produced mainly by the bed-log cultivation method using logs of Quercus serrata (a species of oak), Quercus acutissima (a species of oak), Fagus crenata (Japanese beech) or the like as the bed material. This method includes many problems. The harvest is frequently influenced by weather; bed logs are not readily available in recent years because of the shortage of material wood and the manpower for lumbering the same; and the cultivation period is long (requiring 1.5 to 2 years for harvesting after inoculation), resulting in considerably high production costs.

Recently, a sawdust-medium cultivation method has been established for Flammulina velutipes, Pleurotus ostreatus, Lyophyllum ulmarium and Pholiota nameko, in which the mushrooms are cultivated in a bottle or box filled with a sawdust culture medium containing rice bran. This method ensures a constant harvest at all seasons throughout the year. As a result, mushroom cultivation which was of a small-scale production type and tended to be conducted as a side business by farmers is now being shifted to the sawdust-medium cultivation system which employs readily available materials and can be conducted on an industrial scale by enterprises.

However, this new sawdust-medium cultivation method also has the problem that the production cost is still high because of the low product yield and long cultivation period required in continuous, large-scale production. Hence, there has been a demand for enhanced productivity.

The object of this invention is to provide a method of cultivating mushrooms with a higher yield.

In brief, this invention relates to a method of cultivating mushrooms in a culture medium which contains aluminum and/or an aluminum compound.

In order to solve the problems associated with the conventional method, we made extensive studies on the effect of various aluminum compounds added to the sawdust medium. As a result, it was found that aluminosilicates and aluminates (e.g., magnesium aluminometasilicate, magnesium aluminate, sodium aluminosilicate, sodium aluminate, calcium aluminosilicate and barium aluminosilicate), water-soluble aluminum salts (e.g., aluminum chloride and ammonium aluminum sulfate), insoluble aluminum salts such as aluminum silicates and aluminum salts of fatty acids (e.g., aluminum stearate and aluminum laurate), aluminum oxides and hydroxides (e.g., activated alumina and aluminum hydroxide gel), synthetic hydrotalcites, and many other aluminum compounds have the effect of improving the yield of mushrooms. In addition, it was also demonstrated that addition of aluminum powder to the sawdust medium is also effective in improving the product yield. We thus concluded that the aluminum atom itself has such a desirable effect, and accomplished this invention.

Aluminum is an element widely found on the earth--the most abundant metal element in the earth's crust. It exists in the form of various metal aluminosilicates in rocks and soil as an important component thereof. Bauxite and kaolin are typical examples of ores containing this element. Aluminum is produced on an industrial scale by molten salt electrolysis of cryolyte or alumina (HeroultHall's method). It is a light-weight, soft metal of silver-gray color showing high ductility and malleability and resistant to corrosion, and is therefore used, as metal or alloys, in a variety of fields (construction and transportation materials, chemical apparatuses, household necessaries, thermite, paint, power cables, etc.). Its compounds are primarily produced from aluminum hydroxide, and are also employed in diversified fields (catalysts, dyeing agents, medicines, metal soaps, adsorbents, Portland cement, earthenware, material for glass, fluidity promoters, thickening agents, etc.). Many of these aluminum compounds are used as industrial materials and are hence available at relatively low costs.

The present invention is described below in more detail.

The culture medium used in this invention may be prepared by adding a proper amount of water to a mixture of carbon source (such as sawdust, wheat bran and chaff) and nitrogen source (such as rice bran and soybean meal), and pressing the resulting mixture into a bottle or a box. When sawdust is used as the carbon source, its amount may be in the range from 20 to 90% based on the weight of total culture medium on a dry basis, and the suitable amount varies with the type of nitrogen source used in combination. When rice bran is used as nitrogen source, for example, it is preferable to mix equal weights of sawdust and rice bran together, to add water to the resulting mixture in such an amount that the final water content will be in the range of 60 to 65%, and to press the culture medium thus obtained into a wide-mouthed bottle.

Sawdust of a broad-leaved tree or that of a coniferous tree may be used either alone or in combination.

