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Cubero J.I. (ed.), Saxena M.C. (ed.).

Present status and future prospects of faba bean production and improvement in the Mediterranean countries

Zaragoza : CIHEAM

Options Méditerranéennes : Série A. Séminaires Méditerranéens; n. 10 1991

pages 105-110

Article available on lin e / Article dispon ible en lign e à l’adresse :

--- http://om.ciheam.org/article.php?ID PD F=92605141

--- To cite th is article / Pou r citer cet article

--- Martín A., Cabrera A., López Medina J. An tin u trition al factors in faba bean . Tan n in con ten t in Vicia faba: possibilities for plan t breedin g. In : Cubero J.I. (ed.), Saxena M.C. (ed.). Present status and future prospects of faba bean production and improvement in the Mediterranean countries. Zaragoza : CIHEAM, 1991. p. 105-110 (Options Méditerranéennes : Série A. Séminaires Méditerranéens; n. 10) ---

http://www.ciheam.org/

http://om.ciheam.org/

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Antinutritional. factors in faba bean.

Tannin content in Vicia faba:

possibilities for plant breeding

A. MARTiN*

A. CABRERA**

J. LOPEZ MEDINA***

*CS” INSTITUTO DE AGRONOMíA Y PROTECCIóN VEGETAL APDO. 246, 14080 CóRDOBA, SPAIN

**ESCUELA TECNICA SUPERIOR DE INGENIEROS AGRóNOMOS APDO. 3048, 14080 CóRDOBA, SPAIN

***CENTRO DE INVESTIGACION Y DESARROLLO AGRARIO (CIDA) APDO. 246, 14080 CóRDOBA, SPAIN

- Vicia faba. the

amount of condensed tannins in the testa of faba bean, mainly linked to is available in

A to with

been found. The of tannins in the physiology of the to

- “Facteurs antinutritionnels de la fève. Teneur en tannins chez Vicia faba: possibilités d’amélioration”. Les tannins condensés sont un des facteurs antinlltritionllels les plus inlportants de Vicia faba. La variabilité génétique pour la quantité de tannins condensés dans la testa de la fève, liée principalement à des gènes qui contrôlent la couleur de la peur ou de la graine, est disponible dans des populations naturelles. a été trouvé une réponse positive à la sélection des graines àfaible teneur en tannins dans des lignées de fève ri peurs colorées. Le rôle des tannins dans la physiologie de la plante en relation avec

l‘amélioration génétique est traité.

Introduction

Among the of plant metabolism,

tannins have the attention of plant

mainly because of two nega-

tive effect on the quality of the

uced, and the they play in defence mechan- isms against pathogens and pests.

The of tannins is complex and not well it is difficult to it with the tannin

effects which of to plant Tannins

classified into two condensed tannins which of flavonols and yield anthocyanidins when heated in acid solution, tannins which

gallic acid The

easily eliminated with the action of the juices and do not a in animal feeding.

this not included in analysis.

Flavan, the basic unit of condensed tannins is made up of two benzene linked by a

unit is also the basic of anthocyanidins and glycosides (antho-

cyanins), the being the

in plants glycosidation possible modifications of the basic unit of

sulting in of the physiological and

biochemical of these substances.

ties could be as basic as the auxin

1988), of tissues

against visible UV (Salatino et al., 1988), of nodulation genes

et al., 1986).

biosynthetic pathway

tannins C2) in by adding leucoc-

flavan-3,4-diols, flavan-3-01). The of tion is a of high biological

significance. activity of tannins (a the of digestibility) in-

with size, and it 3 and

(3)

10 Swain, 1963). These to

such as the of

ghum seeds 1982) and the in infestation of Vicia faba by Callosobruchus maculatus

et al., 1986). The has been

posed to be a nonenzymatic

ences in the of in could

be genetic as it is a of some

et al., 198l), although such as biochemical components of the

seed could also be The analytical in

the evaluation of tannin quality and quantity un- solved.

this we the of

on the study of tannins in the seeds of Vicia faba.

Genetics of testa tannin content and its relation with flower and grain colour

As mentioned, tannins some

with anthocyanin pigments in biosynthetic pathway. This is"the the well known

ship between whitè plants and absence of tan- nins in seeds et al., 1957).

mutants have played an in the elucidation of the biosynthetic pathway of anthocyanidins and

decided to study the between testa and tannin content in Vicia faba. In Table 1 we have the of the analysis

of 55 lines with of selfing. The

lationship of with tannin content of the whole seed is significant. As found by

white lines lack tannin in seeds. The spot- ted lines have less tannin in the testa than lines with diffuse pigmentation in the and

found in plants with yellow in lines

with less evident, be-

cause the genetics of seed is complex than

that of 1988).

plants with seed coat and spotted have low tannin content.

