Miniaturized yeast identification system

Claim 2

A culture container of a size to fit on a conventional microscope viewing stand for the identification of fungal pathogens, comprising: (a) a well means for containing fungal differentiation media, the dimensions of said well means adapted to contain a quantity of up to about 5.0 milliliters of media at a depth of up to about 4.5 millimeters, for the growth of a specimen; and (b) a fungal differentiation media present in said well means in the amount of said quantity comprising a composition effective to induce a different observable effect in at least one species of fungi as compared with another species of fungi and effective to induce germ tube production and conventional morphological characteristics, said composition including purified saponin, oxgall, a substrate for phenol oxidase in sufficient quantity to allow differentiation of Cryptococus neoformans, water and ammonium ions.

Claim 3

The culture container of claim 1, further comprising a lid adapted to removable engage with said container.

Claim 4

The culture container of claim 1, wherein said fungal differentiation media further comprises a carrying agent.

Claim 5

The culture container of claim 1, wherein said substrate for phenol oxidase is caffeic acid.

Claim 6

The culture container of claim 1, wherein said substrate for phenol oxidase comprises from about 0.005 to about 0.5 weight percent of the weight of said water.

Claim 7

The culture container of claim 5, wherein said substrate for phenol oxidase comprises from about 0.012 to about 0.12 weight percent of the weight of said water.

Claim 8

The culture container of claim 6, wherein said substrate for phenol oxidase comprises about 0.06 weight percent of the weight of said water.

Claim 9

The culture container of claim 1, wherein said saponin comprises from about 0.1 to about 5.0 weight percent of the weight of said water.

Claim 10

The culture container of claim 8, wherein said saponin comprises from about 0.1 to about 2.5 weight percent of the weight of said water.

Claim 11

The culture container of claim 9, wherein said saponin comprises about 1.0 weight percent of the weight of said water.

Claim 12

The culture container of claim 3, wherein said carrying agent is present in an amount of from about 1.0 to about 5.0 weight percent of the weight of said water.

Claim 13

The culture container of claim 11, wherein said carrying agent is present in an amount of 2.0 weight percent of the weight of said water.

Claim 14

The culture container of claim 3, wherein said carrying agent is agar.

Claim 15

The culture container of claim 1, wherein said oxgall is present in an amount from about 0.25 to about 30.0 weight percent of the weight of said water.

Claim 16

The culture container of claim 14, wherein said oxgall is present in an amount from about 0.5 to about 5.0 weight percent of the weight of said water.

Claim 17

The culture container of claim 15, wherein said oxgall is present in an amount of about 1.0 weight percent of the weigth of said water.

Claim 18

The culture container of claim 1, wherein said ammonium ions are present in an amount from 0.001 M to about 0.5 M.

Claim 19

The culture container of claim 17, wherein said ammonium ions are present from about 0.005 M to about 0.05 M.

Claim 20

The culture container of claim 18, wherein said ammonium ions are present at about 0.01 M.

Claim 21

The culture container of claim 1, wherein said well means is cylindrical.

Claim 22

The culture container of claim 1, wherein said well means is pie-shaped.

Claim 23

The culture container of claim 1, wherein said well means has a perimeter of rectangular or square shape.

Claim 24

The culture container of claim 1, further comprising at least one additional well means for containing fungal differentiation media.

Claim 25

The culture container of claim 1, wherein said quantity is from about 2.5 milliliters to about 5.0 milliliters at a depth of up to about 4.5 millimeters.

Claim 26

The culture container of claim 23 further comprising at least one additional media for fungal differentiation or growth, each of said additional medias situated in one of said additional well means.

Claim 27

The culture container of claim 23, wherein a second fungal differentiation media is present in at least one of said additional well means in the amount of said quantity comprising a media effective to induce a different observable effect in at least one species of fungi subjected to a previous carbohydrate depletion step as compared to another species of fungi subjected to said carbohydrate depletion step, wherein said second fungal differentiation media is adapted in composition to produce an observable effect of positive or negative carbohydrate assimilation in carbohydrate depleted fungal cells within from about 3 hours to about 24 hours from inoculation.

Claim 28

The culture container of claim 23 wherein a second fungal differentiation media is present in at least one of said additional well means in the amount of said quantity comprising a media adapted in composition to induce a different observable effect in a fungal species metabolizing urea as compared to a fungal species which does not within from about 1 hour to about 3 hours after inoculation.

