Dear Label_Name,

Greetings! I hope you are well.

I am writing on behalf of an international publishing house, Science and Education Publishing, USA (http://www.sciepub.com).

Science and Education Publishing (SciEP) is a multidisciplinary open access publisher of Journals covering the fields of Science, Technology and Medicine. All SciEP publications are subject to high-quality peer review, editorial and production processes and are freely available online.

Welcome to the April, 2013 edition of SciEP newsletter, providing monthly summaries of articles on science & education related topics of interest to scientist and professionals. The mission of our journals is to provide an open access forum for publishing new findings on issues pertinent to scientific and academic field. We also invite you to submit original research papers, review articles, short reports, or case studies are considered for publication in our Multidisciplinary Journals.

American Journal of Public Health Research
DOI: 10.12691/ajphr-1-1-3

The Implementation of a Tele-Homecare System with Service Oriented Architecture and HL7 Message Transmission Standard
Ching-Sung Wang

American Journal of Medical and Biological Research
DOI: 10.12691/ajmbr-1-1-2

The Influence of Ethanol on Pyruvate Kinases Activity in Vivo, in Vitro, in Silico
Lelevich Sergey Vladimirovich, Khrustalev Vladislav Victorovich, Barkovsky Eugene Victorovich, Shedogubova Tatyana Aleksandrovna

American Journal of Medical Sciences and Medicine
DOI: 10.12691/ajmsm-1-1-1

Clinical and Histological Features in Wegener Granulomatosis
Li Cavoli Gioacchino, Passantino Rita, Bono Luisa, Tortorici Calogera, Ferrantelli Angelo, Giammarresi Carlo, Rotolo Ugo

American Journal of Infectious Diseases and Microbiology
DOI: 10.12691/ajidm-1-1-2

The Curse of Lymphatic Filariasis: Would the Continual Use of Diethylcarbamazine Eliminate this Scourge in Papua New Guinea?
Anne Lanham, Lillian Mwanri

We have released issues of some journals on February 2013.
American Journal of Public Health Research
American Journal of Medical Sciences and Medicine
American Journal of Medical and Biological Research
American Journal of Pharmacological Sciences
American Journal of Clinical Medicine Research
American Journal of Nursing Research
American Journal of Cancer Prevention
American Journal of Medicine Studies
American Journal of Infectious Diseases and Microbiology
American Journal of Cardiovascular Disease Research
American Journal of Biomedical Research
American Journal of Mechanical Engineering
American Journal of Microbiological Research
Journal of Preventive Medicine
American Journal of Food and Nutrition
American Journal of Hypertension Research
American Journal of Sports Science and Medicine
Journal of Cancer Research and Treatment
American Journal of Zoological Research
Journal of Biomedical Engineering and Technology
American Journal of Microbiological Research
Biomedical Science and Engineering

We are pleased to announce that submissions are now being accepted for peer review for all the journals across all our subject areas in SciEP.

Please submit your manuscript via our online submission system:
http://www.sciepub.com/author/signin

To unsubscribe from our mailing list, please click on the following link: unsubscribe

I am looking forward to hearing from you.

Kind regards,

David Rain
Email:join@sciepub.com
Science and Education Publishing (http://www.sciepub.com)

Variation of Nutrients and Functional Properties within Young Shoots of a Bamboo Species (Yushania alpina) Growing at Mt. Elgon Region in Western Kenya

Paul N. Karanja*, Glaston M. Kenji, Simon M. Njoroge, Daniel N. Sila, Christine A. Onyango, Hiroshi Koaze, Naomichi Baba

Food Science and Technology, Jomo Kenyatta University of Agriculture and Technology, Nairobi, Kenya