Table 2 we show a study but

instead of lines, F2 plants of in

tannin content, pigmentation

used and 1989b). The data on tannin content given as of testa weight. An

imate of both studies can be made by assum- ing that the seed coat was constant at 15% of total weight of the seed. Even this adjustment, the values of tannin content in both tables not because of analytical used in each study. A modified Folin method (Singlenton and 1965), used in the study gives an of tannin content as to the Vanillin

cific method tannins and its used in the second and Jones, 1978). The

between and tannin content is also mani- fested in the second study. the influence of the

located in

et al., 1989), on tannin content became evident, because of the homogeneous genetic

of the analysed.

the analytical the between

and seed coat and tannin content of the seed is obvious. when studying the genetic basis of tannin content in the testa we found that although additiveness was the main component, domi- nant was also significant in

if the plant with gains diffuse pigmen- tation in eliminated, the dominant component

of the and the additive component is

and 1989a).

Table 1. (%) in grain of faba bean pure lines in relation to flower and testa coloursa.

White

2.3 0.2 -

1.5 f 0.1

-

Yellow-spot

0.1

*

0.0

0.1 zk 0.0

Total 0.1 O.Oa 1.5 k 0.2b

- -

- -

Testa

- -

1.5 0.2

2.2 f 0.0 1.7 5z 0.3

-

2.2 f 0.lc 2.1 f 0.2c

2.5 0.2 2.8 f 0.1

2.3 0.1

-

Total Yellow

-

1.5 f 0.2b

- 0.1 O.Oa

-

2.3 f 0 . 0 ~ 2.4 0 . 3 ~

2.5 0.lc 2.5 -t 0.4 -

2.3 5z 0 . 2 ~ -

- 2.3 0.0 1.8 O.lb

2.3 f 0.2

with in the same l i e column statistically (p < 0.01)

- 106 -

(4)

Table 2. of F, plants of faba bean in relation to flower and testa coloura.

r

Testa

White Yellow-spot

-

- -

0.4 -+_ 0.0

- 1.7 f 0.1 yellow

4.2 zk 0.0 3.0 -1. 0.0

2.7 f 0.1

- - 3.6 -1. 0.1

- - - 4.4 -1. 0.1

4 . 1 f O . O ~ 3 . 0 z k O . O ~ 2.5-1.0.1 b

0.4-1.0.0a Total

4.8 0.1 3.2 f 0.1

2.6 & 0.1 -

Total

-

k 0.1 b 3.9 -1. 0.1

0.4 f 0.0 a 3.6 f 0.0 b 4.2 -1. 0.0

- 4.4 f 0.2 c 5.1 f 0.4 4.5 0.1 c 4.2 -1. 0.0 c

in the same line column statistically (p C 0.01)

conclusion is that the main of the quantita- tive detected on tannin content of the testa in

Vicia faba is a of genes, mainly

coat (Rh), diffuse pigmentation (Sdphdp) and

yellow (Yf/yf) genes, the of being

influenced by

The role of tannins in faba bean

The condensed tannins in faba bean have bio- logical effects and biochemical to those

sent in et al., 1977). The

of of condensed

tannins of developing seeds in 1982),

with well

known. Likewise, in the genetic have been classified into

of of tannins contained in them. In Vicia faba, as we know, no such study has been pub-

lished Tena have

studied the evolution of tannin with development

in and found the same as in

ghum. The shows an of condensed tan- seed coat with time which

30 days and is followed by

a decline in tannin content associated with an

in the of They have also studied

the changes of of tannins in the seed coat wilt time of faba bean lines having diffuse pigmen- tation, VF91 (yellow), VF118 (violet) and VF123

dimension

The evolution of tannin content level found, although W 9 1 kept a noticea-

ble amount of catechin) and oligom-

six months, indicating a in the level of

linked to pigment

some white flow- plants a linked to changes in pig-

mentation. in not

black at and this may be to be be- cause of the in the levels of enzymes oxidis- ing phenols plausibly as a change in the sub-

of these enzymes common to both genetic plants with yellow

pigmentation in the seed 1989a).

some white plants do turn black

at have found that these

the allele Yf pigmentation while plants that kept a light the yf yellow pigmenta- tion. This means that anthocyanidins and com- pounds not involved in this change of

.is change in seed associated to and of the seed coat of Vicia faba, linked with and with a biological impact. is well known that the testa

with time due to the oxidation of

phenolic compounds. in plants with the in individual plants is

not light

be obtained. The of each is not maintained in

the next selfing.

