Research on Chemical Composition and Ensiling

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Nan Zhao. 1e. ,. Yimin Cai. 2f. , Mao Li. 3g. , Hanlin Zhou. 3h*. 1 Hainan University, Haikou, Hainan 570228, China. 2 Japan International Research Center for ...
Advanced Materials Research Vols. 347-353 (2012) pp 1647-1651 Online available since 2011/Oct/07 at www.scientific.net © (2012) Trans Tech Publications, Switzerland doi:10.4028/www.scientific.net/AMR.347-353.1647

Research on Chemical Composition and Ensiling Characteristics of Banana Stems and Leaves Jinsong Yang1a , Haisheng Tan1b, Hairui Zhai1c, Qian Wang1d, Nan Zhao1e, Yimin Cai2f, Mao Li3g, Hanlin Zhou3h* 1 Hainan University, Haikou, Hainan 570228, China 2 Japan International Research Center for Agricultural Sciences 3 Chinese Academy of Tropic Agriculture Sciences, Hainan 571737, China a

[email protected], [email protected], [email protected], [email protected], e [email protected], [email protected], [email protected], *Hanlin Zhou: Corresponding author, Email: [email protected]

Keywords: :banana stems and leaves, silage, fermentation quality.

In order to investigate the nutritive and ensiling characteristics of banana stems and leaves, the chemical compositions of banana stems and leaves were analyzed and the effects of additives on fermentation quality were measured. The research results showed: Banana stems and leaves had high fiber content (stem>58% DM, leaf >72% DM), nitrogen free extract content (>50% DM), and water soluble carbohydrate contents (WSC>5% DM), with certain nutritive value. Tannins of banana stem and leaf were 0.11% DM and 0.24% DM. There were lactic acid bacteria (>105cfu/g FM) in the banana stems and leaves; they might be well preserved with some treatments. Abstract.

Introduction Banana (or Musa paradisiacal) was one kind of popular tropical fruit. The growth area in china increased 5%~10% in 2010 to about 5.30 million acres with a total output of 8.50 tons. At the mean time of producing big amount of it, banana stems and leaves of about the same quantity were also produced and abandoned as waste in a long term; hence, it became an important topic about how to dispose of them [1]. There are certain content of protein, crude fat, and crude fiber in banana stems and leaves which made it a very potential non-convention plant feed [2]. There was a big amount of tannin in banana stem and leaf. The combination of tannin and glycoprotein, which was used in oral lubrication, was insoluble and tasted bitter leading to fewer feed intake [3]. Another factor causing banana stem and leaf bad taste and low digestibility was huge amount of fiber contained. Thus, it would help to make full of banana stem and leaf by improve the fiber’s nutritive value and remove or inactivate tannin. There were many methods to processing banana stem and leaf, and in comparative to others, ensiling was relatively low cost one. The energy and protein digestibility of silage was higher than dryer one; in addition, content of digestible crude protein, total nutrient and energy content in dry matter of silage were also high. What’s more, digestibility of silage’s cell wall after silage fermentation was apparently increased [4]. In order to use the by-products as feeds for dairy cows well, the chemical compositions of banana stem leaf were analyzed and the effects of wilting and additives on their fermentation quality were measured.

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Materials and Methods Silage preparation. Banana stems and leaves were obtained from Banana plantations in Hainan province, China. The materials were chopped to approximately 2cm, wilting and were ensiled directly or after treated with 5% molasses (II group), 1% lactic acid bacteria (LAB, Lactobacillus plantarum HN1) inoculation at 1.0×108 cfu/g FM (III group), 5% molasses +1% LAB (IV group). The control (I group) was made without additives. Each 200g treated material was packed into a plastic film bag and the bags were degassed, sealed and kept at ambient temperature for 40 days. Chemical analysis. Dry matter (DM) content was determined by oven drying at 70˚C for 48 h. Crude ash content was measured after incinerated for 3 h at 550˚C. Crude protein (CP) and ether extract were analyzed according to AOAC methods [5]. Water soluble carbohydrate (WSC) content was determined using the anthrone method [6]. The buffering capacity was determined as described by Playne and McDonald [7]. Tannin content was determined by the use of Phosphor molybdatetungstic acid colorimetric method [8] Microbial analysis. Ten gram of material was shaken well with 90mL of sterilized saline solution (0.85% NaCl), and serial dilutions (10-1-10-6) were made in sterile saline solution. LAB was counted on MRS medium agar (Difco Laboratories, Detroit, Mich, USA.) after incubation in an anaerobic incubator (N2:H2:CO2 =85:5:10, YQX-II, CIMO Medical Instrument Manufacturing Co., Ltd, Shanghai, China) at 37˚C for 2 days. Yeasts and molds were counted on potato dextrose agar (Nissui-seiyaku Ltd, Tokyo, Japan) acidified with sterilized tartaric acid solution (10%) to pH 3.5. These agar plates were incubated at 37˚C for 2 days. Fermentation quality. When the bag silos were opened, 20g of silage sample was taken and mixed with 80mL of distilled water and stored in a refrigerator at 4˚C for 18 h. Then, the material was filtered and the filtrate was used for the measurements of pH value, ammonia nitrogen (NH3-N) and organic acids. The pH value was measured with a glass electrode pH meter (PHS-3C, CSDIHO Co., Ltd, Shanghai, China). Concentration of NH3-N was analyzed by Kjeltech analyzer according to Kjeltech method without a digestion step. The organic acid contents were analyzed by HPLC (column: Sodex RS Pak KC-811, Showa Denko K.K., Kawasaki, Japan; detector: DAD, 210 nm, SPD-20A, Shimadzu Co., Ltd., Kyoto, Japan; eluent: 3 mM HClO4, 1.0 mL/min; temperature: 60˚C). The pH changes of samples after exposure to the air for 48, 96 and 144 hours were measured. Data analysis. The data were analyzed by analysis of variance and means. Then it was compared for significance by Duncan’s multiple range method. All statistical procedures were performed using the statistical packages for the SAS and Excel.