Abstract: Yushania alpina is an indigenous bamboo species growing at Mt. Elgon forest in Western Kenya and its young shoots are consumed by the local people as a vegetable. This study was done to determine some physico-chemical properties and their distribution within the shoot. Each shoot was divided into the upper and lower portions which were analyzed separately, and results were expressed in dry weight basis. On proximate composition, there was no significant difference (p<0.05) between the two portions in terms of moisture, protein, ash and fat content, which ranged 92.2-92.4% fresh weight, 33.0-33.4% dry weight basis (dwb), 17.0-17.1% dwb and 2.0% dwb, respectively. Significant difference was found in fiber and carbohydrates, whose content was 23.9 and 23.6% dwb in the upper portion compared to 30.7 and 17.3% dwb in the lower part, respectively. The upper portion contained Ca of 2,670, Mg of 4,300, K of 35,900 and P of 7,630 µg/g dwb, whereas the lower portion had Ca of 1,060, Mg of 1,270, K of 27,600 and P of 4,810 µg/g dwb. The upper portion was found to contain thiamine, riboflavin and vitamin C of 2.2, 8.4 and 78.2 µg/g dwb, respectively, whereas the lower part contained 1.8, 7.3 and 51.2 µg/g dwb, respectively. Fructose was found to differ significantly with the upper portion having 2.19 % against 0.62 % in the lower portion. Total polyphenol and flavonoid content of 27.6 and 24.6 mg/g dwb, respectively, were observed in the upper part compared to 25.9 and 20.1 mg/g dwb, respectively in the lower part. The upper portion was observed to exhibit better antioxidant activity with LC50 of 1 mg/ml compared to 5 mg/ml for the lower part, and higher Hunter’s L* value.

Keywords: Yushania alpina, bamboo, nutrients’ distribution, minerals, polyphenol, flavonoids, antioxidant activity

Citation: Paul N. Karanja, Glaston M. Kenji, Simon M. Njoroge, Daniel N. Sila, Christine A. Onyango, Hiroshi Koaze, Naomichi Baba, Variation of Nutrients and Functional Properties within Young Shoots of a Bamboo Species (Yushania alpina) Growing at Mt. Elgon Region in Western Kenya. Journal of Food and Nutrition Research, 3 (10). 675-680. January 2015. doi:10.12691/jfnr-3-10-10

1. Introduction

Bamboo belongs to the grass family Poaceae and has over 1,250 species worldwide, although most of them are found in South East Asia [1]. Yushania alpina (Y. alpina), formerly known as Arundinaria alpina K. Schum and which is also commonly referred to as the alpine bamboo, is an indigenous species found in Kenya and other Eastern Africa highlands at altitudes of between 2,400 and 3,400 m. The species is currently estimated to cover about 150,000 ha and grows on the Aberdare ranges, Mt Elgon, Mt Kenya, Mau escarpment and Cherangany Hills, amongst other areas [2, 3]. This species is also found in Ethiopia on altitudes of 2,200-4,000 m and consumption of the shoots has been reported, although the bamboo is mainly used as construction material [4]. Some exotic varieties belonging to the genera of Bambusa, Dendrocalamus, Gogantochloa, Oxytenanthera and others, have also been planted in Kenya [5].

Several researchers [6,7,8] have reported the nutritive value of over 20 edible species of bamboo all over the world and have found them to be very rich in protein, dietary fiber, amino acids, minerals and vitamins, among others. It has been reported that bamboo shoots are good sources of dietary fiber with beneficial effect on lipid profiles in the body and bowel functions in young women [9]. They are low in fat and contain phytosterols forming good diet and maintaining low cholesterol level in the body [1]. Due to their distinct characteristics, bamboo shoots have been termed as vegetable with health promoting functionalities [10,11]. The nutritional composition of shoots of Y. alpina, Dendrocalamus giganteus and Bambusa vulgaris growing in Kenya has been studied and found to possess great potential in fighting malnutrition and ill-health [12].

Traditionally, bamboo has been used by some communities in various ways but its potential as a food source remains unexploited [6]. In Kenya, bamboo is used for fencing, basketry, making flower props, tooth picks and furniture. However, some consumption of the shoots of Y. alpina by local people living around Mt. Elgon has been reported, although its usage as a food has been ranked the least important amongst the different uses mentioned above [5]. The shoots are therefore underutilized resource, despite the fact that they have potential of improving life of the rural population [7]. Kigomo [13] found that lack of adequate technical information on the local bamboo resource was a hindrance to its utilization. Choudhury et al. [8] has also pointed out that research on bamboo shoots is inadequate, and that bamboo-based products are lacking in the international market, while Sood et al. [14] reported underutilization of bamboo as food.

The shoots of Y. alpina, unlike those of the giant bamboo species, are relatively slender. They are harvested after the onset of rain around May and June each year when they are about 60 cm tall. There is however, no scientifically guided approach in harvesting these shoots in order to get the most nutrient-rich part and therefore, variation of nutrients and other bio-actives within the shoot needs to be investigated. Thammawong et al. [15] found variation in sugars between different sections of the shoot of Phyllostachys pubescens Mazel from the apex to the bottom. The age of the shoots was found to affect the concentration of nutrients and other biochemical constituents of Dendrocalamus asper, D. strictus and Bambusa tulda, particularly for proteins, phenolics, fiber and carbohydrates [16]. There is however, little information available on these aspects of the shoot and more research on bamboo from different agro-ecological regions as a food resource is recommended [6].