The suitable mixing ratio of aluminum and/or an aluminum compound to sawdust greatly varies depending on the type of the former component, and the effect of increasing the mushroom yield is highly dependent on this mixing ratio. When magnesium aluminometasilicate is used, for example, the weight ratio is preferably 1.about.20:100, most preferably 7.about.13:100. The preferable mixing ratio and the most preferable ratio are 1.about.20:100 and 5.about.10:100 with magnesium aluminate, 1.about.20:100 and 5.about.12:100 with sodium aluminosilicate, 0.2.about.6.0:100 and 1.0.about.3.0:100 with sodium aluminate (40% aqueous solution), 1.about.20:100 and 7.about.15:100 with calcium aluminosilicate, 1.about.20:100 and 7.about.20:100 with barium aluminosilicate, 4.8.times.10.sup.-3 .about.3.0:100 and 4.8.times.10.sup.-2 .about.1.0:100 with aluminum chloride hexahydrate), 9.1.times.10.sup.-3 .about.5.6:100 and 9.1.times.10.sup.-3 .about.1.9:100 with ammonium aluminum sulfate (dodecahydrate), 3.6--21.5:100 and 7.2.about.14.3:100 with aluminum monostearate, 3.3.about.13.0:100 and 6.5.about.13.0:100 with aluminum laurate, 0.56.about.25:100 and 5.8.about.17.5:100 with aluminum trisilicate, 4.0.about.25:100 and 18.about.25:100 with aluminum nonasilicate, 1.about.13:100 and 3.about.7:100 with synthetic hydrotalcite, and 0.1.about.10.0:100 and 0.8.about.3.0:100 with aluminum powder.

However, the amounts of these compounds to be added are not limited by the above-mentioned values. In addition, aluminum or any of the aluminum compounds may be used either alone or in combination.

Mushrooms to which the method of this invention can be applied are those which can be cultivated, for example, Flammulina velutipes, Pleurotus ostreatus, Lyophyllum ulmarium and Pholiota nameko.

The following examples will further illustrate the invention but are not intended to limit its scope.

EXAMPLE 1

To an intimate mixture of 50 g broad-leaved tree's sawdust (Fagus crenata), 50 g coniferous tree's sawdust (Cryptomeria japonica, Japanese cedar) and 100 g rice bran, was added 0, 1, 3, 5, 7, 10, 13, 15 or 20 g of magnesium aluminometasilicate (Neusilin.RTM.; product of Fuji Chemical Industry Co., Ltd.), and water was further added in such an amount that the final water content will be 63%. Each of the culture media thus obtained was pressed into a wide-mouthed, plastic bottle (850 ml), a hole about 1 cm in diameter was bored at the center of the pressed medium, and the bottle was stoppered with a cap and autoclaved at 120.degree. C. for 90 minutes. After cooling, spawn of Lyophyllum ulmarium was inoculated in the usual way and cultivated in the dark at 25.degree. C. and 55% R.H. for 30 days (the step of allowing mycelium to cover the surface of the sawdust medium), and cultivation was further continued for an additional 55 days. After removing the cap, the culture medium was turned up to a depth of about 1 cm to comb out its surface layer with mycelium (a process to promote the formation of fruiting bodies), and the remaining medium was sprinkled with 20 ml tap water. After standing for four hours, the water left unabsorbed on the surface of the medium was removed, cultivation was continued at a temperature of 15.degree. C., a relative humidity of 95% and a luminous intensity of 20 lux for ten days to form primordia of fruiting bodies. The luminous intensity was then raised to a level of 200 lux, and cultivation was further continued for 15 days, thereby examining the effect of magnesium aluminometasilicate upon the yield of fruiting bodies. The result obtained is summarized in Table 1.

TABLE 1______________________________________Amt. of M alumino- Yield of fruit- Rate of increasemetasilicate added (g) ing bodies (g) in Yield (%)______________________________________0 109 1001 115 1063 132 1215 158 1457 174 16010 174 16013 169 15515 159 14620 150 138______________________________________

As can be seen from the above table, addition of magnesium aluminometasilicate to the culture medium drastically increased the yield of Lyophyllum ulmarium.