Claim 29

The culture container of claim 23 wherein a second fungal differentiation media is present in at least one of said additional well means in the amount of said quantity comprising a media effective to induce a different observable effect in at least one species of fungi subjected to a previous carbohydrate depletion step as compared to another species of fungi subjected to said carbohydrate depletion step, wherein said second fungal differentiation media is adapted in composition to produce an observable effect to positive or negative carbohydrate assimilation in carbohydrate depleted fungal cells within from about 3 to about 24 hours from inoculation, and a third fungal differentiation media is present in another of said additional well means adapted in composition to induce a different observable effect in a fungal species metabolizing urea as compared to a fungal species which does not within from about 1 hour to about 3 hours after inoculation.

Claim 30

A culture container of a size to fit on a conventional microscope viewing stand for the identification of fungal pathogens, comprising: (a) a well means for containing fungal differentiation media, the dimensions of said well means adapted to contain a quantity of up to about 5.0 milliliters of media at a depth of up to about 4.5 millimeters, for the growth of a specimen; and (b) a fungal differentiation media present in said well means in the amount of said quantity, comprising about 1.0 weight percent purified saponin, about 1.0 weight percent oxgall, about 0.06 weight percent caffeic acid, about 0.01 M ammonium ions, about 2.0 weight percent agar, and water, said weight percentages based on the weight of said water.

Claim 31

A culture container of a size to fit on a conventional microscope viewing stand for the identification of fungal pathogens, comprising: (a) a well means for containing fungal differentiation media, the dimensions of said well means adapted to contain a quantity of up to about 5.0 milliliters of media at a depth of up to about 4.5 millimeters, for the growth of a specimen; and (b) a fungal differentiation media present in said well means in the amount of said quantity, comprising about 1.0 weight percent purified saponin, about 1.0 weight percent oxgall, about 0.06 weight percent caffeic acid, about 0.01 M ammonium ions, about 2.0 weight percent agar, and water, said weight percentages based on the weight of said water.

Claim 32

A culture container of a size to fit on a conventional microscope viewing stand for the identification of fungal pathogens, comprising: (a) at least two well means for containing fungal differentiation media, the dimensions of each of said two well means adapted to contain a quantity of up to about 5.0 milliliters of media at a depth of up to about 4.5 millimeters, each of said well means for the growth of a specimen; and (b) a first fungal differentiation media present in one of said well means in the amount of said quantity comprising purified saponin, oxgall, a substrate for phenol oxidase, ammonium ions, a carrying agent, and water, and a second fungal differentiation media present in the other of said well means in the amount of said quantity comprising a media effective to induce a different observable effect in at least one species of fungi subjected to a previous carbohydrate depletion step as compared to another species of fungi subjected to said carbohydrate depletion step, wherein said second fungal differentiation media is adapted in composition to produce an observable effect of positive or negative carbohydrate assimilation in carbohydrate depleted fungal cells within from about 3 hours to about 24 hours from inoculation.

Claim 33

A culture container of a size to fit on a conventional microscope viewing stand for the identification of fungal pathogens, comprising: (a) at least two well means for containing fungal differentiation media, the dimensions of each of said two well means adapted to contain a quantity of up to about 5.0 milliliters of media at a depth of up to about 4.5 millimeters, each of said well means for the growth of a specimen; and (b) a first fungal differentiation media present in one of said well means in the amount of said quantity comprising purified saponin, oxgall, a substrate for phenol oxidase, ammonium ions, a carrying agent, and water, and a second fungal differentiation media present in the other of said well means in the amount of said quantity comprising a media effective to induce a different observable effect in at least one species of fungi subjected to a previous carbohydrate depletion step as compared to another species of fungi subjected to said carbohydrate depletion step, wherein said second fungal differentiation media is adapted in composition to produce an observable effect of positive or negative carbohydrate assimilation in carbohydrate depleted fungal cells within from about 3 hours to about 24 hours from inoculation.

Claim 34

The culture container of claim 30, further comprising a lid adapted to removably engage with said container.

Claim 35

The culture container of claim 30, wherein said quantity is from about 2.5 milliliters to about 5.0 milliliters at a depth of up to about 4.5 millimeters.