This research work therefore, was undertaken to determine the distribution of nutrients and other functional properties within the shoots of Y. alpina growing in Kenya, in order to maximize its usage as a functional food beneficial to human health.

2. Materials and Methods

2.1. Sample Preparation

About 40 kg of shoots of Y. alpina with heights of about 60 cm were randomly harvested during a peak season in May 2013, inside Mt. Elgon forest in Western Kenya and transported to Food Science Laboratory of Jomo Kenyatta University of Agriculture and Technology. The outer leaves were removed and each of the soft shoot was divided into two parts, making the upper and the lower portions. The upper part was 15 cm long from the apex after peeling, and the lower portion was the remaining part up to the soft part easily cut by a knife as standardized based on local practice. Color and moisture content were determined for the fresh samples and the rest were dried in an air-circulating oven at optimum temperature of 70ºC for 24 hr [17]. After drying, the upper and the lower portions were ground separately, to pass a sieve of 0.84 mm. Each portion was well homogenized and packaged in sealable polyethylene bags and kept at 5°C until analysis. A minimum of three determinations were done for each parameter under consideration and results given in dry weight basis (dwb).

2.2. Reagents and Chemicals

Gallic acid, Follin Ciocalteau reagent and 1,1-diphenyl-2-picrylhydrazyl (DPPH) were purchased from Sigma-Aldrich, Germany. Sucrose, glucose, fructose, thiamine hydrochloride and riboflavin were from BDH Biochemical, England, whereas L-ascorbic acid was purchased from Panreac, Spain. Mineral standards were purchased from Wako Chemicals, Japan. The rest of reagents/chemicals used were of analytical grade, and deionized and distilled water was used.

2.3. Determination of Proximate and Mineral Composition

Determination of proximate composition was performed using AOAC methods [18], where moisture content was determined by drying 5 g of sample at 105°C to constant weight. Protein content was determined by Kjeldahl method and protein content obtained by multiplying percentage nitrogen by 6.25. Fat was extracted by Soxhlet’s method using petroleum spirit and determined gravimetrically. Ash content was determined by incinerating 5 g of the sample at 550°C until constant weight was attained. Fiber was determined by boiling under reflux 2 g of sample in 1.25% H₂SO4 and 1.25% NaOH, consecutively. The residual after filtering was washed with alcohol and ether. It was then dried and incinerated at 500°C for 1 hr and the difference in weight before and after incineration was calculated as a percentage fiber content. Carbohydrate content was obtained by subtracting the sum of moisture, fat, ash, fiber and protein content from 100.

After digesting ground samples with H₂SO₄-H₂O₂ and diluting to 50 ml with deionized water, minerals were determined by an inductively coupled plasma spectrometer (ICPS 8100, Shimadzu Ltd, Japan).

2.4. Determination of Thiamine and Riboflavin

AOAC methods were used with slight modification [18]. Two grams of the sample were mixed with 20 ml of 0.1 N HCl and heated in boiling water for 60 min. The pH was adjusted to 4.0 and 100 mg of taka-diastase was added, mixed and incubated at 40°C for 18 hr. The digest was made to 50 ml with 2 % acetic acid and centrifuged at 5,000 rpm for 10 min and the supernatant was used for HPLC analysis. In case of thiamine, pre-column oxidation with potassium ferricyanide in NaOH solution to give thiochrome form for fluorescence was done before injecting into HPLC (Shimadzu LC-10A) with a reverse phase C18 column of 250 x 4.6 mm, and fluorometric detection at Ex 365 nm and Em 435 nm (Shimadzu RF 1501). The mobile phase for thiamine was methanol: acetate buffer of pH 4.4 (40:60) and for riboflavin was methanol: water: acetic acid (40:59.5:0.5) at UV wavelength of 270 nm (Shimadzu SPD-10A). Thiamine hydrochloride and riboflavin were used to prepare standard solutions for quantification.