EXAMPLE 2

To an intimate mixture of 50 g broad-leaved tree's sawdust (Fagus crenata), 50 g coniferous tree's sawdust (Cryptomeria japonica) and 100 g rice bran, was added 0, 1, 3, 5, 7, 10, 13, 15 or 20 g of magnesium aluminate (Sanalmin.RTM.; product of Kyowa Chemical Industry Co., Ltd.), and water was further added in such an amount that the final water content will be 63%. Each of the culture media thus obtained was pressed into a wide-mouthed, plastic bottle (850 ml), a hole about 1 cm in diameter was bored at the center of the pressed medium, and the bottle was stoppered with a cap and autoclaved at 120.degree. C. for 90 minutes. After cooling, spawn of Lyophyllum ulmarium was inoculated in the usual way and cultivated in the dark at 25.degree. C. and 55% R.H. for 30 days (the step of allowing mycelium to cover the surface of the sawdust medium), and cultivation was further continued for an additional 55 days. After removing the cap, the culture medium was turned up to a depth of about 1 cm to comb out its surface layer with mycelium (a process to promote the formation of fruiting bodies), and the remaining medium was sprinkled with 20 ml tap water. After standing for four hours, the water left unabsorbed on the surface of the medium was removed, cultivation was continued at a temperature of 15.degree. C., a relative humidity of 95% and a luminous intensity of 20 lux for ten days to form primordia of fruiting bodies. The luminous intensity was then raised to a level of 200 lux, and cultivation was further continued for 15 days, thereby examining the effect of magnesium aluminate upon the yield of fruiting bodies. The result obtained is summarized in Table 2.

TABLE 2______________________________________Amt. of manesium Yield of fruit- Rate of increasealuminate added (g) ing bodies (g) in yield (%)______________________________________0 101 1001 106 1053 139 1385 148 1477 157 15510 160 15813 142 14115 138 13720 135 134______________________________________

As can be seen from the above table, addition of magnesium aluminate to the culture medium drastically increased the yield of Lyophyllum ulmarium.

EXAMPLE 3

To an intimate mixture of 50 g broad-leaved tree's sawdust (Fagus crenata), 50 g coniferous tree's sawdust (Cryptomeria japonica) and 100 g rice bran, was added 0, 1, 3, 5, 7, 10, 13, 15 or 20 g of magnesium aluminometasilicate (Neusilin.RTM.; product of Fuji Chemical Industry Co., Ltd.), and water was further added in such an amount that the final water content will be 63%. Each of the culture media thus obtained was pressed into a wide-mouthed, plastic bottle (850 ml), a hole about 1 cm in diameter was bored at the center of the pressed medium, and the bottle was stoppered with a cap and autoclaved at 120.degree. C. for 90 minutes.

After cooling, spawn of Pleurotus ostreatuswas inoculated in the usual way and cultivated in the dark at 25.degree. C. and 55% R.H. for 30 days. After removing the cap, the culture medium was turned up to a depth of about 1 cm to comb out its surface layer with mycelium (a process to promote the formation of fruiting bodies), and the remaining medium was sprinkled with 20 ml tap water. After standing for four hours, the water left unabsorbed on the surface of the medium was removed, cultivation was continued at a temperature of 15.degree. C., a relative humidity of 95% and a luminous intensity of 20 lux for four days to form primordia of fruiting bodies. The luminous intensity was then raised to a level of 200 lux, and cultivation was further continued for an additional ten days, thereby examining the effect of magnesium aluminometasilicate upon the yield of fruiting bodies. The result obtained is summarized in Table 3.

TABLE 3______________________________________Amt. of Mg alumino- Yield of fruit- Rate of increasemetasilicate added (g) ing bodies (g) in yield (%)______________________________________0 91 1001 94 1033 101 1115 109 1207 120 13210 127 14013 126 13815 110 12120 101 111______________________________________

As can be seen from the above table, addition of magnesium aluminometasilicate to the culture medium drastically increased the yield of Pleurotus ostreatus.