Claim 36

A culture container of a size to fit on a conventional microscope viewing stand for the identification of fungal pathogens, comprising: (a) at least two well means for containing fungal differentiation media, the dimensions of each of said two well means adapted to contain a quantity of up to about 5.0 milliliters of media at a depth of up to about 4.5 millimeters, each of said well means for the growth of a specimen; and (b) a first fungal differentiation media present in one of said well means in the amount of said quantity comprising purified saponin, oxgall, a substrate for phenol oxidase, ammonium ions, a carrying agent, and water, and a second fungal differentiation media present in the other of said well means in the amount of said quantity comprising a media adapted in composition to induce a different observable effect in a fungal species metabolizing urea as compared to a fungal species which does not within from about 1 hour to about 3 hours after inoculation.

Claim 37

A culture container of a size to fit on a conventional microscope viewing stand for the identification of fungal pathogens, comprising: (a) at least two well means for containing fungal differentiation media, the dimensions of each of said two well means adapted to contain a quantity of up to about 5.0 milliliters of media at a depth of up to about 4.5 millimeters, each of said well means for the growth of a specimen; and (b) a first fungal differentiation media present in one of said well means in the amount of said quantity comprising purified saponin, oxgall, a substrate for phenol oxidase, ammonium ions, a carrying agent, and water, and a second fungal differentiation media present in the other of said well means in the amount of said quantity comprising a media adapted in composition to induce a different observable effect in a fungal species metabolizing urea as compared to a fungal species which does not within from about 1 hour to about 3 hours after inoculation.

Claim 38

The culture container of claim 33, further comprising a lid adapted to removably engage with said container.

Claim 39

The culture container of claim 33, wherein said quantity is from about 2.5 milliliters to about 5.0 milliliters at a depth of up to about 4.5 milliliters.

Claim 40

A culture container of a size to fit on a conventional microscope viewing stand for the identification of fungal pathogens comprising: (a) at least three well means for containing fungal differentiation media, the dimensions of each of said three well means adapted to contain a quantity of up to about 5.0 milliliters of media at a depth of up to about 4.5 millimeters, each of said well means for the growth of a specimen; and (b) a first fungal differentiation media present in one of said well means in the amount of said quantity comprising purified saponin, oxgall, a substrate for phenol oxidase, ammonium ions, a carrying agent, and water, a second fungal differentiation media present in another of said well means in the amount of said quantity comprising a media effective to induce a different observable effect in at least one species of fungi subjected to a previous carbohydrate depletion step as compared to another species of fungi subjected to said carbohydrate depletion step, wherein said second fungal differentiation media is adapted in compositin to produce an observable effect of positive or negative carbohydrate assimilation in carbohydrate depleted fungal cells within from about 3 to about 24 hours from inoculation, and a third fungal differentiation media in the third of said well means adapted in composition to induce a different observable effect in a fungal species metabolizing urea as compared to a fungal species which does ot within from about 1 hour to about 3 hours after inoculation.

Claim 41

A culture container of a size to fit on a conventional microscope viewing stand for the identification of fungal pathogens comprising: (a) at least three well means for containing fungal differentiation media, the dimensions of each of said three well means adapted to contain a quantity of up to about 5.0 milliliters of media at a depth of up to about 4.5 millimeters, each of said well means for the growth of a specimen; and (b) a first fungal differentiation media present in one of said well means in the amount of said quantity comprising purified saponin, oxgall, a substrate for phenol oxidase, ammonium ions, a carrying agent, and water, a second fungal differentiation media present in another of said well means in the amount of said quantity comprising a media effective to induce a different observable effect in at least one species of fungi subjected to a previous carbohydrate depletion step as compared to another species of fungi subjected to said carbohydrate depletion step, wherein said second fungal differentiation media is adapted in compositin to produce an observable effect of positive or negative carbohydrate assimilation in carbohydrate depleted fungal cells within from about 3 to about 24 hours from inoculation, and a third fungal differentiation media in the third of said well means adapted in composition to induce a different observable effect in a fungal species metabolizing urea as compared to a fungal species which does ot within from about 1 hour to about 3 hours after inoculation.

Claim 42

The culture container of claim 36, further comprising a lid adapted to removably engage with said container.

Claim 43

The culture container of claim 36, wherein said quantity is from about 2.5 milliliters to about 5.10 milliliters at a depth of up to about 4.5 millimeters.