2.5. Determination of Vitamin C

Vitamin C content in the samples was determined by HPLC method [19]. Ten grams were homogenized with 20 ml of 0.8% m-phosphoric acid for 30 min and centrifuged at 10,000 rpm for 10 min at 4°C. The supernatant was micro-filtered with a 0.45 µm filter and injected into HPLC (Shimadzu LC-10A) with a photo diode array detector (Waters PDA 2996) set at 266 nm. Separation was achieved using a reverse phase C18 column of 150 x 4.6 mm and 0.8% m-phosphoric acid at a flow rate of 0.5 ml/min and L-ascorbic acid was used as a standard.

2.6. Determination of β-Carotene

β-Carotene was extracted by acetone, partitioned with petroleum spirit, and isolated using an open column chromatography of 30 X 2.54 cm packed with silica gel (mesh 200-400) and eluted with petroleum spirit [20]. Absorbance was read at 450 nm and results calculated using the standard curve of β-carotene solutions.

2.7. Determination of Soluble Sugars

Soluble sugars were extracted using the method of Osborne and Voogt [21]. About 10 g of sample were refluxed with 50 ml of 96% (v/v) ethanol for 1 hr at 100°C. The extract was filtered and the residue washed with 80% v/v ethanol. The filtrate was evaporated to dryness in a rotary vacuum evaporator at 60ºC and the dry residue was re-constituted with 10 ml distilled water and defatted using diethyl ether. Sample was micro-filtered with 0.45 µm filter and 20 µl injected into the HPLC (Shimadzu LC-10A) equipped with a refractive index detector (Shimadzu RID-6A). The mobile phase consisted of acetonitrile:water (80:20) at a flow rate of 0.5 ml/min on NH₂ column of 250 x 4.6 mm.

2.8. Determination of Total Polyphenols, Total Flavonoids and Antioxidant Activity

2.8.1. Determination of Total Polyphenols

Total polyphenol content was determined by the method of Waterman and Mole [22], where 10 mg of ground sample were extracted using aqueous 50% methanol at 80°C for 1 hr. One milliliter of the extract was reacted with Follin Ciocalteau reagent and the absorbance was read at 760 nm against gallic acid as a standard.

2.8.2. Sample Extraction for Flavonoids and Antioxidants

The method by Harborne [23] was applied for sample extraction for analysis of flavonoids and antioxidant activity. Five grams of ground sample were weighed into 250 ml flasks and 100 ml of methanol added. The flasks were closed with parafilm, covered with aluminum foil and shaken for 3 hr. The samples were kept in the dark to extract for 72 hr. They were then filtered and concentrated to 20 ml, and kept in closed vials until analysis. Working solutions were prepared from these extracts.

2.8.3. Determination of Total Flavonoids

The method according to Jagadish et al. [24] was used to determine flavonoid content. In a 10 ml volumetric flask, 4 ml of distilled water and 1 ml of plant extract were added. After 3 min, 0.3 ml of 5% sodium nitrite solution were added and left to stand for 3 min, after which 0.3 ml of 10% aluminum chloride was added and held for 5 min. Two milliliters of 1 M NaOH were added and the volume was made up to 10 ml with distilled water. The absorbance was read at 415 nm using a spectrophotometer. Total flavonoids were calculated from a calibration curve prepared using quercetin as a standard.

2.8.4. Determination of Free Radical Scavenging Activity

The antioxidant activity of the extracts against 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical was determined using the method of Molyneux [25]. Concentrations of the extract were prepared in 0.01, 0.1, 1.0, 2.0, 5.0 and 10.0 mg/ml in methanol, and the results were expressed on dry matter basis. L-ascorbic acid was used as a standard at the same concentrations as the extracts. One milliliter each of the extract and the standard was put in a test tube and 3.0 ml of methanol added, followed by 0.5 ml of 1 mM DPPH in methanol. A blank solution was prepared using methanol and DPPH. Absorbance was measured at 517 nm after keeping the mixture in the dark for 30 min. The DPPH radical scavenging activity was calculated using Equation 1 below.

[picture] | (1)

Where Ab is the absorbance of the reference (blank) and Aa is the absorbance of the sample.

2.9. Measurement of Color

Color was measured using a color spectrophotometer NF 333 (Nippon Denshoku, Japan) using the CIE L*a*b* color scale. The color of the sample was measured and expressed in terms of Hunter’s L* (lightness), a* (redness/greenish) and b* (yellowness/bluish). Hue angle and chroma values were computed from a* and b* values.