(1974) have studied the between seed phenolic compounds, levels of enzymes oxidising pheno- lics compounds, and the of the seed coat in the genus They concluded that seed

bility to to phenolic content and its level of oxidation and in

the position of the seed in the plant. We also

found in to

of

amounting to 80% of its weight 10

seeds plants

- 107 -

(5)

weight by 46% and light

20%. 24 no

The of seeds

in Vicia faba.

the most to this

change of was the absence of infestation by Bruchrts rufimanus of light while

ones and white plants infested

in 100% of the cases field conditions. We to find a between and situation in the plant of the but unlike in was no

Table 3 some and light

seeds the same plant lines and

F3 plants analysed. in of

seed coat not significant. No dif-

found between both seed in sec- tions of seed coats. the tannin index of both was significantly which seems to indicate a in phenols content. On the con- the to vanillin was not significant, al- though a between values of and vanil- lin is evident. The values of the vanillin test could

be as a level of of tan-

nins in light testas, because this test only takes into account the unit of the and the

in could two

of phenols oxidation, of

genetic the development

of the seed. Glennie (1981) has stud- ied the changes in polyphenols content, and in and polyphenol oxidase activities.

found a between tannin evolution

and the activity of both enzymes, with the decline of not as as that of tannins These enzymes and have been associated with de- fence mechanisms. to be a definite of development in which the could be in- fested and also a in which the high level of

idase and tannin such

infestation. White do not change testa and susceptible to Bruchus.

have two types of those with testa sensitive to Bruchus infestation because they pass quickly to high levels

oxidase and activities, and with testa

take time in the same

tion level and immune to Bruchus infestation.

Breeding strategies

of faba bean using

the white genes is the easiest way of solving the

of these

yield and establish-

ment of isogenic lines than

tannin-containing These not un-

usual and the of yield could be a consequence of susceptibility of to pathogens and pests. In Table 4 we data on mean seed weight, of seed plant and yield plant of F2 plants of by tannin-containing lines.

The five lines used of seed size (seed weight of line 14=0.41, 15=0.50, 23=0.41, and 44=0.33, 59=0.40 g). The only that seems to 'be in plants is seed weight and in of yield

it is by a of seeds

white plant. is well known that seeds white flow- plants have a of testa than tannin containing plants and 1986). This fact

could account the The establish-

ment could also be a of

tion a and testa.

a of

have to be tested.

of selection low condensed tannin content in faba bean populations scanty. Sjödin et al. (1981) selected low and high content of total phenolics, populations with

testa two cycles. the cycle

a of 0.33 units was found between high and low tannin containing plants while in the second cycle

significant

The weight was affected by sel-

ection, and the testa which was significantly in the population with high content of total pheno-

affected. The change in testa

could account the change in phenolics content.

seems that selection low tannin content in populations with homogeneous testa and pigmenta- tion in is not effective. the tannin

Table 3. Characteristics of seed coat of individual Vicia faba plants differing in darkening.

Light

X SE X SE

Seed coat %

1.58 ns 3.14 0.20

3.65 & 0.25 Vanillin

4.74

***

5.44 0.14 6.79

& 0.24

6.58

***

5.41 0.11 6.66 & 0.15

T.1.b

2.34

*

5.49 0.31 6.97 &

0.69 ns 13.99 3Z 0.63

13.43 k 0.37

1.21 ns 16.25 3Z 0.47

15.38 k 0.55

lines bF3 plants - 108 -

(6)

X f SE 0.44 f. 0.01 58.01 f. 5.06 26.28 f. 2.32 0.50 f 0.05 56.17 f. 3.20 28.16 f 1.23 0.44 f 0.01 45.34 f. 3.91 20.34 f. 1.86 0.44 f 0.06 59.28 2.78 25.98 f 1.25 0.45 f. 0.01 66.82 ? 8.05 30.29 f 3.67 0.48 f 0.06 52.13 f 2.63 25.04 f 1.24 0.47 f 0.03 55.90 f 1.40 26.09 f. 0.66

N

70

162

62

156

38

127

615

content estimated by the was

in one cycle of selection

and population

et al., 1989). A composite pop- ulation was by mixing F, plants

among lines in and seed coat Selection low and high tannin content was done. The

tannin content using

Two distinctive

obtained. The two selected populations with high and low content of tannins tested and seed

coat was that the two populations

these The low tannin population had 96.5% plants with spotted

yellow spots) and 3.5% with solid pigmentation, in the high tannin population the

to 40%. With to seed coat we found that 64% of the low tannin content population had