EXAMPLE 4

To an intimate mixture of 50 g broad-leaved tree's sawdust (Fagus crenata), 50 g coniferous tree's sawdust (Cryptomeria japonica) and 100 g rice bran, was added 0, 1, 3, 5, 7, 9, 12, 15, 18 or 20 g of sodium aluminosilicate (synthetic zeolite; product of Japan Builder Co., Ltd.), and water was further added in such an amount that the final water content will be 63%. Each of the culture media thus obtained was pressed into a wide-mouthed, plastic bottle (850 ml), a hole about 1 cm in diameter was bored at the center of the pressed medium, and the bottle was stoppered with a cap and autoclaved at 120.degree. C. for 90 minutes. After cooling, spawn of Lyophyllum ulmarium (M-8171 strain, deposited at Fermentation Research Institute, Agency of Industrial Science and Technology, under the deposit number of FERM BP-1415 ) was inoculated in the usual way and cultivated in the dark at 25.degree. C. and 55% R.H. for 30 days (the step of allowing mycelium to cover the surface of the sawdust medium), and cultivation was further continued for an additional 30 days. After removing the cap, the culture medium was turned up to a depth of about 1 cm to comb out its surface layer with mycelium (a process to promote the formation of fruiting bodies), and the remaining medium was sprinkled with 20 ml tap water. After standing for four hours, the water left unabsorbed on the surface of the medium was removed, cultivation was continued at a temperature of 15.degree. C., a relative humidity of 95% and a luminous intensity of 20 lux for ten days to form primordia of fruiting bodies. The luminous intensity was then raised to a level of 200 lux, and cultivation was continued for 15 days, thereby examining the effect of sodium aluminosilicate upon the yield of fruiting bodies. The result obtained is summarized in Table 4.

TABLE 4______________________________________Amt. of Na alumino- Yield of fruit- Rate of increasesilicate added (g) ing bodies (g) in yield (%)______________________________________0 116 1001 121 1043 157 1355 171 1477 167 1449 165 14212 140 12115 128 11018 123 10620 119 103______________________________________

As can be seen from the above table, addition of sodium aluminosilicate to the culture medium drastically increased the yield of Lyophyllum ulmarium (M-8171 strain, FERM BP-1415).

EXAMPLE 5

To an intimate mixture of 50 g broad-leaved tree's sawdust (Fagus crenata), 50 g coniferous tree's sawdust (Cryptomeria japonica) and 100 g rice bran, was added 0, 0.2, 0.5, 1.0, 1.5, 2.0, 3.0, 4.0, 5.0 or 6.0 g of sodium aluminate (product of Osaka Soda Co., Ltd.; 40% aqueous solution), and water was further added in such an amount that the final water content will be 63%. Each of the culture media thus obtained was pressed into a wide-mouthed, plastic bottle (850 ml), a hole about 1 cm in diameter was bored at the center of the pressed medium, and the bottle was stoppered with a cap and autoclaved at 120.degree. C. for 90 minutes. After cooling, spawn of Lyophyllum ulmarium (M-8171 strain, FERM BP-1415) was inoculated in the usual way and cultivated in the dark at 25.degree. C. and 55% R.H. for 30 days (the step of allowing mycelium to cover the surface of the sawdust medium), and cultivation was further continued for an additional 30 days. After removing the cap, the culture medium was turned up to a depth of about 1 cm to comb out its surface layer with mycelium (a process to promote the formation of fruiting bodies), and the remaining medium was sprinkled with 20 ml tap water. After standing for four hours, the water left unabsorbed on the surface of the medium was removed, cultivation was continued at a temperature of 15.degree. C., a relative humidity of 95% and a luminous intensity of 20 lux for ten days to form primordia of fruiting bodies. The luminous intensity was then raised to a level of 200 lux, and cultivation was continued for 15 days, thereby examining the effect of sodium aluminate upon the yield of fruiting bodies. The result obtained is summarized in Table 5.

TABLE 5______________________________________Amt. of sodium Yield of fruit- Rate of increasealuminate added (g) ing bodies (g) in yield (%)______________________________________0 105 1000.2 112 1070.5 129 1231.0 168 1601.5 166 1582.0 160 1523.0 150 1434.0 139 1325.0 126 1206.0 125 119______________________________________

As can be seen from the above table, addition of sodium aluminate to the culture medium drastically increased the yield of Lyophyllum ulmarium (M-817) strain, FERM BP-1415).