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Results and Discussion Characteristics of banana stems and leaves Banana stems and leaves had higher contents of crude fiber, lower contents of crude fat and nitrogen free extract, lower contents of crude protein and water soluble carbohydrate (Table 1). Table 1 Nutrition and tannins content of banana stems and leaves (DM, %) Sample

DM

CP

CF

NDF

ADF

WSC

NFE

Tannins

22.11a

11.21b

2.87c

67.63ab

33.98c

6.52a

54.76bc

0.66a

Medium plantain

17.11a

14.96a

3.34b

67.92ab

39.30bc

6.24a

54.44bc

0.46b

Brazil banana

17.99a

8.16c

5.65a

72.57a

46.78b

6.43a

51.32c

0.24c

4.59b

1.53f

1.58d

73.88a

56.45a

5.64b

51.26c

0.08d

Medium plantain

4.67b

2.01e

2.18cd

64.05b

53.25a

5.48b

53.18b

0.10d

Brazil banana

4.52b

4.49d

1.35d

58.37c

46.96b

5.82b

54.55a

0.11d

Average

11.85

7.06

2.83

67.40

46.12

6.21

53.25

0.28

Banana leaves Dwarf banana Dongguan

Banana stems Dwarf banana Dongguan

DM, dry matter; CP, Crude protein; CF, Crude fat; WSC, water-soluble carbohydrate; NFE, Nitrogen free extract; ND, not detect; Neutral Detergent Fibre, NDF; Acid Detergent Fibre, ADF; Water soluble carbohydrate, WSC.

Remark: different letter in the same range stands for obvious differentiation (P<0.01).

Average value of DM, CP, EE, NDF, ADF, Nitrogen free extract and Tannins in banana stem and leaf were 11.85%, 7.06%, 2.83%, 67.40%, 46.12%, 6.21%, 53.25%, and 0.28%, in which content of DM, CP, EE, and Tannins were obviously higher than banana stem(P<0.01). Because of the big amount of yield of Brazil banana, its leaf and stem (about 99% stem) were chosen as silage experiment material. Adhering microbes in banana stems and leaves. Microbes adhering to banana stems and leaves in three species of banana were analyzed. Analysis result was shown in Table 2. Table 2: The micro-organisms attached to the banana stems and leaves (cfu/g FM) Aerobic Sample

LAB

Bacilli

bacteria

Yeast

Mold

Dwarf banana leaf

6.5x105

ND

6.4x106

1.8x106

1.0x102

Dongguan medium plantain leaf

2.1x104

6.5x103

5.2x105

3.4x104

1.0x102

Brazil banana leaf

6.8x105

4.5x103

4.4x106

2.8x105

2.0x102

1.4x106

5.0x103

5.8x107

4.0x106

ND

6

4

8

6

1.0x102

6.5x106

2.0x102

Banana leaf

Banana stem Dwarf banana stem Dongguan medium plantain stem

2.8x10

Brazil banana stem

6.0x106

2.5x10

6.5x103

2.3x10

6.4x107

7.0x10

ND:not detect. LAB: Lactic acid bacteria.

There were many LAB in Brazil banana leaf and stem which was 6.8x105 cfu/g FM, 6.0x106 respectively. There was a big amount of Bacilli in Dongguan medium banana leaf and stem which were 6.5x103cfu/g FM, 2.5x104 respectively. There were many Aerobic bacteria in Dongguan medium plantain stem, and the second most was in Brazil banana stem. There were a big amount of

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Yeast in Dongguan medium plantain; the second most was in Brazil banana stem. Except for Dwarf banana stem, there were a few mould adhere in banana stems and leaves. Aerobic bacteria, followed by Yeast and LAB, ranked first in quantity among microbes adhering in banana stems and leaves. Fermentation quality of banana stems and leaves silage Organic acid content was the main indicator valuing fermentation quality of silage. Analysis result of organic acid in banana stems and leaves silage was shown in Table 3. Table 3 The ratio of concentrations of organic acid of banana stems and leaves silage (%FM) Group number I(contrast) II III IV

Lactic acid d

0.84 0.90c 1.32b 1.62a

Acetic acid 0.42b 0.43b 0.46a 0.45a

Propionic acid 0.16b 0.19a 0.14c 0.17b

Butyric acid 0.03a 0.03a 0.01a 0.00a

pH 4.6a 4.3b 4.1c 3.9d

Remark: different letters in the same range shown significant difference (p