2.10. Data Analysis

All samples were analyzed at least in triplicates and data presented as mean ± standard deviation (n≥3). The means were subjected to simple ANOVA for significance test (p<0.05) using SPSS version 17.0.

3. Results and Discussions

3.1. Proximate Composition

The proximate composition was determined for the upper and the lower portions of the shoot and is shown in Table 1 below. There was no significant difference (p<0.05) in moisture, protein, fat and ash content between the two portions. Analysis of similar species from three different sites in Ethiopia revealed moisture content of 91.9-93.3%, protein content of 25.9-38.9%, fat content of 0.64-1.50% and ash content of 14.2-17.1% on dry weight basis [4]. These values compare well with the findings of this study even though their focus was not in different sections of the shoot. However, fiber and carbohydrates contents were found to have significant difference between the two portions (p<0.05), where fiber content in the upper and the lower portions were 23.9 and 30.7% dwb, respectively. Higher fiber content observed in the lower portion was due to toughening near the base as the culm develops for structural support [26].

Table 1. Proximate Composition of Upper and Lower Portions Expressed in % dwb

3.2. Mineral Composition

The shoots were found to contain high ash content of up to 17% in both the upper and the lower portions as shown in Table 1 above. However, a comparison of specific minerals contained in the upper and the lower portions, as shown in Table 2, indicates presence of significant differences (p<0.05) for all except iron.

Table 2. Composition of Minerals in Upper and Lower Portions Expressed in µg/g dwb

The results show that the upper portion contains large quantities of all major minerals and these mineral contents reduce towards the lower part of the shoot. The quantities of calcium, magnesium and copper in the upper portion were more than double the content in the lower part. Potassium, which is the major mineral in the shoot, was found to be about 1.3 times higher in the upper portion than in the lower. Therefore, by selecting the right portion of the shoot during harvesting time, the shoot can help to boost the intake of minerals towards meeting the recommended daily allowance (RDA) for calcium, magnesium and potassium, which are 1,000 mg, 350 mg, and 2,000-6,000 mg, respectively [27]. Potassium is a vital electrolyte charged with maintaining proper flow of water inside and outside body cells and is important particularly for athletes. This high amount of potassium may also provide protective effect against hypertension [28].

3.3. Vitamin Composition

Some vitamins found in the shoots of Y. alpina are shown in Table 3 below.

Significant difference (p<0.05) was noted in the content of thiamine, vitamin C and β-carotene. The upper portion contained more thiamine and vitamin C, while β-carotene was significantly more in the lower. It is thus more beneficial to consume the upper part of the shoot. Sood et al. [14] reported vitamin C content of 5.3 mg/100g in fresh bamboo samples. The value obtained in our study is lower than reported by Sood et al. [14] because the samples were dried before analysis and therefore, some heat labile vitamins such as vitamin C may have been degraded.

Table 3. Comparison of Vitamins in Upper and Lower Portions Expressed in µg/g dwb

3.4. Sugar Content

Three sugars namely, fructose, glucose and sucrose were found in the shoots as shown in Table 4 below. Fructose was found to be the dominant sugar in the upper portion and varied significantly from 2.19% to 0.62% in the lower (p<0.05). However, sucrose content was not significantly different between the two portions.

Table 4. Comparison of Sugars in Upper and Lower Portions Expressed in % dwb

Other researchers found significant difference in sugar content between four portions of shoots measured from the apex to the basal part of Phyllostachys pubescens Mazel, where higher glucose, fructose and total sugars were found at the basal part of the shoots underground [15]. This report shows the opposite of our findings, where fructose was found to be higher in the upper portion. However, our results agree with their observation that there was no significant difference in sucrose content in different portions of the shoots, which had just emerged from the ground.

3.5. Total Polyphenols, Flavonoids and Antioxidant Activity Content

The total polyphenol and flavonoid contents were determined and results are shown in Table 5 below. There was no significant difference in total polyphenol content between the upper and the lower portions. However, the total flavonoid content varied significantly (p<0.05) between the two portions, where the upper portion contained 24.6 mg/g dwb compared to 20.1 mg/g dwb in the lower part. It was also observed that the upper portion had higher antioxidant activity with LC50 of 1.0 mg/ml compared to LC₅₀ of 5.0 mg/ml in the lower portion as shown in Figure 1 below.

This high inhibition against the DPPH radical may be due to synergic effect caused by higher vitamin C, polyphenol and flavonoid contents observed in the upper portion of the shoot.