EXAMPLE 6

To an intimate mixture of 50 g broad-leaved tree's sawdust (Fagus crenata), 50 g coniferous tree's sawdust (Cryptomeria japonica) and 100 g rice bran, was added 0, 0.2, 0.5, 1.0, 1.5, 2.0, 3.0, 4.0, 5.0 or 6.0 g of sodium aluminate (product of Osaka Soda Co., Ltd.; 40% aqueous solution), and water was further added in such an amount that the final water content will be 63%. Each of the culture media thus obtained was pressed into a wide-mouthed, plastic bottle (850 ml), a hole about 1 cm in diameter was bored at the center of the pressed medium, and the bottle was stoppered with a cap and autoclaved at 120.degree. C. for 90 minutes. After cooling, spawn of Lyophyllum ulmarium (1-2 strain) was inoculated in the usual way and cultivated in the dark at 25.degree. C. and 55% R.H. for 30 days (the step of allowing mycelium to cover the surface of the sawdust medium), and cultivation was further continued for an additional 55 days. After removing the cap, the culture medium was turned up to a depth of about 1 cm to comb out its surface layer with mycelium (a process to promote the formation of fruiting bodies), and the remaining medium was sprinkled with 20 ml tap water. After standing for four hours, the water left unabsorbed on the surface of the medium was removed, cultivation was continued at a temperature of 15.degree. C., a relative humidity of 95% and a luminous intensity of 20 lux for ten days to form primordia of fruiting bodies. The luminous intensity was then raised to a level of 200 lux, and cultivation was continued for 15 days, thereby examining the effect of sodium aluminate upon the yield of fruiting bodies. The result obtained is summarized in Table 6.

TABLE 6______________________________________Amt. of sodium Yield of fruit- Rate of increasealuminate added (g) ing bodies (g) in yield (%)______________________________________0 113 1000.2 118 1040.5 132 1171.0 169 1501.5 170 1502.0 163 1443.0 155 1374.0 138 1225.0 130 1156.0 128 113______________________________________

As can be seen from the above table, addition of sodium aluminate to the culture medium drastically increased the yield of Lyophyllum ulmarium (1-2 strain).

EXAMPLE 7

To an intimate mixture of 50 g broad-leaved tree's sawdust (Fagus crenata), 50 g coniferous tree's sawdust (Cryptomeria japonica) and 100 g rice bran, was added 0, 1, 3, 5, 7, 10, 15 or 20 g of calcium aluminosilicate or barium aluminosilicate (Ca-A type zeolite, Ba-A type zeolite; products of Japan Builder Co., Ltd.), and water was further added in such an amount that the final water content will be 63%. Each of the culture media thus obtained was pressed into a wide-mouthed, plastic bottle (850 ml), a hole about 1 cm in diameter was bored at the center of the pressed medium, and the bottle was stoppered with a cap and autoclaved at 120.degree. C. for 90 minutes. After cooling, spawn of Lyophyllum ulmarium (M-8171 strain, FERM BP-1415 ) was inoculated in the usual way ahd cultivated in the dark at 25 C. and 55% R.H. for 30 days (the step of allowing mycelium to cover the surface of the sawdust medium), and cultivation was further continued for an additional 30 days. After removing the cap, the culture medium was turned up to a depth of about 1 cm to comb out its surface layer with mycelium (a process to promote the formation of fruiting bodies), and the remaining medium was sprinkled with 20 ml tap water. After standing for four hours, the water left unabsorbed on the surface of the medium was removed, cultivation was continued at a temperature of 15.degree. C., a relative humidity of 95% and a luminous intensity of 20 lux for ten days to form primordia of fruiting bodies. The luminous intensity was then raised to a level of 200 lux, and cultivation was continued for 15 days, thereby examining the effects of calcium and barium aluminosilicates upon the yield of fruiting bodies. The result obtained is summarized in Table 7.

TABLE 7______________________________________Type of com- Amount added Yield of fruit- Rate of increasepound added (g) ing bodies (g) in yield (%)______________________________________Ca alumino- 0 119 100silicate 1 135 113 3 142 119 5 148 124 7 168 141 10 175 147 15 179 150 20 158 133Ba alumino- 1 124 104silicate 3 127 107 5 139 117 7 157 132 10 165 139 15 170 143 20 163 137______________________________________

As can be seen from the above table, addition of calcium or barium aluminosilicate to the culture medium drastically increased the yield of Lyophyllum ulmarium (M-8171 strain, FERM BP-1415)