15% seed coat The of the

plants had yellow seed coat

in the high tannin content population 92.75% of the plants had and yellow seed coat

White X SE 0.24 f 0.01 61.98 f 6.08 26.06 f 2.75 0.47 f 0.01 65.47 f 3.47 30.49 f 1.57 0.42 f 0.01 48.03 f 5.79 20.21 f 2.42 0.41 f 0.01 65.69 f 5.03 26.83 t- 2.00 0.43 f 0.01 68.54 5.76 29.97 f. 2.81 0.45 f 0.01 56.73 f 5.02 25.76 2.32 0.43 f. 0.04 61.74 t- 2.09 26.91 f 0.93

N

43

59

34

55

35

44

270

-

t

15.38

***

0.50 ns 0.06 ns 3.16

**

2.19

*

1.17 ns 1.05 ns 0.38 ns 0.04 ns 3.44

***

1.11 ns 0.36 ns 1.71 ns 0.17 ns 0.07 ns 3.19

**

0.79 ns 0.27 ns 8.33

***

2.31

*

. 0.72 ns

seeds found. as

the genetics of in

the

of

using the white genes, genes that

tannin content, should be

tested. A plant with and lemon spot

could be the basis of low tannin content without the negative effect of white genes.

is well established that phenol compounds play an in plant metabolism and in the

of plants with

1983). In the section

some on the

at plant level of Vicia

faba, like of of the

same plant associated with testa and sus- ceptibility tÒ infestation by Bruchus rufinzanus.

to selection

ful. We not able to find a between seed and situation in the plant, but this does not mean it does not exist. a plant with only light - 109 -

(7)

could be obtained it would be to Bruchus infestation with only a small in tannin content.

Once elucidated the of genes with the tannin content of the testa, main objective will be the study of tannin content in the vegetative of the plant, with the aim of obtaining faba bean with the highest level of tannin in the vegetative and the lowest in

the The study of the influence in

the tannin content of the seed and the elucidation of the

genetic basis of the in levels,

if they do exist, will be the goals

Acknowledgements

Financial the de Educación

y Ciencia, Spain

acknowledged. could not have been done without the facilities of the of The editing help of Jean i s

References

Annual Cam-

GELON,

fluence des tanins condensés du tégument de fèves (Vicia faba) le développement de Callosobruchus maculatzm Entomol. Exp.

Appl. 42~125-132.

and JONES, W.E. (1978): Analysis of con- densed tannins using acidified vanillin. J. Sci. Food

J.O. and

yphenolic changes in J. Food

Chem. 29:973-981.

L.G. (1982): of of

ghum tannin seed development and J. Food

Chem. 30:1090-1094.

of in Vicia faba

A., J. A. (1989):

The genetics of tannin content in faba bean (Vicia faba L.).

297-300 in advances of in in

L. 22:3-7.

legume seeds: animal feed technology, analytical methods and

Wageningen, The

A. and A. (1986): in tannin con-:

A. Genetics of tannin con-

tent and its with and testa in Vicia faba. J.

tent in Vicia faba L. J. Sci. Camb. 106:377-382.

and A. (1989b): Analysis of genetic link- age in faba bean (Vicia faba L.). 24:3-5.

and

beans suitable canning. and 16:1275- 1503.

J.L., L. and

A.W. (1986): Flavonoid activation of nodulation genes in

by compounds in plants. 32490-92.

changes in polyphenols, idase, and polyphenol oxidase in J. Food Chem.

29~33-36.

T. (1963): Changes in tannins in 2:371-383.

auxin Science 241:346-349.

of in

genetic of the of to cat-

echin and 49503-524.

of seed coats to conditions and metabolism of pheno-

lics. 545317420.

A.T. and EVANS, L.E. (1978):

and tannin-containing of faba beans (Vicia faba). Can. J. Sci. 58:753-760.

(1988): localization of phenolic deposits in shoot apices of common species of Annals of

total

phenolics with acid Am. J.

Enol. Vitic.

J., T. (1981):

Selection substances in field bean (Vicia faba). Z.

86231-247.

en el contenido y de. de los taninos condensado!. de

haba (Vicia faba L.) la del 284A-

in del de Química de la

Sociedad Española de Química, Spain.

*

(1983): Tannins: does func-

tion? An ecological Am. Nat.

- 110 -

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