Table 5. Total Polyphenol and Flavonoid Contents Expressed in mg/g dwb

Figure 1. Antioxidant activity of the extracts of the upper and the lower portions of Yushania alpina expressed in dry weight basis

3.6. Color Variation within the Shoot

The Lab Hunter’s values were applied for color measurement. The L* value measures the lightness or brightness of a substance and ranges from 0 for black surface to 100 for white. Hue angle indicates whether the object is red, orange, green, blue or violet and ranges from 0 to 359°, whereas chroma or saturation value is a measure of color intensity and defines a range from pure color (100%) to gray color (0%) at a constant lightness [29]. The results for color variation are shown in Table 6 below. Significant difference between the upper and the lower portions (p<0.05) was noted for L*, b*, Hue angle and chroma values. The upper portion with L* value of 82.1 was therefore, found to be brighter than the lower portion. Negative values of a* and positive values of b* were also observed, indicating that the color was in the yellow-greenish region, which was confirmed by the value of Hue angle. The chroma value shows that greenish-yellow color was stronger in the lower portion than the upper. This means that the color near the tip is more whitish than the lower part. These results are consistent with the fact that the lower portion was found to contain more β-carotene than the upper, and thus influencing the apparent color.

Table 6. Color Variation

3.7. Conclusion

The upper portion of the shoot of Y. alpina was found to contain less fiber and higher carbohydrates, minerals, sugars and vitamins than the lower. It also had higher polyphenols and flavonoids, and exhibited higher antioxidant activity than the lower. The color of the upper portion was brighter than the lower part, and this implies that whiter shoots are potentially rich in nutrients and superior to the greenish ones. Furthermore, the result of the present study provides important baseline information on Y. alpina as valuable vegetable source, as well as potential nutrient supplement.

Acknowledgement

The authors are grateful to the Forest Officer at Kaberwa in Mt. Elgon region for allowing sampling to be done at the forest. Special thanks go to Mr. S. Ndiema and Mr. Daiki Murayama for their technical assistance. The partial funding received from Japan International Cooperation Agency (JICA) is highly appreciated.