EXAMPLE 8

To an intimate mixture of 50 g broad-leaved tree's sawdust (Fagus crenata), 50 g coniferous tree's sawdust (Cryptomeria japonica) and 100 g rice bran, was added 0, 4.8.times.10.sup.-3, 4.8.times.10.sup.-2, 0.48, 1.0 or 3.0 g of aluminum chloride hexahydrate (Guaranteed reagent; Nakarai Chemicals Co., Ltd.), or 9.1.times.10.sup.-3, 9.1.times.10.sup.-2, 0.91, 1.9 or 5.6 g of ammonium aluminum sulfate dodecahydrate (Guaranteed reagent; Nakarai Chemicals Co., Ltd.), and water was further added in such an amount that the final water content will be 63%. Each of the culture media thus obtained was pressed into a wide-mouthed, plastic bottle (850 ml), a hole about 1 cm in diameter was bored at the center of the pressed medium, and the bottle was stoppered with a cap and autoclaved at 120.degree. C. for 90 minutes. After cooling, spawn of Lyophyllum ulmarium (M-8171 strain, FERM BP-1415) was inoculated in the usual way and cultivated in the dark at 25.degree. C. and 55 % R.H. for 30 days (the step of allowing mycelium to cover the surface of the sawdust medium), and cultivation was further continued for an additional 30 days. After removing the cap, the culture medium was turned up to a depth of about 1 cm to comb out its surface layer with mycelium (a process to promote the formation of fruiting bodies), and the remaining medium was sprinkled with 20 ml tap water. After standing for four hours, the water left unabsorbed on the surface of the medium was removed, cultivation was continued at a temperature of 15.degree. C., a relative humidity of 95% and a luminous intensity of 20 lux for ten days to form primordia of fruiting bodies. The luminous intensity was then raised to a level of 200 lux, and cultivation was continued for 15 days, thereby examining the effects of aluminum chloride and ammonium aluminum sulfate upon the yield of fruiting bodies. The result obtained is summarized in Table 8.

TABLE 8______________________________________Type of com- Amount added Yield of fruit- Rate of increasepound added (g) ing bodies (g) in yield (%)______________________________________Aluminum 0 126 100chloride 4.8 .times. 10.sup.-3 136 108 4.8 .times. 10.sup.-2 142 113 0.48 158 125 1.0 150 119 3.0 142 113Ammonium alu- 9.1 .times. 10.sup.-3 169 134minum sulfate 9.1 .times. 10.sup.-2 170 135 0.91 165 131 1.9 155 123 5.6 145 115______________________________________

As can be seen from the above table, addition of aluminum chloride or ammonium aluminum sulfate to the culture medium drastically increased the yield of Lyophyllum ulmarium (M-8171 strain, FERM BP-1415).

EXAMPLE 9

To an intimate mixture of 50 g broad-leaved tree's sawdust (Fagus crenate), 50 g coniferous tree's sawdust (Cryptomeria japonica) and 100 g rice bran, was added 0, 3.6, 7.2, 14.3 or 21.5 g of aluminum monostearate (Nakarai Chemicals Co., Ltd.), or 3.3, 6.5 or 13.0 g of aluminum laurate (Extra pure reagent; Kanto Chemical Co., Ltd.), water was further added in such an amount that the final water content will be 63%, and each of the culture media thus obtained was pressed into a widemouthed, plastic bottle (850 ml). Separately, culture media containing 2.9, 5.9, 11.8 and 17.7 g of stearic acid (SA-420; Asahi Denka Kogyo Co., Ltd.) were prepared as the control group. A hole about 1 cm in diameter was bored at the center of each pressed medium, and the bottle was stoppered with a cap and autoclaved at 120.degree. C. for 90 minutes. After cooling, spawn of Lyophyllum ulmarium (M-8171 strain, FERM BP-1415 ) was inoculated in the usual way and cultivated in the dark at 25.degree. C. and 55% R.H. for 30 days (the step of allowing mycelium to cover the surface of the sawdust medium), and cultivation was further continued for an additional 30 days. After removing the cap, the culture medium was turned up to a depth of about 1 cm to comb out its surface layer with mycelium (a process to promote the formation of fruiting bodies), and the remaining medium was sprinkled with 20 ml tap water. After standing for four hours, the water left unabsorbed on the surface of the medium was removed, cultivation was continued at a temperature of 15.degree. C., a relative humidity of 95% and a luminous intensity of 20 lux for ten days to form primordia of fruiting bodies. The luminous intensity was then raised to a level of 200 lux, and cultivation was continued for 15 days, thereby examining the effects of aluminum monostearate, aluminum laurate and stearic acid upon the yield of fruiting bodies. The result obtained is summarized in Table 9.

TABLE 9______________________________________Type of com- Amount added Yield of fruit- Rate of increasepound added (g) ing bodies (g) in yield (%)______________________________________Aluminum 0 133 100monostearate 3.6 158 119 7.2 171 129 14.3 190 143 21.5 139 105Aluminum 3.3 140 105laurate 6.5 189 142 13.0 181 136Stearic acid 2.9 132 99 5.9 137 103 11.8 128 96 17.7 112 84______________________________________

As can be seen from the above table, addition of aluminum monostearate or aluminum laurate to the culture medium drastically increased the yield of Lyophyllum ulmarium (M-8171 strain, FERM BP-1415).

Furthermore, addition of stearic acid brought no increase in the yield, and this indicates that the effect of aluminum stearate is caused by the aluminum atom involved.

EXAMPLE 10

To an intimate mixture of 50 g broad-leaved tree's sawdust (Fagus crenata), 50 g coniferous tree's sawdust (Cryptomeria japonica) and 100 g rice bran, was added 0, 0.56, 1.2, 3.5, 5.8, 11.7, 17.5 or 25 g of aluminum trisilicate Extra pure reagent; Nakarai Chemicals Co., Ltd.), or 4.0, 10.0, 18.0 or 25 g of aluminum nonasilicate (Kyowaad-700.RTM.; product of Kyowa Chemical Industry Co., Ltd.), and water was further added in such an amount that the final water content will be 63%. Each of the culture media thus obtained was pressed into a wide-mouthed, plastic bottle (850 ml), a hole about 1 cm in diameter was bored at the center of the pressed medium, and the bottle was stoppered with a cap and autoclaved at 120.degree. C. for 90 minutes. After cooling, spawn of Lyophyllum ulmarium (M-8171 strain, FERM BP-1415) was inoculated in the usual way and cultivated in the dark at 25.degree. C. and 55 % R.H. for 30 days (the step of allowing mycelium to cover the surface of the sawdust medium), and cultivation was further continued for an additional 30 days. After removing the cap, the culture medium was turned up to a depth of about 1 cm to comb out its surface layer with mycelium (a process to promote the formation of fruiting bodies), and the remaining medium was sprinkled with 20 ml tap water. After standing for four hours, the water left unabsorbed on the surface of the medium was removed, cultivation was continued at a temperature of 15.degree. C., a relative humidity of 95% and a luminous intensity of 20 lux for ten days to form primordia of fruiting bodies. The luminous intensity was then raised to a level of 200 lux, and cultivation was continued for 15 days, thereby examining the effects of aluminum trisilicate and aluminum nonasilicate upon the yield of fruiting bodies. The result obtained is summarized in Table 10.

TABLE 10______________________________________Type of com- Amount added Yield of fruit- Rate of increasepound added (g) ing bodies (g) in yield (%)______________________________________Aluminum 0 118 100trisilicate 0.56 159 135 1.2 160 136 3.5 162 137 5.8 167 142 11.7 177 150 17.5 175 148 25.0 139 118Aluminum 4.0 128 108nonasilicate 10.0 141 119 18.0 146 124 25.0 153 130______________________________________

As can be seen from the above table, addition of aluminum trisilicate or aluminum nonasilicate to the culture medium drastically increased the yield of Lyophyllum ulmariuim (M-8171 strain, FERM BP-1415 ).