References

[1]   | Nongdam, P., Tikendra, L., The nutritional facts of bamboo shoots and their usage as important traditional foods of North East India, Hindawi Publishing Corporation International Scholarly Research Notices, Vol 2014, page 17, July 2014, article ID 679073.
[2]   | Kibwage, J.K., Odondo, A.J., Momanyi, G.M., Structure and performance of formal retail market for bamboo products in Kenya, 2008, www.academic.reasearch.microsft.com.
[3]   | Ministry of Environment and Natural Resources (MENR), Kenya Forestry Master Plan: Development programs. Nairobi, Kenya, 422, 1994.
[4]   | Feleke, S., “Site factor on nutritional content of Arundinaria alpina and Oxytenanthera abyssinica bamboo shoots in Ethiopia”, Journal of Horticulture and forestry, 5 (9), 115-121, September 2013.
[5]   | Ongugo, P.O., Sigu, G.O., Kariuki, J.G., Luvanda, A.M, Kigomo, B.N., “Production-to-consumption systems: A case study of the bamboo sector in Kenya”, KEFRI/INBAR Project working paper, No. 27, Nairobi, Kenya, Kenya Forestry Research Institute (KEFRI), April 2000.
[6]   | Satya, S., Singhal, P., Bal, L.M., Sudhakar, P., “Bamboo shoots: a potential source of food security”, Mediterranean Journal of Nutrition and Metabolism, 5 (1), 1-10, April 2012.
[7]   | Chongtham, N., Bisht, M.S., Haorongbam, S., “Nutritional Properties of Bamboo Shoots: Potential and Prospects for Utilization as a Health Food”, Comprehensive Reviews in Food Science and Food Safety, 10: 153-168, 2011.
[8]   | Choudhury, D., Sahu, J.K., Sharma, G.D., “Bamboo Shoots: Microbiology, Biochemistry and Technology of Fermentation, a review”, Indian Journal of Traditional Knowledge, 11: 242-249, April 2012.
[9]   | Park, E.J., Jihon, D.Y., “Effects of bamboo shoots consumption on lipid profiles and bowel functions in healthy young women”, Journal of Nutrition, 25 (7-8), 723-728, 2009.
[10]   | RFRI, Bamboo as food and medicine. Report of Rain Forest Research Institute (RFRI), Jorhat, India, 2008, www.icfre.gov.in/new/rfri/bamboo
[11]   | Singhal, P., Bal, L.M., Satya, S., Sudhakar, P., Naik, S.N., “Bamboo shoots: a novel source of nutrition and medicine”, Crititical Reviews in Food Science and Nutrition, 53 (5): 517-534, 2003.
[12]   | Karanja, P.N., Kenji, G.M., Njoroge, S.M., Sila, D.N., Onyango, C.A., Koaze, H., Baba, N., “Compositional characteristics of young shoots of selected Bamboo species growing in Kenya and their potential as food source”, Journal of Food and Nutrition Research, 3 (9), 607-612, 2015.
[13]   | Kigomo, B.N., An overview of Bamboo and Rattan sector in Kenya. Kenya Forestry Research Institute (KEFRI). P. O. Box 20412 NAIROBI, Kenya, 1995.
[14]   | Sood, S., Walia, S., Gupta, M., Sood, A., “Nutritional characterization of shoots and other edible products of an edible bamboo-Dendrocalamus hamiltonii”, Current Research in Nutrition and Food Science, 1 (2), 2013.
[15]   | Thammawong, M., Nei, D., Roy, P., Nakamura, N., Shiina, T., “Characterization of sugar content in different sections and harvest maturity of bamboo shoots”, HortScience, 44 (7) 1941-1946, December 2009.
[16]   | Pandey, A.K., Ojha, V., “Standardization of harvesting age of bamboo shoots with respect to nutritional and anti-nutritional components”, Journal of Forestry Research, 24 (1), 83-90, 2013.
[17]   | Santosh, S., Lalit, M.B., Poonam, S., Naik, S.N., “Bamboo shoots processing: food quality and safety aspect (a review)”, Trends in Food Science and Technology, 21, 181-189, 2010.
[18]   | AOAC, Official methods of analysis, 16th ed., Association of Official Analytical Chemists, Washington, DC, USA, 1995.
[19]   | Vikram V.B., Ramesh M.N. and Prapulla, S.G., “Thermal degradation kinetics of nutrients in orange juice heated by electromagnetic and conventional methods”, Journal of Food Engineering, 69, 31−40. 2005.
[20]   | Rodriguez, A., Delia B., Kimura M., HarvestPlus, Handbook for Carotenoid Analysis. Harvestplus Technical Monogragh 2, Washington, DC and Cali: International Food Policy Research Institute (IFPRI) and International Center for Tropical Agriculture (CIAT), 2004.
[21]   | Osborne, D.R. and Voogt, P., Extraction of the sugars: Analysis of Nutrients in Foods, Academic Press, pp 142-144, 1978.
[22]   | Waterman, P.G., Mole, S., Analysis of polyphenolic plant metabolites, Methods in Ecology. Blackwell Scientific Publications, London, 238, 1994.
[23]   | Harborne, J.B., Phytochemical methods, Chapman and Hall Ltd., London, 1973.
[24]   | Jagadish, L.K., Krishnan, V.V., Shenbhagaraman, R., Kaviyarasan, V., “Comparative study on the antioxidant, anticancer and antimicrobial property of Agaricus bisporus Imbach before and after boiling”, African Journal of Biotechnology, 8, 654-661, 2009.
[25]   | Molyneux, P., “The use of stable free radical 1,1-dipheny-2-picrylhydraxyl (DPPH) for estimating antioxidant activity”, Journal of Science and Technolology, 26, 211-219, 2004.
[26]   | George, M., Marya, B., Using Stage of Maturity to Predict the Quality of Annual Range Forage. Oakland, CA: University of California Division of Agriculture and Natural Resources Publication, 8019, 7, 2001.
[27]   | Silvermam, H.M., Romano J., Elmer G., The Vitamin Handbook; the complete guide to vitamins, minerals, and the most effective herbal remedies and dietary supplements, 1999, www.thevitaminbook.com.
[28]   | Bellows, L., Moore, R., Potassium and the Diet Extension, Fact sheet No. 9.355, Food and Nutrition series, Health, Colorado State University, Fort Collins, CO 80523-4061, 2013.
[29]   | Ali, M., Shahin, R., Zahra, E., Alireza, K., “Kinetic models for color changes in Kiwi fruit slices during hot air drying”, World Journal of Agricultural Sciences, 4 (3), 376-383, 2008.