EXAMPLE 11

To an intimate mixture of 50 g broad-leaved tree's sawdust (Fagus crenata), 50 g coniferous tree's sawdust (Cryptomeria japonica)and 100 g rice bran, was added 0, 1, 3, 5, 7 or 13 g of synthetic hydrotalcite (Kyowaad-1000.RTM.; product of Kyowa Chemical Industry Co., Ltd.), and water was further added in such an amount that the final water content will be 63%. Each of the culture media thus obtained was pressed into a wide-mouthed, plastic bottle (850 ml), a hole about 1 cm in diameter was bored at the center of the pressed medium, and the bottle was stoppered with a cap and autoclaved at 120.degree. C. for 90 minutes. After cooling, spawn of Lyophyllum ulmarium (M-8171 strain, FERM BP-1415 ) was inoculated in the usual way and cultivated in the dark at 25.degree. C. and 55% R.H. for 30 days (the step of allowing mycelium to cover the surface of the sawdust medium), and cultivation was further continued for an additional 30 days. After removing the cap, the culture medium was turned up to a depth of about 1 cm to comb out its surface layer with mycelium (a process to promote the formation of fruiting bodies), and the remaining medium was sprinkled with 20 ml tap water. After standing for four hours, the water left unabsorbed on the surface of the medium was removed, cultivation was continued at a temperature of 15.degree. C., a relative humidity of 95% and a luminous intensity of 20 lux for ten days to form primordia of fruiting bodies. The luminous intensity was then raised to a level of 200 lux, and cultivation was continued for 15 days, thereby examining the effect of synthetic hydrotalcite upon the yield of fruiting bodies. The result obtained is summarized in Table 11.

TABLE 11______________________________________Amt. of synthetic Yield of fruit- Rate of increasehydrotalcite added (g) ing bodies (G) in yield (%)______________________________________0 132 1001 138 1053 164 1245 161 1227 153 11613 135 102______________________________________

As can be seen from the above table, addition of synthetic hydrotalcite to the culture medium drastically increased the yield of Lyophyllum ulmarium (M-8171 strain, FERM BP-1415).

EXAMPLE 12

To an intimate mixture of 50 g broad-leaved tree's sawdust (Fagus crenata), 50 g coniferous tree's sawdust (Cryptomeria japonica) and 100 g rice bran, was added 0, 0.1, 0.3, 0.5, 0.8, 1.0, 3.0, 5.0 or 10.0 g of aluminum powder (Chemical pure reagent; Nakarai Chemicals Co., Ltd.), and water was further added in such an amount that the final water content will be 63%. Each of the culture media thus obtained was pressed into a wide-mouthed, plastic bottle (850 ml), a hole about 1 cm in diameter was bored at the center of the pressed medium, and the bottle was stoppered with a cap and autoclaved at 120.degree. C. for 90 minutes. After cooling, spawn of Lyophyllum ulmarium (M-8171 strain, FERM BP-1416) was inoculated in the usual way and cultivated in the dark at 25.degree. C. and 55% R.H. for 30 days (the step of allowing mycelium to cover the surface of the sawdust medium), and cultivation was further continued for an additional 30 days. After removing the cap, the culture medium was turned up to a depth of about 1 cm to comb out its surface layer with mycelium (a process to promote the formation of fruiting bodies), and the remaining medium was sprinkled with 20 ml tap water. After standing for four hours, the water left unabsorbed on the surface of the medium was removed, cultivation was continued at a temperature of 15.degree. C., a relative humidity of 95% and a luminous intensity of 20 lux for ten days to form primordia of fruiting bodies. The luminous intensity was then raised to a level of 200 lux, and cultivation was continued for 15 days, thereby examining the effect of aluminum powder upon the yield of fruiting bodies. The result obtained is summarized in Table 12.

TABLE 12______________________________________Amt. of aluminum Yield of fruit- Rate of increasepowder added (g) ing bodies (G) in yield (%)______________________________________0 124 1000.1 128 1030.3 139 1120.5 145 1170.8 155 1251.0 155 1253.0 186 1505.0 133 10710.0 129 104______________________________________

As can be seen from the above table, addition of aluminum powder to the culture medium drastically increased the yield of Lyophyllum ulmarium (M-8171 strain, FERM BP-1415).

Effects Achieved by the Invention

As is apparent from the foregoing, mushrooms can be cultivated with high yields by the method of this invention.

Claims

1. A method of cultivating mushrooms which comprises conducting the cultivation in a culture medium containing at least one member selected from the group consisting of magnesium aluminometasilicate, magnesium aluminate, sodium aluminosilicate, sodium aluminate, calcium aluminosilicate, barium aluminosilicate, and synthetic hydrotalcites.